Bicalutamide and Ridaforolimus in Men With Prostate Cancer (MK-8669-002)

PHASE2CompletedINTERVENTIONAL
Enrollment

22

Participants

Timeline

Start Date

October 31, 2008

Primary Completion Date

May 31, 2011

Study Completion Date

June 30, 2011

Conditions
Prostate Cancer
Interventions
DRUG

ridaforolimus (MK8669)

Three 10 mg tablets administered daily for 5 consecutive days each week followed by 2 days without ridaforolimus and one 50 mg tablet of bicalutamide administered once daily for 7 days each week. Treatment will continue until disease progression.

DRUG

Comparator: Placebo

Three tablets of matching placebo to ridaforolimus administered daily for 5 consecutive days each week followed by 2 days without matching placebo and on 50 mg tablet of bicalutamide administered once daily for 7 days each week. Treatment will continue until disease progression.

DRUG

open-label ridaforolimus (MK8669)

Single dose of three 10 mg tablets ridaforolimus on Day 1, and 50 mg bicalutamide once daily starting on Day 2. On Day 8, patients will begin taking three 10 mg tablets of ridaforolimus daily for 5 consecutive days each week followed by 2 days without ridaforolimus and one 50 mg tablet of bicalutamide once daily for 7 days each week. Treatment will continue until disease progression.

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Ariad Pharmaceuticals

INDUSTRY

lead

Merck Sharp & Dohme LLC

INDUSTRY

NCT00777959 - Bicalutamide and Ridaforolimus in Men With Prostate Cancer (MK-8669-002) | Biotech Hunter | Biotech Hunter