Classifications

• • 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
  • A61K9/08—Solutions
• • 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
  • A61K31/16—Amides, e.g. hydroxamic acids
  • A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
• • 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
  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5355—Non-condensed oxazines and containing further heterocyclic rings
• • 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
  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5375—1,4-Oxazines, e.g. morpholine
  • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
• • 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
  • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
  • A61K47/12—Carboxylic acids; Salts or anhydrides thereof
• • 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
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
  • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
  • C07B2200/13—Crystalline forms, e.g. polymorphs

Definitions

• the present invention relates to a pharmaceutical formulation comprising 1 - (4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl- 1 ,3,5-triazin-2-yl)phenyl]urea, or a pharmaceutically acceptable salt thereof.
• the present invention relates to a pharmaceutical aqueous formulation comprising 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6- dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea, or a pharmaceutically acceptable salt thereof, that is a clear solution.
• a pharmaceutical aqueous formulation comprising 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6- dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea, or a pharmaceutically acceptable salt thereof, that is a clear solution.
• a pharmaceutically acceptable salt thereof that is a clear solution.
• the compound is an inhibitor of PI3 kinase and mTOR that is useful for the treatment of cancer.
• 4-yl-1 ,3,5-triazin-2-yl)phenyl]urea may be prepared in crystalline form and is chemically and physically stable at 25°C and 60% Relative Humidity (RH) for up to 3 years in this form.
• RH Relative Humidity
• this free base is insufficiently water soluble to allow the preparation of an aqueous solution formulation suitable for intravenous or parenteral administration at the therapeutic dosage levels required.
• the formulation is suitable for intravenous administration of 1 -(4-
• an intravenous formulation of any drug is a solution to facilitate safe and effective administration to a patient. It must be particle-free, and not form a gel or suspension. A clear, aqueous solution is preferred.
• a clear solution is defined as a visually clear solution essentially free from any visible particulates that can be observed on a visual inspection. Generally, if any particulate matter is observed, the formulation is not suitable for intravenous administration and should not be utilised as occlusion of blood vessels may occur. Accordingly, in view of the qualitative nature of the visual test, the term "essentially free from any visible particulates" is usually applied when no visible particulate matter is observed.
• Particulate matter may be defined as follows:
• ⁇ particulates with a definite shape or characteristic can be described as glasslike, metallic-looking, etc.
• the visual inspection can be conducted in accordance with the method defined in European Pharmacopoeia Method 2.9.20 entitled " Particulate
• Figure 2 "Figure 2.9.20.-1 " shown in Figure 2) consists of a viewing station comprising:
• an adjustable lampholder fitted with a suitable, shaded, white-light source and with a suitable light diffuser (a viewing illuminator containing two 13 Watt fluorescent tubes, each 525 mm in length, is suitable).
• the intensity of illumination at the viewing point is maintained between 2000 lux and 3750 lux, although higher values are preferable for coloured glass and plastic containers.
• the Method states: "Remove any adherent labels from the container and wash and dry the outside. Gently swirl or invert the container, ensuring that air bubbles are not introduced, and observe for about 5 seconds in front of the white panel. Repeat the procedure in front of the black panel. Record the presence of any particles. "
• Such a formulation can be directly administered to the patient (in order to avoid degradation occurring), intravenously or parenterally, preferably with the addition of a tonicity modifier.
• a formulation optionally containing a bulking agent and/or tonicity modifier, may be first freeze-dried to prepare a lyophilised solid composition that is chemically stable on storage for preferably at least 2 years, and which lyophilised solid composition then can be constituted, or reconstituted, to provide a clear aqueous solution, preferably with the addition of a tonicity modifier, as necessary, immediately prior to administration to a patient by the intravenous (or parenteral) route.
• the invention provides a pharmaceutical aqueous solution formulation comprising 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea, lactic acid and water, wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of less than 6mg/ml and sufficient lactic acid is present to provide a clear solution.
• the concentration of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3- [4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea in the formulation of the invention may be from 1 to 5.5 mg/ml, from 2 to 5.5 mg/ml, or from 3 to 5.5mg/ml (calculated as the named free base),
