US20150057321A1 - Soft chewable pharmaceutical products - Google Patents
Soft chewable pharmaceutical products Download PDFInfo
- Publication number
- US20150057321A1 US20150057321A1 US14/390,040 US201314390040A US2015057321A1 US 20150057321 A1 US20150057321 A1 US 20150057321A1 US 201314390040 A US201314390040 A US 201314390040A US 2015057321 A1 US2015057321 A1 US 2015057321A1
- Authority
- US
- United States
- Prior art keywords
- methyl
- active pharmaceutical
- product
- pharmaceutical ingredient
- trifluoromethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- 0 CC.[2*]C1(C2=CC=CC=C2)CC([3H]C)=NO1 Chemical compound CC.[2*]C1(C2=CC=CC=C2)CC([3H]C)=NO1 0.000 description 16
- RDMGQFGRPDWBCN-UHFFFAOYSA-N CCOC(N)=C(C)C.COC(N)=C(C)C Chemical compound CCOC(N)=C(C)C.COC(N)=C(C)C RDMGQFGRPDWBCN-UHFFFAOYSA-N 0.000 description 3
- SUSGNSUHZQFCEG-UHFFFAOYSA-N C1=CC2=CC=CN2C=C1.C1=CC2=NC=CN2C=C1.C1=CC=C2/C=C\C=C/C2=C1.[Y]C1=CC=CC=C1.[Y]C1=CSC=C1 Chemical compound C1=CC2=CC=CN2C=C1.C1=CC2=NC=CN2C=C1.C1=CC=C2/C=C\C=C/C2=C1.[Y]C1=CC=CC=C1.[Y]C1=CSC=C1 SUSGNSUHZQFCEG-UHFFFAOYSA-N 0.000 description 1
- HLEBYURTMZEBDD-UHFFFAOYSA-N CC1=C(C(=O)CC2CSC2)C=CC(C2=NOC(C3=CC(Cl)=CC(Cl)=C3)(C(F)(F)F)C2)=C1.CC1=C(C(=O)CCC(=O)NCC(F)(F)F)SC(C2=NOC(C3=CC(Cl)=CC(Cl)=C3)(C(F)(F)F)C2)=C1.O=C(CCC(=O)C1=C2C=CC=CC2=C(C2=NOC(C3=CC(Cl)=CC(C(F)(F)F)=C3)(C(F)(F)F)C2)C=C1)NCC(F)(F)F Chemical compound CC1=C(C(=O)CC2CSC2)C=CC(C2=NOC(C3=CC(Cl)=CC(Cl)=C3)(C(F)(F)F)C2)=C1.CC1=C(C(=O)CCC(=O)NCC(F)(F)F)SC(C2=NOC(C3=CC(Cl)=CC(Cl)=C3)(C(F)(F)F)C2)=C1.O=C(CCC(=O)C1=C2C=CC=CC2=C(C2=NOC(C3=CC(Cl)=CC(C(F)(F)F)=C3)(C(F)(F)F)C2)C=C1)NCC(F)(F)F HLEBYURTMZEBDD-UHFFFAOYSA-N 0.000 description 1
- KKDIPOVLAZLSJL-UHFFFAOYSA-N CC1=C(C(=O)CCC(=O)NCC(F)(F)F)C=CC(C2=NOC(C3=CC(Cl)=CC(Cl)=C3)(C(F)(F)F)C2)=C1 Chemical compound CC1=C(C(=O)CCC(=O)NCC(F)(F)F)C=CC(C2=NOC(C3=CC(Cl)=CC(Cl)=C3)(C(F)(F)F)C2)=C1 KKDIPOVLAZLSJL-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
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- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
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- A61K47/20—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing sulfur, e.g. dimethyl sulfoxide [DMSO], docusate, sodium lauryl sulfate or aminosulfonic acids
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- 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
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- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
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- B—PERFORMING OPERATIONS; TRANSPORTING
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Definitions
- the invention relates to the field of orally administrable pharmaceutical dosage units such as soft chews, especially for administration to non-human animals.
- Chewable pharmaceutical products for drug delivery are well known. Formulation of a drug into a chewable dosage form can increase (animal) patient acceptance of the medication that tend to resist swallowing hard tablets or capsules.
- Texture is important for the acceptance of such oral products by (animal) patients.
- One of the most commonly used form for chewable pharmaceutical products is a chewable compressed tablet, whose ingredients, however, can make the tablet gritty or otherwise unappealing, especially to non-human animals.
- a preferred alternative dosage form for non-human animals is the “soft chew” generally a meat-like mass also widely found in consumable pet treats.
- U.S. Pat. No. 6,387,381 discloses an extrudate which is formed of a matrix having starch, sugar, fat, polyhydric alcohol and water.
- WO 2004/014143 relates to compositions and processes for the delivery of an additive to an organism in a form suitable for consumption, and in particular, in the form of a soft chew.
- US 2009/0280159 and US 2011/0223234 relate to palatable edible soft chewable medication vehicles.
