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Study identifier: NCT06425926 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Safety and Tolerability Study of GIM-531 in Advanced Solid Tumors

Condition: Melanoma Stage IV · Solid Tumor  ·  Sponsor: Georgiamune Inc

PhasePhase 1/Phase 2
Planned participants117
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

GIM-531 is a first-in-class, orally bioavailable small molecule that is being developed for the treatment of advanced solid tumors as a single agent and rescue therapy. GIM-531 exhibits its primary effect through selective inhibition of regulatory T-cells (Tregs).

This description comes directly from the study's public registry record.

Talk to the study team

Jayadev Sureddi, CBCC CRO  ·  (661) 616-6453  ·  jayadev.sureddi@cbcc.global

Always discuss trial participation with your own doctor first.

Locations (11)

HonorHealth Research InstituteScottsdale, Arizona, United StatesRecruiting
Comprehensive Blood and Cancer CenterBakersfield, California, United StatesRecruiting
Providence Medical FoundationFullerton, California, United StatesRecruiting
The Angeles Clinic and Research Institute, A Cedars-Sinai AffiliateLos Angeles, California, United StatesRecruiting
UCSF Helen Diller Family Comprehensive Cancer CenterSan Francisco, California, United StatesRecruiting
Massachusetts General HospitalBoston, Massachusetts, United StatesRecruiting
Intermountain Health St. Vincent Regional Hospital - Cancer Centers of MontanaBillings, Montana, United StatesRecruiting
Weill Cornell Medicine - New York Presbyterian HospitalNew York, New York, United StatesRecruiting
University of Cincinnati Cancer CenterCincinnati, Ohio, United StatesRecruiting
Tennessee Oncology, PLLCNashville, Tennessee, United StatesRecruiting
Virginia Commonwealth UniversityRichmond, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06425926