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Spots Global Cancer Trial Database for FT500 as Monotherapy and in Combination With Immune Checkpoint Inhibitors in Subjects With Advanced Solid Tumors

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Trial Identification

Brief Title: FT500 as Monotherapy and in Combination With Immune Checkpoint Inhibitors in Subjects With Advanced Solid Tumors

Official Title: FT500 as Monotherapy and in Combination With Immune Checkpoint Inhibitors in Subjects With Advanced Solid Tumors (Phase 1)

Study ID: NCT03841110

Study Description

Brief Summary: FT500 is an off-the-shelf, iPSC-derived NK cell product that can bridge innate and adaptive immunity, and has the potential to overcome multiple mechanisms of immune checkpoint inhibitor (ICI) resistance. The preclinical data provide compelling evidence supporting the clinical investigation of FT500 as monotherapy and in combination with ICI in participants with advanced solid tumors.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

UCSD Moores Cancer Center, San Diego, California, United States

University of Minnesota Masonic Cancer Center, Minneapolis, Minnesota, United States

Hackensack University Medical Center/John Theurer Cancer Center, Hackensack, New Jersey, United States

MD Anderson Cancer Center, Houston, Texas, United States

Contact Details

Name: Fate Trial Disclosure

Affiliation: FateTrialDisclosure@fatetherapeutics.com

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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