An Expanded Access Study of Brigatinib for Patients With ALK-positive Advanced Non-Small Cell Lung Cancer

Sponsor

Ariad Pharmaceuticals (Industry)

Overall Status

No longer available

CT.gov ID

NCT02784158

Collaborator

(none)

Locations

Study Details

Study Description

Brief Summary

The purpose of this study is to provide brigatinib for those patients with locally advanced and/or metastatic patients with ALK+ NSCLC on an expanded access basis due to their inability to meet eligibility criteria for on-going recruiting trials, inability to participate in other clinical trials (e.g., poor performance status, lack of geographic proximity), or because other medical interventions are not considered appropriate or acceptable.

Condition or Disease	Intervention/Treatment	Phase
Non-small Cell Lung Cancer Lung Cancer Advanced Malignancies Carcinoma	Drug: Brigatinib

Study Design

Study Type:

Expanded Access

Outcome Measures

Primary Outcome Measures

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Inclusion Criteria:

Have histologically or cytologically confirmed locally advanced or metastatic NSCLC that is determined to have an ALK-rearrangement detected according to local standard procedure.
Resistant to or intolerant of at least 1 prior ALK TKI.
Recovered from toxicities related to prior anticancer therapy to NCI CTCAE, v4.0) grade ≤2.
Are a male or female patient ≥18 years old.
Have adequate organ and hematologic function, as defined by the study protocol.
Have Eastern Cooperative Oncology Group (ECOG) performance status ≤2.
Have normal QT interval on screening electrocardiogram (ECG) evaluation, defined as QT interval corrected (Fridericia) (QTcF) of ≤450 ms in males or ≤470 ms in females.
For female patients of childbearing potential, a negative pregnancy test must be documented prior to enrollment (<7 days prior to the first dose).
Female and male patients who are fertile must agree to use a highly effective form of contraception as defined by the study protocol.
Must provide a signed and dated informed consent indicating that the patient has been informed of all pertinent aspects of the study, including the potential risks, and is willingly participating.

Exclusion Criteria:

Received an ALK TKI within 10 days prior to the first dose of brigatinib.
Received cytotoxic chemotherapy, investigational agents, or radiation within 14 days, except stereotactic radiosurgery (SRS) or stereotactic body radiosurgery.
Received prior brigatinib therapy.
Received monoclonal antibodies within 30 days of the first dose of brigatinib.
Had major surgery within 30 days of the first dose of brigatinib.
Have current spinal cord compression.
Have significant, uncontrolled, or active cardiovascular disease within 6 months prior to first dose, as defined by the study protocol.
Have a history or the presence of pulmonary interstitial disease, drug-related pneumonitis, or radiation pneumonitis.
Have a known or suspected hypersensitivity to brigatinib or its excipients.
Have any condition or illness that, in the opinion of the investigator, would compromise patient safety.
Are pregnant or breastfeeding.
Are eligible for and have reasonable access to participate in another ongoing brigatinib clinical study.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	UC San Diego Moores Cancer Center (Site 099)	La Jolla	California	United States	92093-0698
2	UCI Medical Center-Chao Family Comprehensive (Site 210)	Orange	California	United States	92868-3201
3	Karmanos Cancer Institute (Site 070)	Detroit	Michigan	United States	48201