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A Phase II Single-Arm Prospective Clinical Study of Adebrelimab Combined with Chemotherapy With or Without Bevacizumab as First-Line Treatment for Recurrent/Persistent/Metastatic Cervical Cancer

A Phase II Single-Arm Prospective Clinical Study of Adebrelimab Combined with Chemotherapy With or Without Bevacizumab as First-Line Treatment for Recurrent/Persistent/Metastatic Cervical Cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107989
Enrollment
Unknown
Registered
2025-08-21
Start date
2025-08-26
Completion date
Unknown
Last updated
2025-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent/Persistent/Metastatic Cervical Cancer

Interventions

Recurrent/Persistent/Metastatic Cervical Cancer:Adebrelimab combined with chemotherapy with or without bevacizumab

Sponsors

First Hospital Of Nanping
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Histologically confirmed recurrent/persistent/metastatic cervical cancer (squamous cell carcinoma/adenocarcinoma/adenosquamous carcinoma); 2.Not eligible for curative surgery/radiotherapy; 3.No prior systemic therapy for recurrent/metastatic disease; 4.PD-L1 expression unrestricted (but status must be documented); 5.ECOG PS 0-2 with life expectancy >= 6 months; 6.At least one measurable lesion per RECIST v1.1; 7.Patients voluntarily signed informed consent forms;

Exclusion criteria

Exclusion criteria: 1.Uncontrolled hypertension and cardiac dysfunction (NYHA class III-IV); 2.Myocardial infarction or stroke within the past 6 months; 3.Active infection, immunodeficiency, or requirement for long-term immunosuppressive therapy; 4.Severe hepatic/renal dysfunction (ALT/AST >3×ULN, Cr >1.5×ULN) and other risk factors; 5.Major surgery within 6 weeks; 6.Hypersensitivity or contraindications to any component of the investigational drug;

Design outcomes

Primary

MeasureTime frame
Objective Response Rate(ORR);

Countries

China

Contacts

Public ContactRenliang Fan

First Hospital Of Nanping

523221402@qq.com+86 599 8605951

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026