Study to Evaluate the Safety, Tolerability, PK, and PD of PB2452 With and Without Ticagrelor Pretreatment in Chinese Healthy Volunteers

NCT05162131 · clinicaltrials.gov ↗
PHASE1
Phase
TERMINATED
Status
34
Enrollment
INDUSTRY
Sponsor class

Stopped After recruitment of Cohorts 1-4 was completed, Sponsor decided to terminate study, initially due to COVID and then considering that PK data from the dose planned to be tested in Cohort 5 (18000 mg) would be available from the ongoing Phase 3 study.

Conditions

Interventions

Sponsor

SFJ Pharmaceuticals, Inc.