- the processes described herein relate to the problem that heat generated during the extrusion process causes deterioration in the stability of the active ingredient in the mixture.
- Machines for the high volume production of molded food patties have been described to be useful for the manufacturing of soft chews for administration to non-human animals.
- Such machines are molding machines developed for use in producing molded food products, for example Formax F6TM molding machine made by the Formax Corporation or the molding machines disclosed in U.S. Pat. Nos.
- Such machines are originally used to form hamburger patties from a supply of ground beef by forcing the ground beef under pressure into a multi-cavity mold plate which is rapidly shuttled on a linear slide between a fill position and a discharge position in which vertically reciprocable knock-outs push the patties from the mold cavities.
- a dough mass is prepared with ingredients that lead to the meat-like texture of the resulting soft chew after forming and drying.
- a veterinary medicament on an industrial scale it is necessary to produce the soft chews by a forming machine that is able to produce high volume.
- Salts of pamoic acid are known as pamoates or embonates and are conventionally used as a counter ion of certain basic active ingredients to obtain long-acting pharmaceutical formulations.
- Examples of pamoate salts of active ingredients in veterinary medicine are the anthelmintic compounds pyrantel pamoate and oxantel pamoate and the antihistamine hydroxycine pamoate.
- a number of active ingredients used in human health are pamoate salts, e.g. as disclosed in WO 94/25460, WO 05/016261, WO 04/017970, or WO 05/075454.
- pamoic acid or a pharmaceutically acceptable salt thereof as excipient in soft chew formulations has not been described.
- the soft chews that comprise pamoic acid or a pharmaceutically acceptable salt thereof can be easily processed in a forming machine and that pamoic acid or a pharmaceutically acceptable salt thereof facilitates manufacturing of such soft chews on an industrial scale using a forming machine.
- the invention provides a new soft chewable pharmaceutical product for administration to non-human animals and a process for its manufacture.
- the present invention relates to a soft chewable veterinary pharmaceutical product (a “soft chew”) comprising as ingredients,
- the product comprises sodium pamoate.
- the amount of pamoic acid or the pharmaceutically acceptable salt thereof is between 1.5 and 30% w/w, preferably between 2 and 5% w/w.
- a soft chewable veterinary pharmaceutical product comprising as ingredients,
- R 1 halogen, CF 3 , OCF 3 , CN,
- R 2 ⁇ C 1 -C 3 -haloalkyl, preferably CF 3 or CF 2 Cl,
- T 5- or 6-membered ring, which is optionally substituted by one or more radicals Y,
- Y methyl, halomethyl, halogen, CN, NO 2 , NH 2 —C ⁇ S, or two adjacent radicals Y form together a chain, especially a three or four membered chain;
- Q X—NR 3 R 4 or a 5-membered N-heteroaryl ring, which is optionally substituted by one or more radicals;
- R 3 hydrogen, methyl, haloethyl, halopropyl, halobutyl, methoxymethyl,methoxyethyl, halomethoxymethyl, ethoxymethyl, haloethoxymethyl, propoxymethyl, ethylaminocarbonylmethyl, ethylaminocarbonylethyl, dimethoxyethyl, propynylaminocarbonylmethyl, N-phenyl-N-methyl-amino, haloethylaminocarbonylmethyl, haloethylaminocarbonylethyl, tetrahydrofuryl, methylaminocarbonylmethyl, (N,N-dimethylamino)-carbonylmethyl, propylaminocarbonylmethyl, cyclopropylaminocarbonylmethyl, propenylaminocarbonylmethyl, haloethylaminocarbonylcyclopropyl,
- Z A hydrogen, halogen, cyano, halomethyl (CF 3 );
- R 4 hydrogen, ethyl, methoxymethyl, halomethoxymethyl, ethoxymethyl, haloethoxymethyl, propoxymethyl, methylcarbonyl, ethylcarbonyl, propylcarbonyl, cyclopropylcarbonyl, methoxycarbonyl, methoxymethylcarbonyl, aminocarbonyl, ethylaminocarbonylmethyl, ethylaminocarbonylethyl, dimethoxyethyl, propynylaminocarbonylmethyl, haloethylaminocarbonylmethyl, cyanomethylaminocarbonylmethyl, or haloethylaminocarbonylethyl;
- R 3 and R 4 together form a substituent selected from the group consisting of:
- the active pharmaceutical ingredient is 4-[5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methyl-N-[(2,2,2-trifluoro-ethylcarbamoyl)-methyl]-benzamide.
- the active pharmaceutical ingredient is 4-[5-[3-Chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-1-naphthalenecarboxamide.
- the active pharmaceutical ingredient is 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-N-(thietan-3-yl)benzamide.
- the active pharmaceutical ingredient is 5-[5-(3,5-Dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-3-methyl-N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-2-thiophenecarboxamide.
- more than one active pharmaceutical ingredient is present.
- the combination of active pharmaceutical ingredients comprises one or more antiparasitics.
- Another aspect of the current invention is a process for the manufacture of a product as described above in a forming machine comprising the steps of
- the pamoic acid or the pharmaceutically acceptable salt thereof is mixed with the other ingredients.
