RecruitingPhase 2NCT06917092

QL1706-Based Therapy Post-PD-1/L1 Failure in Advanced Endometrial Cancer

A Phase II Study to Evaluate the Efficacy and Safety of QL1706 Combination Therapy in Immunotherapy-Pretreated Recurrent or Metastatic Endometrial Cancer


Sponsor

Tianjin Medical University Cancer Institute and Hospital

Enrollment

30 participants

Start Date

May 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a prospective, single-arm, multicenter Phase II study evaluating the efficacy and safety of QL1706 combined with chemotherapy in patients with advanced recurrent or metastatic endometrial cancer who progressed after prior anti-PD-1/L1 therapy.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination immunotherapy called QL1706 in patients with advanced endometrial (uterine) cancer whose disease has progressed after PD-1/PD-L1 immunotherapy. It targets patients who initially responded well to immunotherapy but have since relapsed. **You may be eligible if...** - You are between 18 and 70 years old with advanced or recurrent endometrial cancer confirmed by pathology or imaging - You previously received PD-1/PD-L1 immunotherapy and had a progression-free period of at least 6 months - Your cancer is measurable on imaging - You have received no more than 2 prior lines of systemic therapy - Your general health is good (ECOG 0-1) and your organs are functioning adequately **You may NOT be eligible if...** - Your cancer is currently progressing while on immunotherapy (you must have had a gap of at least 5 drug half-lives since your last immunotherapy dose) - You have had more than 2 prior chemotherapy regimens Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGQL1706 combined with chemotherapy ± Bevacizumab

* Drug: QL1706: 5 mg/kg IV every 3 weeks until progression, unacceptable toxicity, completion of 1 year of treatment, or meeting protocol-defined discontinuation criteria, whichever occurred first. * Drug: Chemotherapy: physician's choice chemotherapy for 3-6 cycles. * Drug: Bevacizumab (optional): 15 mg/kg IV every 3 weeks until progression, unacceptable toxicity, completion of 1 year of treatment, or meeting protocol-defined discontinuation criteria, whichever occurred first.


Locations(1)

Tianjin Medical University Cancer Institute & Hospital

Tianjin, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06917092


Related Trials