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NCT06925724PHASE2RECRUITING

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

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Key Facts

Study type
INTERVENTIONAL
Conditions
Endometrial Cancer, Cervical Cancer
Interventions
Ivonescimab
Enrollment
50 participants
Primary completion
Apr 2027
Study completion
Apr 2027
First posted
Apr 2025
Last updated
Mar 2026

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

Expert commentary on why this trial matters and what to watch for.

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Source

Open on ClinicalTrials.gov