- the current invention is directed to the use of pamoic acid or a pharmaceutically acceptable salt thereof in the process as described above to increase lubricity of a product as described above when filling the mold with dough or when removing the dough from the mold or both.
- the current invention is directed to the use of the soft chewable veterinary pharmaceutical product as described above in the manufacture of a medicament for controlling a parasitic insect, acarid or nematode infestation of an animal.
- Another aspect of the current invention is a soft chewable veterinary pharmaceutical composition
- a soft chewable veterinary pharmaceutical composition comprising an isoxazoline compound of Formula (I) for use in a method of controlling a parasitic insect, acarid or nematode infestation of an animal
- Soft chew or “Soft chewable veterinary pharmaceutical product” is intended to mean a product which is solid at room temperature and that is soft to chew and which is functionally chewy because the product has some plastic texture during the process of mastication in the mouth. Such soft chews have a softness that is similar to a cooked ground meat petty.
- Pamoic acid also called embonic acid, is a naphthoic acid derivative.
- the chemical name of pamoic acid is 4,4′-methylenebis(3-hydroxy-2-napthalenecarboxylic acid).
- a salt of pamoic acid is used.
- the pharmaceutically acceptable salt of pamoic acid is the sodium or potassium salt.
- sodium pamoate is used, especially disodium pamoic acid.
- Salts of pamoic acid are readily commercially available, e.g. pamoic acid disodium salt from APAC Pharmaceutical LLC, Columbia, US.
- Different hydrate forms of pamoic acid salts are suitable for use in the current invention.
- the monohydrate form is used.
- the anhydrate form is used.
- esters of pamoic acid can be used in the current invention.
- the active pharmaceutical ingredient by itself does not provide a lubricating effect and pamoic acid or salts thereof are included in the soft chew composition as an (non-active) ingredient or excipient.
- the composition comprises pamoic acid or salts thereof provided that such pamoic acid or pharmaceutically acceptable salt thereof is not an active pharmaceutical ingredient.
- pamoic acid or salts is sodium pamoate.
- the soft chew can comprise a pamoate salt of an active pharmaceutical ingredient.
- the invention relates to a product of the invention wherein a pamoate salt of an active pharmaceutical ingredient is present in the soft chew of the current invention, but no additional pamoic acid or salts thereof are included as non-active ingredient, provided that such active pharmaceutical ingredient is not pyrantel pamoate or oxantel pamoate.
- pamoic acid or a pharmaceutically acceptable salt thereof has been proven to increase the lubricity of the soft chew so that the soft chew can now be processed in a forming machine.
- the amount of pamoic acid or a pharmaceutically acceptable salt thereof necessary to provide the required lubricity depends on the specific composition of the various ingredients and can be determined by the skilled person in each case. In general, a w/w % of at least 1% already displays the favourable processing parameters of the soft chew.
- the invention relates to a product according to the invention wherein the amount of pamoic acid or the pharmaceutically acceptable salt thereof is between 1 and 50% w/w. In another aspect the amount of pamoic acid or the pharmaceutically acceptable salt thereof is between 1.5 and 30% w/w. In still another aspect the amount of pamoic acid or the pharmaceutically acceptable salt thereof is not higher than 10% w/w. In a further aspect, the amount of pamoic acid or the pharmaceutically acceptable salt thereof is between 2.0 and 5.0% w/w.
- pamoic acid or a pharmaceutically acceptable salt thereof in the manufacture of a soft chew.
- the addition of pamoic acid, or a pharmaceutically acceptable salt thereof to a soft chew dough improves the processability of such soft chew dough in the forming equipment by increasing lubricity on the surface of the soft chew product when filling the mold with dough or when removing the dough from the mold or both.
- Lubricity means and refers to the measure of the reduction in friction including reduction of adherence of soft-chew mixture to the mold plate or knock out cups.
- the pamoic acid or pharmaceutically acceptable salt thereof is not an active pharmaceutical ingredient.
- the soft chew according to the invention in general comprises an active pharmaceutical ingredient.
- an active pharmaceutical ingredient is a substance used in a pharmaceutical product, intended to furnish pharmacological activity or to otherwise have direct effect in the diagnosis, cure, mitigation, treatment or prevention of disease, or to have direct effect in restoring, correcting or modifying physiological functions in humans or animals.
- any orally administrable pharmaceutically active ingredient or other biologically active compound may be provided in the soft chews of the invention.
- active ingredients may include, without limitation, antibiotics, analgesics, antivirals, antifungals, antiparasitics such as endo- and ecto-parasticides, hormones and/or derivatives thereof, anti-inflammatories (including non-steroidal anti-inflammatories), steroids, behavior modifiers, vaccines, antacids, laxatives, anticonvulsants, sedatives, tranquilizers, antitussives, antihistamines, decongestants, expectorants, appetite stimulants and suppressants, cardiovascular drugs, minerals and vitamins.
