The Beta Klotho pipeline drugs market research report outlays comprehensive information on the Beta Klotho 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 Beta Klotho 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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Data Insights Beta Klotho - Drugs In Development, 2024

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The report also covers products from therapy areas such as Gastrointestinal, Metabolic Disorders, Musculoskeletal Disorders, and Respiratory which include the indications Metabolic Dysfunction-Associated Steatohepatitis (MASH), Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD), Type 2 Diabetes, Obesity, Fibrosis, and Idiopathic Pulmonary Fibrosis. It also reviews key players involved in Beta Klotho targeted therapeutics development with respective active and dormant or discontinued products.

The Beta Klotho pipeline targets constitutes close to 12 molecules. Out of which, approximately 11 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase III, Phase II, Phase I, Preclinical, and Discovery stages are 1, 5, 2, 2, and 1 respectively. Similarly, the universities portfolio in Preclinical comprises 1 molecule.

Beta Klotho overview

Beta Klotho (KLB) is a single-pass transmembrane protein and is a fundamental component in fibroblast growth factor receptor (FGFR) signaling, as it serves as an obligatory coreceptor for the endocrine hormones fibroblast growth factor 19 (FGF19) and fibroblast growth factor 21 (FGF21).

For a complete picture of Beta Klotho’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.