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

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LG Chem

Status

Enrolling

Conditions

Idiopathic Short Stature
Small for Gestational Age
Chronic Renal Failure
Turner Syndrome
Growth Hormone Deficiency

Study type

Observational

Funder types

Industry

Identifiers

NCT01604395
LG-HGOS001

Details and patient eligibility

About

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).

Enrollment

6,000 estimated patients

Sex

All

Ages

2+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • short stature children aged 2 years or more
  • children with GHD,TS, CRF, SGA or ISS
  • written informed consent from the person, person's parent or legal guardian

Trial design

6,000 participants in 1 patient group

growth hormone

Trial contacts and locations

1

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Central trial contact

YoungHwan Jang

Data sourced from clinicaltrials.gov

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