US20160256557A1 - Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity - Google Patents
Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity Download PDFInfo
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- US20160256557A1 US20160256557A1 US14/937,689 US201514937689A US2016256557A1 US 20160256557 A1 US20160256557 A1 US 20160256557A1 US 201514937689 A US201514937689 A US 201514937689A US 2016256557 A1 US2016256557 A1 US 2016256557A1
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- Prior art keywords
- sodium chloride
- pharmaceutical composition
- amino
- isoquinoline
- aminoethyl
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/473—Quinolines; Isoquinolines ortho- or peri-condensed with carbocyclic ring systems, e.g. acridines, phenanthridines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/02—Inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention relates to injectable pharmaceutical compositions containing 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate (from now on also referred to as “BBR 2778”) as active ingredient in the form of a lyophilised powder with a carrier selected from lactose and dextran, mixed with sodium chloride.
- BBR 2778 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate
- BBR 2778 is a novel anthracenedione derivative with anti-tumoral activity which acts as a DNA intercalating agent and topoisomerase II inhibitor. Pre-clinical studies demonstrate that its cardiotoxicity is lower than that of other known drugs belonging to the same class. BBR 2778 has proved more active than mitoxantrone against haematological tumours, especially ascitic L1210 leukaemia and YC-8 lymphoma, in a wide range of doses.
- BBR2778 in injectable liquid pharmaceutical compositions has proved problematic in terms of stability in solution using common solvents suitable for parenteral administration, especially intravenous administration.
- a lyophilised formulation to be reconstituted with a suitable solvent such as saline immediately before use has therefore been considered.
- a first aspect of the invention therefore provides injectable pharmaceutical compositions containing 6,9-bis[(2-aminoethyl)amino]benzo[q]isoquinoline-5,10-dione dimaleate (BBR 2778) as active ingredient in the form of a lyophilised powder with a carrier selected from lactose and dextran, mixed with sodium chloride, to be reconstituted with a solvent suitable for reconstituting the lyophilisate and suitable for parenteral administration, which solvent is preferably contained in a separate ampoule.
- BBR 2778 6,9-bis[(2-aminoethyl)amino]benzo[q]isoquinoline-5,10-dione dimaleate
- a further aspect of the invention relates to a process for the preparation of said compositions.
- the weight ratio between the carrier and sodium chloride is critical, and is typically between 1:1 and 3:1.
- the weight ratio between BBR 2778 and the carrier is preferably between 1:2 and 1:6.
- the particularly preferred carrier is lactose.
- the unit dose of BBR 2778 will usually be between 25 and 200 mg, and preferably between 50 and 100 mg.
- the unit dose currently being tested in clinical trials is 50 mg.
- the preferred compositions according to the invention will contain 100 to 200 mg of sodium chloride and 100 to 300 mg of lactose.
- compositions of the invention can also contain other excipients commonly used for parenteral formulations, such as antioxidants, buffers, local anaesthetics, salts, amino acids and the like.
- the vials or ampoules of sterile lyophilised powder will then be reconstituted at the time of use with sterile solvents constituted by sterile pyrogen-free water or sterile saline, in volumes of approx. 5 ml to 20 ml, depending on the active ingredient content.
- compositions of the invention are prepared by a process which comprises lyophilisation of an aqueous solution of BBR 2778, lactose or dextran and sodium chloride by means of
- compositions according to the invention are stable at room temperature for at least 24 months.
- the lyophilised product is not subject to deliquescence, and maintains its appearance unchanged over time.
- a further advantage of the invention is the reduction in lyophilisation times and the consequent reduction in the cost of the process.
- a lyophilisation stopper is placed on the mouth of the vials.
- the pre-stoppered vials are then loaded directly onto lyophilisation shelves and frozen at ⁇ 45° C. ⁇ 5° C. for at least 3 hours.
- Primary drying is conducted by increasing the temperature of the shelves in the vacuum freeze-dryer from ⁇ 45° C. to ⁇ 30° C. ⁇ 3° C. in 3 hours, and maintaining the temperature at ⁇ 30° C. for 40 hours.
