Extramammary Paget Disease

3

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

Condition / disease
Location
Status: Recruiting

Gynecologic Extramammary Paget's Disease

In addition to evaluating treatment outcomes, tissue samples and swabs will be collected as part of this study to allow physicians to better understand Extramammary Paget's Disease (EMPD). The researchers also want to learn more about the microorganisms (microbiome) that live on or near the areas of skin affected by EMPD, in order to better understand this condition.

Participants needed: 100
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Mayo ClinicUpdated: Jan 28, 2026Locations: 1
Eligibility criteria

Females [+3]

Males [+1]

Status: Recruiting

A Study of MQ710 With and Without Pembrolizumab in People With Solid Tumor Cancer

Participants of this study will have a diagnosis of a solid tumor cancer that has come back to its original location or spread beyond its original location (advanced), came back (relapsed) or worsened (refractory) after standard treatments, or no standard treatments are available for the participants' cancer. The purpose of this study if to find the highest dose of MQ710 that causes few or mild side effects in participants with a solid tumor cancer diagnosis.

Participants needed: 56
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Dec 3, 2025Locations: 7
Eligibility criteria

Age 18 or over [+25]

Splenectomy [+25]

Status: Recruiting

A Study of Disitamab Vedotin + Bicalutamide in HER2/AR-Positive Scrotal Paget's Disease

The goal of this clinical trial is to learn if Disitamab Vedotin combined with Bicalutamide works to treat advanced HER2-positive and AR- positive extramammary Paget disease of the scrotum. It will also learn about the safety of this combination. All patients received Disitamab Vedotin every 2 weeks and Bicalutamide everyday. Follow-up was conducted until disease progression, intolerable adverse reactions occur withdrawal of informed consent by the subject, loss to follow-up, or death. Clinical tumor imaging assessments were performed using RECIST during the treatment process.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Fudan UniversityUpdated: Aug 12, 2025Locations: 1
Eligibility criteria

Voluntarily sign the informed consent form and comply with the requirements of t... [+6]

Have a history of immunodeficiency, including HIV positive or other acquired or... [+13]