Evaluation of the Drug-drug Interaction Between FosD and Verapamil When Taken Together in Healthy Volunteers
Launched by ASTRAZENECA · Sep 8, 2010
Trial Information
Current as of May 13, 2025
Completed
Keywords
ClinConnect Summary
An Open-label, Single-Centre Study to Assess the Pharmacokinetics of R406 in Healthy Volunteers when Fostamatinib Disodium 150 mg is Administered Alone and in Combination with Verapamil.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Weight of at least 50 kg (110 lbs) and body mass index (BMI) between 18 and 35 kg/m2, inclusive.
- • Females must be of non-childbearing potential
- Exclusion Criteria:
- • History of clinically significant disease or disorder or presence of GI, hepatic or renal disease
- • Any clinically significant illness, medical/surgical procedure or trauma within 4 weeks of the first administration of the drug
- • Any clinically significant abnormalities in lab safety tests or vital signs as results as judged by the Investigator
- • Use of prescription or over-the-counter drugs within 2 weeks of first administration of investigational product
- • Current smokers or use of nicotine products within 1 month prior to enrollment
About Astrazeneca
AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Overland Park, Kansas, United States
Patients applied
Trial Officials
Mark Layton, MD
Study Director
AstraZeneca
Carlos Prendes, MD
Principal Investigator
Quintiles, Inc.
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials