drugset / Trial / NCT01919164

A Study to Investigate the Safety and Effectiveness of Different Doses of Sprifermin in Participants With Osteoarthritis of the Knee

NCT01919164 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This was a multicenter, randomized, double-blind, placebo-controlled, parallel-group Phase 2 trial of Sprifermin administered intra-articularly in participants with primary osteoarthritis of the knee and Kellgren-Lawrence Grade 2 or 3. The trial was intended to investigate the efficacy and safety of different intra articular dosages of Sprifermin in these individuals.

Timeline

Start
2013-07-29
Primary completion
2016-05-05
Completion
2019-05-07

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Sprifermin (AS902330) 100 mcg/Placebo (2 Cycles); Mean Difference (Final Values) 0.04 (95% CI 0.02 to 0.06) NCT01919164 ↗

registry analysis (superiority test); Placebo vs Sprifermin (AS902330) 100 mcg- 4 Cycles; Mean Difference (Final Values) 0.05 (95% CI 0.03 to 0.07) NCT01919164 ↗

release “The study of 549 patients met its primary endpoint” prnewswire.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sprifermin Protein / enzyme biologic 30 ug Other
Subject Sprifermin Protein / enzyme biologic 100 ug Other

Indications