- Secondary drying is performed by increasing the temperature of the shelves from ⁇ 30° C. to +30° C. ⁇ 3° C. in 10 hours and then maintaining said temperature of +30° C. for a further 8 hours.
- the freeze-dryer is returned to atmospheric pressure with nitrogen filtered under sterile conditions, and the vials are stoppered by activating the stoppering device.
- the vials are unloaded in a sterile environment and crimped.
- the solution When reconstituted with 5 ml of water for injection, the solution has a pH of between 3.0 and 4.5.
- a lyophilisation stopper is placed on the mouth of the vials.
- the pre-stoppered vials are then loaded onto trays, which are placed on the shelves of the freeze-dryer.
- the vials are then frozen in the lyophilisation chamber at ⁇ 45° C. ⁇ 5° C. for at least 3 hours.
- Primary drying is conducted by increasing the temperature of the shelves in the vacuum freeze dryer from ⁇ 45° C. to 0° C. ⁇ 2° C. in 6 hours and maintaining the temperature at 0° C. for 30 hours. The temperature of the product during primary drying is maintained at around ⁇ 30° C.
- Secondary drying is performed by increasing the temperature of the shelves from 0° C. to +30° C. ⁇ 2° C. in 3 hours and then maintaining said temperature of +30° C. for a further hours.
- the freeze-dryer is returned to atmospheric pressure with nitrogen filtered under sterile conditions, and the vials are stoppered by activating the stoppering device.
- the vials are unloaded in a sterile environment and crimped.
- the solution When reconstituted with 5 ml of water for injection. the solution has a pH of between 3.0 and 4.5.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Oil, Petroleum & Natural Gas (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
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Abstract
Injectable pharmaceutical compositions containing 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate as active ingredient in the form of a lyophilised powder with a carrier selected from lactose and dextran, mixed with sodium chloride.
Description
- This application claims the benefit of the filing date of U.S. patent application Ser. No. 10/514,301, filed Jul. 18, 2005, which claims priority from international Patent Application No. PCT/EP03/04871, filed May 9, 2003, which claims priority from Italian Patent Application No. MI2002A001040, filed May 16, 2002, the disclosures of which are incorporated by reference herein
- The present invention relates to injectable pharmaceutical compositions containing 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate (from now on also referred to as “BBR 2778”) as active ingredient in the form of a lyophilised powder with a carrier selected from lactose and dextran, mixed with sodium chloride.
- BBR 2778 is a novel anthracenedione derivative with anti-tumoral activity which acts as a DNA intercalating agent and topoisomerase II inhibitor. Pre-clinical studies demonstrate that its cardiotoxicity is lower than that of other known drugs belonging to the same class. BBR 2778 has proved more active than mitoxantrone against haematological tumours, especially ascitic L1210 leukaemia and YC-8 lymphoma, in a wide range of doses.
- Clinical trials on the use of BBR 2778 in the treatment of non-Hodgkin's lymphoma are at an advanced stage.
- The formulation of BBR2778 in injectable liquid pharmaceutical compositions has proved problematic in terms of stability in solution using common solvents suitable for parenteral administration, especially intravenous administration.
- A lyophilised formulation to be reconstituted with a suitable solvent such as saline immediately before use has therefore been considered.
- Here again, however, unforeseeable problems arose, partly due to the low solubility of BBR 2778 in water and the need to use sodium chloride solutions in concentrations ranging from 0.9 to 4%, in which the drug is progressively more soluble. However, the presence of sodium chloride requires the use of long lyophilisation cycles due to the low glass transition temperature observed.
- The choice of lyophilisation carrier has also proved critical in terms of the stability of the final formulation and in operational terms.
- For example, if mannitol is used as lyophilisation carrier, stable formulations are only obtained if they are stored at temperatures of approx. 5° C. or lower; stability studies conducted at 25° C. with 60% relative humidity (RH) showed unacceptable levels of degradation products after only one month. The characterisation of the finished product in the solid state demonstrates that BBR 2778 is transformed from a crystalline raw material to an amorphous powder in the lyophilisate, with a consequent reduction in stability. The choice of carriers with greater protective properties consequently focused on polymeric substances like polyvinylpyrrolidone (PVP, Povidone).
