New drug combo aims to save wombs in young women with uterine cancer
NCT ID NCT06914297
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a combination of an immune-boosting drug (TQB2450) and a high-dose hormone (progestin) to treat young women (ages 18-45) with a specific type of early-stage endometrial cancer (MMRd). The goal is to eliminate the cancer while preserving the uterus so patients can still have children. Ten participants will receive the treatment and be monitored every 12 weeks to see if the cancer disappears and how long it stays away.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 10 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Apr 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age range from 18 to 45 years. 2. Pathological diagnosis of endometrioid carcinoma by biopsy, diagnostic curettage or hysteroscopy, non-invasive (G1-2); clinical diagnosis by G1-2); clinical diagnosis confirmed by at least two associate senior physicians; 3. Run possible, unknown EC; 4. Intense MRI, enhanced MMRI, enhanced MRI/CT, and pulmonary CT, or PET/CT assessments indicated that the lesions were limited to the endometrial layer or superficial myometrium, and there was no clear deep myometrium, cervix, or extrauterine involvement. 5. , WHFIGO 2023 IA1-IA2; 6. EC molecular typing, resulting in MMRd type (molecular typing is based on the World Health Organization (WHO) classification criteria for female genital tumors (5th edition) ); 7. Those who require or insist on preserving reproductive function, or those who insist on preserving the uterus despite having no fertility requirements. informed 8. The hospital was followed up on schedule. 2. Exclusion criteria 9. and can be followed up regularly in this hospital. Exclusion Criteria: 1. Endometrioid carcinoma FIGO grade G3, type II EC (including serous carcinoma, clear cell carcinoma, carcinosarcoma, undifferentiated carcinoma, dedifferentiated carcinoma, neuroendocrine carcinoma, etc.), or other non-epithelial uterine malignancies (adenosarcoma, stromal sarcoma, etc.); 2. Imaging evaluation indicates deep myometrial involvement, cervical involvement, or the possibility of extrauterine metastases. 3. History of important organ transplantation; 4. Uncontrolled diseases or active infections; 5. Concomitant with severe acute diseases such as stroke, myocardial infarction, etc. 6. Other malignant tumors of the reproductive system (except in patients with Lynch syndrome who also have ovarian cancer). 7. Those who require hysterectomy or other methods of treatment other than conservative medication. 8. Pregnant persons; 9. Those who have received conservative treatment (or medication maintenance treatment) with high-potency progesterone or oral contraceptives for more than 1 month due to endometrial hyperplasia in the past three months; 10. Smoking history, those who smoke more than 15 cigarettes per day; 11. Those who are contraindicated in the use of immunosuppressants or progesterone.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Tenth People's Hospital of Tongji University
RECRUITINGShanghai, Shanghai Municipality, 200072, China
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Other studies related to the condition(s) this trial covers.
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