The ATTAIN Study: A Therapeutic Trial of Afatinib In the Neoadjuvant Setting
NCT02271906 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 2
Last updated 2019-04-30
Summary
The goal of this clinical research study is to learn if it is tolerable for patients with NSCLC to receive afatinib before surgery. The safety of this drug will also be studied.
Conditions
Interventions
- DRUG
-
BIBW 2992
40 mg by mouth daily for a minimum of 14 days, and until the day of surgery.
Sponsors & Collaborators
- collaborator INDUSTRY
-
M.D. Anderson Cancer Center
lead OTHER
Principal Investigators
-
George Simon, MD · M.D. Anderson Cancer Center
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-07-01
- Primary Completion
- 2017-08-16
- Completion
- 2017-08-16
- FDA Drug
- Yes
Countries
- United States
Study Locations
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