The Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) drugs in development market research report provides comprehensive information on the therapeutics under development for Congenital Adrenal Hyperplasia (Adrenogenital Syndrome), complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses key aspects of the companies and drugs in development for Congenital Adrenal Hyperplasia (Adrenogenital Syndrome). Buy the report here.

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The report also covers the descriptive pharmacological action of the therapeutics and the latest news and press releases. Additionally, the report provides an overview of the key players involved in therapeutic development for Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) and features dormant and discontinued products.

GlobalData tracks nine drugs in development for Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) by nine companies/universities/institutes. The top development phase for Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) is phase ii with three drugs in that stage. The Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) pipeline has nine drugs in development by companies and 0 by universities/ institutes. Some of the companies in the Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) pipeline products market are: Neurocrine Biosciences, H. Lundbeck and Spruce Biosciences.

The key targets in the Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) pipeline products market include Corticotropin Releasing Factor Receptor 1 (Corticotropin Releasing Hormone Receptor 1 or CRHR1), Adrenocorticotropic Hormone Receptor (Adrenocorticotropin Receptor or Melanocortin Receptor 2 or ACTHR or MC2R), and Corticotropin Releasing Factor Receptor 2 (Corticotropin Releasing Hormone Receptor 2 or CRHR2).

The key mechanisms of action in the Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) pipeline product include Adrenocorticotropic Hormone Receptor (Adrenocorticotropin Receptor or Melanocortin Receptor 2 or ACTHR or MC2R) Antagonist with three drugs in Phase II. The Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) pipeline products include two routes of administration with the top ROA being Oral and four key molecule types in the Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) pipeline products market including Small Molecule, and Monoclonal Antibody.

Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) overview

Congenital adrenal hyperplasia (CAH) is an autosomal recessive disease emerging from mutations of genes for enzymes that lead to the biochemical steps of production of glucocorticoids, mineralocorticoids, or sex steroids from cholesterol by the adrenal glands. This condition involves the excessive or deficient production of sex steroids that can alter the development of primary or secondary sex characteristics in some affected infants, children, or adults. Sometimes, deficient production of mineralocorticoids can lead to severe salt-wasting, increasing neonatal morbidity, and mortality.

For a complete picture of Congenital Adrenal Hyperplasia (Adrenogenital Syndrome)’s pipeline drug market, buy the report here.

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GlobalData’s pipeline drugs offers detailed profiles of pharmaceutical drugs in all stages of pre-clinical and clinical development, from discovery through to pre-registration. Coverage is limited to novel human medicinal drugs and biosimilars seeking market approval proprietary and is one of two primary repositories of pharmaceutical drug information offered by GlobalData through its Pharmaceutical Intelligence Center.