WO2013072304A1 - Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 - Google Patents
Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 Download PDFInfo
- Publication number
- WO2013072304A1 WO2013072304A1 PCT/EP2012/072482 EP2012072482W WO2013072304A1 WO 2013072304 A1 WO2013072304 A1 WO 2013072304A1 EP 2012072482 W EP2012072482 W EP 2012072482W WO 2013072304 A1 WO2013072304 A1 WO 2013072304A1
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- WIPO (PCT)
- Prior art keywords
- container
- dose
- water
- pharmaceutical preparation
- solution
- Prior art date
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- 239000005495 thyroid hormone Substances 0.000 title claims abstract description 22
- 229940036555 thyroid hormone Drugs 0.000 title claims abstract description 22
- 239000000825 pharmaceutical preparation Substances 0.000 title claims description 16
- AUYYCJSJGJYCDS-LBPRGKRZSA-N Thyrolar Chemical compound IC1=CC(C[C@H](N)C(O)=O)=CC(I)=C1OC1=CC=C(O)C(I)=C1 AUYYCJSJGJYCDS-LBPRGKRZSA-N 0.000 claims abstract description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 65
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 27
- 235000019441 ethanol Nutrition 0.000 claims description 27
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- 229920000573 polyethylene Polymers 0.000 claims description 24
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 18
- -1 polyethylene Polymers 0.000 claims description 18
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- 229940088597 hormone Drugs 0.000 claims description 14
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 10
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
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- RZXDTJIXPSCHCI-UHFFFAOYSA-N hexa-1,5-diene-2,5-diol Chemical compound OC(=C)CCC(O)=C RZXDTJIXPSCHCI-UHFFFAOYSA-N 0.000 claims description 2
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- MXNUCYGENRZCBO-UHFFFAOYSA-M sodium;ethene;2-methylprop-2-enoate Chemical class [Na+].C=C.CC(=C)C([O-])=O MXNUCYGENRZCBO-UHFFFAOYSA-M 0.000 claims description 2
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- 229940035722 triiodothyronine Drugs 0.000 abstract description 4
- XUIIKFGFIJCVMT-GFCCVEGCSA-N D-thyroxine Chemical compound IC1=CC(C[C@@H](N)C(O)=O)=CC(I)=C1OC1=CC(I)=C(O)C(I)=C1 XUIIKFGFIJCVMT-GFCCVEGCSA-N 0.000 abstract description 3
- XUIIKFGFIJCVMT-LBPRGKRZSA-N L-thyroxine Chemical compound IC1=CC(C[C@H]([NH3+])C([O-])=O)=CC(I)=C1OC1=CC(I)=C(O)C(I)=C1 XUIIKFGFIJCVMT-LBPRGKRZSA-N 0.000 abstract description 2
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- 229950008325 levothyroxine Drugs 0.000 abstract description 2
- 238000011169 microbiological contamination Methods 0.000 abstract description 2
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
-
- 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
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J3/00—Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
- A61J3/07—Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms into the form of capsules or similar small containers for oral use
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
- A61K31/198—Alpha-aminoacids, e.g. alanine, edetic acids [EDTA]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
-
- 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
- A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
-
- 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
Definitions
- the present invention relates to a pharmaceutical preparation of thyroid hormones T3 and T4.
- the invention relates to a pharmaceutical preparation of thyroid hormones T3 and T4 in water-alcohol solution, suitable for oral administration and characterised by high physical, chemical and microbiological stability.
- the invention also relates to the use of said pharmaceutical preparation in the treatment of disorders caused by hormone T3 and/or T4 deficiency.
- the thyroid hormones triiodothyronine or liothyronine (T3) and tetraiodothyronine or thyroxine (T4) are secreted by the follicular cells of the thyroid gland in response to the pituitary-gland hormone TSH, the production of which is regulated in turn by the hypothalamic hormone T H.
- TSH pituitary-gland hormone
- T H hypothalamic hormone
- the secretion of thyroid hormones follows a circadian rhythm; the highest levels of T3 and T4 are reached during the night and the early hours of the morning.