- the active ingredients are preferably antiparasitics, more preferably selected from the group consisting of isoxazoline compounds, avermectins (e.g., ivermectin, selamectin, doramectin, abamectin, and eprinomectin); milbemycins (moxidectin and milbemycin oxime); pro-benzimidazoles (e.g., febantel, netobimin, and thiophanate); benzimidazole derivatives, such as a thiazole benzimidazole derivatives (e.g., thiabendazole and cambendazole), carbamate benzimidazole derivatives (e.g., fenbendazole, albendazole (oxide), mebendazole, oxfendazole, parbendazole, oxibendazole, flubendazole, and triclabendazole); imidazothiazoles (
- amino-acetonitrile compounds e.g. monepantel, AAD 1566
- amidine compounds e.g., amidantel and tribendimidin
- pharmaceutically acceptable forms such as salts, solvates or N-oxides.
- the pharmaceutically active ingredient is an isoxazoline compound.
- Isoxazoline compounds are known in the art and these compounds and their use as antiparasitic are described, for example, in US patent application US 2007/0066617, and International Patent applications WO 2005/085216, WO 2007/079162, WO 2009/002809, WO 2009/024541, WO 2009/003075, WO 2010/070068 and WO 2010/079077, the disclosures of which, as well as the references cited herein, are incorporated by reference.
- This class of compounds is known to possess excellent activity against ectoparasites, i.e. parasitic insect and acarids, such as ticks and fleas and endoparasites such as nematodes.
- the soft chewable pharmaceutical product according to the invention comprises an isoxazoline compound of the Formula (I)
- R 1 halogen, CF 3 , OCF 3 , CN,
- n integer from 0 to 3, preferably 1, 2 or 3,
- R 2 ⁇ C 1 -C 3 -haloalkyl, preferably CF 3 or CF 2 Cl,
- T 5- or 6-membered ring, which is optionally substituted by one or more radicals Y,
- Y methyl, halomethyl, halogen, CN, NO 2 , NH 2 —C ⁇ S, or two adjacent radicals Y form together a chain CH—CH ⁇ CH—CH, N—CH ⁇ CH—CH, CH—N ⁇ CH—CH, CH—CH ⁇ N—CH, or CH—CH ⁇ CH—N, HC ⁇ HC—CH, CH—CH ⁇ CH, CH ⁇ CH—N, N—CH ⁇ CH;
- Q X—NR 3 R 4 or a 5-membered N-heteroaryl ring, which is optionally substituted by one or more radicals Z A , Z B Z D ;
- R 3 hydrogen, methyl, haloethyl, halopropyl, halobutyl, methoxymethyl,methoxyethyl, halomethoxymethyl, ethoxymethyl, haloethoxymethyl, propoxymethyl, ethylaminocarbonylmethyl, ethylaminocarbonylethyl, dimethoxyethyl, propynylaminocarbonylmethyl, N-phenyl-N-methyl-amino, haloethylaminocarbonylmethyl, haloethylaminocarbonylethyl, tetrahydrofuryl, methylaminocarbonylmethyl, (N,N-dimethylamino)-carbonylmethyl, propylaminocarbonylmethyl, cyclopropylaminocarbonylmethyl, propenylaminocarbonylmethyl, haloethylaminocarbonylcyclopropyl,
- R 4 hydrogen, ethyl, methoxymethyl, halomethoxymethyl, ethoxymethyl, haloethoxymethyl, propoxymethyl, methylcarbonyl, ethylcarbonyl, propylcarbonyl, cyclopropylcarbonyl, methoxycarbonyl, methoxymethylcarbonyl, aminocarbonyl, ethylaminocarbonylmethyl, ethylaminocarbonylethyl, dimethoxyethyl, propynylaminocarbonylmethyl, haloethylaminocarbonylmethyl, cyanomethylaminocarbonylmethyl, or haloethylaminocarbonylethyl; or
- R 3 and R 4 together form a substituent selected from the group consisting of:
- Z A hydrogen, halogen, cyano, halomethyl (CF 3 ).
- T is selected from
- T-1, T-3 and T-4 the radical Y is hydrogen, halogen, methyl, halomethyl, ethyl, haloethyl.
- R 3 , R 4 , X and Z A are as defined above.
- Preferred compounds of Formula (I) are:
- a more preferred compound has the Formula (II),
- R 1a , R 1b , R 1c are independently from each other hydrogen, Cl or CF 3 , preferably R 1a and R 1c are Cl or CF 3 and R 1b is hydrogen,
- Y is methyl, bromine, Cl, F, CN or C(S)NH 2 , and
- R 3 is H and R 4 is —CH 2 —C(O)—NH—CH 2 —CF 3 , —CH 2 —C(O)—NH—CH 2 —CH 3 , —CH 2 —CH 2 —CF 3 or —CH 2 —CF 3 .
- the compound of Formula (I) is 4-[5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methyl-N-[(2,2,2-trifluoro-ethylcarbamoyl)-methyl]-benzamide (CAS RN 864731-61-3-USAN fluralaner).
- the compound of Formula (I) is (Z)-4-[5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-N-[(methoxyimino)methyl]-2-methylbenzamide (CAS RN 928789-76-8).
