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RECRUITING
NCT06233292
PHASE1/PHASE2

A Study of ZG005 in Patients With Advanced Solid Tumors

Sponsor: Suzhou Zelgen Biopharmaceuticals Co.,Ltd

View on ClinicalTrials.gov

Summary

This is a multi-center, open-label, Phase 1/2 study of ZG005 for the treatment of subjects with advanced solid tumors, and consists of three stages: dose escalation and confirmation of MTD/recommended dose.

Official title: A Phase 1/2 Dose Escalation, Tolerability, Safety and Pharmacokinetics Study of ZG005 in Patients With Advanced Solid Tumors

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

484

Start Date

2022-06-17

Completion Date

2026-01

Last Updated

2024-06-14

Healthy Volunteers

No

Conditions

Interventions

BIOLOGICAL

ZG005 Powder for Injection

The dose groups of ZG005 for dose escalations are set as 0.3 mg/kg, 1mg/kg, 3mg/kg, 10mg/kg, and 20mg/kg, intravenous infusion, once every 3 weeks.

BIOLOGICAL

ZG005 Powder for Injection

Recommended Phase 2 Dose (RP2D) of ZG005 monotherapy, intravenous infusion, once every 3 weeks.

Locations (1)

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, China