- T3 and T4 are essential for the normal body growth of children and for the maturation of the various apparatuses, especially the skeleton, and regulate metabolic activity in the adult, influencing the function of every organ and tissue.
- T3 and T4 increase oxygen consumption at rest, raising the basal metabolism, the body temperature and the daily calorie requirement. They regulate carbohydrate metabolism, promoting glycogenolysis and gluconeogenesis, and increase the activity of the enzymes involved in glucose oxidation.
- the thyroid hormones are involved in lipolysis and lipogenesis, regulate protein synthesis, exercising a trophic effect on the muscle, and affect the cardiovascular system.
- Thyroid hormones are essential to the cardiac function: they increase myocardial contractility (positive inotropic effect), increase the heart rate (positive chronotropic effect) and increase venous return to the heart.
- the effect of the thyroid hormones is mainly anabolic at low doses, whereas they have a catabolic action at high doses.
- a treatment based on T3 and/or T4 is required, administered as such or in the form of sodium salts or hydrates.
- T3 and T4 Treatment with thyroid hormones continues throughout the patient's life, and the posology (dose and frequency of administration) is customized according to the patient's response.
- the initial dose of T3 and T4 is usually low.
- the dose is then gradually increased until the clinical evaluation and laboratory tests indicate an optimum response. Selecting the dose is a critical aspect: an under-dose leads to a poor response, while an excessive dose can produce toxic symptoms of hyperthyroidism such as tachycardia, sweating, weight loss, nervousness, diarrhoea, bone resorption due to activation of the osteoclasts, and heart problems.
- T3 and T4 hormones are on the market in solid form (regular tablets and soft gelatin capsules) and in liquid oral form in drops.
- This last pharmaceutical form makes the hormones immediately available for gastrointestinal absorption, and usually consists of a solution in a single multi-dose glass container with a dropper.
- the use of the dropper makes it difficult to measure accurately the volume of solution dispensed, and therefore the dose administered.
- T4 solution with a concentration of 100 ⁇ g/mL is used, for example, T4 doses of between 3.5 and 200 ⁇ g may be administered. Assuming that each drop (approx.
- 35 ⁇ .) contains 3.5 ⁇ g of T4, the administration of the maximum dose of 200 ⁇ g requires no less than 57 drops to be dispensed (2 mL). Moreover, the volume of the drops dispensed is not precisely replicable. The use of a dropper may therefore not guarantee the necessary dose accuracy, which is provided by other forms of administration such as tablets or soft capsules available in a variety of doses to allow optimum individual treatments.
- formulation ingredients for pharmaceutical use with high vapor pressure in general, such as alcohols, or inert gases, such as nitrogen, can act as solvents of the active ingredients present in the finished product or as preservatives, and can also, in synergy with other ingredients present in the pharmaceutical form, promote the physical and chemical stability of the finished product.
- Volatile organic solvents such as ethanol are used to facilitate the dissolution of hormones T3 and/or T4. Adequate containment of volatile substances is necessary to guarantee the physical and chemical stability of the product. Evaporation of said substances from the formulation through the primary packaging material must be prevented, to avoid a gradual reduction in their concentration over time.
- Patent application WO2010/086030 discloses a single-dose squeezable container for solutions of T3/T4 hormones, which is made of plastic with a Young's modulus of between 10 and 80 MPa, and in particular of a mixture of polyethylene or polypropylene with ethylene vinyl acetate.
- said container presents optimum squeezability characteristics which ensure that the solution is completely emptied, it is unable to preserve the chemical and physical stability of the water-alcohol solutions of hormones T3/T4 it contains, causing a loss of alcohol solvent and increasing the quantity of impurities present in it during storage.
- the purpose of the present invention is therefore to overcome the drawbacks associated with the prior art, in particular the chemical and physical instability of water-alcohol solutions of hormone T3/T4 stored in the containers described in WO2010/086030, while maintaining the convenience and accuracy of dose and administration offered by single-dose squeezable containers.