- the compound of Formula (I) is 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-N-(thietan-3-yl)benzamide (CAS RN 1164267-94-0) that was disclosed in WO2009/0080250—Compound B.
- the compound of Formula (I) is 4-[5-[3-Chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-oxo-2-[(2,2,2-trifluoroethyl)pamino]ethyl]-1-naphthalenecarboxamide (CAS RN 1093861-60-9, USAN—afoxolaner) that was disclosed in WO2007/079162—Compound C.
- the compound of Formula (I) is 5-[5-(3,5-Dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-3-methyl-N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-2-thiophenecarboxamide (CAS RN 1231754-09-8) that was disclosed in WO2010/070068—Compound D.
- Especially preferred compounds of Formula (II) are:
- Isoxazoline compounds are known in the art and these compounds and their use as parasiticide are described, for example, in US patent application No. US 2007/0066617, and International Patent applications WO 2007/079162, WO 2009/002809, WO 2009/024541, WO 2009/003075, WO2009/080250, WO 2010/070068, WO 2010/079077, WO 2011/075591 and WO 2011/124998, the disclosures of which, as well as the references cited herein, are incorporated by reference.
- This class of compounds is known to possess excellent activity against ectoparasites such as ticks and fleas.
- the isoxazoline compounds may exist in various isomeric forms.
- a reference to an isoxazoline compound always includes all possible isomeric forms of such compound.
- a compound structure that does not indicate a particular conformation is intended to encompass compositions of all the possible conformational isomers of the compound, as well as compositions comprising fewer than all the possible conformational isomers.
- the compound is a chiral compound. In some embodiments, the compound is a non-chiral compound.
- Isoxazoline compounds of Formula (I) can be prepared according to one or other of the processes described e.g. in Patent Applications US 2007/0066617, WO 2007/079162, WO 2009/002809, WO 2009/080250, WO 2010/070068, WO 2010/079077, 2011/075591 and WO 2011/124998 or any other process coming within the competence of a person skilled in the art who is an expert in chemical synthesis.
- a person skilled in the art is regarded as having at his disposal, inter alia, the entire contents of “Chemical Abstracts” and of the documents which are cited therein.
- the isoxazoline compound is 4-[5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methyl-N-[(2,2,2-trifluoro-ethylcarbamoylymethyl]-benzamide (CAS RN [864731-61-3])—USAN furalaner—Compound A.
- This invention is also directed to soft chews with combinations comprising more than one pharmaceutically active ingredient.
- Preferred combinations comprising active ingredients selected from the group consisting of isoxazolines of Formula (I) and avermectins and milbemycins.
- the soft chew comprises a combination of isoxazolines, especially fluralaner—compound A, or afoxolaner with ivermectin.
- the soft chew comprises a combination of isoxazolines, especially fluralaner—compound A, or afoxolaner with milbemycin or moxidectin.
- AGRs or IGRs insect or acarid growth regulators
- fenoxycarb e.g. fenoxycarb, lufenuron, diflubenzuron, novaluron, triflumuron, fluazuron, cyromazine, methoprene, pyriproxyfen etc.
- fenoxycarb e.g. fenoxycarb, lufenuron, diflubenzuron, novaluron, triflumuron, fluazuron, cyromazine, methoprene, pyriproxyfen etc.
- each of the components in the final product may be varied considerably, depending upon the nature of the pharmaceutically active ingredients, the weight and condition of the subject treated, and the unit dosage desired. Those of ordinary skill in the art will be able to adjust dosage amounts for particular pharmaceutically active ingredients in the soft chews in light of the teachings of this disclosure.
- the pharmaceutically active ingredients may be provided by range in weight based on the total weight of the composition from about 0.001% to 75% (w/w), more preferably 0.1% to 40%, and most preferably not in excess of 50%.
- the amount of Compound A in the product of the invention is between 5% and 20% w/w, especially about 9% w/w or about 14% w/w.
- the soft chew according to the invention comprises as (non-active) ingredient a liquid component.
- the liquid component includes aqueous and non-aqueous solvents, oils or humectant components or mixtures of any of such liquids.
- the liquid component is oil or a mixture of oils.
- the liquid component comprises one or more oils and one or more non-aqueous solvents.
- the liquid component comprises one or more oils, one or more non-aqueous solvents and a humectant.
- the oil employed in the soft chew may be a saturated or unsaturated liquid fatty acid, its glyceride derivatives or fatty acid derivatives of plant or animal origin or a mixture thereof.
- Suitable sources for vegetable fats or oils can be palm oil, corn oil, castor oil, canola oil safflower oil, cotton-seed oil, soybean oil, olive oil, peanut oil and mixtures thereof.
- animal oil or fats and a mixture of animal or vegetable oils or fats are suitable for use in the product according to the invention.
- Vegetable oils may also be utilized to lubricate the soft chew mixture and maintain its softness.
- the oily component is soybean oil.
- non-aqueous solvent is intended to mean any liquid other than water in which a biological material may be dissolved or suspended and includes both inorganic solvents and, more preferably, organic solvents.
