The Histone Deacetylase 8 pipeline drugs market research report outlays comprehensive information on the Histone Deacetylase 8 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 Histone Deacetylase 8 pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.

The report also covers products from therapy areas such as Oncology, Musculoskeletal Disorders, Central Nervous System, and Gastrointestinal which include the indications Unspecified Cancer, Triple-Negative Breast Cancer (TNBC), Fibrosis, Bone Disorders, Alzheimer’s Disease, and Liver Fibrosis. It also reviews key players involved in Histone Deacetylase 8 targeted therapeutics development with respective active and dormant or discontinued products.

The Histone Deacetylase 8 pipeline targets constitutes close to eight molecules. Out of which, approximately six molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase II, Preclinical, and Discovery stages are 1, 4, and 1 respectively. Similarly, the universities portfolio in Preclinical, and Discovery comprises 1, and 1 molecule.

Histone Deacetylase 8 overview

Histone deacetylase 8 is an enzyme encoded by the HDAC8 gene. It is responsible for the deacetylation of lysine residues on the N-terminal part of the core histones. It plays an important role in transcriptional regulation, cell cycle progression and developmental events.

For a complete picture of Histone Deacetylase 8’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.