The Melatonin Receptor Type 1B pipeline drugs market research report outlays comprehensive information on the Melatonin Receptor Type 1B 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 Melatonin Receptor Type 1B 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, Gastrointestinal, Women’s Health, and Toxicology which include the indications Insomnia, Circadian Rhythm Sleep Disorders, Metabolic Dysfunction-Associated Steatohepatitis (MASH), Polycystic Ovarian Syndrome, and Chemotherapy Induced Oral Mucositis. It also reviews key players involved in Melatonin Receptor Type 1B targeted therapeutics development with respective active and dormant or discontinued products.

The Melatonin Receptor Type 1B pipeline targets constitutes close to 11 molecules. Out of which, approximately nine molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Pre-Registration, Phase III, Phase II, Preclinical, and Discovery stages are 1, 2, 3, 2, and 1 respectively. Similarly, the universities portfolio in Preclinical comprises 2 molecule.

Melatonin Receptor Type 1B overview

Melatonin receptor type 1B (MT1) is a G protein-coupled receptor (GPCR) that plays a crucial role in mediating the effects of melatonin, a hormone involved in the regulation of the sleep-wake cycle and other circadian rhythms. The receptor is also known as MTNR1B, and it is primarily expressed in the brain.

For a complete picture of Melatonin Receptor Type 1B’s drug pipeline, buy the report here.

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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.