- the present invention relates to a single-dose pharmaceutical preparation of thyroid hormones T3 and T4 suitable for oral administration, in ready-for-use packaging consisting of a container prefilled with a water-alcohol solution of hormone T3 and/or T4, said container being selected from:
- plastic container with a thickness of between 200 and 700 ⁇ , squeezable by manual compression, having a Young's modulus of between 10 and 200 MPa and characterised by multiple layers of plastics suitably selected from polyethylene, ethylene vinyl alcohol copolymer resins, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, fluorinated-chlorinated resins, ionomer resins, cyclic olefin copolymers, polyamide, polystyrene, polycarbonate, laminated metals, and in particular aluminium bonded to plastics.
- plastics suitably selected from polyethylene, ethylene vinyl alcohol copolymer resins, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, fluorinated-chlorinated resins, ionomer resins, cyclic olefin copolymers, polyamide, polystyrene, polycarbonate, laminated metals, and in particular aluminiu
- the sachet consists of a film made of several layers of materials according to the following combinations: polyethylene, aluminium and polyester; polyethylene, aluminium and paper; ionomer resins, aluminium and paper.
- the sachet also presents oxygen and water vapor permeability preferably between 0.1 and 0.2 cc/m2/day.
- the water-alcohol solution can contain 1 to 20 g of thyroid hormone T3 and/or 12.5 to 200 g of thyroid hormone T4, ethyl alcohol in quantities preferably ranging between 5 and 30% w/v, glycerol in quantities preferably ranging between 70 and 95% w/v, and water.
- the pharmaceutical preparation according to the invention contains not less than 95% of the initial ethanol concentration, a T3 and/or T4 content of not less than 95% of the initial concentration, and total impurities (excluding impurity T3 in the single-dose T4 container) ⁇ 2.5% of the initial concentration of active ingredient.
- the pharmaceutical preparation according to the invention due to its characteristics, guarantees the absence of microbiological contamination, with TAMC (total aerobic microbial count) values ⁇ 100 CFU/g, TYMC (total yeast and mould count) values ⁇ 10 CFU/g, and absence of E. coli, thus being practical to use and not liable to accidental contamination.
- TAMC total aerobic microbial count
- TYMC total yeast and mould count
- the pharmaceutical preparation according to the invention is conveniently used to treat disorders associated with thyroid hormone T3 and/or T4 deficiency.
- a further aspect of the invention therefore relates to the use of a water- alcohol solution of thyroid hormone T3 and/or T4 in a container as described above, to prepare a medicament for oral administration in the treatment of disorders associated with thyroid hormone T3 and/or T4 deficiency.
- the container In order to be easily squeezable and ensure complete delivery of its contents, the container must be soft and malleable. This state is usually achieved with the use of low-density polyethylene, polypropylene and sometimes with the addition of suitable "softening” agents such as EVA, which produce "loose” crosslinking.
- Squeezable containers are characterised by a plastic material having a sufficiently low Young's modulus. The best results have been obtained with plastics characterised by a Young's modulus of less than 200 MPa. It has been demonstrated that when plastic containers with such a Young's modulus are used, the contents are almost completely extracted by a single manual compression.
- ⁇ ⁇ /1 where ⁇ 1 is the amount by which the length of the object changes and 1 is the original length of the object.
- Plastics with such a Young's modulus are obtainable by injection molding or blowing.
- Suitable pharmaceutical-grade plastics can be polyethylene (PE), ethylene vinyl alcohol copolymer resins (EVOH), polyvinyl chloride (PVC), polyvinylidene chloride (PVdC), polyvinyl acetate (PVA), fluorinated- chlorinated resins, ionomer resins, cyclic olefin copolymers (COC), polyamides (PA), polystyrene (PS), polycarbonate (PC), laminated metals such as aluminium bonded to plastics, blends of the materials listed above in variable percentages, or stratifications of the above-mentioned materials of variable thickness.
