Vaginal Neoplasms

2

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

Condition / disease
Location
Status: Recruiting

Agnostic Therapy in Rare Solid Tumors

The ANTARES study is a phase II basket trial designed to evaluate the tissue-agnostic efficacy of the monoclonal anti-PD1 antibody, nivolumab, in patients with advanced or metastatic rare tumors. The study aims to treat rare malignancies with PD-L1 expression (CPS ≥ 10), regardless of the tumor's tissue type or location. Patients who have not responded to standard treatments will be included, and treatment will last for up to 12 months. The study will assess objective response, progression-free survival, and biomarkers such as PD-L1, ctDNA, and microvesicles, in a multicenter collaborative effort to provide innovative therapeutic options for this underrepresented population

Participants needed: 28
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Instituto do Cancer do Estado de São PauloUpdated: Apr 15, 2026Locations: 8
Eligibility criteria

Age 18 years or older. [+65]

Previous treatment lines with immunotherapy (immune checkpoint inhibitors). [+16]

Status: Recruiting

Image-guided Brachytherapy for Vaginal Cancer (EMBRAVE)

The goal of this clinical study is to improve clinical outcomes of patients with vaginal cancer including vaginal recurrences who are treated with curative intent by primary radio(chemo)therapy and image-guided adaptive brachytherapy (IGABT). Being an observational, prospective registration study, wherein neither an experimental treatment is compared to the standard treatment, nor groups of patients are compared. The specific aims are: * to develop evidence-based recommendations for curative intent treatment with primary radio(chemo)therapy and IGABT. * to identify prognostic parameters for oncological outcomes, morbidity and quality of life. The study aims to enroll at least 300 patients. Oncological events will be evaluated at 2 and 5 years of follow-up. Acute and late morbidity events will be evaluated at end of treatment, 2 and 5 years of follow-up.

Participants needed: 300
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Erasmus Medical CenterUpdated: Aug 19, 2025Locations: 1
Eligibility criteria

Histological proven vaginal recurrence from any gynaecological cancer for whom c... [+6]

Primary vaginal cancers with involvement of the ostium of the cervix or vulva (t... [+9]