drugset / Trial / NCT01090492

PF-00489791 For The Treatment Of Raynaud's

NCT01090492 ↗

Phase 2 Completed 243 enrolled Pfizer
RandomizedCrossoverDouble-blindTreatment

Summary

The investigators propose that once daily administration of PF-00489791, a phosphodiesterase inhibitor, will reduce vasospasm and improve symptoms and signs associated with Primary and Secondary Raynaud's Phenomenon.

Timeline

Start
2010-08-04
Primary completion
2011-05-31
Completion
2011-05-31

Outcome

Met primary endpoint

registry analysis (superiority or other test); PF-00489791 20 mg (PRP) vs Placebo (PRP); p = 0.0057; Adjusted Mean Difference -0.69 (80% CI -0.99 to -0.38); ANCOVA NCT01090492 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-00489791 Small molecule 4 mg —
Subject PF-00489791 Small molecule 20 mg —

Indications