- PE polyethylene
- EVOH ethylene vinyl alcohol copolymer resins
- PVC polyvinyl chloride
- PVdC polyvinylidene chloride
- PVA polyvinyl acetate
- fluorinated- chlorinated resins ionomer resins
- ionomer resins cyclic olefin copo
- the T4 preparation to which the present invention relates proved, in terms of total impurity content, more stable than the solution stored in single- dose primary packaging made of an EVA-PE blend (50%-50%) (Table 2).
- the experiment was conducted by storing the samples at 50°C for ten days. The values are expressed as percentages of the initial active ingredient content.
- T4 preparation according to the invention in single-dose packaging proved more chemically stable than similar formulations in multi-dose amber glass bottles present on the market.
- Table 3 compares the values of the impurities after storage under ICH conditions at 25°C/60% RH for 6 months. The values are expressed as percentages of the active ingredient content.
- Table 4 compares the values of the impurities in samples stored under ICH conditions at 25°C/60% RH for 6 months. The values are expressed as percentages of the initial active ingredient content.
- the extractability of the water-alcohol T4 solution from the single- dose LDPE container containing 1.1 mL of solution was evaluated by means of a squeezability test based on successive squeezes to demonstrate the complete, reproducible release of the expected volume of solution, namely 1.0 mL.
- the test involved a representative population of 60 subjects, matched for gender and age, divided into three groups consisting of 10 males and 10 females aged under 30 years, over 50 years or between 30 and 50 years. The subjects were asked to follow the procedure described below: Hold the softer central part of the container firmly between the thumb and index finger. Applying firm pressure, squeeze the liquid into a glass, then release the container. Repeat this procedure 5 times.
- Suitable single-dose laminated containers which guarantee the physical and chemical stability of the solution they contain were also identified.
- T4 solution 100 ⁇ g/mL was stored at 30°C/65% RH for 30 days
- the process used is similar to the one previously described for the single-dose LDPE container.
- one- component LDPE containers in sealed sachets proved to guarantee the physical and chemical stability of the formulation of T3 and T4.
- Said formulation is used to prepare T4 doses of up to 200 ⁇ g, T3 up to 20 ⁇ g, and combinations of both active ingredients.
- excipients such as ethanol and glycerol are used, the concentrations of which can range between 5 and 30% w/v for the former and 70 to 95% w/v for the latter, with water as required.
- the T4 is solubilized in ethanol in a suitable dissolver, under continuous stirring at ambient temperature.
- glycerol is added, and a homogenous, clear, colourless solution is obtained under gentle stirring at ambient temperature.
- the solution is filtered (0.8 ⁇ ), and is then ready for filling a suitable primary container.
- the Melt Flow Index or Melt Index is the index of fluidity of a molten polymer.
- the prototypes are prepared on a laboratory scale, using an automatic pipette (Gilson P-1000) to fill disposable containers with 1.1 mL of the glycerol-ethanol solution previously described (prepared as described in example 1), after which the containers are sealed with a Pentaseal-lab benchtop sealing machine.
- Table 9 lists the T4 content obtained during a period of three months after preparation, the T3 value and the sum of the impurities, excluding T3, found in the individual single-dose container during the experiment. The values relating to the condition considered most drastic for the product, i.e. 30°C/65% H, are recorded.
- the single-dose LDPE container compared in absolute terms with the other materials selected and described, proved able to preserve the chemical quality of the product to a sufficient extent according to the parameters considered.
- Stratified film with high gas and light barrier Polyester 12 ⁇ , Al 9 ⁇ , Polyethylene 50 ⁇ (values to be considered + 5-6%);
- Oxygen permeability 0.1-0.2 cc/m 2 /day
- the oxygen permeability was measured in accordance with ASTM Standard D-3985.
- the water permeability was measured in accordance with ASTM
- the prototypes are prepared on a laboratory scale, using an automatic pipette (Gilson P-1000) to fill disposable containers with 1.1 mL of the glycerol-ethanol solution previously described (prepared as described in example 1), after which the containers are sealed with a Pentaseal-lab benchtop sealing machine. Part of the batch is packaged in a hermetically sealed sachet of the type described above.
