Vulvar Carcinoma

5

Review clinical trials related to Vulvar Carcinoma. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Tisotumab Vedotin in Squamous Cell Carcinoma of the Vulva

This is an open-label, single arm, phase 2 study designed to evaluate the efficacy of tisotumab vedotin in participants with recurrent or metastatic squamous cell carcinoma of the vulva by estimating the objective response rate. Patients will receive tisotumab vedotin every 3 weeks (21 days plus or minus 3 days). Treatment will continue until either unacceptable toxicity, progression of disease, or investigator/patient request for withdrawal.

Participants needed: 28
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: GOG FoundationUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Age ≥18 years, or considered an adult by local regulations, at time of consent. [+22]

Has primary melanoma, adenocarcinoma, sarcomatoid, or other histologies not ment... [+32]

Status: Recruiting

Vaginal DHEA to Improve Vaginal Health After Radiation for Women With Gynecologic, Anal or Rectal Cancer

This phase II trial tests the feasibility and side effects of vaginal DHEA to improve vaginal health after radiation for women with gynecologic, anal or rectal cancer. Treatment of cancers with radiation to the abdomen can influence the vaginal microbiome (any bacteria, virus, or other organisms found in the vagina). Both menopause and radiation cause a decrease in lubrication and elasticity of the vagina and symptoms including vaginal dryness, vaginal burning and itching, vaginal bleeding, pain or burning during urination, and pain during sexual intercourse. DHEA is a type of hormone replacement therapy. It is use to improve symptoms in women during menopause and may be effective in treating these symptoms for women who have received radiation.

Participants needed: 25
Trial details
Phase: Phase 2Age: 50+Biological sex: FemaleType: InterventionalSponsor: Ohio State University Comprehensive Cancer CenterUpdated: Apr 21, 2026Locations: 1
Eligibility criteria

Any patient with anal, rectal, cervical, vaginal, or vulvar cancer receiving ext... [+4]

Patients with scleroderma, mixed connective tissue disorder, and lupus will be e... [+10]

Status: Recruiting

Cryocompression With or Without Cilostazol for the Prevention of Paclitaxel-induced Neuropathy in Patients With Gynecological Cancers

The phase II trial evaluates the effectiveness of cryocompression therapy alone or in combination with cilostazol in preventing paclitaxel-induced peripheral neuropathy (numbness, pain or tingling in the feet and hands) for patients with gynecologic cancers. Peripheral neuropathy is a common side effect of many chemotherapeutic agents, including paclitaxel. Paclitaxel is in a class of medications called antimicrotubule agents. It stops cancer cells from growing and dividing and may kill them. Cryocompression is a therapy that combines compression garments or dressings with cooling of the treated area. Cilostazol is in a class of medications called platelet-aggregation inhibitors (antiplatelet medications). It works by improving blood flow to the legs. Giving cilostazol together with cryocompression may be safe and tolerable in treating patients with gynecological cancers.

Participants needed: 70
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Emory UniversityUpdated: Aug 27, 2025Locations: 3
Eligibility criteria

Age 18 years or older [+5]

Any patient unable and/or unwilling to cooperate with all study protocols [+27]

Status: Recruiting

HPV Vaccine, Imiquimod, and Metformin Combination Trial

The goal of this clinical trial is to explore whether additional treatments can help strengthen the participant's immune system to fight cancer caused by the Human Papillomavirus (HPV), a virus spread through intimate skin-to-skin contact. The trial will also monitor the safety of these treatments. The main questions it aims to answer are: Does the combination of treatments help the participant's body fight the cancer more effectively when used alongside standard therapy? What side effects or medical issues arise when using these experimental treatments? Researchers will use three experimental therapies along with the participant's standard treatment to find out if these therapies work better together than standard treatment alone. Participants will: Receive HPV vaccinations during the 2nd and 4th week of radiation, and again at weeks 8, 10, 12, and 16 after completing radiation. Have blood samples taken, tumor cells brushed from the surface, and imiquimod cream applied during each visit. Take a daily metformin pill and apply an imiquimod suppository three times a week for two weeks after each visit.

Participants needed: 85
Trial details
Phase: Phase 2Age: 18-64Biological sex: FemaleType: InterventionalSponsor: Baylor College of MedicineUpdated: Nov 13, 2024Locations: 2
Eligibility criteria

Participants must have histologically confirmed locally advanced or metastatic c... [+18]

Patients who are receiving any other investigational agents. [+5]