Malignant Fibrous Histiocytoma of Soft Tissue is an indication for drug development with over 10 pipeline drugs currently active. According to GlobalData, preregistered drugs for Malignant Fibrous Histiocytoma of Soft Tissue 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 Malignant Fibrous Histiocytoma of Soft Tissue 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.
Malignant Fibrous Histiocytoma of Soft Tissue overview
Malignant fibrous histiocytoma (MFH), now known as undifferentiated pleomorphic sarcoma, is a type of cancerous tumor that originates in the bone or soft tissue or other organ parts of the body. It is the most common form of soft tissue tumors generally seen in adults and very rarely in children. It is a painless mass believed to originate from primitive mesenchymal cells arising from soft tissue or bone, usually in the extremities or retroperitoneum. It can occur in any part of the body and may metastasize to lungs, lymph nodes, and bones. The etiology is still unknown, but radiation exposure is believed to be one of the common causes of this condition. Diagnosis is done by MRI and CT scan. Treatment is either surgery or radiotherapy.
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For a complete picture of PTSR and LoA scores for drugs in Malignant Fibrous Histiocytoma of Soft Tissue, buy the report here.
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