- the sachets are then placed in suitable environmental test chambers, and immediately undergo a stability study under ICH conditions; the equipment used is calibrated and instantly monitored for correct operation.
- the samples stored in the protective sachet demonstrate a greater ethanol containment capacity than the unprotected samples.
- the product is industrialized by preparing 50 liters of said formulation (as described in example 1). A rotor dissolver of suitable capacity and a semi-automatic Comas Pentafill SA machine for filling single-dose containers (15 strokes per minute) is used. Part of the batch is packaged in a hermetically sealed sachet of the type described, while the remainder is kept in cardboard boxes but not hermetically protected.
- the samples after being placed in suitable environmental test chambers, immediately undergo a stability study under ICH conditions; the equipment used is calibrated and instantly monitored for correct operation.
- Table 10 lists the residual ethanol values in the individual single- dose container in the sealed sachet, and without the sachet. The values relating to the ICH condition 30°C/65% H are recorded.
- the single-dose LDPE container in the sealed sachet offered the best performance after only three months of the experiment. A year after the start of the experiment, the percentage difference in the ethanol present in the formulation is measurable at around 24%.
- Examples 1 and 2 demonstrate the efficacy of the 1 mL single-dose LDPE container stored in a hermetically sealed sachet (PET/Al/PE).
- T4 Solution 25 /mL in single-dose one-component LDPE container contained in hermetically sealed sachet (PET/Al/PE)
- T4 Solution 50 /mL in single-dose one-component LDPE container contained in hermetically sealed sachet (PET/Al/PE)
- T4 Solution 75 /mL in single-dose one-component LDPE container contained in hermetically sealed sachet (PET/Al/PE)
- T4 Solution 100 /mL in single-dose one-component LDPE container contained in hermetically sealed sachet (PET/Al/PE)
- Samples prepared as described in example 2/D are stored in hermetically sealed sachets consisting of:
- Samples prepared as described in example 2/D are stored in hermetically sealed sachets consisting of:
- the prototypes are prepared on a laboratory scale, using an automatic pipette (Gilson P-1000) to fill 5 -layer laminated disposable containers with 1.1 mL of the glycerol-ethanol solution previously disclosed (prepared as described in example 1), after which the containers are sealed with a manual laboratory sealing machine.
- an automatic pipette Glass P-1000
- the container is made in a specific mould by a blowing technique; it is transparent (but can be opacified to protect it from light), has a wall approx. 600 ⁇ thick, and consists of laminated layers of the following materials: LDPE, EVOH, NF 408 adhesive (PE and maleic anhydride); EVOH performs the main function of a barrier to gas permeation. Specifically, PE is Purell PE 1840 H; EVOH is EVAL 101 B.
- the samples prepared were stored at the temperature of 30°C and 65% relative humidity for 30 days.
- the same Table compares the data obtained from samples stored in single-dose laminated containers with PP but without EVOH, and in single-dose LDPE containers with and without protective sachet. The values determined are expressed as percentages, and shown in Table 15.
- the single-dose laminated container containing PE-EVOH keeps the product in high-quality conditions, and the values measured (impurities and ethanol content) are similar to those obtained with a single-dose one-component LDPE container stored in a hermetically sealed sachet.
- 1.1 mL disposable laminated containers are filled with the glycerol- ethanol solution already described (prepared as shown in example 1), using an automatic pipette (Gilson P-1000).
- Said empty single-dose container is made in a special mould. It is obtained by joining 2 symmetrical half-shells generated by a blowing technique similar to the one used to make blister packs. After volumetric filling it is sealed by a manual laboratory sealing machine.
- the wall of the single-dose container is approx. 400 ⁇ thick, and consists of layers of the following materials: PE, EVOH, PP, ACLA ® .
- the samples prepared were stored at the temperature of 30°C and 65% relative humidity for 30 days.
- the same Table compares the data obtained from samples stored in single-dose LDPE containers with and without protective sachet. The values determined are expressed as percentages, and shown in Table 16.
