Deciphering Afatinib Response and Resistance With INtratumour Heterogeneity

PHASE2CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

December 16, 2016

Primary Completion Date

March 22, 2023

Study Completion Date

March 22, 2023

Conditions
Non-small Cell Lung Cancer
Interventions
DRUG

Afatinib

"40mg, 30mg, 20mg, OD, taken until progression, unacceptable toxicity, intercurrent illness, patient/clinician decision.~EGFR positive mutation patients only: dose escalation to a maximum of 50 mg/day may be considered in patients who tolerate a 40 mg/day dose (i.e. absence of diarrhoea, skin rash, stomatitis, and other adverse reactions with CTCAE Grade \> 1) in the first 3 weeks. The dose should not be escalated in any patients with a prior dose reduction. The maximum daily dose for EGFR mutation positive patients is 50 mg."

Trial Locations (7)

Unknown

Aberdeen Royal Infirmary (NHS Grampian), Aberdeen

Barnet and Chase Farm Hospitals (Royal Free London NHS Foundation Trust), Barnet

Heart of England NHS Foundation Trust, Birmingham

Beatson West of Scotland Cancer Centre (NHS Greater Glasgow & Clyde), Glasgow

The Christie NHS Foundation Trust, Manchester

NW1 2BU

University College London Hospitals NHS Foundation Trust, London

W1T 4TJ

Cr Uk & Ucl Ctc, London

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Boehringer Ingelheim

INDUSTRY

lead

University College, London

OTHER