ERAS 4001
Alternative Names: ERAS-4001Latest Information Update: 23 Jun 2025
At a glance
- Originator Medshine Discovery
- Developer Erasca
- Class Antineoplastics; Small molecules
- Mechanism of Action KRAS protein inhibitors
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Preclinical Solid tumours
Most Recent Events
- 23 Jun 2025 Erasca plans the first-in-human phase I/Ib BOREALIS-1 trial for Solid tumours (Metastatic disease, Late-stage disease, Combination therapy, Monotherapy) (PO), in August 2025 (NCT07021898)
- 02 Jun 2025 Erasca received IND clearance from the US FDA
- 13 May 2025 Pharmacodynamics and pharmacokinetics data from a preclinical trial in Solid tumours released by Erasca