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Study details
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A Phase 1 Dose Escalation Trial of ZG006 in Patients With Small Cell Lung Cancer

Suzhou Zelgen Biopharmaceuticals Co.,Ltd
NCT IDNCT06592638ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

30

Study length

about 2.2 years

Ages

18–75

Locations

6 sites in CA, FL, KY +2

What this study is about

This trial is testing a treatment called ZG006 for people with small cell lung cancer who have not responded to or cannot tolerate standard treatments. The goal is to find the best dose of ZG006 that can be safely used in future studies.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take ZG006

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Maximum Tolerated Dose (MTD) of ZG006, Number of participants with adverse events (AEs), Number of participants with serious adverse events (SAEs), The incidence of dose-limiting toxicity (DLT)

Secondary: AUC from time zero to the last quantifiable concentration after dosing (AUC[0-t]) of ZG006, Disease control rate (DCR), Duration of response (DOR), Maximum plasma concentration (Cmax) of ZG006, Objective response rate (ORR), Terminal phase half-life (t1/2) of ZG006, Time to peak concentration (Tmax)

Body systems

Oncology