Naltrexone LA is under clinical development by BioCorRx and currently in Phase I for Alcohol Dependence. According to GlobalData, Phase I drugs for Alcohol Dependence does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Naltrexone LA 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.

Naltrexone LA overview

Naltrexone is under development for the treatment of alcohol, opioid addiction and methamphetamine use disorder (MUD). It is a long acting implantable naltrexone implant, administered by the subcutaneous route. It acts by targeting mu type opioid receptor.

BioCorRx overview

BioCorRx is a healthcare solutions company that primarily focuses on the development of treatments and programs for substance use disorders. The company’s offerings include the beat addiction recovery program and the UnCraveRx weight loss program. The company distributes its program to healthcare providers, independent licensed clinics and licensed healthcare professionals. BioCorRx offers alcoholism and opioid addiction treatment programs for use in rehabilitation and treatment centers. It primarily targets the healthcare sector in the United States. BioCorRx is headquartered in Anaheim, California, the US.

For a complete picture of Naltrexone LA’s drug-specific PTSR and LoA scores, buy the report here.

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.