US20130209558A1 - Oral Dosage Forms of Bendamustine and Therapeutic Use Thereof - Google Patents

Oral Dosage Forms of Bendamustine and Therapeutic Use Thereof Download PDF

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US20130209558A1
US20130209558A1 US13/701,228 US201113701228A US2013209558A1 US 20130209558 A1 US20130209558 A1 US 20130209558A1 US 201113701228 A US201113701228 A US 201113701228A US 2013209558 A1 US2013209558 A1 US 2013209558A1
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bendamustine
pharmaceutical composition
pharmaceutically acceptable
day
active ingredient
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Ulrich Patzak
Taoufik Ouatas
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Astellas Deutschland GmbH
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Definitions

  • the present invention relates to oral dosage forms comprising bendamustine or a pharmaceutically acceptable ester, salt or solvate thereof and therapeutic use thereof.
  • Bendamustine (4-[5-[bis(2-chloroethyl)amino]-1-methylbenzimidazo-2-yl]butanoic acid, a nitrogen mustard) is an alkylating agent with bifunctional alkylating activity. It corresponds to the following formula (I):
  • Bendamustine appears to be free of any cross-resistance with other alkylating agents, which offers advantages in terms of chemotherapy for patients who have already received treatment with an alkylating agent.
  • Bendamustine was initially synthesized in the German Democratic Republic (GDR).
  • GDR German Democratic Republic
  • the hydrochloric acid of bendamustine was the active ingredient in a commercial product available from 1971 to 1992 under the trade name Cytostasan®. Since that time, it has been marketed in Germany under the trade name Ribomustin® and has been widely used to treat chronic lymphocytic leukemia, non-Hodgkin's lymphoma and multiple myeloma.
  • the marketed product contains a lyophilized powder of bendamustine hydrochloride which is reconstituted with water for injection yielding a concentrate. This is subsequently diluted with an aqueous solution of 0.9% sodium chloride resulting in the final solution for infusion. This final solution is administered to the patient by intravenous infusion over a period of about 30 to 60 minutes.
  • US 2006/0128777 A1 describes methods for treating cancers, characterised by death-resistant cells and bendamustine-containing compositions in general.
  • oral dosage forms which are capsules, tablets, pills, powders or granules, wherein the active compound may be admixed with at least one inert excipient, such as sucrose, lactose or starch.
  • inert excipient such as sucrose, lactose or starch.
  • specific compositions were not exemplified.
  • Bendamustine hydrochloride is only sparingly soluble in water at a pH of 2.0 and is slightly or very slightly soluble in a range of organic solvents. A good solubility has been observed however in ethanol and methanol. Therefore it is not surprising that the oral bendamustine compositions, as investigated by Preiss et al. and Weber gave rise to relatively poor bioavailability results and a large inter-individual variability.
  • compositions are suitable for oral administration and comprise bendamustine or a pharmaceutically acceptable ester, salt or solvate thereof as an active ingredient, and at least one pharmaceutically acceptable excipient, which compositions apart from having a good stability also have a good dissolution profile in acidic media, a good bioavailability and a therapeutically acceptable inter- and intraindividual variability.
  • FIG. 1 shows the mean plasma concentration vs. time curve obtained after administering bendamustine hydrochloride in the form of the prior art capsule (reference example 1) and the liquid filled hard capsule formulation of Example 2 to dogs. It is apparent from FIG. 1 that the liquid filled hard capsule formulation provides for a higher maximum concentration of bendamustine, as compared with the prior art reference capsule formulation.
  • FIG. 2 shows the mean plasma vs. time profile obtained after administering bendamustine hydrochloride in the form of the intravenous preparation, as marketed in Germany under the trademark Ribomustin®, and the liquid filled hard capsule formulation of example 2 to patients with cancer.
  • FIG. 3 shows the mean plasma concentration (tablets versus capsule) vs. time curve obtained after administering bendamustine hydrochloride in the form of prior art capsules and the tablet formulations of Examples 15 to 17 (Tablets 1-3) and example 18 (formulation 3) (Tablet 4) to dogs. It is apparent from FIG. 3 that the tablet formulations provide for higher maximum concentrations of bendamustine, as compared to the prior art capsule.
  • FIG. 4 shows a flow sheet of wet granulation manufacturing trials.
  • the present invention relates to a pharmaceutical composition for oral administration which comprises bendamustine or a pharmaceutically acceptable, ester, salt or solvate thereof as an active ingredient, and a pharmaceutically acceptable excipient and which shows a dissolution of the bendamustine of at least 60% in 20 minutes, 70% in 40 minutes and 80% in 60 minutes, as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of a dissolution medium at a pH of 1.5, and wherein the pharmaceutically acceptable excipient is either a pharmaceutically acceptable non-ionic surfactant, selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide and propylene oxide or a pharmaceutically acceptable saccharide selected from the group consisting of one or more of a monosaccharide, a disaccharide, an oligosaccharide, a cyclic oligosaccharide, a polysaccharide and a saccharide
  • the present invention relates to a pharmaceutical composition for oral administration, the composition comprising bendamustine or a pharmaceutically acceptable, ester, salt or solvate thereof as an active ingredient, and a pharmaceutically acceptable excipient, which is a non-ionic surfactant, selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide and propylene oxide.
  • a pharmaceutically acceptable excipient which is a non-ionic surfactant, selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide and propylene oxide.
  • An embodiment of the first embodiment of the invention is a pharmaceutical composition, comprising bendamustine or a pharmaceutically acceptable ester, salt or solvate thereof and a pharmaceutically acceptable excipient, which is a non-ionic surfactant, selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide and propylene oxide, wherein the composition is suitable for oral administration by including it into a hard gelatine capsule.
  • a pharmaceutically acceptable excipient which is a non-ionic surfactant, selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide and propylene oxide
  • a further embodiment of the first embodiment of the invention is a pharmaceutical composition for oral administration in a solid dosage-form, which is a hard gelatine capsule, the composition comprising bendamustine or a pharmaceutically acceptable ester, salt or solvate thereof and a pharmaceutically acceptable excipient, selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide and propylene oxide and preferably selected from the group consisting of macrogol glycerol hydroxystearate, polyoxyl-35-castor oil and ethylene oxide/propylene oxide block copolymer (Pluronic® L44 NF or Poloxamer® 124), wherein the use of the specific non-ionic surfactant leads to a dissolution profile of at least 60% bendamustine dissolved after 20 minutes, 70% dissolved after 40 minutes and 80% dissolved after 60 minutes, as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of a dissolution
  • a preferred embodiment of the first embodiment is a pharmaceutical composition for oral administration in a solid dosage-form, which is a hard gelatine capsule, the composition comprising bendamustine hydrochloride and a pharmaceutically acceptable excipient, which is macrogol glycerol hydroxystearate, wherein the use of the specific non-ionic surfactant results in a dissolution of at least 60% bendamustine dissolved after 10 minutes, 70% after 20 minutes and 80% after 30 minutes, as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of a dissolution medium at a pH of 1.5.
  • the present invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising bendamustine or a pharmaceutically acceptable ester, salt or a solvate thereof as an active ingredient and at least one pharmaceutically acceptable excipient selected from monosaccharides, disaccharides, oligosaccharides, cyclic oligosaccharides, a polysaccharide and saccharide alcohols.
  • the ratio by weight between the active ingredient and excipient is in the range of 1 to 1-5, preferably 1 to 2-5, more preferably a ratio selected from 1:5 and 1:2.
  • the present invention relates to a pharmaceutical composition in a solid dosage form for oral administration, the composition comprising bendamustine or a pharmaceutically acceptable ester, salt or solvate thereof as an active ingredient, and at least one pharmaceutically acceptable excipient, which is a pharmaceutically acceptable saccharide selected from the group consisting of one or more of a monosaccharide, a disaccharide, an oligosaccharide, a cyclic oligosaccharide, a polysaccharide and a saccharide alcohol, wherein the ratio by weight of the active ingredient to the excipient is in the range of 1:1.
  • a pharmaceutically acceptable saccharide selected from the group consisting of one or more of a monosaccharide, a disaccharide, an oligosaccharide, a cyclic oligosaccharide, a polysaccharide and a saccharide alcohol, wherein the ratio by weight of the active ingredient to the excipient is in the range of 1:1.
  • a pharmaceutical composition in a solid dosage form suitable for oral administration comprising bendamustine or pharmaceutically acceptable ester, salts or solvates thereof as an active ingredient and at least one pharmaceutically acceptable excipient which is a pharmaceutically acceptable saccharide selected from the group consisting of one or more of a monosaccharide, a disaccharide, an oligosaccharide, a cyclic oligosaccharide, a polysaccharide and a saccharide alcohol, wherein the ratio by weight of the active ingredient to the saccharide excipient(s) is in the range of 1:2-5 and which composition shows a dissolution of the bendamustine of at least 60% in 20 minutes, 70% in 40 minutes and 80% in 60 minutes as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of a dissolution medium at a pH of 1.5.
  • a pharmaceutically acceptable excipient which is a pharmaceutically acceptable saccharide selected from the group consisting of one or more of a
  • compositions wherein the pharmaceutically acceptable saccharide is selected from the group consisting of one or more of a monosaccharide, a disaccharide and an oligosaccharide, wherein the ratio by weight of the active ingredient to the saccharide excipient(s) is in the range of 1:2-5 and which composition shows a dissolution of the bendamustine of at least 60% in 20 minutes, 70% in 40 minutes and 80% in 60 minutes as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of a dissolution medium at a pH of 1.5.
