Study identifier:D1532C00069
ClinicalTrials.gov identifier:NCT01974349
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Randomized, Open-label, Single-center, Crossover Study to Assess the Effect of Food on the Pharmacokinetics of a 75 mg Single Oral Dose of Selumetinib (AZD6244; ARRY-142886) (Hyd-Sulfate) in Healthy Male Volunteers Aged 18 to 45 Years
Solid tumours
Phase 1
Yes
selumetinib (oral)
Male
39
Interventional
18 Years - 45 Years
Allocation: Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Basic Science
Verified 01 Oct 2017 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: selumetinib 75mg (oral capsule fasted) Volunteers will recieve selumetinib 75mg administered by mouth, as a capsule, in a fasted state. | Drug: selumetinib (oral) Volunteers will receive: 75 mg selumetinib oral dose in a fasted state (Treatment A) followed by a second 75 mg selumetinib oral dose in the fed state (Treatment B) with a washout period of at least 7 days between doses, or: 75 mg selumetinib oral dose in the fed state (Treatment B) followed by a second 75 mg selumetinib oral dose in the fasted state (Treatment A) with a washout period of at least 7 days between doses. Other Name: AZD6244 |
Experimental: selumetinib 75mg (oral capusle fed) Volunteers will receive selumetinib 75mg administered by mouth, as a capsule, in a fed state. | Drug: selumetinib (oral) Volunteers will receive: 75 mg selumetinib oral dose in a fasted state (Treatment A) followed by a second 75 mg selumetinib oral dose in the fed state (Treatment B) with a washout period of at least 7 days between doses, or: 75 mg selumetinib oral dose in the fed state (Treatment B) followed by a second 75 mg selumetinib oral dose in the fasted state (Treatment A) with a washout period of at least 7 days between doses. Other Name: AZD6244 |