Clinical trial

Study of KRN23 (Burosumab), a Recombinant Fully Human Monoclonal Antibody…

NCT02163577 · Kyowa Kirin, Inc., Industry · Completed

Key facts

NCT number NCT02163577
Title Study of KRN23 (Burosumab), a Recombinant Fully Human Monoclonal Antibody Against Fibroblast Growth Factor 23 (FGF23), in Pediatric Subjects With X-linked Hypophosphatemia (XLH)
Official title A Randomized, Open-Label, Dose Finding, Phase 2 Study to Assess the Pharmacodynamics and Safety of the Anti-FGF23 Antibody, KRN23, in Pediatric Patients With X-linked Hypophosphatemia (XLH)
Lead sponsor Kyowa Kirin, Inc., Industry
Collaborators Kyowa Kirin Co., Ltd. Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions X-linked Hypophosphatemia
Intervention type Biological
Interventions burosumab
Enrollment 52
Start date Jul 2, 2014
Primary completion Oct 30, 2018
Completion Oct 30, 2018
First posted Jun 13, 2014
Last update posted May 6, 2024
Countries France, Netherlands, 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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