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UnknownNCT04395612

Niraparib Combined With Brivanib or Toripalimab in Patients With Cervical Cancer

A Clinical Proof-of-concept Study Evaluating Efficacy and Safety of ZL-2306 (Niraparib) Combined With Brivanib or Toripalimab in Patients With Metastatic, Recurrent, and Persistent Cervical Cancer

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
38 (estimated)
Sponsor
Chongqing University Cancer Hospital · Academic / Other
Sex
Female
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

A Clinical Proof-of-concept Study Evaluating Efficacy and Safety of ZL-2306 (Niraparib) Combined With Brivanib or Toripalimab in Patients With Metastatic, Recurrent, and Persistent Cervical Cancer

Detailed description

A prospective, open-ended, single-arm, phase II clinical study.Patients are with metastatic, recurrent, persistent cervical cancer (squamous cell carcinoma, adenocarcinoma, adenosquamous carcinoma) To observe the efficacy and safety of ZL-2306 (Niraparib) combined with Brivanib or Toripalimab in patients with metastatic, recurrent and persistent cervical cancer, and to explore the biomarkers of effectiveness.

Conditions

Interventions

TypeNameDescription
DRUGniraparib combined with brivanibDrug:Niraparib will be administered as a dose of 200 mg orally every day. Drug:Brivanib will be administered as a dose of 400mg orally every day.
DRUGniraparib combined with toripalimabDrug:Niraparib will be administered as a dose of 200 mg orally every day. Drug:Toripalimab will be administered as a dose of 240mg Intravenously every 21days.

Timeline

Start date
2020-05-08
Primary completion
2022-04-01
Completion
2022-07-01
First posted
2020-05-20
Last updated
2021-05-21

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04395612. Inclusion in this directory is not an endorsement.