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:
Jul. 22, 2025

Filed:

Jan. 08, 2019
Applicant:

Foundry Therapeutics, Inc., Menlo Park, CA (US);

Inventors:

Karun D. Naga, Los Altos, CA (US);

Stephen W. Boyd, San Francisco, CA (US);

Hanson S. Gifford, Iii, Woodside, CA (US);

Mark Deem, Portola Valley, CA (US);

John Morriss, Emerald Hills, CA (US);

Martin Mayse, Wayzata, MN (US);

Honglei Wang, Singapore, SG;

Jingnan Luo, Singapore, SG;

Daniel Boon Lim Seet, Singapore, SG;

Koon Kiat Teu, Singapore, SG;

Wei Li Lee, Singapore, SG;

Assignee:

Foundry Therapeutics, Inc., Menlo Park, CA (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61L 27/58 (2006.01); A61L 27/54 (2006.01); A61L 31/10 (2006.01); A61L 31/14 (2006.01); A61L 31/16 (2006.01);
U.S. Cl.
CPC ...
A61L 27/58 (2013.01); A61L 27/54 (2013.01); A61L 31/10 (2013.01); A61L 31/148 (2013.01); A61L 31/16 (2013.01); A61L 2300/416 (2013.01);
Abstract

The devices, systems, and methods disclosed herein may be directed to a delivery system including a therapeutic member configured for endoluminal placement via the delivery system into the esophagus of the patient, wherein the therapeutic member comprises a treatment portion comprising a film for controlled release of a chemotherapeutic agent. The film may comprise a control region, a therapeutic region, and a substantially impermeable base region. The film is configured to release the chemotherapeutic agent in a direction away from the substantially impermeable base region. The delivery system is configured to enable a treatment provider to position the treatment portion of the therapeutic member proximate to a treatment site associated with the esophagus of the patient, and the therapeutic member is configured to administer a therapeutically effective dose to the treatment site for a sustained period following endoluminal placement of the therapeutic member.


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