The Histone Acetyltransferase pipeline drugs market research report outlays comprehensive information on the Histone Acetyltransferase 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 Acetyltransferase 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 Oncology, Immunology, Toxicology, and Undisclosed which include the indications Solid Tumor, Breast Cancer, Autoimmune Disorders, Radiation Injury, and Unspecified. It also reviews key players involved in Histone Acetyltransferase targeted therapeutics development with respective active and dormant or discontinued products.
The Histone Acetyltransferase pipeline targets constitutes close to 39 molecules. Out of which, approximately 28 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase II, Phase I, IND/ CTA Filed, Preclinical, and Discovery stages are 1, 7, 1, 14, and 5 respectively. Similarly, the universities portfolio in Preclinical, and Discovery comprises 9, and 2 molecule.
Histone Acetyltransferase overview
Histone acetyltransferases (HATs) are enzymes that acetylate lysine amino acids on histone proteins. This modification neutralizes the positive charge of lysine, which may disrupt the interaction between DNA and histone tails. By transferring an acetyl group to the histones, genes can be turned on and off.
For a complete picture of Histone Acetyltransferase’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.
