Trial record 7 of 118 for:    "Expanded Access" [STUDY-TYPES] | Open Studies

Expanded Access Study of Afatinib in Treatment-naive or Chemotherapy Pre-treated Patients With Non-small Cell Lung Cancer (NSCLC)

Expanded access is currently available for this treatment.
Verified August 2014 by Boehringer Ingelheim
Sponsor:
Information provided by (Responsible Party):
Boehringer Ingelheim
ClinicalTrials.gov Identifier:
NCT01931306
First received: August 20, 2013
Last updated: August 20, 2014
Last verified: August 2014
  Purpose

To provide expanded access and to evaluate the safety, tolerability and efficacy of afatinib in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) harboring Epidermal Growth Factor Receptor (EGFR) mutation(s) and have never been treated with an EGFR tyrosine kinase inhibitor (TKI)


Condition Intervention
Carcinoma, Non-Small-Cell Lung
Drug: Afatinib

Study Type: Expanded Access     What is Expanded Access?
Official Title: An Open Label Expanded Access Program of Afatinib (BIBW 2992) in Treatment-naive or Chemotherapy Pre-treated Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) Harboring EGFR Mutation(s)

Resource links provided by NLM:


Further study details as provided by Boehringer Ingelheim:

Study Start Date: August 2013
Estimated Study Completion Date: December 2015
Estimated Primary Completion Date: December 2015 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: Afatinib
    BIBW2992 low to medium dose once daily
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  1. locally advanced or metastatic Non-Small Cell Lung Cancer
  2. Epidermal Growth Factor Receptor mutation positive result per the institution's testing methodology. Any type of EGFR mutation allowed
  3. Treatment naïve or patients who have received one line of chemotherapy, chemotherapy include neo adjuvant and adjuvant chemotherapy within 1 year from enrolment
  4. male or female patients age more than 18 years
  5. Adequate organ function, defined as all of the following:

    1. Absolute Neutrophil Count over 1500 per mm3. ANC over 1000 per mm3 may be considered in special circumstances such as benign cyclical neutropenia as judged by the investigator and in discussion with the sponsor.
    2. Platelet count more than 75,000 per mm3
    3. Serum creatinine below 1.5 times of the upper limit of normal
    4. Total Bilirubin below 1.5 times upper limit of institutional normal. Patients with Gilbert's syndrome total bilirubin must be below 4 times institutional upper limit of normal.
    5. Aspartate Amino Transferase or Alanine Amino Transferase below three times the upper limit of normal, if related to liver metastases below five times ULN.
  6. ECOG score between 0 - 2
  7. written informed consent by patient or guardian prior to admission into the trial that is consistent with International Conference on Harmonisation - Good Clinical Practice guidelines and local law.

Exclusion criteria:

  1. prior treatment with an EGFR tyrosine kinase inhibitor
  2. hormonal anti-cancer treatment within 2 weeks prior to start of trial treatment ,continued use of anti androgens and or gonadorelin analogues for treatment of prostate cancer permitted
  3. radiotherapy within 14 days prior to drug administration, except as follows:

    1. Palliative radiation to organs other than chest may be allowed up to 2 weeks prior to drug administration, and
    2. Single dose palliative treatment for symptomatic metastasis outside above allowance to be discussed with sponsor prior to enrolling.
  4. major surgery within 4 weeks before starting trial treatment or scheduled for surgery during the projected course of the trial
  5. known hypersensitivity to afatinib or any of its excipients
  6. history or presence of clinically relevant cardiovascular abnormalities such as uncontrolled hypertension, congestive heart failure New York Heart Association classification of over 3, unstable angina or poorly controlled arrhythmia as determined by the investigator. Myocardial infarction within 6 months prior to starting trial treatment.
  7. Women of Child-Bearing Potential and men who are able to father a child, unwilling to use adequate contraception prior to trial entry, for the duration of trial participation and for at least 2 weeks after treatment has ended.
  8. childbearing potential who:

    1. are nursing or
    2. are pregnant or
    3. are not using an acceptable method of birth control, or do not plan to continue using this method throughout the trial and,or do not agree to submit to pregnancy testing required by this protocol
  9. any history of or concomitant condition that, in the opinion of the investigator, would compromise the patient's ability to comply with the trial or interfere with the evaluation of safety for the trial drug
  10. previous or concomitant malignancies at other sites, except effectively treated non-melanoma skin cancers, carcinoma in situ of the cervix, ductal carcinoma in situ or effectively treated malignancy that has been in remission for more than 3 years and is considered to be cured.
  11. requiring treatment with any of the prohibited concomitant medications that can not be stopped for the duration of trial participation
  12. known pre-existing interstitial lung disease
  13. presence of poorly controlled gastrointestinal disorders that could affect the absorption of the trial drug
  14. active hepatitis B infection, active Hepatitis C infection
  15. meningeal carcinomatosis
  16. symptomatic brain metastases, patients with asymptomatic brain metastases, who were previously treated, are eligible provided they have had Stable Disease for at least 4 weeks on stable doses of medication
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01931306

Contacts
Contact: Boehringer Ingelheim Call Center 1-800-243-0127 clintriage.rdg@boehringer-ingelheim.com

Locations
Korea, Republic of
1200.193.82003 Boehringer Ingelheim Investigational Site
Bucheon, Korea, Republic of
1200.193.82009 Boehringer Ingelheim Investigational Site
Busan, Korea, Republic of
1200.193.82001 Boehringer Ingelheim Investigational Site
Incheon, Korea, Republic of
1200.193.82010 Boehringer Ingelheim Investigational Site
Jeonnam, Korea, Republic of
1200.193.82002 Boehringer Ingelheim Investigational Site
Jinju, Korea, Republic of
1200.193.82004 Boehringer Ingelheim Investigational Site
Seongnam, Korea, Republic of
1200.193.82007 Boehringer Ingelheim Investigational Site
Seoul, Korea, Republic of
1200.193.82008 Boehringer Ingelheim Investigational Site
Seoul, Korea, Republic of
1200.193.82005 Boehringer Ingelheim Investigational Site
Seoul, Korea, Republic of
1200.193.82006 Boehringer Ingelheim Investigational Site
Seoul, Korea, Republic of
Sponsors and Collaborators
Boehringer Ingelheim
Investigators
Study Chair: Boehringer Ingelheim Boehringer Ingelheim
  More Information

No publications provided

Responsible Party: Boehringer Ingelheim
ClinicalTrials.gov Identifier: NCT01931306     History of Changes
Other Study ID Numbers: 1200.193
Study First Received: August 20, 2013
Last Updated: August 20, 2014
Health Authority: South Korea: Ministry of Food and Drug Safety (MFDS)

Additional relevant MeSH terms:
Carcinoma
Carcinoma, Non-Small-Cell Lung
Lung Neoplasms
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Carcinoma, Bronchogenic
Bronchial Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Lung Diseases
Respiratory Tract Diseases

ClinicalTrials.gov processed this record on August 21, 2014