A Phase 1, Multicenter, Open-label, Dose-escalation Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Clinical Activity of Orally Administered LP-168 in Subjects with Relapsed or Refractory B-cell Malignancies
Administered By
Awarded By
Contributors
- Brander, Danielle Marie Principal Investigator
Start/End
- October 22, 2021 - October 17, 2026