drugset / Trial / NCT04504708

Dose-Escalation and Dose-Expansion Study of ZX-101A in Patients With Relapsed/Resistant or Refractory Advanced Hematologic Malignancies

NCT04504708 ↗

Phase 1/2 Terminated 6 enrolled Hangzhou Zenshine Pharmaceuticals Co., Ltd.
Non-randomizedSequentialOpen-labelTreatment

Summary

ZX-101A-101 is a Phase 1/2a, first-in-human, open-label, multicenter, multiple-ascending dose study to investigate the safety, tolerability, pharmacokinetics, pharmacodynamic, and preliminary antitumor activity of ZX-101A administered orally (PO) once daily (QD) in 28-day cycles in patients with relapsed/resistant or refractory advanced hematologic malignancies \[Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL), indolent NHL, and other NHL subtypes).

Timeline

Start
2021-02-17
Primary completion
2022-07-08
Completion
2022-07-08

Outcome

Outcome not reported

Stopped (Business): “Study terminated early due to business decision.”

Drugs

EvaluationDrugModalityDoseRoute
Subject ZX-101A Unknown — Oral