- Replacing mannitol with Povidone K 17 produced a stable lyophilisate even at 25° C., 60% RH, but Povidone has been removed from the list of excipients approved for parenteral administration in the USA (Fed. Reg. 8 Mar. 1999, Vol. 64, Num. 64) and requires a long lyophilisation cycle due to the low glass transition temperature observed (−37° C.), which requires primary drying to be conducted at a temperature below −37° C.
- Unsatisfactory results were also obtained with the use of other conventional lyophilisation carriers such as urea, glycine, ammonium chloride and TRIS in the presence and absence of sodium chloride, and by lyophilisation of BBR 2778 in the absence of excipients.
- It has now been found that it is possible to obtain stable lyophilised formulations of BBR 2778 in the presence of sodium chloride by using lactose or dextran as lyophilisation carrier.
- A first aspect of the invention therefore provides injectable pharmaceutical compositions containing 6,9-bis[(2-aminoethyl)amino]benzo[q]isoquinoline-5,10-dione dimaleate (BBR 2778) as active ingredient in the form of a lyophilised powder with a carrier selected from lactose and dextran, mixed with sodium chloride, to be reconstituted with a solvent suitable for reconstituting the lyophilisate and suitable for parenteral administration, which solvent is preferably contained in a separate ampoule.
- A further aspect of the invention relates to a process for the preparation of said compositions.
- In the compositions of the invention, the weight ratio between the carrier and sodium chloride is critical, and is typically between 1:1 and 3:1.
- The weight ratio between BBR 2778 and the carrier is preferably between 1:2 and 1:6. The particularly preferred carrier is lactose.
- The unit dose of BBR 2778 will usually be between 25 and 200 mg, and preferably between 50 and 100 mg. The unit dose currently being tested in clinical trials is 50 mg. For this latter quantity of active ingredient, the preferred compositions according to the invention will contain 100 to 200 mg of sodium chloride and 100 to 300 mg of lactose.
- If required, the compositions of the invention can also contain other excipients commonly used for parenteral formulations, such as antioxidants, buffers, local anaesthetics, salts, amino acids and the like.
- The vials or ampoules of sterile lyophilised powder will then be reconstituted at the time of use with sterile solvents constituted by sterile pyrogen-free water or sterile saline, in volumes of approx. 5 ml to 20 ml, depending on the active ingredient content.
- The compositions of the invention are prepared by a process which comprises lyophilisation of an aqueous solution of BBR 2778, lactose or dextran and sodium chloride by means of
- a freezing stage at a temperature below at least −45° C. for at least 3 hours;
- a primary drying stage consisting of increasing the temperature of the product to −35° C.±5° C. in approx. 3 hours and maintaining said temperature for at least 40 hours;
- a secondary drying stage consisting of increasing the temperature of the product to +30° C.±5° C. in 10 hours and maintaining said temperature for at least 8 hours.
- The compositions according to the invention are stable at room temperature for at least 24 months. The lyophilised product is not subject to deliquescence, and maintains its appearance unchanged over time.
- A further advantage of the invention is the reduction in lyophilisation times and the consequent reduction in the cost of the process.
- The following examples illustrate the invention in greater detail.
- Preparation of vials containing lyophilised BBR 2778 in the presence of lactose and sodium chloride.
- A solution containing 10 mg/ml of BBR 2778, 20 mg/ml of NaCl and 60 mg/ml of lactose, prepared by dissolving the various components in water for injection at 20-25° C., is distributed between type I glass vials under sterile conditions at the rate of 5 ml per vial, after sterile filtration. A lyophilisation stopper is placed on the mouth of the vials.
- The pre-stoppered vials are then loaded directly onto lyophilisation shelves and frozen at −45° C.±5° C. for at least 3 hours.
- Primary drying is conducted by increasing the temperature of the shelves in the vacuum freeze-dryer from −45° C. to −30° C.±3° C. in 3 hours, and maintaining the temperature at −30° C. for 40 hours.
