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Real-World Effectiveness of Afatinib (Gilotrif) Following Immunotherapy in the Treatment of Metastatic, Squamous Cell Carcinoma of the Lung: A Multi-Site Retrospective Chart Review Study in the U.S.

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Non-squamous, Non-Small Cell Lung Cancer

Treatments

Drug: other systemic therapy
Drug: Afatinib

Study type

Observational

Funder types

Industry

Identifiers

NCT04750824
1200-0335

Details and patient eligibility

About

Characteristics of patients with Neuregulin-1 (NRG1) gene fusion-positive solid tumors treated with afatinib, and characteristics of those treated with another systemic therapy.

Enrollment

110 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults, 18 years of age or older, at the time of diagnosis with any solid tumor.
  • Confirmed NRG1 gene fusion in any solid tumor.
  • Initiated afatinib or other systemic therapy (in any line of therapy) for treatment of a solid tumor with NRG1 gene fusion on or after 01/01/2017 through 03/31/2020.
  • Followed up for ≥3 months after initiation of afatinib or other systemic therapy (unless deceased prior to 3 months of follow-up).

Exclusion criteria

  • Treatment with any Tyrosine kinase inhibitor (TKI)/ErbB-directed therapy other than afatinib

Trial design

110 participants in 2 patient groups

All afatinib patients
Treatment:
Drug: Afatinib
All non-afatinib (other systemic therapies)
Treatment:
Drug: other systemic therapy

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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