• the invention provides a pharmaceutical aqueous solution formulation wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3- [4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of from 2.5 to 5.5mg/ml.
• the invention provides a pharmaceutical aqueous solution formulation wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3- [4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of about 5mg/ml.
• lactic acid when the free base of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is used, above 2.5 mole equivalents of lactic acid are present in the formulation of the invention. More preferably, from 3 to 10, from above 2.5 to 8.0, or from 3.5 to 4.5 mole equivalents of lactic acid are present in the formulation of the invention. Most preferably, about 4.1 mole equivalents of lactic acid are present in the formulation of the invention.
• the invention provides a pharmaceutical aqueous solution formulation wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of from 5.0 to 5.5mg/ml and at least 2.5 mole equivalents of lactic acid are present.
• the invention provides a pharmaceutical aqueous solution formulation wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of about 5mg/ml and at least 2.5 mole equivalents of lactic acid are present.
• the invention provides a pharmaceutical aqueous solution formulation comprising 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6- dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea, lactic acid and water, wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin- 4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a
• the formulation of the invention may be prepared using the 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea free base or using a lactic acid salt of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea.
• the invention provides a pharmaceutical aqueous solution formulation comprising 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea lactate, lactic acid and water, wherein 1-(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of about 5mg/ml, and at least 1 .5 mole equivalents of lactic acid are present
• DL-lactic acid D-lactic acid or L-lactic acid, or any combination thereof, may be used in the formulation of the invention.
• DL-lactic acid is used, preferably, the pH of the formulation of the invention is not greater than 3.7. More preferably, the pH of the formulation of the invention is from 3.0 to 3.7, from 3.3 to 3.6, or from 3.4 to 3.5.
• the present invention provides a pharmaceutical aqueous solution formulation comprising 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea, lactic acid and water, wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of up to 5.5 mg/ml, and above 2.5 mole equivalents of lactic acid are present and in an amount sufficient to ensure a clear solution is formed with a pH of no greater than 3.7.
• the present invention provides a pharmaceutical aqueous solution formulation comprising 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea, lactic acid and water, wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of about 5mg/ml, and about 4.1 mole equivalents of lactic acid are present and in an amount sufficient to ensure a clear solution is formed with a pH of no greater than 3.7.
• a crystalline form of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3- [4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea L-lactate may be used to prepare the formulation of the invention.
• the invention provides a pharmaceutical aqueous solution formulation comprising 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea, orthophosphoric acid and water, wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin- 1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of less than 4 mg/ml and sufficient orthophosphoric acid is present to provide a clear solution,
• the invention provides a pharmaceutical aqueous solution formulation wherein 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3- [4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of from 3.0 to 3.5mg/ml.
• the invention provides a pharmaceutical aqueous solution formulation wherein at least 5 mole equivalents of orthophosphoric acid are used.
• the invention provides a pharmaceutical aqueous solution formulation wherein from 5 to 7 mole equivalents of orthophosphoric acid are used.
• the present invention provides a pharmaceutical aqueous solution formulation comprising 1-(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea, orthophosphoric acid and water, wherein 1-(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of less than 4mg/ml, from 5 to 7 mole equivalents of orthophophoric acid are present and in an amount sufficient to ensure a clear solution is formed.
• the pH of the formulation prepared is from 2-2.5 prior to
• the pH is then preferably adjusted to from 3.0-4.5 for intravenous administration.
• a bulking agent is preferably added to the formulation prior to the freeze-drying process commencing.
• the primary function of the bulking agent is to provide the freeze-dried solid with a non-collapsible, structural integrity that will allow rapid reconstitution on constitution of the aqueous formulation prior to administration, and it should also facilitate efficient lyophilisation.
• Bulking agents are typically used when the total mass of solutes in the formulation is less than 2g/100ml. Bulking agents may also be added to achieve isotonicity with blood.
• the bulking agent may be selected from a saccharide, sugar alcohol, amino acid or polymer, or be a mixture of two or more of any thereof.
• the bulking agent is a sugar or sugar alcohol, or a mixture thereof.