  • the pharmaceutically acceptable saccharide is selected from the group consisting of one or more of a monosaccharide, a disaccharide and an oligosaccharide, wherein the ratio by weight of the active ingredient to the saccharide excipient(s) is in the range of 1:2-5 and which composition shows a dissolution of the bendamustine of at least 60% in 20 minutes, 70% in 40 minutes and 80% in 60 minutes as measured
  • the present invention is based on the surprising finding that stable compositions of bendamustine having a specific and desirable dissolution profile can be obtained by incorporating into the pharmaceutical composition certain non-ionic surfactants or certain saccharides or saccharide alcohols. It has been found that if a pharmaceutically acceptable non-ionic surfactant, selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide and propylene oxide and preferably selected from the group consisting of macrogol glycerol hydroxystearate, polyoxyl-35-castor oil and ethylene oxide/propylene oxide block copolymer (Pluronic® L44 NF or Poloxamer® 124) is used as an excipient in a pharmaceutical composition comprising bendamustine or a pharmaceutically acceptable ester, a salt or a solvate thereof as an active ingredient, a particularly favourable profile of the composition with respect to stability and degradation products, dissolution, bioavailability and a reduced variability in bioava
  • the incorporation of the above-mentioned non-ionic surfactants in bendamustine-containing compositions results in a dissolution profile of at least 60% bendamustine dissolved after 20 minutes, 70% dissolved after 40 minutes and 80% dissolved after 60 minutes, as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of a dissolution medium at a pH of 1.5 and preferably it results in a dissolution of at least 60% bendamustine dissolved after 10 minutes, 70% after 20 minutes and 80% after 30 minutes.
  • a pharmaceutically acceptable saccharide selected from the group consisting of one or more of a monosaccharide, a disaccharide, an oligosaccharide, a cyclic oligosaccharide, a polysaccharide or a saccharide alcohol and preferably selected from the group consisting of one or more of a monosaccharide, a disaccharide and an oligosaccharide is used as an excipient in a pharmaceutical composition comprising bendamustine or pharmaceutically acceptable ester, salt or solvate thereof as an active ingredient, a particularly favourable profile of the composition as regards stability, tabletting properties, dissolution and impurity formation is achieved.
  • the above saccharides result in a composition which shows a dissolution of the bendamustine of at least 60% in 20 minutes, 70% in 40 minutes and 80% in 60 minutes as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of a dissolution medium at a pH of 1.5.
  • any combination of one or more of a monosaccharide, a disaccharide, an oligosaccharide, a cyclic oligosaccharide, a polysaccharide and a saccharide alcohol may be used.
  • saccharides of the composition according to the second embodiment of the present invention are dextrose anhydrous, dextrose monohydrate, lactitol monohydrate, trehalose, sorbitol, erythritol, maltose monohydrate, mannitol, lactose anhydrous, lactose monohydrate, maltitol, xylitol, sucrose, sucrose 97%+maltodextrin 3%, ⁇ -cyclodextrin, D-raffinose pentahydrate, D-melezitose monohydrate and microcrystalline cellulose.
  • the pharmaceutical compositions according to the present invention show good tabletting characteristics, fast dissolution and a pharmaceutically acceptable stability.
  • the above saccharides constitute preferred embodiments of the second embodiment of the present invention and any combination thereof may be used.
  • the ratio between the active ingredient and the above saccharides is in the range of 1:1-5, preferably 1:2-5 and more preferably a ratio selected from 1:5 and 1:2.
  • a further preferred embodiment of the second embodiment of the invention is a pharmaceutical composition in a solid dosage form for oral administration, the composition comprising bendamustine or a pharmaceutically acceptable ester, salt or solvate thereof as an active ingredient and at least one pharmaceutically acceptable excipient selected from dextrose anhydrous, dextrose monohydrate, lactitol monohydrate, trehalose, sorbitol, erythritol, maltose monohydrate, mannitol, lactose anhydrous, lactose monohydrate, maltitol, xylitol, sucrose, sucrose 97%+maltodextrin 3%, ⁇ -cyclodextrin, D-raffinose pentahydrate, D-melezitose monohydrate and microcrystalline cellulose and which composition shows a dissolution of the bendamustine of at least 60% in 10 minutes, 70% in 20 minutes and 80% in 30 minutes.
  • saccharides are mannitol, maltitol, erythritol, xylitol, lactose, sucrose, glucose, sorbitol, maltose, trehalose, lactitol and dextrose (anhydrous or monohydrate) and the weight ratio of the active ingredient to said saccharide is preferably in the range of 1:2-5. Combinations of two or more saccharides within the scope of the above saccharides are also included within the present invention.
  • a person skilled in the art is well in a position to select suitable combinations within the saccharide excipients mentioned above and obtain a composition which shows a dissolution of bendamustine of at least 60% in 20 minutes, 70% in 40 minutes and 80% in 60 minutes as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of a dissolution medium at a pH of 1.5.
  • composition in the form of a tablet, a granulate, or a pill.
  • a preferred dosage form is a tablet, preferably an immediate release tablet, which means that the tablet releases the active ingredient very fast after being placed in an aqueous medium, preferably an acidic medium.
  • the term tablet also comprises fast-disintegrating tablets, amongst which are dispersible tablets and effervescent tablets.
  • Direct compression involves compressing a mixture containing the active ingredient(s) and the excipient(s) on a tablet press (L. Lachman et al., in: The Theory and Practice of Industrial Pharmacy, 3rd ed., 1986).
  • the mixture to be compressed must possess both good flow and compression properties in order to produce tablets having a uniform content of the active ingredient(s).
  • Good flow properties cannot always be achieved by adding appropriate excipients, such as lubricants, anti-adhesive agents and flow-promoters to the mixture. Hence frequently the mixture is granulated prior to compression.
  • Granulation is a process by which sphere-like or regularly shaped aggregates called granules are formed out of the powder mixture. This can be achieved by dry granulation methods and wet granulation methods. Granulation is also used for converting a mixture of powders with poor cohesion into aggregates, which when compressed result in tablets that have good cohesion properties.
  • the active ingredient(s), optionally in admixture with one or more excipients is (are) advantageously provided with a coating in order to mask the taste of such ingredient(s) and/or to protect the same against possible harmful effects by light and/or moisture and in the case of bendamustine to protect the mucosa in the mouth against the harmful effects exerted by the active compound.
  • a granulate preferably is prepared and processed as further outlined below.
  • granulate refers to aggregates of particles, sometimes called granules.
  • a granulate in general is prepared by compaction and/or compression techniques (dry granulation) or by wet granulation techniques, using a liquid in which optionally a wet granulation binding agent is dissolved (Remington's Pharmaceutical Sciences 18th ed. 1990, page 1641).
  • Wet granulation techniques also include extrusion techniques.
  • the term granulate also comprises pellets, spherules, and extrudates, of which pellets preferably are used as examples of a granulate.
  • a pellet may be described as a small particle of approximately 1.0-1.6 mm in diameter and having a certain density, which particle is prepared by application of the pharmaceutical processes of extrusion and spheronisation to powder mixtures.
  • the active ingredient(s), optionally in admixture with one or more excipients, may be advantageously provided with a coating in order to mask the taste of such ingredient and/or to protect the same against possible harmful effects by light and/or moisture and/or to protect the mucosa in the mouth against the harmful effects exerted by the active compound.
  • Pills are small, round solid dosage forms, prepared by adding the active ingredient to a doughy mixture of triglycerides. The mixture is rolled into a long string, which is then cut into pieces and rolled (J. T. Carstensen: Pharmaceutical principles of solid dosage forms, 1993, Technomic Publishing Company, Inc. page 63).
  • the dosage forms according to the invention are prepared by dry compaction techniques. Suitable techniques are for example described in Remington's Pharmaceutical Science 18th. ed. 1990, page 1644. They comprise dry granulation, roller compaction and direct compression. When tablets are prepared by these techniques, it is even more advantageous to use direct compression.
  • the dosage forms according to the present invention are preferably provided with a coating.
  • the coating has different purposes: it may serve for masking the taste of the active ingredient(s) used in the composition, whilst at the same time it is protecting the active ingredient against possible harmful effects by light and/or moisture such as oxidation, degradation, etc. Furthermore, the coating layer may prevent the subject from damage of the oral mucosa by the active ingredient.
  • the coating layer can be applied to the dosage forms by techniques well-known in the art such as spray-coating and microencapsulation.
  • tablets it can be in the form of a film-coating, a saccharide-coating or a compression coating.
  • a film-coating process is used (Remington's Pharmaceutical Sciences 18th ed. 1990, page 1666).
  • an active ingredient requires the application of a coating for fast-disintegrating tablets the individual granules can suitably be provided with a coating prior to compression into tablets.
  • esters with alkyl alcohols and sugar alcohols examples include C 1-6 -alkyl alcohols such as methanol, ethanol, propanol, isopropanol, butanol and tert-butanol.
  • alkyl alcohols C 1-6 -alkyl alcohols such as methanol, ethanol, propanol, isopropanol, butanol and tert-butanol.
  • sugar alcohols are mannitol, maltitol, sorbitol, erythritol, glycol, glycerol, arabitol, xylitol and lactitol.
  • Preferred examples of the bendamustine esters are the ethyl ester, the isopropyl ester, the mannitol ester and the sorbitol ester, most preferred is the ethylester thereof.
  • pharmaceutically acceptable salt thereof describes any pharmaceutically acceptable salt of bendamustine that administered to a patient (directly or indirectly) provides bendamustine. This term further comprises the pharmaceutically acceptable salt of a bendamustine ester. Nevertheless, it will be considered that the pharmaceutically non-acceptable salts also are included within the limits of this invention since these compounds can be useful in the preparation of pharmaceutically acceptable salts.
  • pharmaceutically acceptable salts of bendamustine are synthesized from the corresponding compound that contains an acid or basic group, by conventional chemical methods.
