Status:
COMPLETED
Evaluate Severe Hepatic Impairment on Dacomitinib PK
Lead Sponsor:
Pfizer
Conditions:
Severe Hepatic Impairment
Eligibility:
All Genders
18-75 years
Phase:
PHASE1
Brief Summary
This is a post approval requirement to study the effect of severe hepatic impairment on the pharmacokinetics of dacomitinib.
Detailed Description
This is a Phase 1, open label, parallel group study to investigate the effect of severe hepatic impairment on the plasma PK, safety and tolerability after a single oral 30 mg dose of dacomitinib under...
Eligibility Criteria
Inclusion
- Inclusion Criteria
- Participants are eligible to be included in the study only if all of the following criteria apply:
- Male and/or female participants of non childbearing potential must be 18 to 75 years of age, inclusive, at the time of signing the informed consent document (ICD).
- Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures.
- Weight:
- Body mass index (BMI) of 17.5 to 40 kg/m2; and a total body weight \>50 kg (110 lb).
- Capable of giving signed informed consent as described in Appendix 1, which includes compliance with the requirements and restrictions listed in the ICD and in this protocol.
- Exclusion Criteria:
- Participants are excluded from the study if any of the following criteria apply:
- Any condition possibly affecting drug absorption (eg, gastrectomy).
- Other acute or chronic medical or psychiatric condition including recent (within the past year) or active suicidal ideation or behavior or laboratory abnormality that may increase the risk associated with study participation or IP administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the participant inappropriate for entry into this study.
- History of or current positive results for human immunodeficiency virus (HIV).
- Previous administration with an investigational drug within 30 days (or as determined by the local requirement) or 5 half lives preceding the first dose of IP used in this study (whichever is longer).
- Hypersensitivity to dacomitinib or its excipients.
- A positive urine drug test. Participants with severe hepatic impairment (Cohort 1) will be eligible to participate if their urine drug test is positive with a drug for a prescribed condition that is not expected to interfere with the PK of dacomitinib.
- Blood donation (excluding plasma donations) of approximately 1 pint (500 mL) or more within 60 days prior to dosing.
- History of sensitivity to heparin or heparin induced thrombocytopenia.
- Unwilling or unable to comply with the criteria in the Lifestyle Considerations section of this protocol.
- Investigator site staff members directly involved in the conduct of the study and their family members, site staff members otherwise supervised by the investigator, or Sponsor employees, including their family members, directly involved in the conduct of the study.
Exclusion
Key Trial Info
Start Date :
April 5 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 24 2019
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT03865446
Start Date
April 5 2019
End Date
October 24 2019
Last Update
November 6 2020
Active Locations (3)
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1
Investigational Drug Services (IDS) University of Miami Hospitals and Clinics, Research Pharmacy
Miami, Florida, United States, 33136
2
University of Miami Division of Clinical Pharmacology
Miami, Florida, United States, 33136
3
Orlando Clinical Research Center
Orlando, Florida, United States, 32809