drugset / Trial / NCT03575871

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

NCT03575871 ↗

Phase 3 Completed 391 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

B7451013 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
2018-06-29
Primary completion
2019-08-13
Completion
2019-08-13

Outcome

Met primary endpoint

registry analysis (superiority test); PF-04965842 100 mg vs Placebo; p = 0.0008; Difference in Percentage 19.3 (95% CI 9.6 to 29.0) NCT03575871 ↗

registry analysis (superiority test); PF-04965842 200 mg vs Placebo; p <0.0001; Difference in Percentage 28.7 (95% CI 18.6 to 38.8) NCT03575871 ↗

registry analysis (superiority test); PF-04965842 100 mg vs Placebo; p <0.0001; Difference in Percentage 33.9 (95% CI 23.3 to 44.4) NCT03575871 ↗

registry analysis (superiority test); PF-04965842 200 mg vs Placebo; p <0.0001; Difference in Percentage 50.5 (95% CI 40.0 to 60.9) NCT03575871 ↗

Publications

Drugs

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

Indications