The Double Stranded RNA Specific Adenosine Deaminase pipeline drugs market research report outlays comprehensive information on the Double Stranded RNA Specific Adenosine Deaminase 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 Double Stranded RNA Specific Adenosine Deaminase 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, and Gastrointestinal which include the indications Unspecified Cancer, Triple-Negative Breast Cancer (TNBC), and Metabolic Dysfunction-Associated Steatohepatitis (MASH). It also reviews key players involved in Double Stranded RNA Specific Adenosine Deaminase targeted therapeutics development with respective active and dormant or discontinued products.
The Double Stranded RNA Specific Adenosine Deaminase pipeline targets constitutes close to eight molecules. Out of which, approximately seven molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Preclinical, and Discovery stages are 4, and 3 respectively. Similarly, the universities portfolio in Preclinical comprises 1 molecule.
Double Stranded RNA Specific Adenosine Deaminase overview
Double stranded RNA specific adenosine deaminase (ADAR) is responsible for RNA editing by site-specific deamination of adenosines. ADAR destabilizes double-stranded RNA through conversion of adenosine to inosine.
For a complete picture of Double Stranded RNA Specific Adenosine Deaminase’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.