- Secondary drying is performed by increasing the temperature of the shelves from −30° C. to +30° C.±3° C. in 10 hours and then maintaining said temperature of +30° C. for a further 8 hours. The freeze-dryer is returned to atmospheric pressure with nitrogen filtered under sterile conditions, and the vials are stoppered by activating the stoppering device. The vials are unloaded in a sterile environment and crimped.
- When reconstituted with 5 ml of water for injection, the solution has a pH of between 3.0 and 4.5.
- Accelerated stability tests conducted on the lyophilisate at 40° C. for 12 months have demonstrated a reduction in BBR 2778 titre within the limits of the specifications approved for the product, and a purity exceeding 95%. The stability is also confirmed at 25° C. even after the 12-month observation period.
- Preparation of vials containing lyophilised BBR 2778 in the presence of dextran and sodium chloride.
- A solution containing 10 mg/ml of BBR 2778, 20 mg/ml of NaCl and 60 mg/ml of dextran 40000, prepared by dissolving the various components in water for injection at 20-25° C., is distributed between type I glass vials under sterile conditions, at the rate of 5 ml per vial, after sterile filtration. A lyophilisation stopper is placed on the mouth of the vials.
- The pre-stoppered vials are then loaded onto trays, which are placed on the shelves of the freeze-dryer. The vials are then frozen in the lyophilisation chamber at −45° C.±5° C. for at least 3 hours.
- Primary drying is conducted by increasing the temperature of the shelves in the vacuum freeze dryer from −45° C. to 0° C.±2° C. in 6 hours and maintaining the temperature at 0° C. for 30 hours. The temperature of the product during primary drying is maintained at around −30° C.
- Secondary drying is performed by increasing the temperature of the shelves from 0° C. to +30° C.±2° C. in 3 hours and then maintaining said temperature of +30° C. for a further hours. The freeze-dryer is returned to atmospheric pressure with nitrogen filtered under sterile conditions, and the vials are stoppered by activating the stoppering device. The vials are unloaded in a sterile environment and crimped.
- When reconstituted with 5 ml of water for injection. the solution has a pH of between 3.0 and 4.5.
- Accelerated stability tests conducted on the lyophilisate at 40° C. for 4 months have demonstrated a reduction in BBR 2778 titre within the limits of the specifications approved for the product, and a purity exceeding 96%.
Claims (11)
1. A pharmaceutical composition comprising 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate and: i) a lactose carrier mixed with sodium chloride; or ii) a dextran carrier mixed with sodium chloride,
wherein the composition is in the form of a lyophilized powder.
2. The pharmaceutical composition of claim 1 , wherein the carrier is lactose.
3. The pharmaceutical composition of claim 1 , further comprising an antioxidant.
4. The pharmaceutical composition of claim 1 , wherein the weight ratio of the carrier to the sodium chloride is between 1:1 and 3:1.
5. The pharmaceutical composition of claim 1 , wherein the weight ratio of the 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate to the carrier is between 1:2 and 1:6.
6. An aqueous composition comprising 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate and: i) a lactose carrier mixed with sodium chloride; or ii) a dextran carrier mixed with sodium chloride,
wherein the concentration of the 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate in the composition ranges from 7-15 mg/ml.
7. The aqueous composition of claim 6 , comprising from 10 to 40 mg/ml sodium choloride and from 20 to 60 mg/ml lactose.
8. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises a unit dose of between 25 and 200 mg of 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate.
9. The pharmaceutical compositions of claim 8 , wherein the unit dose comprises 50 mg of 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate.
10. A kit comprising the pharmaceutical composition of claim 1 , and an ampoule containing a sterile solvent suitable to reconstitute the lyophilized powder, such that the lyophilized powder is suitable for parenteral administration.