  • these salts are, for example, prepared by means of the reaction of free acidic or basic forms of these compounds in a stoichiometric amount with a corresponding base or acid in water or an organic solvent or a mixture of both.
  • Nonaqueous media like ether, ethyl acetate, isopropanol or acetonitrile are generally preferred.
  • acids which may be used for the salt formation of pharmaceutically acceptable salts of bendamustine include inorganic acids such as hydrochloride, hydrobromide, hydriodide, sulphuric, nitric, and phosphoric acids, and organic acids such as acetic, maleic, fumaric, citric, oxalic, succinic, tartaric, malic, lactic, methylsulphonic and p-toluenesulphonic acids.
  • inorganic acids such as hydrochloride, hydrobromide, hydriodide, sulphuric, nitric, and phosphoric acids
  • organic acids such as acetic, maleic, fumaric, citric, oxalic, succinic, tartaric, malic, lactic, methylsulphonic and p-toluenesulphonic acids.
  • Pharmaceutically acceptable salts of bendamustine may be derived from either inorganic or organic bases to yield ammonium salts; alkali metal salts (lithium, sodium, potassium, etc.), alkaline earth salts like calcium or magnesium, aluminium salts, lower alkylamine salts like methylamine or ethylamine salts, lower alkyldiamine salts like ethylenediamine salts, ethanolamine, N,N-dialkyleneethanolamine, triethanolamine, and glucamine salts, as well as basic salts of amino acids.
  • acid salts prepared from the hydrochloride, the hydrobromide, and the hydroiodide whereas the hydrochloride salt is the most preferred pharmaceutically acceptable salt of bendamustine.
  • the pharmaceutically acceptable salts are produced by conventional techniques well-known in the art.
  • the expression “pharmaceutically acceptable solvate thereof” describes any pharmaceutically acceptable solvate that, administered to a patient (directly or indirectly) provides bendamustine.
  • This term further comprises the pharmaceutically acceptable solvate of a bendamustine ester.
  • the solvate is a hydrate, a solvate with an alcohol such as methanol, ethanol, propanol, or isopropanol, a solvate with an ester such as ethyl acetate, a solvate with an ether such as methyl ether, ethyl ether or THF (tetrahydrofuran) or a solvate with DMF (dimethylformamide), of which a hydrate or a solvate with an alcohol such as ethanol is more preferred.
  • a solvent for constituting the solvate is preferably a pharmaceutically acceptable solvent.
  • the active ingredient in the invention's compositions is bendamustine or a pharmaceutically acceptable salt thereof. It is most preferred that the active ingredient is bendamustine hydrochloride.
  • the dose of the active ingredient in the pharmaceutical composition may readily be determined by the skilled artisan depending on the patient's condition, sex, body weight, body surface area (m 2 ; average approximately 2 m 2 per person), or age, especially depending on the patient's body weight and body surface area. It is preferred that the daily dosage ranges from about 50 to about 1000 mg, preferably from about 100 to about 500 mg of the active ingredient, more preferably from about 200 to about 400 mg and most preferably about 280 mg.
  • the daily dosage may be taken as a single dose or as multiple doses such as twice or three-times daily, most preferably as a single daily dose.
  • the daily dose may be taken once a week or several times a week.
  • the minimum oral single dose is 50 mg.
  • the above doses relate to bendamustine and may easily be recalculated in relation to a pharmaceutically acceptable ester, salt or solvate thereof.
  • the dose can be expressed in absolute amounts (mg), but in oncology normally the dose is expressed in mg/m 2 , taking into account the patient's body surface area.
  • the maximum tolerated dose (MTD) and the effective dose of bendamustine is dependent on the cumulative amount given per cycle. Based on the reproducible BA of bendamustine the MTD is reached at a cumulative dose of 1000 mg per cycle.
  • the lower limit of effective cumulative dose is between 350 mg and 500 mg per cycle. Therefore a cumulative dose per cycle of 350 mg to 1000 mg needs to be given orally.
  • the preferred cumulative oral dose per cycle is 500 mg to 700 mg.
  • Bendamustine can be given in effective single doses from 50 mg to 900 mg.
  • the preferred range of a single oral dose is 200-300 mg.
  • the maximum tolerated dose is about 1000 mg bendamustine within one cycle (3-4 week cycle). In sensitive/compromised patients the cumulative dose is about 350-500 mg bendamustine within one cycle (3-4 weeks), preferably about 365 mg within 4 weeks.
  • Possible and preferred oral dosage regimens are:
  • the treatment with bendamustine is effected in therapeutic cycles, wherein bendamustine and optional additional agents are dosed for 1 to 5 days and then the treatment is repeated after an interruption of 2 to 4 weeks.
  • the repetitions of the therapeutic cycle are continued until the respective condition to be treated has improved.
  • the number of repetitions is within the discretion of a medical doctor.
  • the therapeutic cycle is repeated 4 to 15 times, preferably 4 to 12 times, more preferably 4 to 6 times.
  • Oral 145 mg/m 2 or 261 mg (1.8 m 2 ): range 100-200 mg/m 2 or 150-350 mg per day.
  • Oral 174 mg/m 2 or 313 mg (1.8 m 2 ): range 100-250 mg/m 2 or 150-400 mg per day.
  • bendamustine is combined with vincristine and prednisone in first line non-Hodgkin's lymphoma.
  • Oral 174-217 mg/m 2 or 313-391 mg (1.8 m 2 ): range 100-250 mg/m 2 or 150-400 mg per day.
  • Oral 130 mg/m 2 or 235 mg (1.8 m 2 ): range 100-200 mg/m 2 or 150-350 mg per day.
  • the invention thus relates to a pharmaceutical composition as defined above for use for the oral treatment of a medical condition which is selected from chronic lymphocytic leukaemia, acute lymphocytic leukaemia, chronic myelocytic leukaemia, acute myelocytic leukaemia, Hodgkin's disease, non-Hodgkin's lymphoma, multiple lymphoma, breast cancer, ovarian cancer, small cell lung cancer and non-small cell lung cancer, wherein the dosage regimen comprises at least the administration of a dose of 100 to 600 mg/m 2 /per person of bendamustine on day 1 and day 2, optionally a dose of 50 to 150 mg/m 2 i.v.
  • a medical condition which is selected from chronic lymphocytic leukaemia, acute lymphocytic leukaemia, chronic myelocytic leukaemia, acute myelocytic leukaemia, Hodgkin's disease, non-Hodgkin's lymphoma, multiple lymphoma
  • the invention relates to the pharmaceutical composition as defined above for the use as defined above, wherein the active ingredient bendamustine is administered in a dosage regimen selected from 200-300 mg on day 1 and day 2, optionally followed by a maintenance dose of 50 mg once a day, 50 mg each day from day 1 up till and including day 14, or 150 mg once a week for 3 weeks.
  • the invention further relates to the pharmaceutical composition as defined above for the use as defined above, wherein the patient is one having non-Hodgkin's lymphoma and the dosage regimen comprises administering a total amount of 200 mg/person/day of active ingredient bendamustine on days 1 to 5, 2 mg i.v. of vincristine on day 1 and 100 mg/m 2 i.v. of prednisone on days 1 to 5 and repeating said treatment every three weeks until the non-Hodgkin's lymphoma has improved.
  • the invention further relates to the pharmaceutical composition as defined above for the use as defined above wherein the patient is one having multiple myeloma and the dosage regimen comprises administering an amount of 100-250, preferably 174 to 217 mg/m 2 body surface area bendamustine hydrochloride on days 1 and 2, 60 mg/m 2 i.v. or orally of prednisone on days 1 to 4 and repeating said treatment every four weeks until the multiple myeloma has improved.
  • the invention further relates to the pharmaceutical composition as defined above for the use as defined above, wherein the patient is one having chronic lymphocytic leukaemia and the dosage regimen comprises administering an amount of 100 to 200, preferably 145 mg/m 2 body surface area bendamustine hydrochloride on days 1 and 2 and 60 mg/m 2 i.v. or orally of prednisone on days 1 to 4 and repeating said treatment every four weeks until the chronic lymphocytic leukaemia has improved.
  • the invention moreover relates to the pharmaceutical composition as defined above for the use as defined above, wherein the patient is one having follicular, indolent or mantle cell lymphoma and the dosage regimen comprises administering a dose of 375 mg/m 2 rituximab on day 1 plus 100 to 200, preferably 130 mg/m 2 oral bendamustine on days 1 and 2 every 28 days until the respective lymphoma has improved.
  • the dosage form may contain the amount of a single daily dose or parts thereof. It is preferred that the dosage form of the present invention comprises about 10 to about 1000 mg, preferably about 25 to about 600 mg, more preferably about 50 to about 200 mg and most preferably about 50 mg or about 100 mg of the active ingredient.
  • non-ionic surfactant refers to an amphiphilic compound having a polar, hydrophilic group and a non-polar, lipophilic group or chain and wherein the hydrophilic and lipophylic properties of the compound are characterised by the so-called Hydrophilic-Lipophilic Balance (HLB) value.
  • HLB Hydrophilic-Lipophilic Balance
  • the non-ionic surfactant to be used for preparing the compositions of the present invention preferably has an HLB-value between 10 and 20 and preferably between 12 and 18.
  • the non-ionic surfactant further has a melting point, pour point or melting range between 5° C. and body temperature (37° C.) and preferably between just below room temperature (20° C.) and body temperature.
  • the material can be in a liquid or a semi-solid state at room temperature.
  • the amphiphilic material is a carrier for the bendamustine active ingredient, which can be present in a dissolved form, a suspended form or partly in a dissolved and partly in a suspended form.
  • non-ionic surfactants that are advantageously used for the preparation of the compositions according to the first embodiment of the present invention are selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide/propylene oxide, provided the materials have the afore-mentioned HLB-value and melting point, pour point or melting range.
