Adneuris Therapeutics, Inc.
The purpose of this study is to evaluate the safety and effectiveness of cebranopadol in treating acute pain.
Inclusion Criteria: * Adults 18 to 75 years of age. * Able to provide informed consent. * Experiencing moderate to severe acute pain related to: 1) An ambulatory surgical procedure expected to cause pain lasting at least 72 hours, or 2) A traumatic or non-traumatic musculoskeletal condition. * Have a pain score of at least 4 on a 0 to 10 pain rating scale before starting study treatment. * Willing and able to comply with study requirements Exclusion Criteria: * Chronic pain condition that requires ongoing pain medication. * Significant medical or psychiatric condition that could affect part…
Participants receive Cebranopadol 400 mcg once per day for 14 days or until pain resolves, whichever occurs first.