Neurofibromatoses Type I (Von Recklinghausen’s Disease) is an indication for drug development with over 20 pipeline drugs currently active. According to GlobalData, preregistered drugs for Neurofibromatoses Type I (Von Recklinghausen’s Disease) have a 100% 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 Neurofibromatoses Type I (Von Recklinghausen’s Disease) 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.
Neurofibromatoses Type I (Von Recklinghausen’s Disease) overview
Neurofibromatosis type 1 (NF1), also called von Recklinghausen’s disease, is a rare genetic disorder characterized by the development of multiple noncancerous (benign) tumors of nerves and skin (neurofibromas). This is transmitted on chromosome 17 and is caused by mutation of the NF1 gene. Symptoms include liver enlargement, glioma, Lisch nodules, and pheochromocytoma. Treatment includes pain medications, surgery, chemotherapy, and radiation therapy.
For a complete picture of PTSR and LoA scores for drugs in Neurofibromatoses Type I (Von Recklinghausen’s Disease), buy the report here.
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