The Fatty Acid Amide Hydrolase pipeline drugs market research report outlays comprehensive information on the Fatty Acid Amide Hydrolase targeted therapeutics, complete with analysis by indications, stage of development, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses the drugs in the Fatty Acid Amide Hydrolase pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.
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The report also covers products from therapy areas such as Central Nervous System, Respiratory, Immunology, and Genito Urinary System which include the indications Post-Traumatic Stress Disorder (PTSD), Substance (Drug) Abuse, Chronic Cough, Inflammation, and Overactive Bladder. It also reviews key players involved in Fatty Acid Amide Hydrolase targeted therapeutics development with respective active and dormant or discontinued products.
The Fatty Acid Amide Hydrolase pipeline targets constitutes close to 21 molecules. Out of which, approximately 17 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase III, Phase II, Phase I, IND/ CTA Filed, Preclinical, and Discovery stages are 1, 2, 2, 1, 8, and 3 respectively. Similarly, the universities portfolio in Preclinical, and Discovery comprises 2, and 2 molecule.
Fatty Acid Amide Hydrolase overview
Fatty acid amide hydrolase (FAAH) catalyzes the hydrolysis of endogenous amidated lipids like the sleep-inducing lipid oleamide, the endocannabinoid anandamide, as well as other fatty amides, to their corresponding fatty acids, thereby regulating the signaling functions of these molecules.
For a complete picture of Fatty Acid Amide Hydrolase’s drug pipeline, 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.
Global Markets Direct’s report features investigational drugs from across globe covering over 20 therapy areas and nearly 3,000 indications. The report is built using data and information sourced from Global Markets Direct’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third-party sources.
Drug profiles featured in the report undergo periodic review following a stringent set of processes to ensure that all the profiles are updated with the latest set of information. Additionally, various dynamic tracking processes ensure that the most recent developments are captured on a real time basis.
