Recessive X Chromosome Disorders is an indication for drug development with over 200 pipeline drugs currently active. According to GlobalData, preregistered drugs for Recessive X Chromosome Disorders have a 87.5% 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 Recessive 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.
Recessive X Chromosome Disorders overview
A recessive X chromosome disorder, also known as an X-linked recessive disorder, is a genetic condition caused by a mutation on one of the X chromosomes, one of the two sex chromosomes. Typically, males have one X and one Y chromosome (XY), while females have two X chromosomes (XX). In recessive X-linked disorders, the mutated gene is located on the X chromosome and typically affects males more severely, as they have only one X chromosome. Common examples include hemophilia, Duchenne muscular dystrophy, and red-green color blindness. Carrier females, with one affected X chromosome and one normal X chromosome, often do not show symptoms but can pass the disorder to their offspring.
For a complete picture of PTSR and LoA scores for drugs in Recessive X Chromosome Disorders, buy the report here.
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