Royalty Pharma plc RPRX
Royalty Pharma plc (Nasdaq: RPRX) is a life-science royalty company. Its next catalyst on record is Neladalkib (Nuvalent/GSK; royalty-funded candidate): FDA PDUFA date (licensee-sponsored) (November 27, 2026).
Upcoming catalysts
- November 27, 2026Neladalkib (Nuvalent/GSK; royalty-funded candidate) — FDA PDUFA date (licensee-sponsored)
In May 2026, Nuvalent announced the FDA accepted its NDA for neladalkib for filing and granted the application Priority Review with a PDUFA date of November 27, 2026.
- April 23, 2027Deucrictibant (Pharvaris; royalty-funded candidate) — FDA PDUFA date (licensee-sponsored)
In July 2026, Pharvaris announced that the FDA accepted its NDA for deucrictibant immediate-release for the on-demand treatment of hereditary angioedema attacks and assigned a PDUFA date of April 23, 2027.
Recent results and decisions
- submitted Novartis completed regulatory submission for pelabresib in myelofibrosis in the European Union based on the positive Phase 3 MANIFEST-2 study.
In October 2026, Novartis announced that the regulatory submission for pelabresib in myelofibrosis was completed in the European Union, based on the positive Phase 3 MANIFEST-2 study.
Filing - adcomm positive European Medicines Agency's CHMP adopted a positive opinion of Rasonque for metastatic pancreatic adenocarcinoma.
In October 2026, Revolution Medicines announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) had adopted a positive opinion of Rasonque for the treatment of adult patients with metastatic pancreatic adenocarcinoma who have received at least one prior sys
Filing - missed Phase 2 MAXPIRe trial of Niktimvo in idiopathic pulmonary fibrosis did not meet its primary endpoint; Syndax does not plan further development in IPF.
In October 2026, Syndax Pharmaceuticals (Syndax) announced that the Phase 2 MAXPIRe trial of Niktimvo in idiopathic pulmonary fibrosis (IPF) did not meet its primary endpoint.
Filing
15 more on record.
For subscribers
- Cash runway against each catalyst, with the company's own runway statement
- Track record: every Phase 3 readout, FDA decision and guidance slip since 2014
- Expected move for each dated catalyst, from comparable past events
- Phase 2 evidence behind each Phase 3 readout
- Companies on the same target or class
- Full catalyst list with filing sentences, deals, registered trials, Excel export
The free Monday brief
Last week's readouts and FDA decisions and the dated catalysts in the week ahead, each with its filing sentence.