A Comparative Single-Dose Pharmacokinetic (PK) and Safety Study of Azilsartan Medoxomil in Children With Hypertension and in Healthy Adults

PHASE1TerminatedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

May 31, 2010

Primary Completion Date

July 31, 2013

Study Completion Date

September 30, 2013

Conditions
Hypertension
Interventions
DRUG

Azilsartan medoxomil (TAK-491)

Azilsartan medoxomil 80 mg, tablets, orally, one day only

DRUG

Azilsartan medoxomil (TAK-491)

Azilsartan medoxomil 20 mg to 60 mg (based on participant weight), tablets, orally, one day only

DRUG

Azilsartan medoxomil (TAK-491)

Azilsartan medoxomil 20 mg to 60 mg (based on participant weight), tablets, orally, one day only

DRUG

Azilsartan medoxomil (TAK-491)

Azilsartan medoxomil 0.66 mg/kg participant body weight, granules, reconstituted orally, one day only

Trial Locations (8)

Unknown

Little Rock

Atlanta

Louisville

Toledo

Birmingham

Bristol

London

Manchester

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Takeda

INDUSTRY