- non-aqueous solvents include, but are not limited to, the following: acetone, acetonitrile, benzyl alcohol, butyl diglycol, dimethylacetamide (DMA), dimethylsulfoxide (DMSO), dimethylformamide, N,N-diethyl-3-methylbenzamide, dipropylene glycol n-butyl ether, ethyl alcohol, isopropanol, methanol, butanol, phenylethyl alcohol, isopropanol, ethylene glycol monoethyl ether, ethylene glycol monomethyl ether, monomethylaceamide, dipropylene glycol monomethyl ether, liquid polyoxyethylene glycols, propylene glycol, N-methylpyrrolidone (NMP), 2-pyrrolidone, limonene, eucalyptol, dipropylene glycol monomethyl ether, diethylene glycol monoethyl ether, ethylene glycol, dieth
- the term “humectant” means and refers to a hygroscopic substance. It can be a molecule with several hydrophilic groups, e.g. hydroxyl groups, but amines and carboxyl groups, sometimes esterified, can be encountered as well; the affinity to form hydrogen bonds with molecules of water is crucial here.
- the humectant has the effect of keeping the soft chew dough moist.
- humectants include propylene glycol, glyceryl triacetate, vinyl alcohol and neoagarobiose.
- Others can be sugar polyols such as glycerol, sorbitol, xylitol and maltitol, polymeric polyols like polydextrose, or natural extracts like quillaia, lactic acid, or urea.
- the humectant is glycerol.
- the liquid component comprises about 5% to about 50% w/w of the soft chew. In an alternate embodiment, a liquid component comprises about 7.5% to about 40% w/w of the soft chew. In an alternate embodiment, a liquid component comprises about 10% to about 30% w/w of the soft chew. In an alternate embodiment, a liquid component comprises about 15% to about 25% w/w of the soft chew.
- the forming agent is important for the texture of the soft chew and the possibility to form single soft chews from the dough that stay intact and separate.
- the term “former” or “forming agent” means and refers to an agent providing texture to the soft chew product, like for example polyethylene glycol (PEG) or polyvinylpyrrolidone (PVP).
- a forming agent of choice is polyethylene glycol (PEG).
- PEG polyethylene glycol
- different molecular weight PEG may be utilized.
- PEG 3350 is utilized.
- the PEG chosen is a matter of choice and the molecular weight may be higher or lower than 3350, but preferably higher than 600.
- PEG 8000 might be used.
- the forming agent comprises about 1% to about 40% w/w of the soft chew. In an alternate embodiment, a forming agent comprises about 5%to about 30% w/w % of the soft chew. In an alternate embodiment, a forming agent comprises about 10% to about 20%w/w of the soft chew. In case the forming agent is polyvinylpyrrolidone e.g. 2, 4, 5, 6 or 9% w/w are present in the soft chew.
- the product according to the current invention conventionally further comprise physiologically acceptable formulation excipients known in the art e.g. as described in “Gennaro, Remington: The Science and Practice of Pharmacy” (20th Edition, 2000) incorporated by reference herein. All such ingredients, carriers and excipients must be substantially pharmaceutically or veterinary pure and non-toxic in the amounts employed and must be compatible with the pharmaceutically active ingredients.
- excipients that can be present in the soft chew are e.g. a filler, a flavour, or sugar components.
- filler or “filler component” means and refers to those food-stuffs containing a preponderance of starch and/or starch-like material.
- filler are cereal grains and meals or flours obtained upon grinding cereal grains such as corn, oats, wheat, milo, barley, rice, and the various milling by-products of these cereal grains such as wheat feed flour, wheat middlings, mixed feed, wheat shorts, wheat red dog, oat, hominy feed, and other such material.
- Alternative non-food stuff fillers such as e.g. lactose may be used.
- the filler is starch, corn starch being preferred.
- Flavours are commonly added to soft chewable pharmaceutical products to enhance their palatability.
- a veterinary medication might include animal product-based flavourings such as beef, pork, chicken, turkey, fish and lamb, liver, milk, cheese and egg may be utilized.
- Non-animal origin flavourings are plant proteins, such as soy protein, yeasts, or lactose to which edible artificial food-like flavourings has been added.
- other non-animal flavourings could include anise oil, carob, peanuts, fruit flavours, herbs such as parsley, celery leaves, peppermint, spearmint, garlic, or combinations thereof.
- the sugar component may act as a sweetener, filler or flavour or provides a texture that is appealing to the animal, e.g. crunchy texture.
- saccharide which is at least partially soluble in moisture, non-toxic, and preferably not provide any undesirable taste effects.
- saccharide which is at least partially soluble in moisture, non-toxic, and preferably not provide any undesirable taste effects.
- sugar shall include a “sugar substitute” or an “artificial sweetener”.