11. A process for preparing the pharmaceutical composition of claim 1 , the process comprising:
lyophilizing an aqueous solution of 6,9-bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate in the presence of: i) lactose and sodium chloride; or ii) dextran and sodium chloride, wherein the step of lyophilizing comprises:
freezing the solution at a temperature below at least −45° C. for at least 3 hours;
drying the frozen solution to form a product, by increasing the temperature of the frozen solution to −35° C.±5° C. in approximately 3 hours and maintaining said temperature for at least 40 hours; and
then drying the product by increasing the temperature of the product to +30° C.±5° C. in 10 hours and maintaining said temperature for at least 8 hours.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US14/937,689 US20160256557A1 (en) | 2002-05-16 | 2015-11-10 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
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ITMI2002A001040 | 2002-05-16 | ||
IT2002MI001040A ITMI20021040A1 (en) | 2002-05-16 | 2002-05-16 | INJECTABLE PHARMACEUTICAL COMPOSITIONS OF AN ANTHROCENEDIONAL DERIVATIVE WITH ANTI-TUMOR ACTIVITY |
US10/514,301 US20060199831A1 (en) | 2002-05-16 | 2003-05-09 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
PCT/EP2003/004871 WO2003097101A1 (en) | 2002-05-16 | 2003-05-09 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
US12/964,861 US9211262B2 (en) | 2002-05-16 | 2010-12-10 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
US14/937,689 US20160256557A1 (en) | 2002-05-16 | 2015-11-10 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
Related Parent Applications (1)
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US12/964,861 Continuation US9211262B2 (en) | 2002-05-16 | 2010-12-10 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
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US20160256557A1 true US20160256557A1 (en) | 2016-09-08 |
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US10/514,301 Abandoned US20060199831A1 (en) | 2002-05-16 | 2003-05-09 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
US12/964,861 Active 2024-08-09 US9211262B2 (en) | 2002-05-16 | 2010-12-10 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
US14/937,689 Abandoned US20160256557A1 (en) | 2002-05-16 | 2015-11-10 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
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US10/514,301 Abandoned US20060199831A1 (en) | 2002-05-16 | 2003-05-09 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
US12/964,861 Active 2024-08-09 US9211262B2 (en) | 2002-05-16 | 2010-12-10 | Injectable pharmaceutical compositions of an anthracenedione derivative with anti-tumoral activity |
Country Status (12)
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US (3) | US20060199831A1 (en) |
EP (1) | EP1503797B1 (en) |
JP (1) | JP4624780B2 (en) |
AT (1) | ATE381944T1 (en) |
AU (1) | AU2003240613A1 (en) |
CA (1) | CA2486001C (en) |
DE (1) | DE60318310T2 (en) |
ES (1) | ES2298521T3 (en) |
FR (1) | FR12C0064I2 (en) |
IT (1) | ITMI20021040A1 (en) |
MX (1) | MXPA04011348A (en) |
WO (1) | WO2003097101A1 (en) |
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EP2106788A1 (en) * | 2008-04-04 | 2009-10-07 | Ipsen Pharma | Liquid and freeze dried formulations |
CN105769757B (en) * | 2016-03-26 | 2018-05-25 | 青岛市肿瘤医院 | A kind of parenteral solution for treating non-Hodgkin lymphoma and preparation method thereof |
CN105769776B (en) * | 2016-03-26 | 2018-05-11 | 青岛市肿瘤医院 | A kind of freeze-dried composition for treating non-Hodgkin lymphoma and preparation method thereof |
