Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Genitourinary Tumors With Sacituzumab Tirumotecan

RINGQUEST is a Phase 2, open-label, single arm, basket, investigator-initiated clinical trial of sacituzumab tirumotecan in patients with: * Cohort 1: papillary renal carcinoma (pRCC). * Cohort 2: less frequent bladder tumors such as variant histology urothelial carcinoma (VH-UC). The most common VH-UC are nested, microcystic, micropapillary, lymphoepithelioma-like, plasmacytoid, giant cell, poorly differentiated, lipid-rich, clear cell, sarcomatoid) bladder cancer and non-urothelial bladder cancer of epithelial origin including squamous cell carcinoma and adenocarcinoma (urachal and non-urachal).

Participants needed: 100
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Alianza multidisciplinar para la investigación de los tumores genitourinarios -GUARDUpdated: Jul 23, 2026Locations: 1
Eligibility criteria

The participant provides written informed consent for the study. [+18]

Symptomatic brain metastases or leptomeningeal disease. Note: Participants with... [+16]

Status: Not yet recruiting

Radium-223 for High-Volume Metastatic Hormone Sensitive Prostate Cancer

GUARD-QUANTUM is a prospective, phase II, single-arm, non-randomized, non-blinded, investigator-initiated study. The rationale behind studying this combination lies in the potential additive or synergistic benefits that may arise from concurrently targeting androgen receptor signaling pathways and bone metastases.

Participants needed: 50
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Alianza multidisciplinar para la investigación de los tumores genitourinarios -GUARDUpdated: Jul 21, 2026Locations: 12
Eligibility criteria

Patients must be fully informed about the study and sign the informed consent fo... [+20]

Presence of tumor lesion in central nervous system through radiologically confir... [+29]

Status: Recruiting

Phase III Randomized International Open Label Clinical Trial of Treatment Intensification With Docetaxel Plus Apalutamide in Patients With Metastatic Hormone-sensitive Prostate Cancer Who Did Not Achieve a Deep PSA Response After Initial Treatment With Apalutamide: REINFORCE Trial.

This is a phase III, randomized, open-label, multi-center study to assess the efficacy of treatment intensification with docetaxel plus apalutamide and ADT, assessed by event-free survival, in patients with mHSPC who do not achieve deep PSA response (≤0,2 ng/ml or PSA90 response in combination with a PSA ≤ 4 ng/ml) after initial treatment with apalutamide and ADT. A non-deep PSA response is defined as PSA \> 0.2 ng/ml in combination with a PSA response \< 90%, or a PSA response ≥90% in combination with a PSA \> 4 ng/ml.

Participants needed: 320
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: Alianza multidisciplinar para la investigación de los tumores genitourinarios -GUARDUpdated: Jun 17, 2026Locations: 56
Eligibility criteria

Written informed consent. Each patient must sign an informed consent form (ICF)... [+19]

Presence of neuroendocrine histology. [+22]