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 Neuroendocrine Carcinoma.
Overview
- Phase
- Phase 1
- Intervention
- ZG006
- Conditions
- Neuroendocrine Carcinoma
- Sponsor
- Suzhou Zelgen Biopharmaceuticals Co.,Ltd
- Enrollment
- 78
- Locations
- 1
- Primary Endpoint
- Objective response rate (ORR)
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief 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 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 Neuroendocrine Carcinoma.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- •Participants were deemed unsuitable for participating in the study by the investigator for any reason.
Arms & Interventions
Dose Escalation
A total of six dose escalations were preset: 0.1 mg, 0.3 mg, 1 mg, 3 mg.
Intervention: ZG006
Dose Expansion
Participants will receive the RP2D identified in Dose Escalation Study .
Intervention: ZG006
Outcomes
Primary Outcomes
Objective response rate (ORR)
Time Frame: Up to approximately 2 years
ORR is defined as the percentage of participants achieving a confirmed complete response (CR) or partial response(PR) based on RECIST 1.1 criteria.
Secondary Outcomes
- Number of participants with adverse events (AEs)(Up to approximately 2 years)