A Phase 1, Open-Label, First-In-Human, Dose-Escalation Study With Expansion to Assess the Safety, Tolerability, and Pharmacokinetics of Orally Administered TRE-515 in Subjects With Solid Tumors
Latest Information Update: 31 May 2024
At a glance
- Drugs TRE 515 (Primary)
- Indications Myelodysplastic syndromes; Solid tumours
- Focus Adverse reactions; First in man
- Sponsors Trethera
- 17 Apr 2024 Planned number of patients changed from 36 to 85.
- 17 Apr 2024 Planned End Date changed from 1 Jul 2023 to 1 Jun 2027.
- 17 Apr 2024 Planned primary completion date changed from 1 May 2023 to 31 Dec 2026.