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Clinical Trial Details — Status: No longer available

Administrative data

NCT number NCT03178071
Other study ID # B7461020
Secondary ID
Status No longer available
Phase
First received
Last updated

Study information

Verified date October 2019
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

This expanded access study has being designed following a demand from the FDA, given the increase in the number of request for single patient INDs for lorlatinib


Description:

Given that an Expanded Access study does not meet the definition of a controlled clinical investigation, and as such, is not considered an applicable drug clinical trial per NIH, Basic Results for such studies are not required to be reported. Protocol B7461020 has been identified as an Expanded Access trial, and has been registered to ClinicalTrials.gov, however Basic Results will not be posted. This statement has been placed in the Detailed Description section of the protocol registration on ClinicalTrials.gov.


Recruitment information / eligibility

Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Ineligibility for participation in any ongoing clinical study of the investigational product

- Age =18 years

- Histologically or cytologically diagnosis of metastatic NSCLC that carries an ALK rearrangement or a ROS1 rearrangement

- For ALK positive patients: failure to prior treatment with at least one ALK-TKI. If prior ALK-TKI was crizotinib, additional prior treatment required with at least one second generation ALK-TKI registered and commercially available. For patients with resistance mutations not covered by other inhibitors (eg, ALK G1202R resistance mutation), prior treatment with an ALK/ROS1 inhibitor is not required.

- For ROS1 positive patients: failure to prior treatment with at least crizotinib

- Adequate bone marrow, liver, renal, pancreatic functions

- Negative pregnancy test at screening

Exclusion Criteria:

- Previous surgery, chemotherapy, radiotherapy or other anti cancer therapy or participation in other studies with investigational drugs within the timeframe indicated in the protocol

- History of interstitial fibrosis or interstitial lung disease

- Concomitant use of prohibited medication

- Clinically significant cardiovascular disease: cerebral vascular accident/stroke, myocardial infarction, unstable angina, congestive heart failure, second degree or third degree atrioventricular block (unless paced) or any AV block with PR >220 msec

- Ongoing cardiac dysrhythmias, uncontrolled atrial fibrillation,bradycardia, ECG with QTc >470 msec, or congenital long QT syndrome

- History of or predisposing characteristics for acute pancreatitis

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Lorlatinib
oral tablets, administered daily, continuously

Locations

Country Name City State
United States University of Michigan Comprehensive Cancer Center Ann Arbor Michigan
United States University Cancer & Blood Center, Llc Athens Georgia
United States Brigham and Women's Hospital Boston Massachusetts
United States Dana Farber Cancer Institute Boston Massachusetts
United States Dana Farber Cancer Institute/Pharmacy Boston Massachusetts
United States Massachusetts General Hospital Boston Massachusetts
United States Charleston Hematology Oncology Associates, PA Charleston South Carolina
United States University of Chicago Medical Center Chicago Illinois
United States University of Chicago Medical Center, CCD Chicago Illinois
United States University of Cincinnati Medical Center Cincinnati Ohio
United States Ohio State University East Hospital Columbus Ohio
United States Stefanie Spielman Comprehensive Breast Center Columbus Ohio
United States The Ohio State University Columbus Ohio
United States The Ohio State University Investigational Drug Services Columbus Ohio
United States The Ohio State University James Cancer Hospital Columbus Ohio
United States The Ohio State University Martha Morehouse Medical Plaza Columbus Ohio
United States Siteman Cancer Center - West County Creve Coeur Missouri
United States Texas Oncology-Baylor Charles A. Sammons Cancer Center Dallas Texas
United States Henry Ford Health System Detroit Michigan
United States Henry Ford Hospital Detroit Michigan
United States Karmanos Cancer Institute Detroit Michigan
United States North Shore Hematology Oncology Associates East Setauket New York
United States Elmhurst Memorial Hospital Nancy W. Knowles Cancer Center Elmhurst Illinois
United States Karmanos Cancer Institute Weisberg Cancer Treatment Center Farmington Hills Michigan
United States CarePoint Gahanna Gahanna Ohio
United States Pacific Shores Medical Group Huntington Beach California
United States Pacific Shores Medical Group Irvine California
United States Pacific Shores Medical Group Long Beach California
United States Pacific Shores Medical Group Long Beach California
United States Edward Cancer Center Naperville Illinois
United States Rutgers Cancer Institute Of New Jersey New Brunswick New Jersey
United States Breast and Imaging Center - 12th floor New York New York
United States Memorial Sloan Kettering Cancer Center New York New York
United States Memorial Sloan Kettering Cancer Center New York New York
United States Kaiser Permanente, Oakland Medical Center Oakland California
United States UC Irvine Health / Chao Family Comprehensive Cancer Center Orange California
United States University of California Irvine/Chao Family Comprehensive Cancer Center Orange California
United States North Shore Hematology Oncology Associates Patchogue New York
United States Memorial Cancer Institute at Memorial Hospital West Pembroke Pines Florida
United States UPMC Hillman Cancer Center - Patient Clinic Pittsburgh Pennsylvania
United States North Shore Hematology Oncology Associates Port Jefferson Station New York
United States Kaiser Permanente, South Sacramento Medical Center Sacramento California
United States Siteman Cancer Center - South County Saint Louis Missouri
United States Washington University School of Medicine Saint Louis Missouri
United States Siteman Cancer Center - St Peters Saint Peters Missouri
United States Kaiser Permanente, San Francisco Medical Center San Francisco California
United States Seattle Cancer Care Alliance Seattle Washington
United States Arizona Oncology Associates, PC - NAHOA Sedona Arizona
United States Kaiser Permanente, Vallejo Medical Center Vallejo California

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Country where clinical trial is conducted

United States,