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: Recruiting

A Trial to Evaluate Multiple Regimens in Newly Diagnosed and Recurrent Glioblastoma

Glioblastoma (GBM) adaptive, global, innovative learning environment (GBM AGILE) is an international, seamless Phase II/III response adaptive randomization platform trial designed to evaluate multiple therapies in newly diagnosed (ND) and recurrent GBM. All institutions are enrolling Newly Diagnosed participants. Institutions also enrolling Recurrent participants are marked with an asterisk (\*).

Participants needed: 2,250
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Global Coalition for Adaptive ResearchUpdated: Jul 13, 2026Locations: 63
Eligibility criteria

Age ≥ 18 years. [+9]

Received any prior treatment for glioma including: a. Prior prolifeprospan 20 wi... [+12]

Status: Recruiting

A Trial to Evaluate Multiple Regimens in Newly Diagnosed and Recurrent Glioblastoma

Glioblastoma (GBM) adaptive, global, innovative learning environment (GBM AGILE) is an international, seamless Phase II/III response adaptive randomization platform trial designed to evaluate multiple therapies in newly diagnosed (ND) and recurrent GBM. All institutions are enrolling Newly Diagnosed participants. Institutions also enrolling Recurrent participants are marked with an asterisk (\*).

Participants needed: 2,250
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Global Coalition for Adaptive ResearchUpdated: Jun 26, 2026Locations: 63
Eligibility criteria

Age ≥ 18 years. [+9]

Received any prior treatment for glioma including: a. Prior prolifeprospan 20 wi... [+12]

Status: Not yet recruiting

Department of Defense PTSD Adaptive Platform Trial - Intervention B - Vilazodone

This is a Phase 2 randomized, double-blinded, placebo-controlled study that will evaluate multiple potential pharmacotherapeutic interventions for PTSD utilizing an adaptive platform trial design. Intervention B - Vilazodone will assess the safety and efficacy of vilzodone in participants with PTSD. Please see NCT05422612 for information on the S-21-02 Master Protocol.

Participants needed: 200
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: Global Coalition for Adaptive ResearchUpdated: May 20, 2026
Eligibility criteria

Not listed