Overview

A Phase 1 Study of ZSP1602 in Participants With Advanced Solid Tumors

Status:
Recruiting
Trial end date:
2021-07-31
Target enrollment:
Participant gender:
Summary
The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics, and determine the maximum tolerated dose of ZSP1602 in participants with basal cell carcinoma, adenocarcinoma of esophagogastric junction, small cell lung cancer, neuroendocrine neoplasm and other advanced solid tumors.
Phase:
Phase 1
Details
Lead Sponsor:
Guangdong Zhongsheng Pharmaceutical Co., Ltd.