IDYA

IDEAYA Biosciences

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3Trials in this database
6Recorded changes · last 12 months
Partial coverageOnly the trials and history collected so far

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.

Completion dates · Pro

Which trial dates moved later?

Pro summarizes how far estimated completion dates moved later and counts trials with edits to their main study measures, using the history available here. View Pro features
TrialSponsorPhaseStatusPrimary completion
(Neo)Adjuvant IDE196 (Darovasertib) in Patients With Localized Ocular MelanomaNCT05907954IDEAYA BiosciencesPhase 2Active not recruiting2027-04-30Estimated
IDE196 (Darovasertib) in Combination With Crizotinib as First-line Therapy in Metastatic Uveal MelanomaNCT05987332IDEAYA BiosciencesPhase 2, Phase 3Active not recruiting2027-01-15Estimated
Neoadjuvant Darovasertib in Primary Uveal MelanomaNCT07015190IDEAYA BiosciencesPhase 3Recruiting2030-10Estimated

Latest recorded trial changes

· 2 fields changed

Main study measure wording changed

Text changed; whether the study measures changed has not been verified. Saved text may be shortened.

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− Before

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

+ After

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.

Recruitment status changed

− Before

Recruiting

+ After

Active not recruiting

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· 3 fields changed

Main study measure wording changed

Text changed; whether the study measures changed has not been verified. Saved text may be shortened.

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− Before

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

+ After

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

Planned enrollment increased by 78 participants

− Before

82 participants (planned)

+ After

160 participants (planned)

Primary completion date changed

− Before

31 Jan 2026

+ After

30 Apr 2027

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