X Chromosome Disorders is an indication for drug development with over 100 pipeline drugs currently active. According to GlobalData, preregistered drugs for X Chromosome Disorders have a 50% likelihood of approval (LoA) indication benchmark. GlobalData’s report assesses how phase transition success rate (PTSR) and likelihood of approval (LoA) scores for pipeline drugs in X Chromosome Disorders compared to historical benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
X Chromosome Disorders overview
X chromosome disorders, also termed X-linked disorders, arise from mutations in genes residing on the X chromosome, a pivotal determinant of an individual’s sex. These conditions impact both males and females, albeit with distinct consequences. In X-linked recessive disorders, such as hemophilia and Duchenne muscular dystrophy, males, possessing only one X chromosome, are more susceptible, while females, often asymptomatic carriers, can transmit the disorder. X-linked dominant disorders, exemplified by Rett syndrome, tend to be more severe in females, lacking the compensatory second X chromosome found in males. Sex chromosome aneuploidies, like Turner syndrome (XO) in females and Klinefelter syndrome (XXY) in males, disrupt development and fertility. Disorders like X-linked agammaglobulinemia may stem from irregularities in the natural process of X chromosome inactivation in females, underscoring the complexity of X chromosome-related genetic conditions.
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For a complete picture of PTSR and LoA scores for drugs in X Chromosome Disorders, buy the report here.
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