Study of Cadonilimab Combined With Bevacizumab and Standard Chemotherapy as First Line Therapy in Unresectable Pleural Mesothelioma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorSun Yat-sen University

About this trial

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 criteria

Qualifiers

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.

Disqualifiers

Primitive peritoneal, pericardial and tunica vaginalis testis mesothelioma.

Active, untreated central nervous system (CNS) metastasis.

Use of Chinese herbal medicine or immunomodulatory agents with anti-tumor indications within 14 days prior to the first dose of study treatment.

Known active autoimmune diseases.

Trial design

Treatments tested in this trial

  • Cadonilimab+Bevacizumab+Pemetrexed+Carboplatin

Treatment groups

38 Participants
are divided into 1 treatment group

Sponsors and collaborators