Friday, May 1: Veppanu’s FDA Approval, Daraxonrasib Expanded Access, and Jakafi XR
BioBrief by BioBrief
Episode notes
BioBrief covers three high-signal biopharma developments from Friday, May 1, 2026. The FDA approved the first targeted protein degrader drug, Revolution Medicines moved closer to access in pancreatic cancer, and Incyte added a once-daily formulation to defend the Jakafi franchise.
- Arvinas / Pfizer — Veppanu
- Mechanism: Oral estrogen receptor PROTAC / targeted protein degrader
- Indication: ER-positive, HER2-negative, ESR1-mutated advanced or metastatic breast cancer
- Stage: FDA approval
- Key result: Median progression-free survival of 5.0 months versus 2.1 months for fulvestrant in 270 ESR1-mutated patients
- Why it matters: First FDA-approved PROTAC, validating targeted protein degradation while raising launch questions in a narrow breast cancer label
- Revolutio ...