A Study to Evaluate Nutropin AQ for the Treatment of Growth Restriction in Children With Cystic Fibrosis

NCT ID: NCT00079742

Last Updated: 2008-06-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 68 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-09-30
• Study Completion Date: 2007-05-31

Brief Summary

This is a Phase II, multicenter, randomized, controlled, open-label trial of the safety and efficacy of Nutropin AQ administered subcutaneously (SC) daily in prepubertal children with CF and growth restriction.

Conditions

Cystic Fibrosis

Keywords

Growth restriction in children with cystic fibrosis

Study Design

• Primary Study Purpose: TREATMENT

Interventions

Nutropin AQ [somatropin (DNA origin) injection]

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Ability of parent or legal guardian to provide written informed consent and, if applicable, pediatric assent and compliance with study assessments for the full duration of the study
• Diagnosis of CF by sweat or genetic testing
• Between the ages of 5 and 12 years for girls and 5 and 13 years for boys
• Ability to perform pulmonary function tests in a reproducible manner, per American Thoracic Society guidelines for spirometry
• Height <= 10th percentile for age and sex
• Prepubertal, Tanner Stage 1
• Bone age of the non-dominant hand and wrist obtained no more than 6 months prior to study entry (bone age must be <= 10 years for girls and <= 11 years for boys as read using the method of Greulich and Pyle)
• Adequate caloric intake (following the CFF guidelines is encouraged; caloric intake must be documented at screening using a 24-hour food diary)
• Normal thyroid function

Exclusion Criteria

• Prior or current rhGH use
• History of short stature due to GHD
• History within the 12 months prior to screening of glucose intolerance (impaired glucose tolerance) or CF-related diabetes (CFRD) as defined by at least one of the following: fasting serum glucose of >= 126 mg/dL on two or more occasions; fasting serum glucose of >= 126 mg/dL plus any casual (previously called random) glucose level >= 200 mg/dL; casual (previously called random) glucose of >= 200 mg/dL on two or more occasions; fasting serum glucose of <= 126 mg/dL but 2-hour post oral glucose load of 140-199 mg/dL (impaired glucose tolerance) on two or more occasions; if a subject meets the criteria for impaired glucose tolerance or CFRD in the screening glucose tolerance test, even if there is no history of impaired glucose tolerance, the subject will not be eligible for the study.
• Infection with Burkholderia cepacia
• Qualitative change in antibiotic treatment (e.g., for exacerbation of lung infection) within 14 days of study entry
• Hospitalization or treatment with systemic corticosteroids during the 30 days prior to study entry
• Inability to adhere to previously documented adequate nutrition
• Active neoplasia
• Participation in any other investigational study (including investigational drug studies) within 30 days of enrollment or during the study if in the treatment arm, except for participation in observational and questionnaire studies (untreated)
• Subjects who require, as part of the their medical care, scheduled elective hospitalizations for IV antibiotic therapy

• Minimum Eligible Age: 5 Years
• Maximum Eligible Age: 13 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Genentech, Inc.

INDUSTRY

Sponsor Role: lead

Principal Investigators

Barbara Lippe, M.D.

Role: STUDY_DIRECTOR

Genentech, Inc.

Countries

United States

Other Identifiers

L2762g

Identifier Type: -

Identifier Source: org_study_id