A Study of Ivonescimab in People With Endometrial and Cervical Cancers
A Phase 2 Study of Ivonescimab (Bispecific Antibody Against PD1 and VEGF) For the Treatment of Endometrial (EC) and Cervical (CC) Cancers
Sponsor: Memorial Sloan Kettering Cancer Center + Summit Therapeutics
No open prediction endpoints
Endpoints are classified and published by ProgramSignal analysts.
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Primary Endpoints (CT.gov)
Overall response rate (ORR)
Time frame: 27 weeks
Eligibility Criteria
Inclusion Criteria: * Histologically confirmed metastatic/recurrent endometrial or cervical cancer that has progressed after treatment with at least one platinum-based regimen. 1. Endometrial cancer histologies can include: endometrioid, serous, clear cell, dedifferentiated/undifferentiated, mixed epithelial, adenocarcinoma NOS, and carcinosarcoma. 2. Cervical cancer histologies can include: squamous cell carcinoma, adenocarcinoma, and adenosquamous cell carcinoma * Measurable disease per RECIST v 1.1 criteria * Subjects must have an Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 to 2. * All patients must have received at least 1 line of platinum-based therapy. Prior PD1 or VEGF therapy is allowed. * Adequately controlled blood pressure (BP) with or without antihypertensive medications, defined as BP ≤160/90 mmHg. * Have adequate laboratory values as defined in the following table: * Hematologic * Absolute neutrophil count (ANC) ≥1500/mm3 (≥1.5 × 103/µL…
Read full criteria on CT.gov →✦ Analyst Commentary
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