Tris Pharma Initiates Pivotal P-III Study to Evaluate Cebranopadol for Moderate-to-Severe Acute Pain
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- Tris Pharma reported the initiation of a pivotal P-III (ALLEVIATE-1 & ALLEVIATE-2) study assessing the efficacy & safety of cebranopadol (TRN-228) for moderate-to-severe acute pain patients (n=500)
- ALLEVIATE-1 (n=300; US 6 clinical study) & ALLEVIATE-2 (n=240; US 8 clinical study) is a P-III study, a randomized, double-blind, placebo-controlled trial, that 1EP assessing the analgesic efficacy of cebranopadol vs PBO in treating moderate-to-severe pain following full abdominoplasty & bunionectomy as measured by pain intensity assessments respectively
- 2EP includes evaluating the safety & tolerability efficacy of cebranopadol vs oxycodone (ALLEVIATE 1 & 2) and efficacy using rescue medication ((ALLEVIATE 2)
Ref: Tris Pharma | Image: Tris Pharma
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Disha is a content writer at PharmaShots. She is passionate and curious about recent updates and developments in MedTech and Pharma industry. She covers news related to clinical trial results and updates. She can be contacted at connect@pharmashots.com.