• the sugar is sucrose.
• the sugar alcohol is mannitol.
• Reconstitution of the lyophilized solid composition may be achieved by addition of the requisite quantity of water that was present prior to lyophilisation in order that a clear solution is obtained.
• a tonicity modifier may then be added prior to use.
• Constitution of the lyophilized solid composition may be achieved using an appropriate quantity of water and/or an aqueous solution of a suitable tonicity modifier in order to ensure that a clear solution is obtained.
• a tonicity modifier must be present prior to intravenous or parenteral administration of the formulation to a patient by injection to avoid crenation or hemolysis of red blood cells, and to mitigate or avoid pain and discomfort to the patient. This requires that the formulation to be administered to the patient has an effective osmotic pressure that is approximately the same as that of the blood of the patient.
• Suitable tonicity modifiers are non-ionic tonicity modifiers such as glycerol, sorbitol, mannitol, sucrose, propylene glycol or dextrose, or a mixture of any 2 or more thereof.
• the non-ionic tonicity modifier is dextrose, sucrose or mannitol, or is a mixture of any 2 or more thereof.
• Aqueous pharmaceutical formulations that are suitable for intravenous administration generally have a pH of from 3 to 9.
• the formulations of the invention that are to be intravenously administered preferably have a pH of from 3 to 4.5.
• the formulation of the invention may be used for the curative, palliative or prophylactic treatment of cancer in a mammal, including a human being.
• the cancer to be treated may be selected from the group consisting of leukemia, skin cancer, bladder cancer, breast cancer, uterus cancer, ovary cancer, prostate cancer, lung cancer, colon cancer, pancreas cancer, renal cancer, gastric cancer and brain cancer.
• the weekly dose of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3- [4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea to be administered by the intravenous route for the treatment of cancer using the formulations disclosed herein is preferably in the range of from 100-400mg/ml per week.
• the solution was sterile filtered through an in-line 0.45 pm clarification filter and 0.22 pm filter assembly. This solution was then filled into 50 ml_ vials with a target fill volume of 20.8 ml_ for each vial.
• the vials were each partially stoppered (not sealed) with a 20mm Gray Lyo D777-1 V10-F597W FluroTec Siliconised (trade mark) stopper.
• the freeze dryer was back-filled with sterile filtered nitrogen to a set point of ca. 700mbar (70,000 Pascals), and the vials were fully closed using the stoppers. The freeze dryer was then vented to atmospheric pressure using sterile filtered air and the vials were unloaded from the freeze dryer.
• Each vial contained the freeze dried (lyophilised) formulation as a white solid.
• EXAMPLE 3 Reconstitution of a 5mq/ml pharmaceutical aqueous solution formulation comprising 1 -(4- ⁇ r4-(dimethylamino)piperidin-1 -yl1carbonyl)phenyl)-3-r4-(4,6-dimorpholin-4-yl- 1 ,3,5-thazin-2-yl)phenyl1urea, DL-lactic acid and mannitol from a lyophilised solid composition
• the vials of lyophilised solid composition samples prepared in Example 2(b) were reconstituted as follows.
• One of the reconstituted vials was visually inspected using a method based on that of European Pharmacopoeia Method 2.9.20 described above. The method is designed to observe the presence of any visible particles.
• the solution in the vial was assessed for the presence of sub-visible particles using a HIAC apparatus (trade mark) by using a sub-visible particulate determination method that is based on that defined in United States Pharmacopoeia 36 ⁇ 788> Method 1 ("Light Obscuration Particle Count Test').
• Method 1 Light Obscuration Particle Count Test'
• the results must comply with the criteria for "Test 1 . B" for USP 36 ⁇ 788> Method 1 as these define the widest possible acceptable limits for sub-visible particulate matter.
• This Test states as follows: "Test 1.B (Solutions for parenteral infusion or solutions for injection supplied in containers with a nominal content of less than 100 mL) -The preparation complies with the test if the average number of particles present in the units tested does not exceed 6000 per container equal to or greater than 10 pm and does not exceed 600 per container equal to or greater than 25 pm".
• 1 ,3,5-triazin-2-yl)phenyl]urea (52mg) was weighed into a 2ml vial.
• the slurry was heated to 60°C at a rate of 5°C/minute, held at 60°C for 20min. and then cooled at 0.1 °C/minute to 5°C where it was held until it was isolated (24 hours after the start of the heating step).
• the slurry was filtered through a 0.2 pm nylon centrifuge filter to isolate the crystalline title compound.
• Citric Acid at pH 2.94 13.3mM Citric Acid at pH 2.94
• 5.47772g of Citric Acid Anhydrous was added to approximately 75ml_ of WFI.
• 1.42293g of Sodium Citrate Dihydrate was added to this solution. This was then made to 1 L volume in a volumetric flask using WFI. pH was then recorded.
• Acid at pH 1.79 0.38864g of Maleic Acid was dissolved in approximately 75ml_ of WFI. This was then made up to 100ml_ volume in a volumetric flask using WFI. pH was then recorded. Acid at pH 2.46 (9) 0.44667g of Malic Acid was dissolved in approximately 75ml_ of WFI. This was then made to 100ml_ volume in a volumetric flask using WFI. pH was then recorded.
• Acid* was dispensed into a 100ml_ volumetric flask and made up to volume using WFI. pH was then recorded.
