Patents by Inventor Stephen D. Collins
Stephen D. Collins has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).
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Publication number: 20240165125Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: ApplicationFiled: June 16, 2023Publication date: May 23, 2024Inventors: James CLOYD, Angela BIRNBAUM, Ilo LEPPIK, Stephen D. COLLINS
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Publication number: 20230090653Abstract: The present application discloses pharmaceutical compositions and methods of treating neurological disorders and seizure disorders with the high dose modified release compositions of huperzine. The pharmaceutical compositions and methods described herein, allow for higher dosing of huperzine, while avoiding rapid peak plasma levels, thereby avoiding the dose-limiting adverse events associated with the immediate release formulations.Type: ApplicationFiled: June 3, 2022Publication date: March 23, 2023Applicant: Supernus Pharmaceuticals, Inc.Inventors: Stephen D. COLLINS, Peter J. GOLDSTEIN, Joshua T. JOHNSTONE
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Publication number: 20220265547Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: ApplicationFiled: October 14, 2021Publication date: August 25, 2022Inventors: James CLOYD, Angela BIRNBAUM, Ilo LEPPIK, Stephen D. COLLINS
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Patent number: 11351120Abstract: The present application discloses pharmaceutical compositions and methods of treating neurological disorders and seizure disorders with the high dose modified release compositions of huperzine. The pharmaceutical compositions and methods described herein, allow for higher dosing of huperzine, while avoiding rapid peak plasma levels, thereby avoiding the dose-limiting adverse events associated with the immediate release formulations.Type: GrantFiled: November 19, 2019Date of Patent: June 7, 2022Assignee: Supernus Pharmaceuticals, Inc.Inventors: Stephen D. Collins, Peter J. Goldstein, Joshua T. Johnstone
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Publication number: 20210353552Abstract: The present application discloses pharmaceutical compositions for modified release of huperzine. The pharmaceutical compositions and methods described herein, allow for dosing of huperzine at higher therapeutic thresholds, while avoiding rapid serum peak plasma levels, thereby avoiding the adverse nausea and vomiting associated with the immediate release pharmaceutical compositions. Methods of treating neurological disorders and/or seizure disorders with the modified release compositions is also described.Type: ApplicationFiled: July 28, 2021Publication date: November 18, 2021Applicant: Biscayne Neurotherapeutics, Inc.Inventors: Stephen D. Collins, Peter Goldstein, Joshua T. Johnstone
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Publication number: 20210196623Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: ApplicationFiled: July 27, 2020Publication date: July 1, 2021Inventors: James CLOYD, Angela BIRNBAUM, Ilo LEPPIK, Stephen D. COLLINS
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Publication number: 20200155456Abstract: The present application discloses pharmaceutical compositions and methods of treating neurological disorders and seizure disorders with the high dose modified release compositions of huperzine. The pharmaceutical compositions and methods described herein, allow for higher dosing of huperzine, while avoiding rapid peak plasma levels, thereby avoiding the dose-limiting adverse events associated with the immediate release formulations.Type: ApplicationFiled: November 19, 2019Publication date: May 21, 2020Inventors: Stephen D. COLLINS, Peter P. GOLDSTEIN, Joshua T. JOHNSTONE
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Publication number: 20180333365Abstract: The present application discloses pharmaceutical compositions for modified release of huperzine. The pharmaceutical compositions and methods described herein, allow for dosing of huperzine at higher therapeutic thresholds, while avoiding rapid serum peak plasma levels, thereby avoiding the adverse nausea and vomiting associated with the immediate release pharmaceutical compositions. Methods of treating neurological disorders and/or seizure disorders with the modified release compositions is also described.Type: ApplicationFiled: May 21, 2018Publication date: November 22, 2018Inventors: Stephen D. COLLINS, Peter GOLDSTEIN, Joshua T. JOHNSTONE
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Publication number: 20180153797Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: ApplicationFiled: July 24, 2017Publication date: June 7, 2018Inventors: James CLOYD, Angela BIRNBAUM, Ilo LEPPIK, Stephen D. COLLINS
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Patent number: 9770407Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: GrantFiled: October 11, 2013Date of Patent: September 26, 2017Assignee: LUNDBECK PHARMACEUTICALS LLCInventors: James Cloyd, Angela Birnbaum, Ilo Leppik, Stephen D. Collins
