40 Comprehensive efficacy and integrated safety results from the late-phase clinical program of the sufentanil sublingual tablet 30 MCG

Conclusion The sufentanil sublingual tablet 30 mcg, while still under FDA review, has shown potential benefit as a non-invasive analgesic modality in medically supervised settings requiring short-term treatment of acute moderate-to-severe pain. Conflict of interest Drs. J. Miner and Z. Rafique were principal investigators in the phase 3 clinical trial. Dr. R. Leto and M. Tyler have served as consultants to AcelRx Pharmaceuticals Funding Development of the Sufentanil Sublingual Tablet 30 mcg is funded in part by the Clinical and Rehabilitative Medicine Research Program (CRMRP) of the U.S. Army Medical Research and Materiel Command (USAMRMC) under contract No. W81XWH-15-C-0046. The CRMRP was established in 2008 to foster research and technology advances for regeneration, restoration, and rehabilitation of traumatic injuries.
Source: BMJ Open - Category: General Medicine Authors: Source Type: research