S. Esmail Tabibi - Rockville MD Emmanuel I. Ezennia - Baltimore MD B. Rao Vishnuvajjala - Rockville MD Shanker Gupta - Rockville MD
Assignee:
The United States of America as represented by the Department of Health and Human Services - Washington DC
International Classification:
A61K 9127
US Classification:
424450, 264 41, 264 43, 264 46
Abstract:
The present invention provides a drug delivery system comprising a water-insoluble drug, a water-miscible organic solvent for the water-insoluble drug, a surfactant, and water, as well as a process for preparing the same. This invention further provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier and such a drug delivery system. In addition, the present invention provides a method of delivering a drug to a host by administering to the host the drug delivery system of the present invention.
Louis Plamondon - Watertown MA Louis Grenier - Medford MA Julian Adams - Brookline MA Shanker Lal Gupta - Rockville MD
Assignee:
The United States of America as represented by the Department of Health and Human Services - Washington DC Millennium Pharmaceuticals, Inc. - Cambridge MA
The invention relates to the formulation of pharmaceutical compounds. More particularly, the invention provides stable, pharmaceutically acceptable compositions prepared from boronic acid compounds and methods for preparing the compositions. The invention also provides novel boronate ester compounds. The invention further provides boronic acid anhydride compounds useful in the methods of the invention.
The present invention provides stable compounds prepared from boronic acid and lyophilized compounds thereof of the formula (1): in which Z and Z are moieties derived from sugar. The invention also provides methods for preparing such compounds. Lyophilizing a mixture comprising a boronic acid compound and a moiety derived from sugar produces a stable composition that readily releases the boronic acid compound upon reconstitution in aqueous media.
S. Esmail Tabibi - Rockville MD, US Emmanuel I. Ezennia - Baltimore MD, US B. Rao Vishnuvajjala - Rockville MD, US Shanker Gupta - Rockville MD, US
Assignee:
The United States of America as represented by the Department of Health and Human Services - Washington DC
International Classification:
A61K 9127
US Classification:
424450, 264 41, 264 43, 264 46
Abstract:
The present invention provides a drug delivery system comprising a water-insoluble drug, a water-miscible organic solvent for the water-insoluble drug, a surfactant, and water, as well as a process for preparing the same. This invention further provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier and such a drug delivery system. In addition, the present invention provides a method of delivering a drug to a host by administering to the host the drug delivery system of the present invention.
The present invention provides stable compounds prepared from boronic acid and lyophilized compounds thereof of the formula (1): in which Zand Zare moieties derived from sugar. The invention also provides methods for preparing such compounds. Lyophilizing a mixture comprising a boronic acid compound and a moiety derived from sugar produces a stable composition that readily releases the boronic acid compound upon reconstitution in aqueous media.
Louis Plamondon - Watertown MA, US Louis Grenier - Cambridge MA, US Julian Adams - Brookline MA, US Shanker Lal Gupta - Rockville MD, US
Assignee:
The United States of America as represented by the Department of Health and Human Services - Washington DC Millennium Pharmaceutical, Inc. - Cambridge MA
The invention relates to the formulation of pharmaceutical compounds. More particularly, the invention provides stable, pharmaceutically acceptable compositions prepared from boronic acid compounds and methods for preparing the compositions. The invention also provides novel boronate ester compounds. The invention further provides boronic acid anhydride compounds useful in the methods of the invention.
Pharmaceutical Compositions Of Fenretinide Having Increased Bioavailability And Methods Of Using The Same
A pharmaceutical composition for parenteral delivery, comprising a retinide such as fenretinide in combination with a solvent capable of dispersing or solubilizing the retinide. The solvent comprises an alcohol, such as ethanol, in combination with an alkoxylated castor oil, such as CREMOPHOR EL, or comprising a retinide, such as fenretinide, in an emulsion composed of a lipoid dispersed in an aqueous phase, a stabilizing amount of a non-ionic surfactant, optionally a solvent, and optionally an isotonic agent. In addition, a method of use in the treatment of hyperproliferative disorders, such as cancers is described.
Pharmaceutical Compositions Of Safingol And Methods Of Using The Same
Shanker Gupta - Rockville MD, US C. Patrick Reynolds - Sherman Oaks CA, US Barry J. Maurer - Sylmar CA, US B. Rao Vishnuvajjala - Rockville MD, US
Assignee:
Childrens Hospital Los Angeles - Los Angeles CA
International Classification:
A61K 31/19 A61K 31/13
US Classification:
514557, 514667
Abstract:
The present invention provides stable aqueous solutions consisting essentially of: (a) a sphingolipid; (b) lactic acid; and (c) optionally a stabilizing agent; wherein the solution has a molar ratio of lactic acid to sphingolipid of 1:1 to 10:1. The present invention further provides an emulsion formulation consisting essentially of: (a) lactic acid; (b) a sphingolipid, wherein the sphingolipid is present in an amount of about 0. 1 to about 30 mg/ml of emulsion; (b) optionally an isotonic agent; and (c) a phospholipid present in an amount of about 0. 2 to about 200 mg/ml of emulsion. Methods of making and using the compositions are also provided.