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 Study to Learn About the Investigational Drug Rinzimetostat (ORIC-944) in Patients With mCRPC Who Were Previously Treated With Abiraterone Acetate (Himalayas-1)

Himalayas-1 is a randomized, open-label, global, multicenter phase 3 study evaluating whether the combination of rinzimetostat with darolutamide is more effective compared to physician's choice of control; ARPI (darolutamide or enzalutamide) or docetaxel for treating patients with metastatic castration resistant prostate cancer (mCRPC) who were previously treated with abiraterone acetate. The primary objective of this study is to demonstrate superiority in radiographic progression free survival (rPFS) of the investigational arm of rinzimetostat + darolutamide combination versus physician's choice of control: ARPI (darolutamide or enzalutamide) or docetaxel.

Participants needed: 600
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: ORIC PharmaceuticalsUpdated: Jul 23, 2026Locations: 2
Eligibility criteria

Histologically or cytologically confirmed adenocarcinoma of the prostate without... [+4]

Treatment with first-generation antiandrogen agents (eg, bicalutamide, flutamide... [+5]

Status: Recruiting

Study of ORIC-944 in Patients With Metastatic Prostate Cancer

The purpose of this study is to establish the safety and preliminary antitumor activity of ORIC-944 as a single agent and in combinations with ARPIs in patients with metastatic prostate cancer.

Participants needed: 275
Trial details
Phase: Phase 1Age: 18+Biological sex: MaleType: InterventionalSponsor: ORIC PharmaceuticalsUpdated: Jul 9, 2026Locations: 27
Eligibility criteria

Patients with metastatic prostate cancer [+10]

History or presence of CNS metastases, unless previously treated and stable [+5]

Status: Recruiting

ORIC-114 in Combination With Subcutaneous Amivantamab in Patients With EGFR Exon20 Insertion Mutant NSCLC

The purpose of this study is to establish the recommended phase 2 dose (RP2D), safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity of ORIC-114 in combination with subcutaneous (SC) amivantamab in patients with advanced or metastatic NSCLC harboring an EGFR exon 20 insertion mutation.

Participants needed: 76
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: ORIC PharmaceuticalsUpdated: Apr 24, 2026Locations: 4
Eligibility criteria

Histologically or cytologically confirmed metastatic NSCLC with a documented EGF... [+7]

Known small cell lung cancer transformation [+5]

Status: Recruiting

Study of ORIC-114 in Patients With Advanced Solid Tumors Harboring an EGFR or HER2 Alteration

The purpose of this study is to establish the recommended Phase 2 dose (RP2D) and/or maximum tolerated dose (MTD), safety, pharmacokinetics (PK), pharmacodynamics (PD), and antitumor activity of ORIC-114 as a Single Agent or in Combination with Chemotherapy when administered to patients with advanced solid tumors harboring an EGFR or HER2 alteration.

Participants needed: 350
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: ORIC PharmaceuticalsUpdated: Aug 5, 2025Locations: 42
Eligibility criteria

Histologically or cytologically confirmed locally advanced or metastatic solid t... [+20]

Known EGFR T790M mutation [+7]