FindMyKOL
Clinical trialNCT06816992RecruitingPhase 1Interventional

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

SponsorORIC PharmaceuticalsEnrollment76EGFR Exon 20 Insertion MutationsEGFR-mutated NSCLCNSCLCSolid Tumors
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Australia
  • Peter Maccallum Cancer Centre

    Melbourne, Victoria, Australia

    Not, yet, recruiting
Canada
  • the Princess Margaret Hospital

    Toronto, Ontario, Canada

    Not, yet, recruiting
United States
  • Nyu Langone Health

    New York, New York, United States

    Recruiting
  • Virginia Cancer Specialists

    Fairfax, Virginia, United States

    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

ORIC-114 Dose 1 + amivantamabORIC-114 Dose 2 + amivantamabORIC-114 Dose 3 + amivantamab
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
27 Feb 2025
Primary completion
31 Dec 2026
Completion
31 Dec 2027
Last update posted
24 Apr 2026
Registered enrollment
76
Registry id
NCT06816992

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.