• the stability testing was conducted using three ca. 3mg/ml samples of 1 -(4- ⁇ [4- (dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5- triazin-2-yl)phenyl]urea for each acid buffer prepared above.
• orthophosphoric acid would not be suitable for the preparation of pharmaceutical aqueous solution formulations for intravenous administration to a patient at a required API (active pharmaceutical ingredient) concentration.
• API active pharmaceutical ingredient
• the stability testing was conducted using three ca. 3mg/ml samples of 1 -(4- ⁇ [4- (dimethylamino)piperidin-l -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5- triazin-2-yl)phenyl]urea for each acid buffer prepared above.
• Citric Acid at pH 2.98 13.3mM Citric Acid at pH 2.98
• 0.27346g of Citric Acid Anhydrous was dissolved in approximately 40ml_ of WFI.
• 0.07284g of Sodium Citrate Dihydrate was also added to this solution. This was then dispensed into a 50ml_ volumetric flask and made to volume using WFI. pH was then recorded.
• the stability testing was conducted using three ca. 4mg/ml samples of 1 -(4- ⁇ [4- (dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5- triazin-2-yl)phenyl]urea for each acid buffer prepared above.
• the buffer solutions are prepared using WFI in 10ml (*20ml where indicated in the Table below) volumetric flasks using the following DL-lactic acid weights (** 90% W W DL-LACTIC ACID IN WATER):
• Samples 1 - 1 1 were placed on a roller bed at room temperature and at 50rpm for ca. 21 .5 hours.
• Samples 12 and 13 were placed on a roller bed at room temperature and at 50rpm for ca. 23 hours.
• Samples 14 and 15 were placed on a roller bed at room temperature and at 50rpm for ca. 25 hours.
• the solution concentration of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3- [4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea must be less than 6mg/ml and more than 2.5 mole equivalents of DL-lactic acid must be used in the formulation.
• Samples 1 -1 1 were stored at room temperature without rolling for further time to provide a total experimental period of ca. 72 hours. It was observed that some samples became a solution at the end of the total 72 hour period that were not in solution after the initial ca. 21 .5 hour rolling period.
• Samples 14 and 15 were stored with rolling at room temperature for further time to provide a total experimental period of ca. 73 hours.
• a clear solution is also achievable using a solution concentration of 3mg/ml of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3- [4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea where above 2.5 mole equivalents of DL-lactic acid are used in the formulation.
• the results above for Samples 14 and 15 show that clear solutions are achievable at a solution
• a ca. 33.3mM aqueous orthophosphoric acid solution was prepared as follows. 0.32569g of orthophosphoric acid was dispensed into ca. 80mL of water for irrigation. This was made to 100mL volume using water for irrigation in a volumetric flask and the pH was recorded as 1 .92. A 3mg/ml_ concentration of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)- 3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea was desired and this had to take account of a drug potency of 97.1 %.
• the 3 samples were therefore each diluted to 0.5mg/ml_, 0.1 mg/ml_ and 0.05mg/ml_ to identify if the pH increased to a suitable pH for intravenous administration.
• the diluted samples were placed on a roller bed overnight in order to reach equilibrium. The pH was also measured. The pH of the samples was as follows:
• Each of the samples was visually assessed using a light box as described in European Pharmacopoeia Method 2.9.20 (above), inspecting the samples against a black and a white background.
• the sample was also tested by illumination using a narrow (Tyndall) beam light source and then visually inspected from a direction perpendicular to the light beam in order to identify undissolved solid particles. Each sample was observed to be a visually clear solution.
• Lactic acid is therefore generally more suitable than orthophosphoric acid for the preparation of an aqueous solution formulation for intravenous administration of 1 -(4- ⁇ [4- (dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5- triazin-2-yl)phenyl]urea according to the invention. 5. Investigation regarding 3mq/ml, 4mq/ml and 5mq/ml aqueous
• API Three concentrations of API (3, 4 and 5mg/ml_) were desired which had to be corrected to take account of an API potency of 97.1 %.
• the API weights were determined according to the following calculations.
• the samples were placed on a roller bed at room temperature and visually assessed using a light box as described in European Pharmacopoeia Method 2.9.20 (above), inspecting the samples against a black and a white background.
• the sample was also tested by illumination using a narrow (Tyndall) beam light source and then visually inspected from a direction perpendicular to the light beam in order to identify undissolved solid particles.
• the visual analysis was carried out at 24 hour, 48 hour, 72 hour and 6 day periods.
• the pH of the samples was assessed as follows:
• orthophosphoric acid dispensed into ca. 75 mL of water for irrigation. This was made to 100 mL volume using water for irrigation in a volumetric flask and the pH was recorded as 1 .94. 3 and 3.5 mg/mL formulations of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea was desired and this had to take account of a drug potency of 97.1 %.
• the 3mg/ml aqueous formulation used contained ca. 6.8 mole equivalents of orthophosphoric acid.
• the samples were placed on a roller bed at room temperature for 15 hours.
• Lactic acid is therefore preferable for the preparation of a clear, particle-free aqueous solution formulation of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6- dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea that is suitable for intravenous or parenteral administration.
• the powder X-ray diffraction (PXRD) analysis was carried out on a Bruker D4 (trade mark) diffractometer using copper radiation (wavelength: 1 .5406A).
• the tube voltage and amperage were set to 35 kV and 40 mA, respectively.
• the divergence slit used was v6 and the scattering slit was set at 0.499 mm.
• a variable receiving slit was used.
• Diffracted radiation was detected by a Vantec detector.
• a theta-two theta continuous scan at 5.4 min (0.2 sec/0.018° step) from 2.0 to 55 ° 2 ⁇ was used.
• a corundum standard was analyzed to check the instrument alignment. The data were collected and analysed using Bruker AXS software.
• the samples were prepared by placing them on a silicon wafer.
• DIFFRAC.EVA V3.1 software was used to visualize and evaluate the PXRD spectra.
• the PXRD data files (.raw) were not processed prior to peak searching.
• a threshold value of 1.3 and a width value of 0.3 were used to make the preliminary peak assignments.
• the output of automated assignments was visually checked to ensure validity and adjustments manually made if necessary.
• peaks were manually assigned within the spectra, if appropriate. A peak at 28.1 ° 2-theta that related to the mounting medium was manually removed from the list.
• the sample is typically placed onto a flat silicon plate.
• the sample powder is pressed by a glass slide or equivalent to ensure a random surface and proper sample height.
• the sample holder is then placed into the instrument.
• the incident X-ray beam is directed at the sample, initially at a small angle relative to the plane of the holder, and then moved through an arc that continuously increases the angle between the incident beam and the plane of the holder.
• X-ray powder analyses result from a variety of factors including: (a) errors in sample preparation (e.g., sample height), (b) instrument errors (e.g. flat sample errors), (c) calibration errors, (d) operator errors (including those errors present when determining the peak locations), and (e) the nature of the material (e.g. preferred orientation and transparency errors). Calibration errors and sample height errors often result in a shift of all the peaks in the same direction. Small differences in sample height when using a flat holder will lead to large displacements in the PXRD peak positions.
• this correction factor will bring the measured peak positions from the Bruker into agreement with the expected peak positions and may be in the range of from 0 to 0.2 degree 2-theta.
• This crystalline form of 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea L-lactate is distinguished from other known (semi-crystalline) forms of this salt by having characterizing peaks at about 6.5, 15.9, 20.9, 22.1 and 23.1 degrees 2-theta (+/- 0.2 degrees 2-theta).
• Samples of a lyophilised solid formulation prepared in accordance with the method of Example 2 in 50ml_ clear vials were analysed for chemical degradation after storage at 25°C/60% Relative Humidity (RH) and 40°C/75% RH at a variety of different timepoints. Several samples were evaluated for each condition to allow representative results at the selected timepoints. The 40°C/75% RH samples were tested after 6 months.
• RH Relative Humidity
• the 25°C/60% RH samples were tested after 6 months, 12 months, 24 months and 36 months.
• the samples were tested for chemical purity using High Performance Liquid
• HPLC Chromatography
• Sample solvent Add 3 mL of 0.1 N aqueous hydrochloric acid into a 1000 mL volumetric flask and dilute to set volume with the Diluent (Acetonitrile/water, 1 : 1 v/v). Mix well.
• Standard and Check standard preparations • Accurately prepare two solutions of ca. 2 mg/mL (+/- 10%) of 1 -(4- ⁇ [4- (dimethylamino)piperidin-1 -yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl- 1 ,3,5-triazin-2-yl)phenyl]urea Reference Standard in Sample solvent, and record the concentrations accurately of both. These are the Standard and Check standard solutions. Produce Standard and Check standard
• Example 2 by adding 20 mL of water to each vial, shaking the vial to dissolve the solid and wait for the bubbles to disappear. Transfer the solution into a l OOOmL volumetric flask. Rinse each vial at least twice with Diluent and transfer the washings into the volumetric flask. Dilute to the set volume with Diluent.
• Liquid chromatographic system e.g. Waters 2695 (trade mark) or Agilent 1 100 (trade mark) machine
• test samples are injected between standard preparation injections.
• For each injection standard and sample, measure the retention time and area of the 1 -(4- ⁇ [4-(dimethylamino)piperidin-1 - yl]carbonyl ⁇ phenyl)-3-[4-(4,6-dimorpholin-4-yl-1 ,3,5-triazin-2-yl)phenyl]urea peak in each chromatogram.
• For each sample injection also measure the retention times and peak area of any peaks present in the sample injection that do not appear in the blank injection.
• Degradants 3, 5 and 6 were identified as process related impurities which did not change on stability, and so were not reported at the 36 month timepoint.
• samples of a lyophilised solid formulation prepared in accordance with the method of Example 2 in a 50ml_ clear vial are chemically stable for at least 36 months at 25°C/60% RH and for at least 6 months at 40°C/75% RH.