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Patent number: 9629797Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: GrantFiled: July 12, 2012Date of Patent: April 25, 2017Assignee: LUNDBECK PHARMACEUTICALS LLCInventors: James Cloyd, Angela Birnbaum, Ilo Leppik, Stephen D. Collins
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Publication number: 20150335624Abstract: A method of treating a seizure disorder is described wherein an acetylcholinesterase(AChE) inhibitor is administered to a subject having a seizure disorder and an increased risk of a cardiac event from the seizure disorder, wherein the AChE inhibitor decreases the risk of such cardiac event. Further described are methods of decreasing the risk of a cardiac event in subjects with or without a seizure disorder by administering a therapeutically effective amount of an AChE inhibitor. Methods of treating kidney disease and reducing an elevated CRP level by administering an AChE inhibitor are also described.Type: ApplicationFiled: January 6, 2014Publication date: November 26, 2015Inventors: Stephen D. COLLINS, Stephen P. WANASKI, Holli A. CARLSON, David KOLB
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Publication number: 20140080812Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: ApplicationFiled: October 11, 2013Publication date: March 20, 2014Applicant: LUNDBECK LLCInventors: James CLOYD, Angela BIRNBAUM, Ilo LEPPIK, Stephen D. COLLINS
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Publication number: 20120283246Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: ApplicationFiled: July 12, 2012Publication date: November 8, 2012Inventors: James Cloyd, Angela Birnbaum, IIo Leppik, Stephen D. Collins
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Publication number: 20120004225Abstract: The present invention provides bumetanide, furosemide, piretanide, azosemide, and torsemide analogs and compositions comprising such analogs. The present invention also provides pharmaceutical compositions containing these bumetanide, furosemide, piretanide, azosemide, and torsemide analogs and methods for their use. All of these analogs are particularly useful for the treatment and/or prophylaxis of conditions that involve the Na+K+Cl? co-transporter or GABAA receptor including but not limited to addictive disorders, Alzheimer's Disease, anxiety disorders, ascites, autism, bipolar disorder, cancer, depression, endothelial corneal dystrophy, edema, epilepsy, glaucoma, Huntington's Disease, insomnia, ischemia, migraine, migraine with aura, neuropathic pain, nociceptive neuralgia, nociceptive pain, ocular diseases, pain, Parkinson's disease, personality disorders, postherpetic neuralgia, psychosis, schizophrenia, seizure disorders, tinnitus, and withdrawal syndromes.Type: ApplicationFiled: January 22, 2010Publication date: January 5, 2012Applicant: NeuroTherapeutics Pharma, Inc.Inventors: Stephen Wanaski, John J. Partridge, Stephen D. Collins
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Publication number: 20100204178Abstract: The present invention is directed to a carbamazepine-cyclodextrin inclusion complex useful for the parenteral administration of carbamazepine. The carbamazepine-cyclodextrin inclusion complex is prepared by the admixture of a modified cyclodextrin and carbamazepine in a physiologically acceptable fluid. Modified cyclodextrins include 2-hydroxypropyl-beta-cyclodextrin and sulfoalkyl cyclodextrins. More particularly, the sulfoalkyl cyclodextrins are those described and disclosed in U.S. Pat. Nos. 5,134,127 and 5,376,645. A physiologically acceptable fluid includes sterile isotonic water, Ringer's lactate, D5W (5% dextrose in water), physiological saline, and similar fluids suitable for parenteral administration.Type: ApplicationFiled: September 30, 2009Publication date: August 12, 2010Inventors: James Cloyd, Angela Birnbaum, Ilo Leppik, Stephen D. Collins
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Patent number: 6872734Abstract: (R)-N-[4,4-Bis(3-methyl-2-thienyl)-3-butenyl]nipecotic acid and salts thereof are effective GABA uptake inhibitory compounds and exert pharmacological effects on pain associated with diabetic neuropathy and migraine.Type: GrantFiled: October 18, 2001Date of Patent: March 29, 2005Assignee: Abbott LaboratoriesInventors: Stephen D. Collins, Roger L. Deaton, William J. Giardina, Adrienne L. Gilbert
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Publication number: 20020103236Abstract: (R)-N-[4,4-Bis(3-methyl-2-thienyl)-3-butenyl]nipecotic acid and salts thereof are effective GABA uptake inhibitory compounds and exert pharmacological effects on pain associated with diabetic neuropathy and migraine.Type: ApplicationFiled: October 18, 2001Publication date: August 1, 2002Inventors: Stephen D. Collins, Roger L. Deaton, William J. Giardina, Adrienne L. Gilbert