A Phase 1 Study of EPI-326 in EGFR-mutant NSCLC and HNSCC

Part of paid clinical trials in Los Angeles, California.

Sponsor
EpiBiologics
Study ID
NCT07462377
Phase
PHASE1
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • EPI-326 — DRUG
    EPI-326 is a tissue-selective bispecific antibody for EGFR-driven cancers. EPI-326 will be administered in the clinic via IV infusion.

Study Details

A phase 1 study to determine the safety, tolerability, PK, PD, and preliminary anti-tumor activity of ascending doses of EPI-326 administered to patients with locally advanced or metastatic HNSCC and to patients with any documented EGFR-mutant locally advanced or metastatic NSCLC.

Key Dates

Start date
Mar 31, 2026
Status verified
Jun 2026
Primary completion
Jul 31, 2029
Completion
Jul 31, 2029

Study Design

Enrollment
110 participants (estimated)
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Experimental: EPI-326
    Experimental: Dose Escalation

Primary Outcome Measure

Evaluation of the safety and tolerability of EPI-326 [ Time Frame: Up to 3 years. ]

Central Contacts

Locations (6)

FacilityCityStateZIPSite coordinators
START Los AngelesLos AngelesCalifornia90025
EpiBiologics Clinical Trials
650-955-7486
Astera Cancer CareEast BrunswickNew Jersey08816
EpiBiologics Clinical Trials
650-955-7486
START New York Long IslandLake SuccessNew York11042
EpiBiologics Clinical Trials
650-955-7486
Sarah Cannon and HCA Research InstituteNashvilleTennessee37203
EpiBiologics Clinical Trials
650-955-7486
MD Anderson Cancer CenterHoustonTexas77030
EpiBiologics Clinical Trials
650-955-7486
South Texas Accelerated Research Therapeutics (START)San AntonioTexas78229
EpiBiologics Clinical Trials
650-955-7486

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