- the sugar component may comprise white sugar, corn syrup, sorbitol, mannitol, oligosaccharide, isomalto oligosaccharide, fructose, lactose, glucose, lycasin, xylitol, lactitol, erythritol, mannitol, isomaltose, polydextrose, raffinose, dextrin, galactose, sucrose, invert sugar, honey, molasses, polyhydric alcohols and other similar saccharides oligomers and polymers and mixture thereof or artificial sweeteners such as saccharine, aspartame and other dipeptide sweeteners.
- the sweetener is aspartame.
- Various embodiments further comprise additional excipients such as surfactants, stabilizer, flow agents, disintegration agents, preservatives and/or lubricating agents.
- surfactant components are well-known in the art.
- a suitable surfactant is e.g. sodium lauryl sulphate.
- Suitable stabilizer components are citric acid, sodium citrate, and/or the like and antioxidants such as BHT, BHA, Ascorbic acid, Tocopherol, EDTA.
- Flow agents typically may include silica dioxide, modified silica, fumed silica, talc and any other suitable material to assist bulk movement of active components and/or the combination during delivery and/or manufacture.
- Disintegration agents typically may include sodium starch glycolate, pregelatinized corn starch (Starch 1500), crospovidone (Polyplasdone XLTM, International Specialty Products), and croscarmellose sodium (Ac-Di-SolTM, FMC Corp.), and derivatives thereof and any other suitable material to help breakdown the dosage form and to assist in delivery of active ingredients.
- Preservative for oral formulations are known in the art and are included in order to retard growth of microorganisms such as bacteria and fungi.
- An embodiment of preservative includes products such as potassium sorbate, sodium benzoate or calcium propionate.
- Lubricating agents are e.g. magnesium stearate, fumaric acid, sodium stearyl fumarate.
- dry ingredients of the chew mixture are blended first; then the liquid components (e.g., oil, humectants or solvents) are added and blended therein to form a thoroughly blended mixture.
- the soft chew mixture is discharged from a port through the blender into a suitable container for processing into individual dosage units by hand or preferably with a forming machine.
- a variety of forming equipment may be utilized in the invention, but those particularly preferred for use are molding machines developed for use in producing molded food products, such as pre-formed hamburger patties and chicken nuggets.
- molding machines developed for use in producing molded food products, such as pre-formed hamburger patties and chicken nuggets.
- Preferred forming equipment for use in the invention includes the Formax F6TM molding machine made by the Formax Corporation.
- the F6 machine has the capabilities of 60 strokes per minute.
- a square forming die of 6′′ by 6′′ can be used to form approximately 16-25 chunk-like soft chew units per stroke, each unit weighing 4 grams and being approximately 5 ⁇ 8′′ by 5 ⁇ 8′′ in size. Dies for production of other sizes or shapes (e.g., bone shaped chews) may also be utilized.
- Each batch of chews may be packaged in bulk or, preferably, each soft chew is then individually packaged for storage.
- suitable packaging materials include HDPE bottles, blister or foil/foil packaging.
- the product of the invention is intended for use for controlling a parasitic insect- and acarid or helminth, especially parasitic nematode infestation.
- controlling a parasitic insect- and acarid infestation refers to preventing, reducing or eliminating an infestation by such parasites on animals preferably by killing the insects and/or acarids or nematode parasites within hours or days.
- parasitic insect- and acarid refers to ectoparasites e.g. insect and acarine pests that commonly infest or infect animals.
- ectoparasites include the egg, larval, pupal, nymphal and adult stages of lice, fleas, mosquitoes, mites, ticks biting or nuisance fly species. Especially important are the adult stages of fleas and ticks.
- the product according to the invention will contain an effective amount of the active ingredients, meaning a non-toxic but sufficient amount to provide the desired control effect.
- an appropriate “effective” amount in any individual case. Such an amount will depend on the age, condition, weight and type of the target animal.
- the soft chews may be formulated to contain an amount of active ingredients that is adjusted to animals in a specific weight range.
- the animals may receive a dosage every 2, 3, 4, 5 or 6 months or receives a monthly, weekly or daily dosage.
- the treatment can, for example, be continuing or seasonal.
- the product according to the current invention can be administered to all species of animals that have insect- or acarid- or helminth parasite infestation.
- the recipient of the product may be a livestock animal, e.g. sheep, cattle, pig, goat or poultry; a laboratory test animal, e.g. guinea pig, rat or mouse; or a companion animal, e.g. dog, cat, rabbit, ferret or horse.
- the product according to the invention is especially suitable for use in companion animals, e.g. dogs, cats or ferrets.
- w/w designates weight/weight
- w/v designates weight/volume
- mg/kg designates milligrams per kilogram of body weight.
- % w/w represents the percentage by weight of an ingredient in the recipe of the product.
- Dry powdery ingredients which exhibited aggregates were sieved through an 800 ⁇ m screen. All dry powdery ingredients were weighed in and placed in the mixing vessel of a horizontal ploughshare or planetary mixing blender and mixed until the blend was visually practically homogeneous, i.e. approximately 10 minutes.
- the defined amount of glycerol was added slowly followed by a short mixing. Oily components were added slowly followed again by a short mixing. If necessary, the mixer was heated to a temperature inhibiting a too fast precipitation of the PEG which introduced in the next step.