  • the non-ionic surfactant is a polyethoxylated castor oil.
  • a polyethoxylated castor oil is sold under the tradename Cremophor®. Cremophor® products of various purities and viscosities are produced and may be used in the present invention. In particular macrogol glycerol hydroxystearate (Cremophor® RH 40) and polyoxyl-35-castor oil (Cremophor® EL or Cremophor® ELP) can be used. Cremophor®ELP and Cremophor® EL are known as nonionic solubilizers and emulsifiers, produced by reacting castor oil with ethylene oxide in a molar ratio of 1 to 35.
  • Macrogol glycerol hydroxystearate (commercially available as Cremophor® RH 40) is a semi-solid material at 25° C., having a viscosity range at the same temperature of 20-40 cps (as a 30% aqueous solution). It is known as a nonionic solubiliser and emulsifier. It is produced by reacting castor oil with ethylene oxide in a molar ratio of 1 to 45. Its HLB-value ranges from 14-16 and the melting range is from 20-28° C. In experiments it was shown that macrogol glycerol hydroxystearate can advantageously be used on its own for the preparation of compositions according to the present invention.
  • Pluronic® block copolymers consist of ethylene oxide and propylene oxide blocks.
  • the ethylene oxide units have a hydrophilic character whereas the propylene oxide units have a lipophilic character Variations in the number of hydrophilic ethylene oxide units and lipophilic propylene oxide units results in copolymers with a different molecular mass and different hydrophilic-lipophilic-balance (HLB).
  • HLB hydrophilic-lipophilic-balance
  • Examples of block copolymers of propylene oxide (“PEO”)-polypropylene oxide (“PPO”) meeting the requirements of the HLB-value and the melting point or pour point or melting range for making the compositions according to the present invention include the commercially available types Pluronic® L35, Pluronic® L 44, Pluronic® L64, Pluronic® P85 and Pluronic® P105.
  • Pluronic® L44 is a preferred non-ionic surfactant.
  • non-ionic surfactants are all liquids having a viscosity value which may be too low to avoid sedimentation of the bendamustine hydrochloride.
  • the additional problem to be solved was to find an excipient or a combination of excipients that would allow for a total value for the viscosity of the mixture that would be high enough to avoid segregation of the bendamustine chloride when added to the mixture.
  • compositions according to the first embodiment of the present invention that contain a liquid non-ionic surfactant, advantageously further contain a viscosity improving agent.
  • Suitable viscosity-improving agents include a powder such as colloidal silicon dioxide (commercially available under the trademark Aerosil®) or a semi-solidwaxy material, such as lauroyl macrogol glycerides (commercially available under the trademark Gelucire® 44/14).
  • the amount of the powder or the semi-solid material to be added to the liquid non-ionic surfactant depends on the viscosity of the liquid non-ionic surfactant. Different concentrations have been tested in order to find the minimum suitable amount of viscosity improving agent to be added to visually avoid sedimentation of the active ingredient.
  • Typical relative concentrations of colloidal silicon dioxide to be added range from about 1% to about 8%, but are preferably as low as 1.7% or 2.0% in order not to have a negative impact on the dissolution characteristics of the active ingredient.
  • Typical relative concentrations of lauroyl macrogol glycerides range from 5 to 50%, and are preferably about 10% and about 45%.
  • compositions according to the first embodiment of the present invention are disclosed in example 4 and comprise bendamustine hydrochloride in combination with:
  • compositions according to the first embodiment of the present invention are advantageously filled into a capsule, which can then easily be taken by the patient.
  • capsules Two types of capsule are commonly used and are classified according to the nature and flexibility of the capsule shell: soft and hard capsules.
  • Soft capsules are single unit solid dosage forms comprising a liquid or semi-solid fill. They are formed, filled and sealed in one operation using a rotary die process. They have been used as unit dose containers for liquids for many years, whereas hard capsules have conventionally been used for the delivery of solids in the form of powders, granulates and pellets.
  • Hard capsules are single unit dosage forms, consisting of a cap and a body, which are manufactured separately and which are supplied empty for filling.
  • Soft capsules are most commonly manufactured from gelatine, to which a plasticiser, usually glycerine or sorbitol, is added in addition to water. Also for hard capsules the most commonly used polymer is gelatine. An additional component is water, which acts as a plasticiser. This component however may be responsible for degradation of active ingredients, such as bendamustine hydrochloride. Therefore as an alternative hard capsules may be manufactured from hydroxypropylmethyl cellulose.
  • Both soft and hard capsules in addition can include colouring agents and opacifiers.
  • the preferred type of capsule for the compositions according to the present invention is the hard capsule and more in particular the hard gelatine capsule.
  • the materials to be filled into the capsule are fluid at room temperature, which would avoid heating during the filling operation. Generally, heating could result in an easy degradation of the active component.
  • fill formulations for hard capsules may be Newtonian liquids, such as oils, thixotropic or shear thinning gels or semi-solid matrix products that are filled at elevated temperatures and in which the active ingredient is either dissolved or suspended as a fine dispersion.
  • any excipient or mixture of excipients can be used provided that the viscosity of the fill material confirms to the requirements of the filling process.
  • the uniformity of capsule fill weights is important. Further fill formulations should not show stringing and should allow for a clean break from the dosing nozzle.
  • compositions according to the first embodiment of the present invention can be advantageously administered in hard gelatine capsules.
  • the particular non-ionic surfactants selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide/propylene oxide, and in particular from the group consisting of macrogol glycerol hydroxystearate, polyoxyl-35-castor oil and Pluronic® L44 or Poloxamer® 124, if incorporating bendamustine or a pharmaceutically acceptable ester, salt, or solvate thereof, and after incorporation into hard gelatine capsules result in achieving a good stability, a good dissolution profile and a good bioavailability.
  • Cremophor® A 25 ceteareth-25 or macrogol (25) cetostearyl ether
  • Cremophor® A 6 ceteareth-6 and stearylalcohol or macrogol (6) cetostearyl ether
  • compositions of the present invention can include additional excipients, in particular protective agents, such as anti-oxidants and antimicrobial preservatives, e.g. methyl-, ethyl- and propylparaben, as illustrated in examples 1-3.
  • protective agents such as anti-oxidants and antimicrobial preservatives, e.g. methyl-, ethyl- and propylparaben, as illustrated in examples 1-3.
  • the antioxidant may be d-alpha tocopherol acetate, dl-alpha tocopherol, ascorbyl palmitate, butylated hydroxyanidole, ascorbic acid, butylated hydroxyanisole, butylatedhydroxyquinone, butylhydroxyanisol, hydroxycoumarin, butylated hydroxytoluene, ethyl gallate, propyl gallate, octyl gallate, lauryl gallate, or mixtures thereof.
  • the anti-oxidant is preferably added to compositions containing macrogol glycerol hydroxystearate or polyoxyl-35-castor oil.
  • the saccharides are present in the compositions according to the second embodiment of the invention in a substantial amount, preferably in an amount ranging from 2 to 5 times the weight of the active substance.
  • the saccharides when incorporated into the compositions of the present invention have shown to have a positive effect on the stability of the active compound. In addition to that it was surprisingly found that these excipients result in an increased bio-availability of the active compound, in particular bendamustine hydrochloride, when compared to the reference capsule.
  • saccharides include mannitol, maltitol, erythritol, xylitol, lactose, sucrose, glucose, sorbitol, maltose, trehalose, lactitol and dextrose (anhydrous or monohydrate).
  • composition according to the present invention may comprise further excipients as described in more detail below for lubricants, glidants, fillers (or diluents), binders and disintegrants.
  • Lubricants are substances which may have one or more of the following functions in pharmaceutical compositions and especially in tablet manufacture: preventing adhesion of the tablet material to the surface of parts of the tabletting machine (hopper, dies and punches), reducing interparticle friction, facilitating ejection of the tablets from the dies and improving the flow rate of the mixture (to be tabletted).
  • Said lubricant is typically selected from a group consisting of stearic acid, salts or esters of stearic acid, hydrogenated vegetable oils, magnesium oxide, polyethylene glycol, sodium lauryl sulphate and talc, and mixtures thereof.
  • said lubricant is selected from magnesium stearate, calcium stearate, zinc stearate, glyceryl palmitostearate and sodium stearyl fumarate, and mixtures thereof.
  • Stearic acid is the most preferred alternative.
  • glidant in this application is to be understood as a substance which improves the flow characteristics of the mixture to be tabletted.
  • any suitable glidant such as talc, silicon dioxide and silicagel (Cab-O-Sil®, Syloid®, Aerosil®), starch and calcium silicate may be used.
  • silicon dioxide is used.
  • filler represent excipients which are used to increase the bulk of the materials to be tabletted. This increase in size improves the handling of the solid compositions. Fillers are usually necessary if the dose of drug per solid composition is low and the solid composition would otherwise be too small. Examples of suitable fillers are lactose, sucrose, mannitol, sorbitol, saccharose, starch, pregelatinized starch, microcrystalline cellulose, powdered cellulose, calcium hydrogen phosphate, calcium carbonate and any combinations thereof. In a preferred embodiment the filler is selected from the group consisting of lactose, starch, microcrystalline cellulose, microfine cellulose and any combinations thereof, most preferably anhydrous lactose and microcrystalline cellulose.
  • binder is used for agents that impart cohesiveness to the pharmaceutical formulation, which cohesiveness ensures that the composition remains intact especially in case of tablets after compression.
  • suitable binders are lactose, sucrose, mannitol, sorbitol, saccharose, starch, pregelatinized starch, microcrystalline cellulose, powdered cellulose, calcium hydrogen phosphate, calcium carbonate and any combinations thereof.