CN105997896B (en) * | 2016-05-28 | 2019-07-05 | 长沙秋点兵信息科技有限公司 | The injection freeze-dried powder and preparation method thereof for treating non-Hodgkin lymphoma |
CN106176630B (en) * | 2016-08-03 | 2019-01-04 | 湖北丽益医药科技有限公司 | A kind of preparation method of injection maleic acid Pixantrone aseptic powdery |
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US3590124A (en) * | 1967-06-27 | 1971-06-29 | Us Navy | Blood transfusion fluids having reduced turbulent friction properties |
JP2690009B2 (en) * | 1986-07-10 | 1997-12-10 | エーザイ 株式会社 | Cefalosporin injection |
NZ241868A (en) | 1991-03-08 | 1995-05-26 | Univ Vermont | 6,9-bis(substituted-amino)benzo[g]isoquinoline-5,10-diones, preparation and pharmaceutical compositions thereof |
JP3501471B2 (en) * | 1992-06-15 | 2004-03-02 | 旭化成ファーマ株式会社 | Stabilizing composition and method of calcitonin |
JPH08126685A (en) * | 1994-01-26 | 1996-05-21 | Shionogi & Co Ltd | Lyophilization of dextran compound |
US5587382A (en) * | 1994-03-28 | 1996-12-24 | Boehringer Mannheim Italia, Spa | 6,9-bis[(2-aminoethyl) amino]benzo [g]isoquinoline-5,10- dione dimaleate; an aza-anthracenedione with reduced cardiotoxicity |
MY122499A (en) * | 1997-11-10 | 2006-04-29 | Searle & Co | Use of alkylated iminosugars to treat multidrug resistance |
GB9808922D0 (en) * | 1998-04-24 | 1998-06-24 | Cantab Pharmaceuticals Res Ltd | Virus preparations |
TWI233805B (en) * | 1999-07-01 | 2005-06-11 | Fujisawa Pharmaceutical Co | Stabilized pharmaceutical composition in lyophilized form as antifungal agent |
IT1315253B1 (en) * | 1999-10-22 | 2003-02-03 | Novuspharma Spa | LIPOSOMIAL PREPARATION OF 6,9-BIS- (2-AMINOXYL) AMINO | BENZOG | ISOCHINOLIN-5,10-DIONE DIMALEATO |
-
2002
- 2002-05-16 IT IT2002MI001040A patent/ITMI20021040A1/en unknown
-
2003
- 2003-05-09 JP JP2004505097A patent/JP4624780B2/en not_active Expired - Lifetime
- 2003-05-09 ES ES03729997T patent/ES2298521T3/en not_active Expired - Lifetime
- 2003-05-09 MX MXPA04011348A patent/MXPA04011348A/en active IP Right Grant
- 2003-05-09 AT AT03729997T patent/ATE381944T1/en not_active IP Right Cessation
- 2003-05-09 AU AU2003240613A patent/AU2003240613A1/en not_active Abandoned
- 2003-05-09 WO PCT/EP2003/004871 patent/WO2003097101A1/en active IP Right Grant
- 2003-05-09 EP EP03729997A patent/EP1503797B1/en not_active Expired - Lifetime
- 2003-05-09 US US10/514,301 patent/US20060199831A1/en not_active Abandoned
- 2003-05-09 CA CA2486001A patent/CA2486001C/en not_active Expired - Lifetime
- 2003-05-09 DE DE60318310T patent/DE60318310T2/en not_active Expired - Lifetime
-
2010
- 2010-12-10 US US12/964,861 patent/US9211262B2/en active Active
-
2012
- 2012-10-25 FR FR12C0064C patent/FR12C0064I2/en active Active
-
2015
- 2015-11-10 US US14/937,689 patent/US20160256557A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2003097101A1 (en) | 2003-11-27 |
ATE381944T1 (en) | 2008-01-15 |
US20060199831A1 (en) | 2006-09-07 |
ES2298521T3 (en) | 2008-05-16 |
AU2003240613A1 (en) | 2003-12-02 |
FR12C0064I2 (en) | 2013-08-16 |
ITMI20021040A0 (en) | 2002-05-16 |
DE60318310D1 (en) | 2008-02-07 |
FR12C0064I1 (en) | 2012-12-14 |
DE60318310T2 (en) | 2008-12-11 |
US20110144147A1 (en) | 2011-06-16 |
US9211262B2 (en) | 2015-12-15 |
JP4624780B2 (en) | 2011-02-02 |
EP1503797B1 (en) | 2007-12-26 |
CA2486001A1 (en) | 2003-11-27 |
EP1503797A1 (en) | 2005-02-09 |
MXPA04011348A (en) | 2005-08-15 |
CA2486001C (en) | 2010-04-13 |
ITMI20021040A1 (en) | 2003-11-17 |
JP2005530792A (en) | 2005-10-13 |
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