A Study of Cebranopadol for the Treatment of Acute Pain After Abdominoplasty

Key Inclusion Criteria: * Scheduled to undergo full abdominoplasty procedure without liposuction or other collateral procedures, using anesthesiologic and surgical procedures planned as described in this protocol. * Must be able to adhere to the visit schedule, complete all study assessments, and protocol requirements including self-reported questionnaires. Key Exclusion Criteria: * Any clinically significant disease, medical condition or laboratory finding that in the investigator's opinion may interfere with the study procedures or data integrity or compromise the safety of the subject. * Subject has a current painful condition that could confound the interpretation of efficacy, safety or tolerability data in the study, in the opinion of the investigator. * History of allergy, hypersensitivity or intolerance to any opioid analgesics or anesthetics, including opioid-induced nausea or vomiting.