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Related Experiment Videos

Mecasermin.

Gillian M Keating1

  • 1Wolters Kluwer Health Adis, Auckland, New Zealand. demail@adis.co.nz

Biodrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy
|May 17, 2008
PubMed
Summary
This summary is machine-generated.

Mecasermin, a treatment for growth failure, significantly increased height velocity in children with severe insulin-like growth factor-I (IGF-I) deficiency. This therapy demonstrated sustained growth benefits for up to eight years in clinical trials.

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Area of Science:

  • Pediatric Endocrinology
  • Growth Hormone Therapy
  • Metabolic Disorders

Background:

  • Mecasermin (recombinant human insulin-like growth factor-I [IGF-I]) is approved for treating growth failure in specific pediatric populations.
  • Severe primary IGF-I deficiency or GH gene deletion with neutralizing GH antibodies are key indications.
  • Growth hormone insensitivity (GHI) is a condition where the body does not respond properly to growth hormone.

Purpose of the Study:

  • To evaluate the efficacy of subcutaneous mecasermin in promoting linear growth in children with growth failure and severe IGF-I deficiency associated with GH insensitivity.
  • To assess the long-term effects of mecasermin on growth velocity and height standard deviation scores.

Main Methods:

  • A noncomparative, multicenter trial involving 76 children with growth failure and severe IGF-I deficiency.

Related Experiment Videos

  • Treatment involved subcutaneous mecasermin at 0.12 mg/kg twice daily.
  • Growth velocities and height standard deviation scores were monitored over extended periods (mean 4.4 years, up to 12.5 years).
  • Main Results:

    • Subcutaneous mecasermin significantly increased height velocity in the first year of treatment (from 2.8 cm/year to 8.0 cm/year).
    • Sustained growth velocities above baseline were observed for up to 8 years.
    • In a separate trial, mecasermin therapy for 6.5-7.5 years resulted in a mean increase of +1.4 in height standard deviation score.

    Conclusions:

    • Mecasermin effectively stimulates linear growth in children with growth failure due to severe IGF-I deficiency and GH insensitivity.
    • The treatment provides sustained growth benefits over several years.
    • Mecasermin was generally well tolerated in the studied pediatric population.