The Turner Syndrome drugs in development market research report provides comprehensive information on the therapeutics under development for Turner 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 Turner Syndrome. Buy the report here.
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 Turner Syndrome and features dormant and discontinued products.
GlobalData tracks five drugs in development for Turner Syndrome by five companies/universities/institutes. The top development phase for Turner Syndrome is preclinical with two drugs in that stage. The Turner Syndrome pipeline has five drugs in development by companies and 0 by universities/ institutes. Some of the companies in the Turner Syndrome pipeline products market are: BioMarin Pharmaceutical, Xiamen Amoytop Biotech and Ascendis Pharma.
The key targets in the Turner Syndrome pipeline products market include Growth Hormone Receptor, Matrilin 3, and Insulin Like Growth Factor 1 Receptor.
The key mechanisms of action in the Turner Syndrome pipeline product include Growth Hormone Receptor Agonist with three drugs in Phase III. The Turner Syndrome pipeline products include one routes of administration with the top ROA being Subcutaneous and three key molecule types in the Turner Syndrome pipeline products market including Recombinant Protein, and Recombinant Peptide.
Turner Syndrome overview
Turner syndrome, also referred to as congenital ovarian hypoplasia syndrome, is a chromosomal disorder that affects development in females. It results when a female’s cells have one normal X chromosome and the other sex chromosome is either missing or structurally altered. About half of the population with Turner syndrome have monosomy X (45,XO). The other 50% of the population has a mosaic chromosomal component (45,X with mosaicism). Turner syndrome is typically not inherited, but it can be inherited in rare cases. Some patients with Turner syndrome can have a Y chromosome mosaicism. Although not a cause of Turner syndrome, SHOX (short stature homeobox-containing gene on the X- chromosome) is associated with the short stature found in Turner syndrome.
For a complete picture of Turner Syndrome’s pipeline drug market, buy the report here.
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