- the single-dose laminated container containing PE-EVOH-PP-ACLAR ® only 400 ⁇ thick keeps the product in good quality conditions, and the values measured (impurities and ethanol content) are not very different from those obtained with a single-dose one-component LDPE container stored in a hermetically sealed sachet.
- 1.1 mL disposable laminated containers are filled with the glycerol- ethanol solution already disclosed (prepared as described in example 1), using an automatic pipette (Gilson P-1000).
- Said empty single-dose container is made in a special mould. It is obtained by joining 2 symmetrical half-shells generated by a blowing technique similar to the one used to make blister packs. After volumetric filling it is sealed by a manual laboratory sealing machine.
- the wall of the single-dose container is approx. 300 ⁇ thick, and consists of layers of the following materials: PVC, PVDC, PE.
- the single-dose laminated container containing PVC, PVDC, PE only 300 ⁇ thick keeps the product in good quality conditions, and the values measured (impurities and ethanol content) are not very different from those obtained with a single-dose one-component LDPE container stored in a hermetically sealed sachet.
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Abstract
Description
Claims
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/814,770 US20140179785A1 (en) | 2011-11-14 | 2012-11-13 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 |
DK12798182.7T DK2790638T3 (en) | 2011-11-14 | 2012-11-13 | PHARMACEUTICAL SINGLE DOSAGE PREPARATION OF THYROIDA HORMONES T3 AND / OR T4 |
CA2853880A CA2853880C (en) | 2011-11-14 | 2012-11-13 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 |
ES12798182.7T ES2621009T3 (en) | 2011-11-14 | 2012-11-13 | Pharmaceutical unit dosage of thyroid hormones T3 and / or T4 |
EP16154717.9A EP3056187B2 (en) | 2011-11-14 | 2012-11-13 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 |
PL16154717.9T PL3056187T5 (en) | 2011-11-14 | 2012-11-13 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 |
EP12798182.7A EP2790638B1 (en) | 2011-11-14 | 2012-11-13 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 |
CN201280055960.7A CN103987358B (en) | 2011-11-14 | 2012-11-13 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 |
RU2014119151A RU2688430C2 (en) | 2011-11-14 | 2012-11-13 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 |
HK15101283.7A HK1200692A1 (en) | 2011-11-14 | 2015-02-05 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 t3 / t4 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT002066A ITMI20112066A1 (en) | 2011-11-14 | 2011-11-14 | SINGLE-DOSE ORAL PHARMACEUTICAL PREPARATION OF THYROID ORMONS T3 AND T4 |
ITMI2011A002066 | 2011-11-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013072304A1 true WO2013072304A1 (en) | 2013-05-23 |
Family
ID=45315902
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2012/072482 WO2013072304A1 (en) | 2011-11-14 | 2012-11-13 | Single-dose pharmaceutical preparation of thyroid hormones t3 and/or t4 |
Country Status (14)
Country | Link |
---|---|
US (1) | US20140179785A1 (en) |
EP (2) | EP2790638B1 (en) |
CN (2) | CN103987358B (en) |
CA (1) | CA2853880C (en) |
DK (2) | DK2790638T3 (en) |
ES (2) | ES2698521T5 (en) |
FI (1) | FI3056187T4 (en) |
HK (1) | HK1200692A1 (en) |
HU (1) | HUE033305T2 (en) |
IT (1) | ITMI20112066A1 (en) |
PL (2) | PL2790638T3 (en) |
PT (2) | PT3056187T (en) |
RU (2) | RU2688430C2 (en) |
