drugset / Trial / NCT03349060

Study to Evaluate Efficacy and Safety of PF-04965842 in Subjects Aged 12 Years And Older With Moderate to Severe Atopic Dermatitis

NCT03349060 ↗

Phase 3 Completed 387 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

B7451012 is a Phase 3 study to evaluate PF-04965842 in patients aged 12 years and older with a minimum body weight of 40 kg who have moderate to severe atopic dermatitis. The efficacy and safety of two dosage strengths of PF-04965842, 100 mg and 200 mg taken orally once daily, will be evaluated relative to placebo over 12 weeks of study participation. Eligible patients will have an option to enter a long-term extension study after completing 12 weeks of treatment.

Timeline

Start
2017-12-07
Primary completion
2019-03-26
Completion
2019-03-26

Outcome

Met primary endpoint

registry analysis (superiority test); PF-04965842 100 mg vs Placebo; p = 0.0037; Difference in Percentage 15.8 (95% CI 6.8 to 24.8); NCT03349060 ↗

registry analysis (superiority test); PF-04965842 200 mg vs Placebo; p <0.0001; Difference in Percentage 36.0 (95% CI 26.2 to 45.7); NCT03349060 ↗

registry analysis (superiority test); PF-04965842 100 mg vs Placebo; p <0.0001; Difference in Percentage 27.9 (95% CI 17.4 to 38.3); NCT03349060 ↗

registry analysis (superiority test); PF-04965842 200 mg vs Placebo; p <0.0001; Difference in Percentage 51.0 (95% CI 40.5 to 61.5); NCT03349060 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Abrocitinib Small molecule 100 mg Oral
Subject Abrocitinib Small molecule 200 mg Oral

Indications