The Ornithine Decarboxylase pipeline drugs market research report outlays comprehensive information on the Ornithine Decarboxylase 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 Ornithine Decarboxylase 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, Genetic Disorders, Non Malignant Disorders, and Metabolic Disorders which include the indications Neuroblastoma, Central Nervous System (CNS) Tumor, Familial Adenomatous Polyposis, Adenomas, and Type 1 Diabetes (Juvenile Diabetes). It also reviews key players involved in Ornithine Decarboxylase targeted therapeutics development with respective active and dormant or discontinued products.
The Ornithine Decarboxylase pipeline targets constitutes close to seven molecules. Out of which, approximately seven 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 The molecules developed by companies in Pre-Registration, Filing rejected/ Withdrawn, Phase III, Phase II, Preclinical, and Discovery stages are 1, 1, 1, 1, 2, and 1 respectively.
Ornithine Decarboxylase overview
Ornithine decarboxylase (ODC1) catalyzes the rate-limiting step of polyamine biosynthesis that converts ornithine into putrescine, which is the precursor for the polyamines, spermine, and spermidine.
For a complete picture of Ornithine Decarboxylase’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.
