ARI115148: Study to Compare the Bioavailability of Dutasteride Novel Formulation Form to the Soft Gel Capsule Form in Healthy Male Subjects

Sponsor

GlaxoSmithKline (Industry)

Overall Status

Completed

CT.gov ID

NCT01577693

Collaborator

(none)

Enrollment

Location

Arms

3.6

Actual Duration (Months)

9.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the bioavailability of 0.5mg dutasteride novel formulation compared to the currently marketed 0.5mg dutasteride soft gel capsule in fasted healthy male subjects.

Condition or Disease	Intervention/Treatment	Phase
Prostatic Hyperplasia	Drug: dutasteride Drug: dutasteride	Phase 1

Detailed Description

The purpose of this study is to determine the bioavailability of 0.5mg dutasteride in a novel formulation compared to the currently marketed 0.5mg dutasteride soft gel capsule in fasted healthy male subjects. This will be an open-label, single dose, randomized, two-period crossover study in healthy male subjects. Subjects will receive a single oral dose 0.5mg novel dutasteride formulation and a single oral dose 0.5mg dutasteride soft gel capsule in a fasted state. Each dose of the study medication will be separated by a 28-day washout period. Blood samples for pharmacokinetic analysis will be taken at regular intervals after dosing. Safety will be assessed by measurement of blood pressure, heart rate, laboratory data, and review of adverse events. The study will enrol approximately 35 healthy male subjects to ensure that 30 subjects complete the study. The study will be conducted in the USA.

Study Design

Study Type:

Interventional

Actual Enrollment :

35 participants

Allocation:

Randomized

Intervention Model:

Crossover Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

An Open-label, Single Dose, Randomized, Two-period Crossover Study to Investigate the Bioavailability of a Novel Dosage Form of Dutasteride in Healthy Male Subjects

Actual Study Start Date :

May 12, 2011

Actual Primary Completion Date :

Aug 31, 2011

Actual Study Completion Date :

Aug 31, 2011

Arms and Interventions

Arm	Intervention/Treatment
Experimental: 0.5 mg novel dose form (test) 0.5 mg novel dose form (test)	Drug: dutasteride novel dutasteride
Other: 0.5 mg Soft Gel Capsule 0.5 mg Soft Gel Capsule (reference)	Drug: dutasteride dutasteride soft gel capsule

Arm

Intervention/Treatment

Experimental: 0.5 mg novel dose form (test)

0.5 mg novel dose form (test)

Drug: dutasteride

novel dutasteride

Other: 0.5 mg Soft Gel Capsule

0.5 mg Soft Gel Capsule (reference)

Drug: dutasteride

dutasteride soft gel capsule

Outcome Measures

Primary Outcome Measures

Bioavailability [Change from Day 1 (session 1) compared to Day 29 (session 2), predose, .25, .5, .75, 1, 2, 3, 4, 6, 8, 10, 12, 16, 24, 48, 72]
To assess the dutasteride relative bioavailability of the of 0.5 mg novel formulation compared with the currently marketed 0.5 mg soft gelatin capsule.

Secondary Outcome Measures

Safety [Changes from screening to 3 months]
Changes in blood pressure and pulse rates, review of number of subjects with adverse events, and changes in clinical laboratory data.

Eligibility Criteria

Criteria

Ages Eligible for Study:

20 Years to 45 Years

Sexes Eligible for Study:

Male

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Healthy as determined by a responsible and experienced physician.
Males between 20 and 45 years of age inclusive, at the time of signing the informed consent form.
Male subjects with female partners of child-bearing potential must agree to use one of the contraception.
Body mass index within the range 18-30 kg/m2 (inclusive); weight range 55-95 kg (inclusive).
Capable of giving written informed consent.
Single QTcB < 450 msec.
Aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase, and bilirubin less than or equal to 1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).

Exclusion Criteria:

History of postural hypotension, dizziness, poor hydration, vertigo, vaso-vagal reactions or any other signs and symptoms of orthostasis.
Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
A positive test for human immunodeficiency virus (HIV) antibody.
Subject is mentally or legally incapacitated.
Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements.
History of sensitivity to dutasteride, components thereof or drugs of this class or a history of drug or other allergy.
History of sensitivity to heparin or heparin-induced thrombocytopenia
The subject has participated in a clinical trial for 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
A positive pre-study drug/alcohol screen.
History of regular alcohol consumption.
Consumption of red wine, grapefruit juice, grapefruit and related hybrids, and jufen grapes.
The subject has donated blood or blood products in excess of 500 mL within a 56 day period.
Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 6 months.
Unwillingness or inability to follow the procedures outlined in the protocol.