Cebranopadol is under clinical development by Tris Pharma and currently in Phase II for Chronic Low Back Pain (CLBP). According to GlobalData, Phase II drugs for Chronic Low Back Pain (CLBP) does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Cebranopadol LoA Report. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Cebranopadol overview
Cebranopadol (GRT-6005) is under development for the treatment of acute pain, chronic low back pain, chronic neuropathic pain and opioid addiction. It is an orally administered analgesic agent that exhibits a potent agonist activity on opioid receptor like -1 (ORL1) and mu opioid receptor.
It was also under development for the treatment of chronic nociceptive pain and chronic moderate to severe pain related to cancer, chronic pain due to diabetic peripheral neuropathy, post-operative pain in hallux valgus (Bunion), chronic pain due to knee osteoarthritis (OA), addiction, cancer pain and chronic low back pain
Tris Pharma overview
Tris Pharma discovers, develops and commercializes over-the-counter and generic products. The company’s pipeline product candidates include TRN-110, TRN-124, TRN-125, TRN-167, TRN-123, TRN-152, TRN-148, TRN-213, TRN-219, and TRN-226. Its generic products include colesevelam, dexmethylphenidate, dextroamphetamine, doxycycline Hyclate, doxycycline hyclate, droxidopa, febuxostat, hydrocodone, hydrocodone polistirex, lacosamide, methylphenidate, morphine sulfate and paliperidone ER. Tris Pharma is headquartered in South Brunswick, New Jersey, the US.
For a complete picture of Cebranopadol’s drug-specific PTSR and LoA scores, buy the report here.
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