WO (1) | WO2013072304A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102013017917A1 (en) * | 2013-10-26 | 2015-04-30 | Michael Raschke | L-Thyrogal |
EP3311844A1 (en) | 2016-10-18 | 2018-04-25 | Altergon S.A. | High-stability packaged solutions of t4 thyroid hormone |
IT201900003013A1 (en) | 2019-03-01 | 2020-09-01 | Altergon Sa | Administration regimen of T4 thyroid hormone compositions with high oral absorption |
US11241382B2 (en) | 2019-03-01 | 2022-02-08 | Altergon Sa | Administration regimen of compositions of T4 thyroid hormone with high oral absorption |
IT202100020105A1 (en) | 2021-07-28 | 2023-01-28 | Altergon Sa | Use of T4 thyroid hormone in a highly versatile treatment in patients taking proton pump inhibitors |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2022221480A1 (en) * | 2021-04-15 | 2022-10-20 | Vertice Pharma Llc | Stable liquid oral dosage forms of liothyronine |
EP4295836A1 (en) * | 2022-06-22 | 2023-12-27 | Labomed Pharmaceutical Company S.A. | Sachet comprising a liquid suspension of a sevelamer salt |
CN115645361B (en) * | 2022-09-30 | 2023-11-21 | 天津市眼科医院 | Ophthalmic preparation for enhancing biomechanical property of cornea and application of T3 |
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EP1291021A2 (en) * | 2001-07-02 | 2003-03-12 | Altergon S.A. | Pharmaceutical formulations for thyroid hormones |
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JP2008519147A (en) * | 2004-11-08 | 2008-06-05 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Reinforced polyamide for food packaging and health care applications |
KR20070100720A (en) | 2004-12-27 | 2007-10-11 | 킹 파머슈티칼스 리서치 앤드 디벨로프먼트 아이엔씨 | Oxygen-impervious packaging with optional oxygen scavenger, stabilized thyroid hormone compositions and methods for storing thyroid hormone pharmaceutical compositions |
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DE102008056123B4 (en) * | 2008-11-06 | 2017-11-16 | Klöckner Pentaplast Gmbh | Multilayer film and blister packaging |
-
2011
- 2011-11-14 IT IT002066A patent/ITMI20112066A1/en unknown
-
2012
- 2012-11-13 EP EP12798182.7A patent/EP2790638B1/en active Active
- 2012-11-13 CN CN201280055960.7A patent/CN103987358B/en active Active
- 2012-11-13 PT PT16154717T patent/PT3056187T/en unknown
- 2012-11-13 EP EP16154717.9A patent/EP3056187B2/en active Active
- 2012-11-13 ES ES16154717T patent/ES2698521T5/en active Active
- 2012-11-13 WO PCT/EP2012/072482 patent/WO2013072304A1/en active Application Filing
- 2012-11-13 FI FIEP16154717.9T patent/FI3056187T4/en active
- 2012-11-13 PL PL12798182T patent/PL2790638T3/en unknown
- 2012-11-13 PT PT127981827T patent/PT2790638T/en unknown
- 2012-11-13 ES ES12798182.7T patent/ES2621009T3/en active Active
- 2012-11-13 CA CA2853880A patent/CA2853880C/en active Active
- 2012-11-13 DK DK12798182.7T patent/DK2790638T3/en active
- 2012-11-13 RU RU2014119151A patent/RU2688430C2/en active
- 2012-11-13 DK DK16154717.9T patent/DK3056187T4/en active
- 2012-11-13 RU RU2018140275A patent/RU2018140275A/en unknown
- 2012-11-13 HU HUE12798182A patent/HUE033305T2/en unknown
- 2012-11-13 US US13/814,770 patent/US20140179785A1/en not_active Abandoned
- 2012-11-13 CN CN201710217112.6A patent/CN107049929B/en active Active
- 2012-11-13 PL PL16154717.9T patent/PL3056187T5/en unknown
-
2015
- 2015-02-05 HK HK15101283.7A patent/HK1200692A1/en unknown
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US3128920A (en) * | 1964-04-14 | figure | ||
