Overview

Study of the Safety, Tolerability and Pharmacokinetics of HZ-A-018 in Patients With B Cell Lymphoma

Status:
Recruiting
Trial end date:
2022-02-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to establish the safety, tolerability, pharmacokinetics and RP2D (Recommended Phase II Dose) of orally administered HZ-A-018 in patients with B cell lymphoma who have at least failed or relapsed after first-line treatment.
Phase:
Phase 1
Details
Lead Sponsor:
First Affiliated Hospital of Zhejiang University
Collaborator:
Hangzhou HeZheng Pharmaceutical Co., Ltd