A PHASE 1 FIRST-IN-HUMAN OPEN-LABEL STUDY EVALUATING THE SAFETY, TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS AND PRELIMINARY EFFICACY OF ERAS-4001 MONOTHERAPY AND IN COMBINATION IN PATIENTS WITH ADVANCED SOLID TUMORS
Latest Information Update: 19 Jun 2025
At a glance
- Drugs ERAS 4001 (Primary) ; Panitumumab (Primary) ; Pembrolizumab (Primary)
- Indications Solid tumours
- Focus Adverse reactions; First in man; Pharmacokinetics
- Acronyms BOREALIS-1
- Sponsors Erasca
Most Recent Events
- 19 Jun 2025 Planned number of patients changed to 200.
- 19 Jun 2025 Status changed from planning to not yet recruiting.
- 13 May 2025 According to an Erasca media release, in May 2025, the company announced the submission of an IND application to the FDA .