Adverse EventsThere was a higher rate of treatment-emergent adverse events for repibresib subjects compared to the vehicle, which contributed to increased discontinuation rates.
Clinical Trial ResultsRepibresib did not meet the primary endpoint or key secondary endpoint in the Phase 2b vitiligo trial, leading to the decision to discontinue treatment in the ongoing extension phase and terminate the trial.
Financial StabilityThe company's cash, cash equivalents, and investments are expected to last approximately 1.1 years at the current burn rate.