Study of ZG005 in Combination With Gecacitinib in Participants With Advanced Cervical Cancer

Recruiting Phase 1 Phase 2 Interventional Study
Cervical Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 75
Sex
Female
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
Suzhou Zelgen Biopharmaceuticals Co.,Ltd · Industry
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About This Trial

This is a multicenter, open-label phase I/II study in patients with advanced cervical cancer designed to evaluate the safety, tolerability, and preliminary efficacy of ZG005 in combination with Gecacitinib ± bevacizumab.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Fully understand the study and voluntarily sign the informed consent form. * Female 18-75 years of age; * Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1. * Histologically or cytologically confirmed advanced cervical cancer, including squamous cell carci…
Contacts

Yongsheng Chu

+86-0512-57309965

chuys@zelgen.com

CONTACT