  • the binder is selected from the group consisting of lactose, starch, microcrystalline cellulose, microfine cellulose and any combinations thereof, most preferably anhydrous lactose and microcrystalline cellulose.
  • binders can be used both as a solution and in a dry form.
  • suitable binders there may be mentioned, for example, polyvinylpyrrolidone, dispersible cellulose, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, methylcellulose, starch, pregelatinized starch, partly pregelatinized starch, gum arabic, dextrin, pullulan and the like.
  • dispersible cellulose, polyvinylpyrrolidone, hydroxypropyl cellulose and hydroxypropylmethyl cellulose are more preferred.
  • a disintegrant can be included in a pharmaceutical composition and especially a tablet composition to facilitate its breakup or disintegration after the tablet comes into contact with a physiological aqueous liquid.
  • the disintegrant When the tablet is swallowed, the disintegrant often is responsible for the quick disintegration of the tablet when it comes into contact with body fluids, such as saliva, gastric and intestinal fluids.
  • body fluids such as saliva, gastric and intestinal fluids.
  • Materials serving as disintegrants have been classified chemically as starches, celluloses, cross-linked polymers, etc.
  • starch a modified starch such as sodium starch glycolate (Primojel®), sodium carboxymethyl cellulose, crosslinked carboxymethylcellulose sodium (Ac-Di-Sol®), cross-linked polyvinylpyrrolidone, polacrilin potassium (Amberlite® IRP88) and low-substituted hydroxypropyl cellulose can produce a very good disintegrating effect.
  • a modified starch such as sodium starch glycolate (Primojel®), sodium carboxymethyl cellulose, crosslinked carboxymethylcellulose sodium (Ac-Di-Sol®), cross-linked polyvinylpyrrolidone, polacrilin potassium (Amberlite® IRP88) and low-substituted hydroxypropyl cellulose can produce a very good disintegrating effect.
  • the stability of an aqueous solution of bendamustine is strongly influenced by the pH. A significant hydrolytic decomposition of this compound is observed at pH values higher than about 5. At pH>5, the decomposition proceeds rapidly and the resulting content of by-products is high in this pH range.
  • the main hydrolysis products are 4-[5-[(2-Chloroethyl)-(2-hydroxy-ethyl)amino]-1-methyl-benzimidazo-2-yl]-butanoic acid (HP1), 4-[5-[Bis(2-hydroxyethyl)amino]-1-methyl-benzimidazo-2-yl]-butanoic acid (HP2) and 4-(5-Morpholino-1-methylbenzimidazol-2-yl)-butanoic acid (HP3):
  • Absorption of an orally administered drug usually happens from the stomach, the small intestine and/or the large intestine.
  • the pH in the stomach is about 1 to 3.5, in the small intestine about 6.5 to 7.6, and in the large intestine about 7.5 to 8.0.
  • compositions comprising bendamustine hydrochloride in a pharmaceutically acceptable excipient, which is a non-ionic surfactant, selected from the group consisting of a polyethoxylated castor oil or derivative thereof and a block copolymer of ethylene oxide and propylene oxide, or one of the above saccharides surprisingly show a fast dissolution, and in particular a dissolution of the bendamustine of at least 60% in 20 minutes, 70% in 40 minutes and 80% in 60 minutes, and preferably of at least 60% in 10 minutes, 70% in 20 minutes and 80% in 30 minutes, as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in an artificial gastric fluid.
  • the artificial gastric fluid refers to a solution prepared by dissolving 2 g of sodium chloride in 1000 ml of water and then adjusting the pH to 1.5 ⁇ 0.05 with 5 N hydrochloric acid.
  • the total time of a drug to pass the stomach to the small intestine is between about 20 minutes to 5 hours, usually between about 30 minutes to 3 hours.
  • pharmaceutical compositions according to this invention advantageously should reduce the degradation of bendamustine in the patient since the bendamustine is released and dissolved to a major extent while in the stomach.
  • bioavailability of the bendamustine containing compositions according to the invention may be expected.
  • the oral pharmaceutical compositions may be used for the treatment or prevention of relapse of a medical condition in a human or animal, preferably a human, which medical condition is selected from chronic lymphocytic leukemia (abbreviated as CLL), acute lymphocytic leukaemia (abbreviated as ALL), chronic myelocytic leukaemia (abbreviated as CML), acute myelocytic leukaemiam (abbreviated as AML), Hodgkin's disease, non-Hodgkin's lymphoma (abbreviated as NHL), multiple myeloma, breast cancer, ovarian cancer, small cell lung cancer, non-small cell lung cancer, and an autoimmune disease.
  • CLL chronic lymphocytic leukemia
  • ALL acute lymphocytic leukaemia
  • CML chronic myelocytic leukaemia
  • AML acute myelocytic leukaemiam
  • NHL non-Hodgkin's lymphoma
  • MM multiple my
  • the pharmaceutical compositions in a solid dosage form may be used for the treatment, induction, salvage therapy, conditioning prior to stem cell transplantation, maintenance therapy, treatment of residual disease of a medical condition in a human or animal, preferably a human, which medical condition is selected from chronic lymphocytic leukemia (CLL), acute lymphocytic leukaemia (ALL), chronic myelocytic leukaemia (CML), acute myelocytic leukaemia (AML), Hodgkin's disease, non-Hodgkin's lymphoma (NHL), multiple myeloma, breast cancer, ovarian cancer, small cell lung cancer, non-small cell lung cancer, and an autoimmune disease.
  • CLL chronic lymphocytic leukemia
  • ALL acute lymphocytic leukaemia
  • CML chronic myelocytic leukaemia
  • AML acute myelocytic leukaemia
  • NHL non-Hodgkin's lymphoma
  • multiple myeloma breast cancer
  • the present invention also comprises a method of treatment or prevention of relapse of a medical condition selected from chronic lymphocytic leukemia, acute lymphocytic leukaemia, chronic myelocytic leukaemia acute myelocytic leukaemia, Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma, breast cancer, ovarian cancer, small cell lung cancer, non-small cell lung cancer, and an autoimmune disease, in a human or animal body comprising administering to the human or animal body in need thereof an effective amount of the pharmaceutical preparation of this invention.
  • a medical condition selected from chronic lymphocytic leukemia, acute lymphocytic leukaemia, chronic myelocytic leukaemia acute myelocytic leukaemia, Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma, breast cancer, ovarian cancer, small cell lung cancer, non-small cell lung cancer, and an autoimmune
  • the pharmaceutical composition may be administered in combination with at least one further active agent, wherein said further active agent is given prior, concurrently, or subsequently to the administration of the pharmaceutical composition.
  • This at least one further active agent is preferably an antibody specific for CD20 (an examples is rituximab or ofatumumab), an anthracyclin derivative (an example is doxorubicin or daunorubicin), a vinca alkaloid (an example is vincristine), a platin derivative (an example is cisplatin or carboplatin), daporinad (FK866), YM155, thalidomide and analogues thereof (an example is lenalidomide), or a proteasome inhibitor (an example is bortezumib).
  • an antibody specific for CD20 an examples is rituximab or ofatumumab
  • an anthracyclin derivative an example is doxorubicin or daunorubicin
  • the pharmaceutical composition of this invention may also be administered in combination with at least one corticosteroid, wherein said corticosteroid is given prior, concurrently, or subsequently to the administration of the pharmaceutical composition.
  • corticosteroids are prednisone, prednisolone and dexamethasone.
  • bendamustine can be administered as an oral formulation in a total amount of 200 mg/person/day on days 1-5+vincristine 2 mg i.v. on day 1+prednisone 100 mg/m 2 i.v. on days 1-5 every 3 weeks in patients with NHL.
  • bendamustine can be administered as an oral formulation in a total amount of 400-500 mg/person/day on days 1 and 2+prednisone 60 mg/m 2 i.v. or orally on days 1-4 every 4 weeks.
  • patients with CCL bendamustine can be administered as an oral formulation in a total amount of 200 mg-300 mg/person/day on days 1 and 2) every 4 weeks+prednisone 60 mg/m 2 i.v. or orally on days 1-4 every 4 weeks.
  • liquid filled hard gelatine capsule compositions according to the present invention further is, that the active ingredient(s), optionally in admixture with one or more excipients, do not need to be provided with a coating in order to further mask the taste of such ingredient and/or to protect the same against possible harmful effects by light and/or moisture such as oxidation, degradation, or to prevent that the subject may experience damage of the oral mucosa, due to the interaction with the active ingredient.
  • NP1 4-[6-(2-Chloroethyl)-3,6,7,8-tetra-hydro-3-methyl-imidazo[4,5-h]-[1,4]benzothiazin-2-yl] butanoic acid BM1Dimer: 4- ⁇ 5-[N-(2-Chloroethyl)-N-(2- ⁇ 4-[5-bis(2-chloroethyl)amino-1-methylbenzimidazol-2-yl]butanoyloxy ⁇ ethyl)amino]-1-methylbenzimidazol-2-yl ⁇ butanoic acid BM1EE: 4-[5-[Bis(2-chloroethyl)amino]-1-methyl-benzimidazo-2-yl] butanoic ethyl ester * 2 n.d.: not detectable, i.e. beyond detection limit (area percentage less than 0.05%)
  • the blend was transferred to a capsule filling machine (Zanassi AZ 5) and filled into hard gelatine capsules (size 2) (mean mass: 259.5 mg (begin)-255.3 mg (end)) and hypromellose capsules (size 2) (mean mass: 255.8 (begin)-253.4 mg (end)) respectively.
  • Capsules were stored at 40° C./75% RH in a closed glass vial.
