← Eichor
Study identifier: NCT07726147 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Phase 1, First in Human (FIH), Open-Label, Single-Arm, Ascending Dose Study to Assess the Safety, Tolerability and Preliminary Immunogenicity of ITI-9001 in Japanese Patients With Japanese Red Cedar (JRC) Pollinosis

Condition: Allergen Immunotherapy  ·  Sponsor: Immunomic Therapeutics, Inc.

PhasePhase 1
Planned participants45
Who can joinAll sexes, 18 Months to 65 Years
Healthy volunteersNo

About this study

This is a Phase 1, first-in-human clinical trial to test a new treatment called ITI-9001 for people with allergies to Japanese Red Cedar (JRC) pollen-a common cause of seasonal allergies in Japan. The main goals are to find out if ITI-9001 is safe, how well people tolerate it, and whether it can trigger helpful immune responses.

This description comes directly from the study's public registry record.

Talk to the study team

Scott Wehage, M.S.  ·  301-968-3501  ·  clinicaloperations@immunomix.com

Always discuss trial participation with your own doctor first.

Locations (1)

Medical Corporation Shinanokai SHINANOZAKA ClinicTokyo, Shinjuku-ku, JapanRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07726147