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A placebo controlled, randomized, double-blind phase II clinical trial to evaluate tolerability, safety and efficacy endpoints after administration of recombinant human insulin-like growth factor-I/recombinant human insulin-like growth factor binding protein-3 (rhIGF-I/rhIGFBP-3) [mecasermin rinfabate] for 24 weeks in adults with myotonic dystrophy type 1

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A placebo controlled, randomized, double-blind phase II clinical trial to evaluate tolerability, safety and efficacy endpoints after administration of recombinant human insulin-like growth factor-I/recombinant human insulin-like growth factor binding protein-3 (rhIGF-I/rhIGFBP-3) [mecasermin rinfabate] for 24 weeks in adults with myotonic dystrophy type 1

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 11 Jan 2022

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At a glance

  • Drugs Mecasermin rinfabate (Primary)
  • Indications Muscular dystrophies; Myotonic dystrophy
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Insmed

    • Most Recent Events

    • 08 Dec 2021 Primary endpoints are amended.
    • 08 Dec 2021 Status changed from active, no longer recruiting to completed.
    • 21 Jul 2008 Trial now fully enrolled according to Insmed media release.

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