  • the amount of bendamustine hydrochloride as well as of related substances, like degradation products, by-products of synthesis were measured with HPLC (column: Zorbax Bonus-RP, 5 ⁇ m; temperature of column oven: 30° C.; temperature of autosampler: 5° C.; detector: 254 nm).
  • Table 2b filled in hypromellose capsules
  • 2c filled in gelatine capsules.
  • the blend was transferred to a capsule filling machine (Zanassi AZ 5) and filled into hard gelatine capsules (size 2) (mean mass: 257.9 mg (begin)-255.2 mg (end)) and hypromellose capsules (size 2) (mean mass: 261.1 (begin)-257.8 mg (end)) respectively.
  • Capsules were stored at 40° C./75% RH in a closed glass vial.
  • the amount of bendamustine hydrochloride and of related substances was measured with HPLC, as described above. The results are shown in Table 3b (filled in hypromellose capsules) and 3c (filled in gelatine capsules).
  • the blend was transferred to a capsule filling machine (Zanassi AZ 5) and filled into hard gelatine capsules (size 2) (mean mass: 241.3 mg (begin)-244. mg (end)) and hypromellose capsules (size 2) (mean mass: 243.5 (begin)-243. mg (end)) respectively.
  • Capsules were stored at 40° C./75% RH in a closed glass vial.
  • the amount of bendamustine hydrochloride and of related substances was measured with HPLC, as described above. The results are shown in Table 4b (filled into hypromellose capsules) and 4c (filled in gelatine capsules).
  • Cremophor® RH 40 0.68 g of methylparaben, 0.068 g of propylparaben and 0.068 g of butylhydroxytoluene were weighed and dissolved in 6.14 g of ethanol. Cremophor® RH 40 was melted at 40° C. in a sufficient amount. 5.56 g of the ethanolic solution obtained, 36.83 g of the melted Cremophor® RH 40 and 202.82 g of Pluronic® L44 NF were weighed and mixed at 800 rpm using a mechanical stirrer until the mixture became transparent. The mixture was allowed to solidify by placing it at 10° C.
  • Cremophor® RH 40 0.68 g of methylparaben, 0.068 g of propylparaben and 0.068 g of butylhydroxytoluene were weighed and dissolved in 6.14 g of ethanol. Cremophor® RH 40 was melted at 40° C. in a sufficient amount. 5.56 g of the ethanolic solution obtained and 239.65 g of the melted Cremophor® RH 40 were weighed and mixed at 800 rpm using a mechanical stirrer until the mixture became transparent. The mixture was allowed to solidify and cool to room temperature.
  • the liquid filled capsules so obtained were stored in closed amber glass bottles with screw plugs at 40° C./75% RH, at 30° C./65% RH, at 25° C./60% RH and at 5° C.
  • the amount of bendamustine hydrochloride as well as of related substances, like degradation products, by-products of synthesis was measured with HPLC, as described above.
  • the dissolution test was conducted according to Chapter 2.9.3. of European Pharmacopoeia 6.0, using Apparatus 2 (Paddle-apparatus). The rotation speed of the paddle was 50 rpm, the temperature was 37° C. ⁇ 0.5° C., the amount of dissolution medium was 500 ml.
  • liquid filled hard capsule formulation of example 2 according to the invention shows the preferred fast dissolution profile of bendamustine, which is at least 60% in 10 minutes, 70% in 20 minutes and 80% in 30 minutes, as measured with a paddle apparatus at 50 rpm according to the European Pharmacopoeia in 500 ml of an artificial gastric fluid.
  • the liquid filled hard capsules of example 2 containing 50 mg of bendamustine, were orally administered to male and female beagle dogs in comparison with the capsules of reference example 1 in order to determine the bioavailability of 1 dose (i.e. 50 mg) of bendamustine (AUC and Cmax) and to determine the level of variability in bioavailability of these capsule formulations: (i.e. % CV on AUC and Cmax).
  • a further formulation (formulation X) was also included in the test but since this formulation was outside the scope of the present invention no details are provided.
  • the total number of animals required was 16.
  • the basic study design was a cross-over design with 8 animals per arm.
  • Period 1 Single Dose of Capsule, Day 1:
  • Period 2 (1 Week after Period 1, Single Dose of Either of the Following Formulations, Day 8):
  • the mean plasma profiles vs. time for both the capsule formulation (reference example 1) and the liquid filled capsule formulation of Example 2 are shown in FIG. 1 .
  • bendamustine HCl 100 mg intravenous, 110.2 mg orally was selected based on the safety of the oral formulation in preclinical studies and based on the safety of the registered i.v. formulation.
  • Bendamustine was administered orally as two liquid-filled hard-shell capsules with 250 mL of water or as i.v. infusion over 30 minutes.
  • the total duration of the admission period was 6 days (day ⁇ 1 to 2 and day 7-9) excluding screening and a post study visit.
  • the blood concentration-time curve as obtained after evaluating 6 patients is shown in FIG. 2 .
  • the mean value for the absolute bioavailability, calculated as AUC oral /dose/AUC iv /dose*100% was 58.5%, with a standard deviation of 9.3 and an interindividual variation (expressed as % CV) of 15.9.
  • mixtures containing bendamustine hydrochloride and an excipient at a ratio of 1:1 (m/m) were prepared.
  • the excipients were selected from Opadry®, Eudragit® E PO, sodium carboxymethylcellulose (Avicel® RC 591) and cross-linked polyvinylpyrrolidone (Crospovidone).
  • 253 g of a mixture comprising mannitol as the main excipient and microcrystalline cellulose, Ac-Di-Sol®, colloidal silicon dioxide, talc and stearic acid in the relative quantities mentioned in the following table 2a was prepared by mixing in a 1 liter cube blender (Erweka) for 15 minutes. Thereafter 10.612 g of the mixture and 3.0 g of bendamustine hydrochloride were sieved through a 0.425 mm sieve and then transferred into a Turbula mixer T2A, equipped with a glass vial of 50 ml and subsequently mixed for 10 minutes at 60 rpm.
  • a Turbula mixer T2A equipped with a glass vial of 50 ml and subsequently mixed for 10 minutes at 60 rpm.
  • Mean value diameter 9.1 mm; mean value mass: 247.7 mg; mean value hardness: 81N.
  • Tablets were stored at 40° C./75% RH (glass vial open) or 50° C. (glass vial closed).
  • the amount of bendamustine hydrochloride as well as of related substances, like degradation products, by-products of synthesis were measured with HPLC (column: Zorbax Bonus-RP, 5 ⁇ m; temperature of column oven: 30° C.; temperature of autosampler: 5° C.; detector: 254 nm). The results are shown in Table 12b.
  • NP1 4-[6-(2-Chloroethyl)-3,6,7,8-tetra-hydro-3-methyl-imidazo[4,5-h]-[1,4]benzothiazin-2-yl] butanoic acid
  • BM1Dimer 4- ⁇ 5-[N-(2-Chloroethyl)-N-(2- ⁇ 4-[5-bis(2-chloroethyl)amino-1-methylbenzimidazol-2-yl]butanoyloxy ⁇ ethyl)amino]-1-methylbenzimidazol-2-yl ⁇ butanoic acid
  • BM1EE 4-[5-[Bis(2-chloroethyl)amino]-1-methyl-benzimidazo-2-yl] butanoic ethyl ester * 2 n.d.: not detectable, i.e. beyond detection limit (area percentage less than 0.05%)
  • the capsule formulations were a lot less stable than the tablet formulations according to the invention although the capsule formulations were prepared from pure bendamustine hydrochloride without any further processing steps. Both at 40° C./75% RH (glass vial open) and 50° C. (closed vial) more degradation products are formed within one month of storage. In the case of open vial with 40° C. and 75% RH (relative humidity) the amount of hydrolysis product HP1 is increased by a factor of 4 after one month of storage. For the closed vials the HP1 content is even higher, which might be due to reaction with the capsules. Summarising, tablets provide a much more stable solid dosage form than the capsules.
  • Example 11 8.0 g of hydroxypropylmethyl cellulose and 1.5 g PEG 6000 are dissolved in 88.5 g purified water. Thereafter 2.0 g yellow ferric oxide and 0.5 g titanium oxide are dispersed therein yielding a coating liquid. Tablets as obtained in Example 11 are coated with 3% of this solution per tablet mass using a film coating device.
  • Mean value diameter 9.5 mm; mean value mass: 254.6 mg (begin)-257.2 mg (end); friability 0.1%; mean value hardness: 122N (begin)-128 (end).
  • the tablets were subsequently film-coated with the Opadry® dispersion until a mass increase of 5% had been achieved.
  • the mean mass of the film-coated tablets was 268.4 mg.
  • the tablets were subsequently film-coated with the Eudragit® dispersion until a mass increase of 3% had been achieved.
  • the mean mass of the film-coated tablets was 273.5 mg.
  • the tablets were subsequently film-coated with the Eudragit® dispersion until a mass increase of 3% had been achieved.
  • the mean mass of the film-coated tablets was 253.6 mg. Both the tablet cores and the film-coated tablets were stored at 40° C./75% RH in closed amber glass vials. The amount of bendamustine hydrochloride and of related substances was measured with HPLC, as described above. The results are shown in Tables 18b.1 and 18b.2:
  • composition coated tablets Composition PF1 PF2 PF3 component mg/tablet mg/tablet mg/tablet Bendamustine HCl 55.1 55.1 55.1 Anhydrous dextrose — — 205.8 Dextrose monohydrate 186.0 — — Trehalose — 66.0 — sorbitol — — 43.9 Lactose DCL 21 68.2 185.7 — Avicel ® PH 112 18.7 — 23.0 Crospovidone — 21.0 — Magnesium stearate 2.0 2.2 2.2 Opadry 8.0 8.0 8.0 Total 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 338.0 33
  • the tablet cores were subsequently coated in a coating pan (4M8 ForMate PanCoat) using a 9% Opadry® TM White aqueous suspension and dried.
