Drugs / BCX10013
last change Dec 2024 re-read 3 minutes ago

BCX10013

Developed for
paroxysmal nocturnal hemoglobinuria
Investigated by
BioCryst Pharmaceuticals

Trials 1

202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT06100900 Oct 2023 → Dec 2024 paroxysmal nocturnal hemoglobinuria BioCryst Pharmaceuticals Completed No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2023-11-03 BioCryst Pharmaceuticals Results BioCryst R&D Day Highlights New Diversified Pipeline of First-in-Class/Best-in-Class Therapies with Five Programs Expected in Clinical Development in Next 24 Months biocryst.com ↗
At the R&D Day, the company plans to present data from the recently completed 160 mg cohort of its multiple ascending dose healthy volunteer trial which highlights the strength and duration of alternative pathway suppression achieved at this dose level, supporting once-daily clinical dosing.
2023-01-09 BioCryst Pharmaceuticals Results BioCryst Reports Initial Clinical Data with Oral Factor D Inhibitor BCX10013 Supporting Development as a Once-daily Treatment for Complement-mediated Diseases biocryst.com ↗
BioCryst Pharmaceuticals, Inc. (Nasdaq: BCRX) today announced that initial data from ongoing phase 1 single ascending dose (SAD) and multiple ascending dose (MAD) trials in healthy volunteers show rapid, sustained and >97 percent suppression of the alternative pathway (AP) of the complement system 24 hours following a single 110 mg dose.

Evidence & citations 1 cited value

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as BCX10013 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06100900 ↗