A Phase 1a/1b Open-label, Dose-Escalation and Expansion Study of ACTM-838 as a Single Agent in Patients With Advanced Solid Tumors
Latest Information Update: 20 Mar 2025
At a glance
- Drugs ACTM-838 (Primary)
- Indications Solid tumours
- Focus Adverse reactions; First in man
- Sponsors Actym Therapeutics
- 11 Jul 2024 Status changed from not yet recruiting to recruiting.
- 30 May 2024 According to an Actym Therapeutics media release, company announced that the U.S. Food and Drug Administration (FDA) has approved its Investigational New Drug (IND) application to start a Phase 1 clinical trial.
- 01 Apr 2024 Status changed from planning to not yet recruiting.