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Active, not recruiting Phase 3 Interventional

AZD0901 Compared With Investigator's Choice of Therapy in Participants With Second- or Later-line Advanced or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma Expressing Claudin18.2

ClinicalTrials.gov ID: NCT06346392

Public ClinicalTrials.gov record NCT06346392. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 11, 2026, 5:18 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Multi-center, Open-label, Sponsor-blinded, Randomized Study of AZD0901 Monotherapy Compared With Investigator's Choice of Therapy in Second- or Later-Line Adult Participants With Advanced/Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma Expressing Claudin18.2 (CLARITY Gastric 01)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to measure the efficacy and safety of AZD0901 compared to Investigator's choice of therapy as 2L+ treatment for participants with advanced or metastatic gastric or GEJ adenocarcinoma expressing CLDN18.2.

Study identification

NCT ID
NCT06346392
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
594 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 130 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 3, 2024
Primary completion
May 30, 2026
Completion
Oct 13, 2026
Last update posted
Jul 8, 2026

2024 – 2026

United States locations

U.S. sites
26
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Research Site Mobile Alabama 36604
Research Site Tucson Arizona 85719
Research Site Duarte California 91010
Research Site Irvine California 92618
Research Site Los Angeles California 90048
Research Site Los Angeles California 90089
Research Site Newport Beach California 92663
Research Site Washington D.C. District of Columbia 20007
Research Site Hollywood Florida 33021
Research Site Orlando Florida 32804
Research Site Marietta Georgia 30060
Research Site Boise Idaho 83712
Research Site Lexington Kentucky 40536
Research Site Boston Massachusetts 02114
Research Site Ann Arbor Michigan 48106
Research Site Ann Arbor Michigan 48109
Research Site Kansas City Missouri 64111
Research Site Mineola New York 11501
Research Site New York New York 10016
Research Site New York New York 10032
Research Site New York New York 10065
Research Site Philadelphia Pennsylvania 19111
Research Site York Pennsylvania 17403
Research Site Charlottesville Virginia 22908
Research Site Fredericksburg Virginia 22408
Research Site Olympia Washington 98502

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 132 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06346392, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 8, 2026 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06346392 live on ClinicalTrials.gov.

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