New hope for Hard-to-Treat endometrial cancer: pfizer launches phase 3 trial
NCT ID NCT07578649
First seen Jun 27, 2026 · Last updated Aug 18, 2026 · Updated 3 times
Summary
This Phase 3 trial tests a new biologic drug (PF-08634404) plus chemotherapy against the approved drug Keytruda plus chemotherapy in 600 women with advanced or recurrent pMMR endometrial cancer. The goal is to see if the new combination helps patients live longer without their cancer worsening. Participants will be randomly assigned to one of two groups and receive treatment for up to two years.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- PF-08634404 (a biologic drug) plus chemotherapy
- What this could lead to
- If it works, this could offer a new treatment option for people with advanced or recurrent pMMR endometrial cancer, potentially improving how long they live without the cancer growing.
- What could go wrong
- This is an early-stage Phase 3 trial that hasn't started recruiting yet. The new drug may not be more effective than the existing treatment (Keytruda), and side effects from combining it with chemotherapy are unknown.
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 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 600 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2031
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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 years and older
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Women ≥18 years of age who are confirmed not pregnant at screening. * Histologically or cytologically confirmed endometrial cancer that is recurrent or advanced; carcinosarcomas are eligible but pure sarcomas are excluded. * Newly diagnosed FIGO Stage III disease with measurable disease per RECIST v1.1, newly diagnosed FIGO Stage IV disease with or without measurable disease, or recurrent disease with or without measurable disease for which curative treatment with surgery and/or radiotherapy is unlikely. * For participants with recurrent disease, prior adjuvant systemic anti-cancer therapy is allowed if relapse occurred more than 6 months after the last dose. * Must provide tumor tissue for prospective central assessment of MMR and p53 status. * Proficient mismatch repair (pMMR) endometrial cancer as determined by central testing. * Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1. * Life expectancy of at least 12 weeks. * Adequate organ function as defined in the protocol. Exclusion Criteria: * Prior systemic therapy for first-line advanced or recurrent endometrial cancer. * Prior immunotherapy or anti-angiogenic therapy. * Deficient mismatch repair (dMMR) endometrial cancer by central testing. * Active or untreated central nervous system (CNS) metastases; participants with previously treated and clinically stable brain metastases may be eligible if not requiring steroids and without evidence of progression. * Clinically significant risk of bleeding or fistula, including a history of severe bleeding disorders. * History of another malignancy within 3 years, except for cancers with negligible risk of recurrence or death. * History of allogeneic organ or hematopoietic stem cell transplantation; active autoimmune disease requiring systemic treatment within the past 2 years; or history of immunodeficiency * Interstitial lung disease, pneumonitis, or clinically significant pulmonary disease * Uncontrolled or significant cardiovascular, metabolic, renal, hepatic, or vascular disease * Active or uncontrolled infection. * Recent major surgery or severe trauma within protocol-defined washout periods.
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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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Saitama Medical University International Medical Center
Hidaka, Saitama, 350-1298, Japan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a Weight-Loss drug and an IUD treat early uterine cancer without surgery?
- Your gut bacteria may hold the key to whether immunotherapy works
- AI reads tumor slides to match cancer patients with trials
- Hormone blockers and letrozole tested to spare uterus in early endometrial cancer