Clin2
NCT00903110Possibly a fitRecruiting

Long-term safety registry for Increlex in children

IGF1 Deficiency

Part of Hormones & metabolism clinical trials.

This study is a registry that follows children and teens with severe IGF-1 deficiency who use Increlex (or specific GH gene deletion situations) to better track long-term safety and effectiveness. You would likely join if your child is already starting or planning Increlex and is not in other growth-related drug trials.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
500 people
Ages
2 years to 18 years
Study type
Observational

Who can take part

  • Your child must have severe primary IGF-1 deficiency that fits the Increlex label (or GH gene deletion in the US case).
  • Your child is starting Increlex, planning to start it, or currently taking it (per the approved label where you live).
  • A parent or legal guardian must sign consent before any registry activities begin; your child should give assent when appropriate.
  • Your child must NOT be currently in an Increlex clinical trial.
  • Your child must NOT be currently in another clinical trial for growth (growth retardation).
  • Your child must not have certain reasons to avoid Increlex (like allergy to it, known or suspected tumors/cancer, or growth plate/epiphysis already closed).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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