A First-in-Human, Open-Label, Phase 1/2 Dose-Escalation With Enrichment and Dose-Expansion Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Antitumor Activity of GIM-122 as a Single Agent in Adult Subjects With Advanced Solid Malignancies
Latest Information Update: 02 Mar 2025
At a glance
- Drugs GIM 122 (Primary)
- Indications Solid tumours
- Focus Adverse reactions; First in man; Therapeutic Use
- Sponsors Georgiamune
Most Recent Events
- 31 Jan 2024 Status changed from not yet recruiting to recruiting.
- 31 Aug 2023 Status changed from planning to not yet recruiting.
- 15 Aug 2023 New trial record