A Phase I Dose Escalation Study of Tolerability, Safety, Efficacy, and Pharmacokinetics of ZG006 in Participants With Advanced Small Cell Lung Cancer or Neuroendocrine Carcinoma, Followed by a Phase II Dose Expansion Study in Participants With Advanced Small Cell Lung Cancer

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

This is a multicenter, open-label phase I/II study, divided into 2 parts: Part 1 involves a dose-escalation study of ZG006 in which the safety and tolerability of ZG006 in patients with advanced small cell lung cancer or neuroendocrine carcinoma are explored. Upon completion of Part 1, investigators and the sponsor will discuss and determine two recommended phase II doses (RP2D) based on safety, preliminary efficacy, and pharmacokinetic (PK) results for use in Part 2. Part 2 is a phase II dose-expansion study of ZG006, aiming to investigate the efficacy and safety of ZG006 in patients with advanced small cell lung cancer.

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

• Fully understand the study and voluntarily sign the informed consent form;

• Male or female 18\

⁃ 75 years of age;

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

• Life expectancy ≥ 3 months;

Locations
Other Locations
China
Shanghai Chest Hospital
RECRUITING
Shanghai
Contact Information
Primary
Hewen Yin
yinhw@zelgen.com
+86-0512-57309965
Time Frame
Start Date: 2024-09-02
Estimated Completion Date: 2026-04
Participants
Target number of participants: 105
Treatments
Experimental: Dose Escalation
A total of six dose escalations were preset: 0.1 mg, 0.3 mg, 1 mg, 3 mg, 10 mg, and 30 mg.
Experimental: Dose Expansion
Participants will receive the RP2D identified in Dose exploration of the study.
Sponsors
Leads: Suzhou Zelgen Biopharmaceuticals Co.,Ltd

This content was sourced from clinicaltrials.gov