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NCT07404202Recruiting

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

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

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2100 (estimated)
First submitted
5 Feb 2026
Start date
6 Mar 2026
Primary completion date
31 Dec 2026
Lead sponsor
AstraZeneca
NCT number
NCT07404202

What you commit to

  • Study type: Observational
  • Planned participants: 2100
  • From 6 Mar 2026 to the primary completion date, 31 Dec 2026
  • 12 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 1\. Have a history of other cancers besides NSCLC, BTC, GYN cancers and UC.

Other

  • 2\. Specimens of patients that may affect interpretation evaluated by the researcher (e.g., frozen specimens, decalcified specimens, specimens with limited tumor content, etc.)

Who the study is looking for

  • 1\. Patients must be at least 18 years of age
  • 2\. Male and female patients must have a histological confirmed diagnosis of NSCLC, BTC, GYN cancers, or UC between Jan 01, 2023 and Sep 30, 2025.
  • --For GYN cancers, only cervical cancer, endometrial cancer and ovarian cancer should be included. For each gynecological cancer listed above, at least 5 cases need to be enrolled at each expression level (i.e., IHC 0/1+/2+/3+).
  • 3\. Patients must have sufficient archived tumor tissue available, with at least 15 slides suitable for HER2 status determination. Both resection or biopsy samples are acceptable. The age limit of archived tissue blocks is 5 years.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Research Site
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BeijingChinaRecruiting
Research Site
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ChangshaChinaWithdrawn
Research Site
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ChengduChinaActive, not recruiting
Research Site
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GuangzhouChinaActive, not recruiting
Research Site
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HaerbinChinaActive, not recruiting
Research Site
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JinanChinaActive, not recruiting
Research Site
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NantongChinaActive, not recruiting
Research Site
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ShanghaiChinaWithdrawn
Research Site
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ShenyangChinaActive, not recruiting
Research Site
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SuzhouChinaWithdrawn
Research Site
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ÜrümqiChinaActive, not recruiting
Research Site
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ZhejiangChinaActive, not recruiting

This page is information, not medical advice. Discuss any trial with your doctor.