Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 1

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

NCT05315700 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • DRUG ORIC-114
  • DRUG Chemotherapy drug

Study Locations (20)

California

  • City of Hope — Duarte
  • City of Hope — Huntington Beach
  • City of Hope — Irvine
  • City of Hope — Long Beach
  • University of California, San Francisco — San Francisco

Other

  • Chris O'Brien Lifehouse — Camperdown
  • Peter MacCallum Cancer Centre — Melbourne
  • One Clinical Research, Hollywood Medical Centre — Nedlands

Florida

  • Mayo Clinic — Jacksonville
  • Moffitt Cancer Center — Tampa

Connecticut

  • Yale Cancer Center — New Haven

District of Columbia

  • Georgetown University — Washington D.C.

Illinois

  • Northwestern University — Chicago

Massachusetts

  • Dana Farber Cancer Institute — Boston

Minnesota

  • Mayo Clinic — Rochester

Trial Details

FieldValue
Enrollment Target 350 participants
Start Date 2022-03-10
Est. Completion 2027-09
Phase Phase 1

Sponsor

ORIC Pharmaceuticals

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05315700

The ClinicalTrials.gov registry entry for NCT05315700 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 350 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ORIC Pharmaceuticals, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 2 interventions — of which ORIC-114 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05315700 reports 20 study locations spanning 13 distinct geographic areas — top geographies include California, Other, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05315700 about?

NCT05315700 is a clinical study titled "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 advance...

What is the current status of trial NCT05315700?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 350 participants. The study started on 2022-03-10. Estimated completion is 2027-09.

What conditions does trial NCT05315700 study?

This clinical trial studies the following conditions: Solid Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05315700?

The interventions under investigation include: ORIC-114 (DRUG), Chemotherapy drug (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05315700?

This trial is sponsored by ORIC Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05315700 being conducted?

This trial has 20 study locations across California, Connecticut, District of Columbia, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial