The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Mar. 02, 2021

Filed:

May. 12, 2015
Applicant:

Taris Biomedical Llc, Lexington, MA (US);

Inventors:

Heejin Lee, Bedford, MA (US);

Karen Daniel, Newton, MA (US);

Cheryl Larrivee-Elkins, Framingham, MA (US);

Vikas Agarwal, Andover, MA (US);

Hong Linh Ho Duc, Weston, MA (US);

Assignee:

TARIS Biomedical LLC, Lexington, MA (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61M 31/00 (2006.01); A61L 29/06 (2006.01); A61K 9/00 (2006.01); A61K 9/14 (2006.01); A61K 9/20 (2006.01); A61K 31/167 (2006.01); A61L 29/14 (2006.01); A61L 29/16 (2006.01);
U.S. Cl.
CPC ...
A61L 29/06 (2013.01); A61K 9/0034 (2013.01); A61K 9/14 (2013.01); A61K 9/20 (2013.01); A61K 31/167 (2013.01); A61L 29/14 (2013.01); A61L 29/16 (2013.01); A61M 31/00 (2013.01); A61M 31/002 (2013.01); A61M 31/007 (2013.01); A61L 2300/402 (2013.01); A61M 2205/04 (2013.01); A61M 2210/16 (2013.01);
Abstract

Drug delivery devices are provided in which much of a drug payload within the device remains within an area proximal to a wall of the device through which the drug must pass for release of the drug from the device into a patient. In one case, the device may include a drug reservoir portion which has a drug reservoir lumen bounded by a reservoir wall having an inner surface; a drug located in the drug reservoir lumen; and a core region which does not comprise the drug, wherein the drug is disposed between the inner surface of the reservoir wall and the core region. The device may be elastically deformable between a first shape suited for insertion through a lumen into a body cavity of the patient and a second shape suited to retain the device within the body cavity.


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