Expired Study
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South San Francisco, California 94080


Purpose:

This study is a multicenter, open-label, observational, postmarketing surveillance study that will collect information on the use of Genentech GH preparations to treat GH-deficient subjects with optimal GH dosing during puberty.


Criteria:

Inclusion Criteria: - Adolescent boys who are GH deficient and Tanner Stage 2 or greater (testes 3 mL or greater) - Adolescent girls who are GH deficient and breast Tanner Stage 2 or greater - Current treatment with GH dose of 0.4 to 0.7 mg/kg/wk - Ability to keep follow-up appointments throughout the study - Willingness to remain on therapy until epiphyseal closure is achieved - Prior enrollment in NCGS Core Study 85-036 Exclusion Criteria: - Treatment with non-Genentech GH preparation - Closed epiphyses - Active neoplasia - Treatment with insulin for diabetes


NCT ID:

NCT00097513


Primary Contact:

Study Director
Barbara Lippe, M.D.
Genentech


Backup Contact:

N/A


Location Contact:

South San Francisco, California 94080
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 17, 2017

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