The Apolipoprotein C III pipeline drugs market research report outlays comprehensive information on the Apolipoprotein C III 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 Apolipoprotein C III 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 Metabolic Disorders, Cardiovascular, and Genetic Disorders which include the indications Hypertriglyceridemia, Familial Chylomicronemia (Type I Hyperlipoproteinemia), Hypertension, Atherosclerosis, and Hemochromatosis. It also reviews key players involved in Apolipoprotein C III targeted therapeutics development with respective active and dormant or discontinued products.
The Apolipoprotein C III pipeline targets constitutes close to 11 molecules. Out of which, approximately 11 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Pre-Registration, Filing rejected/ Withdrawn, Phase III, Phase II, Phase I, and Preclinical stages are 1, 1, 1, 1, 2, and 5 respectively.
Apolipoprotein C III overview
Apolipoprotein C-III (APOC3) is a protein that is associated with lipoproteins, which are complex particles that transport lipids (fats) in the bloodstream. ApoC-III is mostly found on triglyceride-rich lipoproteins, including very low-density lipoproteins (VLDL) and chylomicrons. It plays a crucial role in lipid metabolism and the regulation of triglyceride levels in the blood.
For a complete picture of Apolipoprotein C III’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.
