A Phase 1 Dose Escalation Study of the Tolerability, Safety, Efficacy and Pharmacokinetics of ZG006 in Patients With Small Cell Lung Cancer

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This is a multi-center, open-label, Phase 1 clinical study of ZG006 in the US for the treatment of subjects with small cell lung cancer who have failed or are intolerant to available standard treatment. During the dose escalation stage, a standard 3+3 design will be used to assess the MTD/ recommended dose for the subsequent studies.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Small cell lung cancer (SCLC), who failed or intolerant to available standard treatments;

• Tissue sample positive for DLL3 expression;

• Life expectancy ≥ 3 months;

• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1;

• Female and Male patients must agree to use a reliable form of contraception during the study treatment period and for at least 6 months after the last dose of the study drug.

Locations
United States
California
Zelgen Site 105
NOT_YET_RECRUITING
Orange
Florida
Zelgen Site 102
RECRUITING
Plantation
Kentucky
Zelgen Site 103
RECRUITING
Lexington
Ohio
Zelgen Site 101
RECRUITING
Canton
Zelgen Site 104
NOT_YET_RECRUITING
Cleveland
Texas
Zelgen Site 106
NOT_YET_RECRUITING
Houston
Contact Information
Primary
Zelgen
liusc@zelgen.com
+86-02158942758
Time Frame
Start Date: 2025-03-31
Estimated Completion Date: 2027-06
Participants
Target number of participants: 30
Treatments
Experimental: Dose Escalation
Sponsors
Leads: Suzhou Zelgen Biopharmaceuticals Co.,Ltd

This content was sourced from clinicaltrials.gov