Clinical Trial: An Open-Label, Safety and Efficacy Study of Cebranopadol in Participants With Acute Pain With Surgical or Non-Surgical Origin

U.S., Sept. 29 -- ClinicalTrials.gov registry received information related to the study (NCT07845071) titled 'An Open-Label, Safety and Efficacy Study of Cebranopadol in Participants With Acute Pain With Surgical or Non-Surgical Origin' on Sept. 22.

Brief Summary: The purpose of this study is to evaluate the safety and effectiveness of cebranopadol in treating acute pain.

Study Start Date: Sept., 2026

Study Type: INTERVENTIONAL

Condition: Pain

Intervention: DRUG: Cebranopadol 400 ug

Participants receive Cebranopadol 400 mcg once per day for 14 days or until pain resolves, whichever occurs first.

Recruitment Status: RECRUITING

Sponsor: Adneuris Therapeutics, Inc.

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