(Neo)Adjuvant IDE196 (Darovasertib) in Patients With Localized Ocular Melanoma
Trial details
- Registry ID
- NCT05907954
- Phase
- Phase 2
Company identity has not yet been verified
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| (Neo)Adjuvant IDE196 (Darovasertib) in Patients With Localized Ocular MelanomaNCT05907954 | IDEAYA Biosciences | Phase 2 | Active not recruiting | 2027-04-30Estimated |
| IDE196 (Darovasertib) in Combination With Crizotinib as First-line Therapy in Metastatic Uveal MelanomaNCT05987332 | IDEAYA Biosciences | Phase 2, Phase 3 | Active not recruiting | 2027-01-15Estimated |
| Neoadjuvant Darovasertib in Primary Uveal MelanomaNCT07015190 | IDEAYA Biosciences | Phase 3 | Recruiting | 2030-10Estimated |
NCT05907954 · IDEAYA Biosciences
Recruiting
Active not recruiting
NCT05987332 · IDEAYA Biosciences
Text changed; whether the study measures changed has not been verified. Saved text may be shortened.
Measure: Progression-Free Survival (PFS) by blinded independent central review (BICR) of IDE196 + Crizotinib compared to investigator's choice of treatment
Measure: Overall Survival (OS) of IDE196 + Crizotinib compared to investigator's choice of treatment
Measure: Phase 2a: To determine the optimal dose of IDE196 + Crizotinib combination for Phase 2B and Phase 3 by evaluating the following: Measure: Phase 2 Progression-Free Survival (PFS) Measure: Phase 3 Overall Survival (OS) of IDE196 + Crizotinib compared to investigator's choice of treatment.
Recruiting
Active not recruiting
NCT05907954 · IDEAYA Biosciences
Text changed; whether the study measures changed has not been verified. Saved text may be shortened.
Measure: Incidence of Adverse Events (AEs) and significant laboratory abnormalities Measure: Cohort 1 (enucleation): Number of patients converted from requiring enucleation to radiation Measure: Cohort 2 (plaque brachytherapy): Estimated change in modeled radiation dose
Measure: Incidence of Adverse Events (AEs) and significant laboratory abnormalities Measure: Cohort 1 (enucleation): Number of patients converted from requiring enucleation to radiation Measure: Cohort 2 (plaque brachytherapy): Estimated change in modeled radiation dose Measure: Cohort 3 (patients with small UM tumors): Number of patients with clinical benefit per protocol-defined UM response criteria
82 participants (planned)
160 participants (planned)
31 Jan 2026
30 Apr 2027