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

trialsTrialRecruiting

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

A phase 1/2 trial of GIM-531 in melanoma, run by Georgiamune Inc, now recruiting.

Overview Connected2

Overview

Safety and Tolerability Study of GIM-531 in Advanced Solid Tumors is a phase 1/2 interventional study registered as NCT06425926 by Georgiamune Inc, with 117 participants planned, started 2024-05-09 and due to reach its primary completion in 2026-12. Interventions recorded: GIM-531 and Anti-PD-1 monoclonal antibody.

Setting

A Phase 1/2, Open-label, Multi-center Study of the Safety, Tolerability, and Efficacy of GIM-531 as a Single Agent and in Combination With Anti-PD-1 in Advanced Solid Tumors

Phase

Phase 1/2

Sponsor

Georgiamune Inc

Registry

Started

2024-05-09

Enrolled

117 enrolled

Connected

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cancers

companies

Evidence strength18/100 · Preliminary

How much and what kind of evidence, not how big the benefit. Click for the breakdown.

Phase 1/2+8
117 enrolled+10
No structured primary endpoint0
Result: recruiting0
No independent replication recorded0

Formula disclosed on the evidence page.

ProvenanceLast edited 2026-09-16 · Jude Gomila · Registry trials wave 6 and products wave 7 · diff · file

Sources & links

ClinicalTrials.gov NCT06425926

Data

JSON ·

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Cancers

Melanoma

Companies

Georgiamune

Not yet reviewedNeeds expert (clinical) review. Review this page or see the review queue and roster.

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