The Phosphodiesterase 1 pipeline drugs market research report outlays comprehensive information on the Phosphodiesterase 1 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 Phosphodiesterase 1 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, Oncology, and Cardiovascular which include the indications Epilepsy, Parkinson’s Disease, Colorectal Cancer, Unspecified Cancer, Hypertension, and Systolic Heart Failure. It also reviews key players involved in Phosphodiesterase 1 targeted therapeutics development with respective active and dormant or discontinued products.
The Phosphodiesterase 1 pipeline targets constitutes close to six 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, Phase I, and Preclinical stages are 1, 2, and 3 respectively.
Phosphodiesterase 1 overview
Phosphodiesterase 1 (PDE1) is an enzyme that plays a crucial role in regulating the levels of two important signaling molecules in cells: cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP). These signaling molecules are involved in a wide range of cellular processes, including memory, learning, and muscle contraction. PDE1 is found in many different tissues throughout the body, but it is particularly abundant in the brain.
For a complete picture of Phosphodiesterase 1’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.
