Safety and Pharmacokinetic Study of PF-06651600 in Healthy Volunteers
Completed
Pfizer
Phase 1
This study is a first in human study of PF-06651600. PF-06651600 is being developed for
treatment of inflammatory bowel disease. This study will test single and multiple doses of
PF-06651600. The goal of the study is to assess the safety, tolerability, pharmacokinetics
and pharmacodynamics of PF-06651600 in healthy volunteers.
Bioavailability Study Of PF-06651600 In Healthy Subjects
Completed
Pfizer
Phase 1
PF-06651600 is being developed for treatment of inflammatory bowel disease. This study will
test the bioavailability of a solid dose formulation of PF-06651600 compared to an oral
solution formulation under fasting conditions and the effect of a high fat meal on the
bioavailability of the solid dose formulation of PF-06651600 in healthy subjects. Safety and
tolerability of the tablet and oral solution formulations of PF-06651600 will be assessed
under fasting and fed conditions.
Study To Assess The Efficacy And Safety Of Pf-06651600 In Subjects With Rheumatoid Arthritis With An Inadequate Response To Methotrexate
Completed
Pfizer
Phase 2
This is an 8 week study to assess the efficacy and safety profile of PF-06651600 in
seropositive subjects with rheumatoid arthritis with an inadequate response to methotrexate
(up to approximately 50% of subjects may also have had an inadequate response to 1 anti-TNF
biologic).
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