drug
idursulfase
Marketedupdated 3mo agoby Shire Human Genetic Therapies Inc
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Trials studying idursulfase
- phase3A Phase III Study of JR-141 in Patients With Mucopolysaccharidosis II (STARLIGHT)
- —Post-trial Access Program of Idursulfase-IT Along With Elaprase in Children With Hunter Syndrome
- phase4Long-term Evaluation on Height and Weight in Patients With MPS II Who Started Treatment at < 6 Years of Age
- phase4A Study of ELAPRASE in Treatment-naïve Participants With Hunter Syndrome (Mucopolysaccharidosis [MPS] II)
- phase3Extension Study of Idursulfase-IT Along With Elaprase in Children and Adults With Hunter Syndrome and Cognitive Impairment
- phase2An Extension Study of HGT-HIT-045 Evaluating Long-Term Safety and Clinical Outcomes of Idursulfase-IT in Conjunction With Elaprase in Pediatric Participants With Hunter Syndrome and Cognitive Impairment
- phase3A Study to Determine the Efficacy and Safety of Tividenofusp Alfa (DNL310) vs Idursulfase in Pediatric and Young Adult Participants With Neuronopathic (nMPS II) or Non-Neuronopathic Mucopolysaccharidosis Type II (nnMPS II)
- phase3Study of Long Term Safety and Clinical Outcomes of Idursulfase IT and Elaprase Treatment in Pediatric Participants Who Have Completed Study HGT-HIT-094
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