A Phase II, Prospective, Single Arm Trial of Cadonilimab in Combination With Bevacizumab and Standard Chemotherapy as First Line Therapy in Unresectable Pleural Mesothelioma

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Cadonilimab, a tetravalent bispecific antibody targeting PD-1 and CTLA-4, is designed to retain the efficacy benefit of combination of PD-1 and CTLA-4 and improve on the safety profile of the combination therapy. The aim of this study is to evaluate the efficacy and safety of cadonilimab in combination with bevacizumab and standard chemotherapy as first Line therapy in unresectable pleural mesothelioma.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically confirmed pleural malignant mesothelioma not eligible for curative surgery

• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.

• No previous systemic anti-tumor treatment for advanced/metastatic disease

• Measurable disease as per mRECIST v1.1 for assessment of response in malignant pleural mesothelioma.

• Adequate haematological, renal and liver function.

Locations
Other Locations
China
Sun Yat-sen University Cancer Center
RECRUITING
Guangzhou
Contact Information
Primary
Wenfeng Fang, MD
fangwf@sysucc.org.cn
+86-15322302066
Time Frame
Start Date: 2023-11-01
Estimated Completion Date: 2026-07
Participants
Target number of participants: 38
Treatments
Experimental: Cadonilimab+Bevacizumab+Pemetrexed+Carboplatin
Cadonilimab+Bevacizumab+Pemetrexed+Carboplatin for 4 to 6 cycles, followed by Maintenance with Cadonilimab and Bevacizumab
Related Therapeutic Areas
Sponsors
Leads: Sun Yat-sen University

This content was sourced from clinicaltrials.gov

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