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Tris Pharma Reports the P-III (ALLEVIATE-1) Study Results of Cebranopadol to Treat Moderate-to-Severe Acute Pain

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  • The P-III (ALLEVIATE-1) study assessed analgesic efficacy of cebranopadol (400µg, QD) vs PBO for treating moderate-to-severe acute pain post abdominoplasty surgery
  • Study depicted significantly reduced pain intensity as evaluated by Pain Numeric Rating Scale (NRS) AUC4-48 (1.34 mean hourly difference) and a well-tolerated safety with nausea being the common AE
  • Tris will present full results of ALLEVIATE-1 at future conferences and share findings from 2 additional studies: an intranasal abuse potential study & ALLEVIATE-2 (P-III bunionectomy trial) in Q1’25, with an NDA submission planned later. Chronic pain studies for cebranopadol are set to begin in H2’25

Ref: Tris Pharma | Image: Tris Pharma

Related News:- Tris Pharma Initiates Pivotal P-III Study to Evaluate Cebranopadol for Moderate-to-Severe Acute Pain

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