Midomafetamine is under clinical development by Lykos Therapeutics and currently in Pre-Registration for Post-Traumatic Stress Disorder (PTSD). According to GlobalData, Pre-Registration drugs for Post-Traumatic Stress Disorder (PTSD) does not have sufficient historical data to build an indication benchmark PTSR for Pre-Registration. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Midomafetamine 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.

Midomafetamine overview

Midomafetamine is under investigation for the treatment of schizophrenia, post-traumatic stress disorder (PTSD), social anxiety in autism patients and social anxiety in autistic adults. The drug candidate is psychedelic. It is administered through oral route. It is used as an adjunct to psychotherapy. The drug candidate acts by targeting monoamine oxidase (MAO), sodium dependent dopamine transporter (SLC6A3) and sodium dependent noradrenaline transporter (SLC6A2).

Lykos Therapeutics overview

Lykos Therapeutics, a subsidiary of Multidisciplinary Association for Psychedelic studies, is a biotechnology research company engaged in developing novel therapeutics for the treatment of mental health conditions. It is headquartered in San Jose, California, the US.

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

This content was updated on 7 February 2024

Premium Insights

From

The gold standard of business intelligence.

Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.

GlobalData

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.