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Long-term Safety and Effectiveness of Growth Hormone With GHD, TS, CRF, SGA , ISS and PWS in Children

Study acronym: LGS
StatusRecruiting
PhaseNot specified
SponsorLG Chem
Started
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Record History

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  1. Notable Lead sponsor: LG Life Sciences to LG Chemv5 Show 4 more changesShow less
    • Enrollment target: 2000 to 6000
    • Primary completion date: Jan 2020 to Dec 31, 2032
    • Study completion date: Jan 2022 to Dec 31, 2032
    • Study title expanded, about 2 words
  2. Minor Re-verified, no change to tracked fieldsv4
  3. Minor Primary completion date: Jan 2020
    • Study completion date: Jan 2022
    v3
  4. Minor Secondary endpoints revised (3)
    • Study title shortened, about 1 word
    v2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
13 trials monitored
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The purpose of this study is to evaluate the long-term safety and effectiveness of growth hormone (Eutropin Inj./Eutropin plus Inj.) treatment with GHD (Growth Hormone Deficiency), TS (Turner Syndrome),CRF (Chronic Renal Failure), SGA (Small for Gestational Age), and ISS (Idiopathic Short Stature).
Trial Details
NCT Number NCT01604395
Lead Sponsor LG Chem
Conditions
(from sponsor)
Growth Hormone Deficiency, Turner Syndrome, Chronic Renal Failure, Small for Gestational Age, Idiopathic Short Stature
Related terms Dwarfism, Pituitary, Kidney Failure, Chronic, Turner Syndrome
Enrollment 6,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov