A Phase 1 Open-Label, Multi-Center, Safety and Efficacy Study of PRT7732, an Oral SMARCA2 Degrader, in Patients With Advanced or Metastatic Solid Tumors With a SMARCA4
Latest Information Update: 07 Jun 2025
At a glance
- Drugs PRT 7732 (Primary)
- Indications Solid tumours
- Focus Adverse reactions; First in man
- Sponsors Prelude Therapeutics
Most Recent Events
- 06 May 2025 According to a Prelude Therapeutics media release, Enrollment has advanced rapidly, and the company is currently enrolling patients in the fifth dose escalation cohort (60 mg once daily).
- 06 May 2025 According to a Prelude Therapeutics media release, the company expects to provide an initial first-in-human data update at a major medical meeting in the second half of 2025.
- 10 Mar 2025 According to a Prelude Therapeutics media release, company initiated and enrolled first enrollment into the Phase 1 study of once daily, oral PRT7732 and is on track to provide interim data update anticipated in the second half of 2025.