← Eichor
Study identifier: NCT07404202 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Multicenter, Non-interventional, Descriptive Study to Assess Assay Concordance of HER2 IHC Testing in Chinese Pan-tumor Patients

Condition: Pan-tumor(NSCLC, GYN Cancers, BTC and UC)  ·  Sponsor: AstraZeneca

PhaseN/A
Planned participants2100
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

This is a multicenter, non-interventional, descriptive study to retrospectively collect solid tumor samples from focused tumor types (NSCLC, GYN cancers, BTC and UC) and assess both assay concordance and interpretation concordance.

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

Talk to the study team

AstraZeneca Clinical Study Information Center  ·  1-877-240-9479  ·  information.center@astrazeneca.com

Always discuss trial participation with your own doctor first.

Locations (14)

Research SiteBeijing, ChinaRecruiting
Research SiteChangsha, ChinaWithdrawn
Research SiteChengdu, ChinaRecruiting
Research SiteGuangzhou, ChinaRecruiting
Research SiteGuangzhou, ChinaWithdrawn
Research SiteHaerbin, ChinaRecruiting
Research SiteJinan, ChinaRecruiting
Research SiteNantong, ChinaRecruiting
Research SiteShanghai, ChinaWithdrawn
Research SiteShanghai, ChinaRecruiting
Research SiteShenyang, ChinaRecruiting
Research SiteSuzhou, ChinaWithdrawn

+ 2 more locations — full list on the registry record.

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/NCT07404202