  • the mean mass of the tablets was 342.42 mg. Thereafter the tablets were packed into amber glass bottles closed with screw plugs and stored at 40° C./75% RH.
  • the tablet cores were subsequently coated in a coating pan (4M8 ForMate PanCoat) using a 9% Opadry® TM White aqueous suspension and dried.
  • the mean mass of the tablets was 340.1 mg. Thereafter the tablets were packed into amber glass bottles closed with screw plugs and stored at 40° C./75% RH.
  • Sorbitol and anhydrous dextrose were weighed. 140.64 g of Sorbitol was dissolved in 105.48 g of purified water and the solution obtained was subsequently used to granulate 659.36 g of dextrose in a Fluid Bed Granulator (4M8ForMate FluidBed). Thereafter the granulate was dried at 60° C. and sieved through a 850 ⁇ m sieve.
  • the tablets were subsequently coated in a coating pan (4M8 ForMate PanCoat) using a 9% Opadry® TM White aqueous suspension. Mean mass of the tablets: 341.43 mg. Thereafter the tablets were packed into amber glass bottles closed with screw plugs and stored at 40° C./75% RH.
  • the dissolution samples are tested for assay by HPLC (column: Zorbax Bonus-RP, 5 ⁇ m; temperature of column oven: 30° C.; temperature of autosampler: 5° C.; detector: 254 nm).
  • Artificial gastric fluid pH 1.5 was prepared by dissolving 2 g of sodium chloride p.A. in 1000 ml of water and adjusting the pH to 1.5 ⁇ 0.05 with 5 N hydrochloric acid.
  • the dissolution test was conducted according to Chapter 2.9.3. of European Pharmacopoeia 6.0, using Apparatus 2 (Paddle-apparatus). The rotation speed of the paddle was 50 rpm, the temperature was 37° C. ⁇ 0.5° C., the amount of dissolution medium was 500 ml.
  • Example 11 tablette formulation 1
  • Example 12 tablette formulation 2
  • Tablet Tablet formulation formulation Tablet formulation example 18 (PF1) example 18 (PF2) example 18 (PF3) Mean value after Mean value after Mean value after 3 Dissolution 3 months at 3 months at months storage at after 40° C./75% RH 40° C./75% RH 40° C./75% RH 10 minutes 89.7 96.3 60.1 20 minutes 93.7 95.2 88.8 30 minutes 93.2 93.3 94.0
  • tablet formulations of the invention show a fast dissolution of bendamustine.
  • inventive formulations show a dissolution profile of the bendamustine as defined hereinbefore.
  • the objective was to determine the bioavailability of 1 dose (i.e. 50 mg) of bendamustine in 3 tablet formulations (T1-3) and 1 capsule formulation (C) with a total of 4 oral formulations: AUC and Cmax
  • the objective was to determine the bioavailability of 1 dose (i.e. 50 mg) of bendamustine in 1 tablet formulation T4, and 1 capsule formulation (C) with a total of 3 oral formulations: AUC and Cmax
  • Period 1 Single dose of capsule, day 1: Dose # Number of Animal Group Treatment Dose (mg) animals numbers 1 Bendamustine Capsule 50 4 Male + 4 Female 2 Bendamustine Capsule 50 4 Male + 4 Female
  • Example 18 The coated tablets of Example 18 (formulation 3, coated with Opadry® Tablets T4), containing 50 mg of bendamustine, were orally administered to male and female dogs in comparison with the capsules of the reference example.
  • the mean plasma profiles vs. time for both the capsule formulation and the coated tablet of Example 18 are shown in FIG. 3 .
  • coated tablets of Examples 15, 16, or 17 (Tablets T1 to T3), containing 50 mg of bendamustine, were orally administered to male and female dogs in comparison with the capsules of the reference example.
  • the mean plasma profiles vs. time of the capsule formulation and the coated tablets of Examples 15 to 17 are shown in FIG. 3 .
  • microcrystalline cellulose Avicel®PH 112
  • Cross-linked polyvinylpyrrolidone Crospovidone®
  • Table 24 and Table 25 summarize the composition of each Placebo formulation and the results of the analytical tests performed on both the final mixtures and the tablets. In Table 16, observations made during the manufacturing process of placebo batches and/or during their analytical characterization are reported.
  • Batch D001T/005 (filler: ⁇ -cyclodextrin) showed good behaviour in dry manufacturing process, high hardness, low friability but long disintegration time.
  • This formulation was further investigated by employing a super disintegrant (Crospovidone®) and adding the API (see following paragraph).
  • the placebo formulations evaluated as more suitable to manufacture tablets containing the active pharmaceutical ingredient (API) by dry granulation, were modified to include the API and two API/saccharide weight ratios were explored: 1:5 and 1:2.
  • microcrystalline cellulose Avicel®PH 112
  • Crosslinked polyvivylpyrrolidone Crosslinked polyvivylpyrrolidone
  • Magnesium stearate was used as lubricant for all the batches produced.
  • Table 27 summarizes the composition of each API-containing formulation manufactured and the results of the analytical tests performed on the API-containing final mixtures; table 28 summarizes the results of the analytical tests performed on the obtained products.
  • the obtained mixture was tabletted by using a 8 mm diameter punch.
  • microcrystalline cellulose Avicel® PH 112
  • Crosslinked polyvinylpyrrolidone Ccrospovidone®′
  • the Crospovidone® was chosen according to the previous cyclodextrin based formulation manufactured by dry granulation with a 1:5 API/Saccharide (see previous results).
  • Table 29 and Table 30 summarize the composition of each API-containing formulation manufactured by dry granulation with an API/Saccharide weight ratio of 1:2 and the results of the analytical tests performed on both, the final mixtures and the tablets. All API-containing batches showed suitable uniformity of mass, homogeneity of API content and low impurities content. Friability and hardness values are, in the most of the cases, in compliance with the specifications. In the case of batches D001T/093, D001T/095 and D001T/096, the results of the dissolution test performed on 6 tablets showed out of specifications values with a high RSD and the test was extended to a sample of 12 tablets.
  • Cyclodextrin based tablets show good properties with both disintegrants (Avicel® PH 112 and Crospovidone®).
  • saccharides with suitable characteristics to be manufactured by dry granulation were also explored by using direct compression developing tablets with a 1:5 API/Saccharide ratio.
  • microcrystalline cellulose Avicel® PH 112
  • Crosslinked polyvinylpyrrolidone Crosslinked polyvinylpyrrolidone
  • This manufacturing process consisted of the following steps:
  • API-containing batches manufactured by Direct Compression D001T/026 D001T/027 D001T/028 D001T/029 D001T/030 (% w/w ) (% w/w ) (% w/w ) (% w/w ) (% w/w ) Bendamustine HCL 16.6 16.6 15.3 16.6 15.7 Lactose Monohydrate — — 78.4 — — (Supertab 14 SD) Sorbitol 77.1 — — — (Neosorb P60W) ⁇ -Cyclodextrin — — — 77.1 (Kleptose DC) Maltose (Food grade) 77.1 — — — — (Sunmalt S) Sucrose 97% + Maltodextrin 3% — — — — 78.0 (EV Saccharide DC 3.75
  • the API-containing tablets manufactured by direct compression showed no critical differences from the ones produced by dry granulation except for batch D001T/030 (filler: Sucrose 97%+Maltodextrin 3%) that showed a non homogeneous API content and a slight increase in the value of friability.
  • Each saccharide was granulated according to the steps described in the flow-sheet of FIG. 4 . At the end of each step the wet granulated saccharide was dried and a compression trial was performed to evaluate if the granulate was suitable for tabletting. Placebo batches were manufactured only for the granulated saccharides with doubtful results of the compression test. The compositions and the relevant analytical results of the placebo trials are reported in Table 33.
  • Placebo batches were manufactured according to the following steps:
  • Manufacturing trials including a wet granulation process were carried out on all saccharides that turned out to be not suitable for tablet manufacturing by dry granulation or direct compression technologies.
  • Table 33 and Table 34 list the composition of each API-containing formulation manufactured by wet granulation and the results of the analytical tests performed on both, the final mixtures and the tablets.
  • the batches D001T/060, D001T/061, D001T/082, D001T/086 have low values in API assay and for the batches D001T/082 and D001T/086 the Uniformity of Content does not comply, though the granulate was sieved by using 850 micron and 710 micron nets. This result is probably due to poor powders mixing.
  • API-containing batches final mixture composition and analytical results.
  • API-containing Batches manufactured by Wet Granulation D001T/033 D001T/036 D001T/037 D001T/040 D001T/047 D001T/059 Components (% w/w ) (% w/w ) (% w/w ) (% w/w ) (*) (% w/w ) Bendamustine HCl 15.7 15.7 15.7 15.7 14.9 15.7 Dextrose Anhydrous 78 — — — — (Anhydrous Dextrose ST 0.5) Dextrose Monohydrate G — 78 — — — — Mannitol — — 78 — — (Pearlitol 200 SD) Lactitol Monohydrate — — — — 78 — — (Lacty M)(Food grade) D-
  • the fructose was not evaluated at a ratio of 1:2 because the obtained granulate is not suitable for tabletting.
  • step 3 (Dry granulation of the mixture) see above.
  • Table 36 and table 37 report the compositions and the analytical results of the API-containing batches manufactured by using wet granulated saccharides with an API/Saccharide weight ratio of 1:2. Friability is, in the most of the cases, out of specifications. The API/Saccharide weight change does not compromise the technological properties of the D001T/084 batch (Filler: granulated mannitol).