Landscapes

• Health & Medical Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Veterinary Medicine (AREA)
• Medicinal Chemistry (AREA)
• Public Health (AREA)
• Pharmacology & Pharmacy (AREA)
• Animal Behavior & Ethology (AREA)
• Epidemiology (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• General Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Molecular Biology (AREA)
• Biochemistry (AREA)
• Dermatology (AREA)
• Inorganic Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Plural Heterocyclic Compounds (AREA)
• Medicinal Preparation (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Priority Applications (21)

Applications Claiming Priority (4)

Related Child Applications (2)

Publications (1)

Family

ID=54937330

Family Applications (1)

Country Status (25)

Cited By (5)

Citations (2)

Family Cites Families (8)

• 2015
  • 2015-12-10 US US15/534,999 patent/US10172942B2/en active Active
  • 2015-12-10 SG SG11201703826TA patent/SG11201703826TA/en unknown
  • 2015-12-10 KR KR1020177016417A patent/KR102016822B1/ko active Active
  • 2015-12-10 EP EP15813578.0A patent/EP3233054B1/en active Active
  • 2015-12-10 MX MX2017008072A patent/MX380172B/es unknown
  • 2015-12-10 CN CN201580068063.3A patent/CN107205923B/zh active Active
  • 2015-12-10 RS RS20211128A patent/RS62337B1/sr unknown
  • 2015-12-10 PT PT158135780T patent/PT3233054T/pt unknown
  • 2015-12-10 NZ NZ731518A patent/NZ731518A/en unknown
  • 2015-12-10 SI SI201531687T patent/SI3233054T1/sl unknown
  • 2015-12-10 HU HUE15813578A patent/HUE055928T2/hu unknown
  • 2015-12-10 PL PL15813578T patent/PL3233054T3/pl unknown
  • 2015-12-10 DK DK15813578.0T patent/DK3233054T3/da active
  • 2015-12-10 LT LTEPPCT/IB2015/059515T patent/LT3233054T/lt unknown
  • 2015-12-10 WO PCT/IB2015/059515 patent/WO2016097949A1/en not_active Ceased
  • 2015-12-10 ES ES15813578T patent/ES2881214T3/es active Active
  • 2015-12-10 RU RU2017119282A patent/RU2672875C1/ru active
  • 2015-12-10 HR HRP20211446TT patent/HRP20211446T1/hr unknown
  • 2015-12-10 AU AU2015365497A patent/AU2015365497B2/en active Active
  • 2015-12-14 TW TW104141933A patent/TWI660729B/zh active
  • 2015-12-14 CA CA2915199A patent/CA2915199C/en active Active
  • 2015-12-15 JP JP2015243831A patent/JP6420753B2/ja active Active
• 2017
  • 2017-05-08 IL IL252158A patent/IL252158B/en active IP Right Grant
  • 2017-06-01 ZA ZA201703764A patent/ZA201703764B/en unknown
• 2018
  • 2018-11-13 US US16/189,009 patent/US10660959B2/en active Active
• 2021
  • 2021-09-28 CY CY20211100851T patent/CY1124527T1/el unknown

Patent Citations (2)

Non-Patent Citations (2)

Also Published As

Similar Documents

Legal Events