EP1291021A2 (en) * | 2001-07-02 | 2003-03-12 | Altergon S.A. | Pharmaceutical formulations for thyroid hormones |
WO2010086030A1 (en) | 2009-01-30 | 2010-08-05 | Altergon S.A. | Container for pharmaceutical use for the quantitative release of a single dose for oral administration of t3 and t4 thyroid hormones in solution |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
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DE102013017917A1 (en) * | 2013-10-26 | 2015-04-30 | Michael Raschke | L-Thyrogal |
RU2765547C2 (en) * | 2016-10-18 | 2022-02-01 | Альтергон Са | Highly stable packaged solutions of the thyroid hormone t4 |
US11096913B2 (en) | 2016-10-18 | 2021-08-24 | Altergon Sa | High-stability packaged solutions of T4 thyroid hormone |
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US10537538B2 (en) | 2016-10-18 | 2020-01-21 | Altergon Sa | High-stability packaged solutions of T4 thyroid hormone |
EP3528847B1 (en) | 2016-10-18 | 2020-07-22 | Altergon SA | High-stability packaged solutions of t4 thyroid hormone |
CN109789213B (en) * | 2016-10-18 | 2022-05-31 | 阿尔特贡股份公司 | High stability packaging solution for T4 thyroid hormone |
EP3311844A1 (en) | 2016-10-18 | 2018-04-25 | Altergon S.A. | High-stability packaged solutions of t4 thyroid hormone |
WO2018073209A1 (en) | 2016-10-18 | 2018-04-26 | Altergon Sa | High-stability packaged solutions of t4 thyroid hormone |
WO2020178074A1 (en) | 2019-03-01 | 2020-09-10 | Altergon S.A. | Administration regimen of solutions of t4 thyroid hormone with high oral absorption |
US11241382B2 (en) | 2019-03-01 | 2022-02-08 | Altergon Sa | Administration regimen of compositions of T4 thyroid hormone with high oral absorption |
IT201900003013A1 (en) | 2019-03-01 | 2020-09-01 | Altergon Sa | Administration regimen of T4 thyroid hormone compositions with high oral absorption |
EP4321214A2 (en) | 2019-03-01 | 2024-02-14 | Altergon S.a. | Administration regimen of solutions of t4 thyroid hormone with high oral absorption |
IT202100020105A1 (en) | 2021-07-28 | 2023-01-28 | Altergon Sa | Use of T4 thyroid hormone in a highly versatile treatment in patients taking proton pump inhibitors |
WO2023006841A1 (en) | 2021-07-28 | 2023-02-02 | Altergon S.A. | Use of thyroid hormone t4 in a high versatility treatment in patients taking proton pump inhibitors |
Also Published As
Publication number | Publication date |
---|---|
PT2790638T (en) | 2017-04-19 |
ITMI20112066A1 (en) | 2013-05-15 |
CA2853880A1 (en) | 2013-05-23 |
RU2014119151A (en) | 2015-12-27 |
EP3056187A9 (en) | 2016-11-23 |
ES2621009T3 (en) | 2017-06-30 |
DK3056187T3 (en) | 2018-12-10 |
PL2790638T3 (en) | 2017-07-31 |
FI3056187T4 (en) | 2023-09-22 |
ES2698521T5 (en) | 2024-01-22 |
EP3056187A1 (en) | 2016-08-17 |
CN107049929A (en) | 2017-08-18 |
CN103987358B (en) | 2017-04-26 |
RU2018140275A (en) | 2019-01-18 |
EP3056187B1 (en) | 2018-08-22 |
RU2018140275A3 (en) | 2022-03-23 |
CN107049929B (en) | 2020-08-04 |
DK3056187T4 (en) | 2023-09-25 |
EP3056187B2 (en) | 2023-08-30 |
PL3056187T5 (en) | 2023-12-04 |
PL3056187T3 (en) | 2019-02-28 |
RU2688430C2 (en) | 2019-05-21 |
DK2790638T3 (en) | 2017-04-03 |
HUE033305T2 (en) | 2017-11-28 |
EP2790638A1 (en) | 2014-10-22 |
ES2698521T3 (en) | 2019-02-05 |
HK1200692A1 (en) | 2015-08-14 |
EP2790638B1 (en) | 2017-01-04 |
PT3056187T (en) | 2018-11-28 |
CN103987358A (en) | 2014-08-13 |
CA2853880C (en) | 2019-12-10 |
US20140179785A1 (en) | 2014-06-26 |
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