drugset / Trial / NCT02084511

Effectiveness and Safety of Different Doses of BI 1026706 in Patients With Postoperative Dental Pain

NCT02084511 ↗

Phase 1 Completed 80 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

To investigate the effectiveness of BI 1026706 powder for reconstitution of an oral solution compared to placebo and the relative effectiveness compared to Celecoxib.

Timeline

Start
2014-03
Primary completion
2014-10
Completion
2014-10

Outcome

Missed primary endpoint

registry analysis (superiority or other test); BI 50 mg PfOS vs Placebo; Mean Difference (Final Values) 27.39 (95% CI -76.3 to 131.1) NCT02084511 ↗

registry analysis (superiority or other test); BI 200 mg PfOS vs Placebo; Mean Difference (Final Values) 53.48 (95% CI -50.2 to 157.1) NCT02084511 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1026706 Unknown — Oral
Subject Celecoxib Other / unclassified — —

Indications

No indication recorded.