Clinical trial

Safety & Efficacy Study of ORGN001 (Formerly ALXN1101) in Pediatric Patients…

NCT02047461 · Origin Biosciences, Industry · Completed

Key facts

NCT number NCT02047461
Title Safety & Efficacy Study of ORGN001 (Formerly ALXN1101) in Pediatric Patients With MoCD Type A Currently Treated With rcPMP
Official title A Phase 2, Multicenter, Multinational, Open-Label, Dose-Escalation Study to Evaluate the Safety and Efficacy of ORGN001 (Formerly ALXN1101) in Pediatric Patients With Molybdenum Cofactor Deficiency (MoCD) Type A Currently Treated With Recombinant Escherichia Coli-derived Cyclic Pyranopterin…
Lead sponsor Origin Biosciences, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Molybdenum Cofactor Deficiency, Type A
Intervention type Drug
Interventions ORGN001 (formerly ALXN1101)
Enrollment 8
Start date Apr 1, 2014
Primary completion Aug 1, 2022
Completion Oct 1, 2022
First posted Jan 28, 2014
Last update posted Oct 17, 2023
Countries Australia, Netherlands, Tunisia, United Kingdom, United States

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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