- the PEG 3350 was molten.
- the defined amount of the molten PEG was added relatively quickly to the chew mixture, which was then mixed until the mixture was homogeneous and could be separated from the wall.
- the mixture resembled a “cookie dough-like” appearance.
- the mixture was formed into individual chunks using a Formax F6TM molding machine with dies for production of chunk-like shapes, and packaged for storage.
- soft chews according to the invention comprising 4-[5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methyl-N-[(2,2,2-trifluoro-ethylcarbamoyl)-methyl]-benzamide—Compound A as active ingredients are set forth below.
- the mixture was formed into individual chunks using a Formax F6TM molding machine and the processing was without any problems like stopping of the movable parts.
- soft chews that do not contain pamoic acid or salts or esters thereof are set forth below.
- Substance mass [mg] % Result Formulation G Active ingredient 500 8.93 Forming machine stops Flavor 1120 20 while in process.
- the addition Sodium lauryl sulfate 112 2 of further 2% w/w Lactose monohydrate 560 10 soybean oil and 2.5% Soybean oil (BHT- 896 16 w/w magnesium stearate stabilized) did not improve the Glycerol 420 7.5 process.
- the initial formulation containing no sodium pamoate is not processable. After addition of 2.5% sodium pamoate the forming process runs properly.
- composition according to the invention with the following excipients was prepared.
- Excipient Composition (% w/w) Fluralaner- Compound A 4.27% 2-pyrrolidone 10.19% microcrystalline cellulose 24.27% sodium starch glycolate 4.95% flavor 14.56% sodium lauryl sulfate 3.40% sodium pamoate 2.43% aspartame 0.49% magnesium stearate 0.49% glycerol 2.91% soybean oil 16.75% Polyethylene Glycol 8000 15.29%
- Dogs were randomly assigned to 4 treatment groups of 8 animals each, and one untreated control group of 8 animals.
- the dogs in the treatment groups were treated with the composition as described above on Day Zero as shown in Table 6:
- the dogs were infested on Day ⁇ 2 with approximately 50 adult unfed ticks ( R. sanguineus ) and on Day 28 and 56. Ticks were counted approximately 48 h post infestation and on Days 30 and 58 (approximately 48 hour after each post-treatment re-infestation) to evaluate the acaricidal activity in the treated groups.
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US15/386,100 Abandoned US20170100377A1 (en) | 2012-04-04 | 2016-12-21 | Solid Oral Pharmaceutical Compositions for Isoxazoline Compounds |
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US15/390,244 Abandoned US20170105972A1 (en) | 2012-04-04 | 2016-12-23 | Soft chewable pharmaceutical products |
US15/433,901 Abandoned US20170172918A1 (en) | 2012-04-04 | 2017-02-15 | Soft chewable pharmaceutical products |
US15/433,840 Abandoned US20170172986A1 (en) | 2012-04-04 | 2017-02-15 | Soft chewable pharmaceutical products |
US15/613,848 Abandoned US20170266165A1 (en) | 2012-04-04 | 2017-06-05 | Soft Chewable Pharmaceutical Products |
US15/634,924 Active 2034-05-05 US11337917B2 (en) | 2012-04-04 | 2017-06-27 | Soft chewable pharmaceutical products |
US15/982,879 Abandoned US20190117564A1 (en) | 2012-04-04 | 2018-05-17 | Soft Chewable Pharmaceutical Products |
US15/982,904 Abandoned US20190117565A1 (en) | 2012-04-04 | 2018-05-17 | Soft Chewable Pharmaceutical Product |
US16/296,490 Active US11285101B2 (en) | 2012-04-04 | 2019-03-08 | Soft chewable pharmaceutical products |
US16/508,758 Abandoned US20200000718A1 (en) | 2012-04-04 | 2019-07-11 | Solid Oral Pharmaceutical Compositions for Isoxazoline Compounds |
US17/189,939 Active 2033-07-19 US11712416B2 (en) | 2012-04-04 | 2021-03-02 | Solid oral pharmaceutical compositions for isoxazoline compounds |
US17/648,841 Pending US20220142984A1 (en) | 2012-04-04 | 2022-01-25 | Soft Chewable Pharmaceutical Products |
US18/335,415 Pending US20230320981A1 (en) | 2012-04-04 | 2023-06-15 | Solid oral pharmaceutical compositions for isoxazoline compounds |
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US (15) | US20150057321A1 (ja) |
EP (2) | EP2833867B2 (ja) |
JP (2) | JP6088637B2 (ja) |
KR (1) | KR102077874B1 (ja) |
CN (4) | CN104203214B (ja) |
AU (7) | AU2013245008B2 (ja) |
BR (3) | BR122022008957B1 (ja) |
CA (2) | CA2868381C (ja) |
ES (1) | ES2633611T5 (ja) |
NZ (1) | NZ631100A (ja) |
RU (3) | RU2646483C2 (ja) |
WO (2) | WO2013150052A1 (ja) |
ZA (2) | ZA201406968B (ja) |
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