Immunotherapy for Surgery Avoidance in Vulnerable dMMR Endometrial Cancer

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18+
SponsorWomen's Hospital School Of Medicine Zhejiang University

About this trial

Efficacy evaluate of iparomlimab and tuvonralimab (a PD-1/CTLA-4 bispecific antibody) in patients with surgically resectable dMMR endometrial cancer.

Eligibility criteria

Qualifiers

Age:18 years or older.

Histologically confirmed endometrial cancer (excluding carcinosarcoma).

FIGO (2009) stage I to IIIC2 disease that is considered surgically completely resectable.

Must agree to use contraception from the time of informed consent until at least 5 months after the last dose of the investigational product.

Disqualifiers

Myocardial infarction;

Unstable angina pectoris;

Congestive heart failure of New York Heart Association (NYHA) Class III or IV

Poorly controlled hypertension despite appropriate treatment (e.g., sustained systolic blood pressure ≥150 mmHg or diastolic blood pressure ≥90 mmHg for ≥ 24 hours)

Trial design

Treatments tested in this trial

  • Iparomlimab and Tuvonralimab (QL1706)

Treatment groups

30 Participants
are divided into 1 treatment group

Locations

This trial has no locations