5
Participants
Start Date
July 6, 2017
Primary Completion Date
October 24, 2017
Study Completion Date
October 25, 2017
1 mg QD to 15 mg QD PF-06649751
Up titration from 1 mg QD to 15 mg QD PF-06649751
3 mg QD to 15 mg QD PF-06649751
Up titration from 3 mg QD to 15 mg QD PF-06649751
7 mg QD to 15 mg QD PF-06649751
Up titration from 7 mg QD to 15 mg QD PF-06649751
15 mg QD PF-06649751
15 mg QD PF-06649751 remaining at 15 mg QD PF-06649751
1 mg QD to 7 mg QD PF-06649751 (if de-escalated in parent study)
Up titration from 1 mg QD to 7 mg QD PF-06649751 for subject at 1 mg QD who were blindly de-escalated in the parent study
3 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study)
Up titration from 3 mg QD to 7 mg QD PF-06649751 for 3 mg QD subjects who were blindly de-escalated in parent study
7 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study)
7 mg QD to remain at 7 mg QD PF-06649751 for subjects who were blindly de-escalated in parent study
15 mg QD de-escalated to 7 mg QD PF-06649751 in parent study remain at 7 mg QD
7mg QD PF-06649751 for subjects assigned to 15 mg QD who were blindly de-escalated to 7 mg QD PF-06649751 in parent study
Atlanta Center for Medical Research, Atlanta
Parkinson's Disease and Movement Disorders Center of Boca Raton, Boca Raton
University of Toledo, Gardner-McMaster Parkinson Center, Toledo
University of Toledo, Investigational Drug Services, Toledo
The Movement Disorder Clinic of Oklahoma, Tulsa
Hoag Memorial Hospital Presbyterian, Newport Beach
Booth Gardner Parkinson's Care Center, Kirkland
Associated Neurologists of Southern CT, PC, Fairfield
Pharmaceutical Research Associates, Inc., Marlton
Lead Sponsor
Pfizer
INDUSTRY