Sevuparin sodium is under clinical development by Modus Therapeutics and currently in Phase I for Endotoxemia. According to GlobalData, Phase I drugs for Endotoxemia does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Sevuparin sodium LoA Report. Buy the report here.
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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.
Sevuparin sodium overview
Sevuparin sodium (DF-02) is under development for the treatment of malaria, sepsis, endotoxemia, septic shock and chronic kidney disease (CKD) with anemia. It is administered as an intravenous infusion and subcutaneous injection. The drug candidate is a polysaccharide drug derived from heparin, a low anticoagulant heparin (LAH) derivative. It was also under development for the treatment of malaria and acute vaso-occlusive crisis (VOC) associated with sickle cell disease (SCD).
Modus Therapeutics overview
Modus Therapeutics, a subsidiary of Modus Therapeutics Holding AB, is a biotechnology company that develops sevuparin for diseases. The company focuses to develop sevuparin for patients with sepsis, septic shock, a severe and often fatal condition. It develops Sevuparin which is a heparinoid designed to retain its inflammation modifying properties while causing significantly less blood-thinning. Its therapeutic areas include sepsis, malaria and anemia. Modus Therapeutics is headquartered in Stockholm, Sweden.
For a complete picture of Sevuparin sodium’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
