Dinesh Patel - Salt Lake City UT, US David Vollmer - West Jordan UT, US Claire Daugherty - Salt Lake City UT, US John Gebhard - Salt Lake City UT, US
International Classification:
A61K 31/415 A61K 31/202
US Classification:
514406000, 514560000, 514547000
Abstract:
The present invention is related to therapeutic uses of dehydroepiandrosterone (DHEA) congeners. More specifically, the present invention relates to the co-administration of a dehydroepiandrosterone (DHEA) congener in combination with at least one other pharmaceutically active agent to reduce inflammation.
Co-Administration Of Dehydroepiandrosterone (Dhea) Congener With Parthenolide For Treating Inflammation
Dinesh Patel - Salt Lake City UT, US David Vollmer - West Jordan UT, US Claire Daugherty - Salt Lake City UT, US John Gebhard - Salt Lake City UT, US
International Classification:
A61K 31/57 A61K 31/365
US Classification:
514171000, 514468000
Abstract:
The present invention is related to therapeutic uses of dehydroepiandrosterone (DHEA) congeners. More specifically, the present invention relates to the co-administration of a dehydroepiandrosterone (DHEA) congener in combination with a parthenolide to reduce inflammation.
Co-Administration Of Dehydroepiandrosterone (Dhea) Congeners And Other Active Agents For Treating Depression
Dinesh Patel - Salt Lake City UT, US David Vollmer - West Jordan UT, US Claire Daugherty - Salt Lake City UT, US John Gebhard - Salt Lake City UT, US
International Classification:
A61K 31/57
US Classification:
514171000
Abstract:
The present invention is drawn to compositions and methods for treating depression in a subject comprising co-administering therapeutically effective amounts of a DHEA congener and a second antidepressant agent to the subject, wherein the step of co-administrating is more effective in producing an anti-depressive effect compared to the administration of either the DHEA congener or the second antidepressant agent alone at their respective dosages.
Co-Administration Of Dehydroepiandrosterone (Dhea) Congeners And Other Active Agents For Treating Cancer
Dinesh Patel - Salt Lake City UT, US David Vollmer - West Jordan UT, US Claire Daugherty - Salt Lake City UT, US John Gebhard - Salt Lake City UT, US
International Classification:
A61K 31/53 A61K 31/365 A61K 31/415
US Classification:
514171000, 514406000, 514471000
Abstract:
The present invention is related to therapeutic uses of dehydroepiandrosterone (DHEA) congeners. More specifically, the present invention relates to the co-administration of a dehydroepiandrosterone (DHEA) congener in combination with at least one other pharmaceutically active agent to treat or prevent cancer.
John R. Gebhard - Salt Lake City UT, US David Vollmer - West Jordan UT, US Claire Daugherty - Salt Lake City UT, US Dinesh Patel - Salt Lake City UT, US
International Classification:
A61K 47/48 A61K 31/714 C07H 23/00 A61P 35/00
US Classification:
4241781, 514 52, 536 264, 5303871
Abstract:
The present invention is directed to methods and compositions including a taxane covalently bonded to the cobalt atom of a cobalamin. The composition can be delivered by any effective route, but is particularly useful as an oral anti-cancer or antiangiogenic compound. The anti-cancer/anti-angiogenic compound can be used in various chemotherapies including anti-angiogenic chemotherapies, alone or in combination with other anti-cancer/anti-angiogenic compounds.
John R. Gebhard - Cottonwood Heights UT, US David Vollmer - West Jordan UT, US Claire Daugherty - Salt Lake City UT, US Dinesh Patel - Salt Lake City UT, US
Assignee:
Osiris Therapeutics, Inc. - Columbia MD
International Classification:
A61K 31/714 A61P 35/00 A61P 35/02 C07H 23/00
US Classification:
514 52, 536 264
Abstract:
The present invention is directed to methods and compositions including a taxane covalently bonded to the cobalt atom of a cobalamin. The composition can be delivered by any effective route, but is particularly useful as an oral anti-cancer or antiangiogenic compound. The anti-cancer/anti-angiogenic compound can be used in various chemotherapies including anti-angiogenic chemotherapies, alone or in combination with other anti-cancer/anti-angiogenic compounds.
- Cambridge MA, US Yong XU - Midvale UT, US Michael David SAUNDERS - Sandy UT, US Xiaohui LIU - Holladay UT, US Scott Albert PEARCE - Clearfield UT, US Kevin Bret WRIGHT - Cottonwood Heights UT, US Jason Marc FOULKS - Sandy UT, US Kenneth Mark PARNELL - Kaysville UT, US Steven Brian KANNER - Salt Lake City UT, US David Lee VOLLMER - South Jordan UT, US Jihua LIU - San Marcos CA, US
Compounds having activity as PKM2 activators are disclosed. The compounds have the following structure (I):including stereoisomers, tautomers, pharmaceutically acceptable salts and prodrugs thereof, wherein R, R, R, R, Rand Rare as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.
- Lehi UT, US Yong XU - Midvale UT, US Michael David SAUNDERS - Sandy UT, US Xiaohui LIU - Holladay UT, US Scott Albert PEARCE - Clearfield UT, US Kevin Bret WRIGHT - Cottonwood Heights UT, US Jason Marc FOULKS - Sandy UT, US Kenneth Mark PARNELL - Kaysville UT, US Steven Brian KANNER - Salt Lake City UT, US David Lee VOLLMER - South Jordan UT, US Jihua LIU - San Marcos CA, US
Compounds having activity as PKM2 activators are disclosed. The compounds have the following structure (I):including stereoisomers, tautomers, pharmaceutically acceptable salts and prodrugs thereof, wherein R, R, R, R, Rand Rare as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.