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A Multi-Center Retrospective Observational Study to Evaluate PD-L1 Protein Expression in Chinese Patients with Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

A Multi-Center Retrospective Observational Study to Evaluate PD-L1 Protein Expression in Chinese Patients with Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023909
Enrollment
Unknown
Registered
2019-06-17
Start date
2019-08-16
Completion date
Unknown
Last updated
2019-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

NSCLC

Interventions

PD-L1 group:PD-L1 expression (IHC 22C3 pharmDx kit)

Sponsors

Beijing Cancer Hosptial
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: All inclusion and exclusion criteria will be reviewed by the investigator or qualified designee to ensure that the samples qualifies for the study. 1. Patients must have a histologically confirmed primary NSCLC that is stage IIIB/IV, as classified by latest AJCC staging system, at the time of diagnosis. 2. Patients must be =18 years of age at diagnosis. 3. Patients must have a treatment-naive tumor tissue sample that was available for testing PD-L1, and from a site not previously irradiated. 4. Patients must have a formalin-fixed paraffin-embedded (FFPE) tumor tissue block available that is no older than 3 years. 5. Patients must have informed consent form (ICF) signed for any future study or have conditions that are accepted by IRB/ERC to waive ICF, OR are willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: All inclusion will be reviewed by the investigator or qualified designee to ensure that the samples qualifies for the study. No specific exclusion criteria was set for the study.

Design outcomes

Primary

MeasureTime frame
PD-L1 express;

Countries

China

Contacts

Public ContactTang Wenmin
wen.ming.tang@merck.com+86 021-22118756

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026