RecruitingPhase 1Phase 2NCT06253494

Pembrolizumab, Lenvatinib and IL-15 Superagonist N-803 in Combination With HER2 Targeting Autologous Dendritic Cell (AdHER2DC) Vaccine in Participants With Advanced or Metastatic Endometrial Cancer


Sponsor

National Cancer Institute (NCI)

Enrollment

60 participants

Start Date

May 14, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Background: Endometrial cancer (EC) of the uterus is becoming more common in the US. Sometimes EC often has increased levels of a protein called HER2. Cancers with HER2 tend to be more aggressive and have poorer outcomes. Objective: To test 2 study drugs-a vaccine that targets HER2 (AdHER2DC) plus a drug that supercharges immune cells that kill tumor cells (N-803)-combined with 2 FDA-approved cancer treatment drugs in people with EC. Eligibility: Adults aged 18 and older with HER2-positive EC that returned or got worse after treatment. Design: AdHER2DC vaccine is made from each participant s own blood. Participants will undergo apheresis: Blood is removed from the body through a tube attached to a needle. The blood passes through a machine that separates out the target cells. The remaining blood is returned to the body through a second needle. A special catheter may be needed. The first treatment cycle is 28 days; each cycle after that will be 21 days. All participants will get the 2 approved drugs and the vaccine. One drug is a tablet taken by mouth once a day, every day. The other drug is given through a tube attached to a needle inserted into a vein. The vaccine is injected under the skin. Participants will receive the vaccine on day 1 of cycles 1, 2, and 3. Additional doses up to 3 doses will be give if possible. Some participants will receive N-803. This drug is injected under the skin of the abdomen on day 1 of each cycle. Treatment may last up to 1 year. Follow-up visits will continue up to 2 more years.


Eligibility

Min Age: 18 YearsMax Age: 120 Years

Plain Language Summary

Simplified for easier understanding

This trial tests a combination of three treatments — pembrolizumab (immunotherapy), lenvatinib (a targeted cancer drug), and N-803 (an immune-boosting drug) — in women with advanced endometrial cancer whose tumors express a protein called HER2. The combination is designed to activate the immune system more powerfully against the cancer. **You may be eligible if...** - You are 18 or older with confirmed endometrial cancer that has spread or cannot be surgically removed - Your tumor tests positive for HER2 (IHC 1+, 2+, or 3+) - Your cancer has progressed after at least one prior treatment - You have measurable or evaluable disease on imaging - You are in generally good health (ECOG status 0–2) - A tumor tissue sample is available or you are willing to undergo a biopsy **You may NOT be eligible if...** - You have poorly controlled other medical conditions - You have had severe prior immune-related side effects - You have active autoimmune disease requiring systemic treatment 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.

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Interventions

BIOLOGICALAdHER2DC vaccine

AdHER2DC vaccine is given by intradermal injections on Day 1 of cycles 1-3 (priming) followed by optional boost doses (up to 3), on Day 1 of cycles 6, 9, 12

BIOLOGICALPembrolizumab

Pembrolizumab is given by IV infusion on Day 8 of cycle 1 and Day 1 of cycles 2-16

BIOLOGICALN-803

N-803 is given by subcutaneous injections on Day 1 of cycles 1-16

DRUGLenvatinib

Lenvatinib is taken orally on Days 8-28 on cycle 1 and every day of cycles 2-16

DEVICEPATHWAY HER2 (4B5) assay

Used during screening to estimate eligibility


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

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NCT06253494


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