  • Mannitol based tablets were manufactured investigating the following API/mannitol ratios: (1:0.01, 1:0.1, 1:0.5, 1:1.7, 1:4, 1:5, 1:6 and 1:10). The formulation with a 1:5 API/mannitol weight ratio (standard formulation) was reported above.
  • the final mixture was tabletted using the tabletting machine equipped with a suitable punch (8 mm diameter punch for 1:1, 1:1.7 and 1:2 ratios, 10 mm in the case of 1:4 and 1:6 ratios, 12 mm for 1:7 ratio and 14 mm for 1:10 ratio).
  • Table 40 and Table 41 report the results concerning the saccharide combination study.
  • the manufacturing process consisted in direct compression of the unprocessed or granulated saccharide.
  • Saccharide Combination Study API-containing batches final mixture composition and analytical results.
  • Saccharide Combination Study API-containing Batches D001T/049 D001T/074 D001T/100 D001T/101 D001T/102 D001T/103 Components (% w/w ) (% w/w ) (% w/w ) (% w/w ) (% w/w ) Bendamustine HCl 14.89 15.74 15.74 15.74 15.74 15.74 Saccharide combination Oligosaccharide/Monosaccharide 1:1 D-Melezitose monohydrate/Dextrose 78.81 — — — — — anhydrous ST 0.5 Raffinose Pentahydrate/Mannitol — — — — 77.96 — (Pearlitol 200 SD) Saccharide combination Oligosaccharide/Disaccharide 1:1 Raffinose Pentahydrate/Lactose
  • the tablets manufactured for the saccharides combination studies show good properties.
  • the batch D001T/102 (Raffinose Pentahydrate/Mannitol (Pearlitol 200 SD))
  • Tablets containing bendamustine hydrochloride/mannitol in a weight ratio of 1:1.2 were prepared by using either freeze dried material obtained from the commercially available product for intravenous application (Ribomustin®) or using wet granulated mannitol and Bendamustine HCl.
  • the manufacturing processes were performed according to the following experimental operations: the freeze dried powder was removed from the Ribomustin® vials and was sieved using a 850 micron net.
  • the obtained powder and the lubricant (magnesium stearate) were accurately weighed and mixed in a polyethylene bag for 5 minutes.
  • the mixture was slowly transferred in the pressing chamber of the tabletting machine and was manually pressed by using an 8 mm diameter punch in order to obtain small slugs.
  • the slugs were sieved using a 850 micron net and the obtained granulate was manually pressed using a 8 mm diameter punch.
  • composition of the formulations is reported in table 42.
  • Table 43 reports the data concerning the comparison between the tablets obtained using the freeze dried bendamustine hydrochloride/mannitol mixture and the non freeze-dried bendamustine hydrochloride/mannitol mixture.
  • batch D001T/125 showed an out of specification value for HP1 impurity.
  • the results of the dissolution test highlight that, although after 10 minutes the dissolution profile of the tablets, containing the freeze-dried bendamustine hydrochloride/mannitol mixture is faster, for both formulations, after 30 minutes the dissolution is in compliance with the current specifications.
  • the friability is out of specification for batch D001T/126, whereas the test was not performed for batch D001T/125 due to lack of sufficient amounts of material.
  • Bendamustine was provided a) orally as capsules, a LFHC formulation (liquid-filled, hard-shell capsule) and b) intravenously as a solution after reconstituting a powder for the preparation of a solution for injection.
  • the LFHC formulation (per capsule) was prepared from 55.1 mg bendamustine hydrochloride, 1.2 mg methylparaben, 0.12 mg polyparaben, 0.12 mg butylated hydroxytoluene, 10.9 mg ethanol and 532.56 mg Cremophor® RH40.
  • the vial with powder for concentrate for solution was the marketed product in Germany (Ribomustine®) which contains per vial 100 mg of bendamustine hydrochloride and mannitol as an excipient. This product was reconstituted with water for injection to a final concentration of 2.5 mg/ml of bendamustine HCl and was further diluted with 0.9% NaCl until about 500 ml before administration to the patient, in accordance with the instructions of the
  • Bendamustine is metabolized via hydrolysis to the inactive metabolites monohydroxybendamustine (HP 1) and dihydroxybendamustine (HP2) and via cytochrome P450 (CYP 1A2) to the active metabolites ⁇ -hydroxybendamustine (M3) and N-desmethylbendamustine (M4).
  • HP 1 monohydroxybendamustine
  • HP2 dihydroxybendamustine
  • CYP 1A2 cytochrome P450
  • M3 ⁇ -hydroxybendamustine
  • M4 N-desmethylbendamustine
  • bendamustine After oral and intravenous administration of bendamustine the concentration of bendamustine, as well as that of the active metabolites of bendamustine (M3 and M4), were determined in plasma and urine samples on day 1 and day 8. Patients returned to the study site for an end-of-study visit 7 to 14 days after completion of the second treatment period, or after early discharge/withdrawal. Subsequently the pharmacokinetic parameters of bendamustine and its metabolites were calculated.
  • Plasma pharmacokinetic parameters of bendamustine (base), M3 and M4 are shown in Table 44, Table 45 and Table 46, respectively. Based on statistical analysis, the absolute bioavailability (oral versus intravenous ratio of AUC inf ) of bendamustine was 66% (geometric mean; 90% CI: 55%, 78%). C max after oral dosing was 42% of C max after intravenous dosing (90% CI: 32%, 54%).
  • M3 and M4 exposure in plasma was considerably lower than for bendamustine.
  • Mean AUC inf of bendamustine was 10.6 and 88 times higher than for M3 and M4, respectively, after oral administration.
  • M3 and M4 AUC inf values were similar for oral and intravenous administration. Based on statistical analysis, after oral administration AUC inf of M3 was 86% of AUC inf after intravenous administration (90% CI: 76%, 98%). For M4 this was 88% (90% CI: 77%, 102%).
  • Urine pharmacokinetic parameters of bendamustine, M3 and M4 are presented in Table 47, Table 48 and Table 49, respectively.
  • the percentage of the dose excreted in urine unchanged was low (2.6% and 2.1% for oral and intravenous bendamustine, respectively).
  • compositions according to the present invention show many advantages. They can be easily used by the patient without assistance of supervisory medical staff. Hence the time-consuming trips to the hospital may become obsolete, thereby increasing the patient compliance.
  • the dosage forms are solid, they can be swallowed as such, which means that the patient does not need to wait until dissolution of the active ingredient has been achieved. Further due to the good stability of the dosage forms they can be easily stored at room temperature and without the need of any special storage conditions.
  • the dosage forms according to the present invention By using the dosage forms according to the present invention, a considerable reduction of the volume of the dosage form may be achieved.
  • the reduced size is desirable both from a manufacturing and handling standpoint and patient compliance.
  • compositions show a high dissolution in vitro reducing the degradation of bendamustine in vivo, thus resulting in an improved bioavailability of the bendamustine in vivo.

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US20150183747A1 (en) * 2011-09-18 2015-07-02 Purdue Pharmaceutical Products L.P. Pharmaceutical Compositions
US10118901B2 (en) 2012-02-01 2018-11-06 Purdue Pharmaceutical Products L.P. Therapeutic agents
US11419853B2 (en) 2014-05-28 2022-08-23 Purdue Pharmaceutical Products L.P. Compounds for treating brain cancer
US10744120B2 (en) 2014-05-28 2020-08-18 Purdue Pharmaceutical Products L.P. Combination comprising a glucocorticoid and EDO-S101
US12064417B2 (en) 2014-05-28 2024-08-20 Purdue Pharmaceutical Products L.P. Combination comprising a glucocorticoid and EDO-S101
US10406138B2 (en) 2014-05-28 2019-09-10 Purdue Pharmaceutical Products L.P. Pharmaceutical combinations for treating cancer
US12048688B2 (en) 2014-05-28 2024-07-30 Purdue Pharmaceutical Products L.P. Pharmaceutical combinations for treating cancer
US9993482B2 (en) 2014-05-28 2018-06-12 Purdue Pharmaceutical Products L.P. Pharmaceutical combination comprising a class III receptor tyrosine kinase inhibitor and the alkylating histone-deacetylase inhibitor fusion molecule EDO-S101 together with its use in the treatment of cancer
US11541038B2 (en) 2014-05-28 2023-01-03 Purdue Pharmaceutical Products L.P. Combination comprising a glucocorticoid and EDO-S101
US11559516B2 (en) 2014-05-28 2023-01-24 Purdue Pharmaceutical Products L.P. Pharmaceutical combinations for treating cancer
US11766424B2 (en) 2016-10-11 2023-09-26 Purdue Pharmaceutical Products L.P. Hodgkin lymphoma therapy
US11266631B2 (en) 2016-10-11 2022-03-08 Purdue Pharmaceutical Products L.P. Hodgkin lymphoma therapy
US11318117B2 (en) 2017-06-13 2022-05-03 Purdue Pharma L.P. Tinostamustine for use in the treatment of t-cell prolymphocytic leukaemia
US11576899B2 (en) 2017-06-13 2023-02-14 Purdue Pharma L.P. Tinostamustine for use in treating sarcoma
US11786509B2 (en) 2017-06-13 2023-10-17 Purdue Pharma L.P. Compounds for treating TNBC
US11896583B2 (en) 2017-06-13 2024-02-13 Purdue Pharma L.P. Tinostamustine for use in treating ovarian cancer
US11918558B2 (en) 2017-06-13 2024-03-05 Purdue Pharma L.P. Tinostamustine for use in the treatment of T-cell prolymphocytic leukaemia
US11413276B2 (en) 2017-06-13 2022-08-16 Purdue Pharma L.P. Compounds for treating TNBC
CN112848583A (zh) * 2020-12-31 2021-05-28 雅达环保科技(玉田)有限公司 一种阻燃保温板及其制备方法

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