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Not yet taking people in ChinaPhase 3

ZG005 added to etoposide and cisplatin for advanced neuroendocrine carcinoma

Tests ZG005 with etoposide and cisplatin in adults with untreated advanced neuroendocrine carcinoma.

Plain-language title generated from the registry record
Registry title: ZG005 Plus Etoposide and Cisplatin vs. Etoposide and Cisplatin as First-Line Treatment for Advanced Neuroendocrine Carcinoma

Key facts

Where
Zhengzhou, ChinaSee the site
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT07833839, who can take part

Where in China

  • The First Affiliated Hospital of Zhengzhou UniversityZhengzhou, ChinaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Suzhou Zelgen Biopharmaceuticals Co.,Ltd
Trial code
NCT07833839
Record updated
22 September 2026
Original description
This is a randomized, double-blind, controlled, multicenter Phase III study evaluating the efficacy, safety, pharmacokinetics, and immunogenicity of ZG005 combined with the EP regimen (etoposide plus cisplatin) in participants with advanced NEC who are naive to systemic therapy.Read full original descriptionShow less

A Randomized, Double-Blind, Controlled, Multicenter Phase III Clinical Trial of ZG005 in Combination With Etoposide and Cisplatin Versus Etoposide and Cisplatin as First-Line Treatment for Advanced Neuroendocrine Carcinoma

This is a randomized, double-blind, controlled, multicenter Phase III study evaluating the efficacy, safety, pharmacokinetics, and immunogenicity of ZG005 combined with the EP regimen (etoposide plus cisplatin) in participants with advanced NEC who are naive to systemic therapy.

Inclusion: Participant has fully understood the trial, agrees to comply with the study treatment regimen and visit schedule, and voluntarily signs the informed consent form (ICF); Male or female participants aged 18 to 75 years (inclusive) at the time of signing the informed consent form (ICF); Life expectancy of more than 3 months; Histologically confirmed recurrent or metastatic neuroendocrine carcinoma (NEC); The Eastern Cooperative Oncology Group's physical status scoring standard (ECOG) is 0~1.

Exclusion: History, computed tomography (CT), or magnetic resonance imaging (MRI) findings suggestive of central nervous system (CNS) metastases or leptomeningeal metastases.

ClinicalTrials.gov NCT07833839