Clinical trial

Study of Burosumab (KRN23) in Adults With Tumor-Induced Osteomalacia (TIO) or…

NCT02304367 · Kyowa Kirin, Inc., Industry · Completed

Key facts

NCT number NCT02304367
Title Study of Burosumab (KRN23) in Adults With Tumor-Induced Osteomalacia (TIO) or Epidermal Nevus Syndrome (ENS)
Official title A Phase 2 Open-Label Trial to Assess the Efficacy and Safety of KRN23, an Antibody to FGF23, in Subjects With Tumor-Induced Osteomalacia (TIO) or Epidermal Nevus Syndrome (ENS)-Associated Osteomalacia
Lead sponsor Kyowa Kirin, Inc., Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Tumor Induced Osteomalacia (TIO), Epidermal Nevus Syndrome (ENS)
Intervention type Biological
Interventions Burosumab
Enrollment 17
Start date Mar 24, 2015
Primary completion Jul 27, 2017
Completion Jan 21, 2021
First posted Dec 1, 2014
Last update posted May 6, 2024
Countries 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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