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Administration of Growth Hormone to Increase CD4+ Count in Patients Taking Anti-HIV Drugs

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
somatropin
Hepatitis A virus, inactivated
Keyhole-Limpet Hemocyanin
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring HIV Infections, CD4 Lymphocyte Count, Antiretroviral Therapy, Highly Active, Growth Hormone, Cell Division, CD4-Positive T-Lymphocytes, Treatment Experienced

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria HIV positive Minimum of 1 year of treatment with HAART CD4+ cell count <350 cells/mm3 HIV-1 RNA <400 copies/ml for 6 months prior to study entry Acceptable methods of contraception Exclusion Criteria Serious medical illness requiring hospitalization within 14 days prior to study entry Pregnant or breast-feeding Taking certain medications Allergy to r-hGH, hepatitis A vaccine, KLH, or their formulations, including allergies to shellfish Active drug or alcohol dependence Diabetes or uncontrolled hyperglycemia Uncontrolled hypertension History of carpal tunnel syndrome Active neoplasm requiring treatment

Sites / Locations

  • Alabama Therapeutics CRS
  • UCLA CARE Center CRS
  • UC Davis Medical Center
  • Univ. of California Davis Med. Ctr., ACTU
  • Ucsf Aids Crs
  • University of Colorado Hospital CRS
  • Northwestern University CRS
  • Rush Univ. Med. Ctr. ACTG CRS
  • Univ. of Iowa Healthcare, Div. of Infectious Diseases
  • Beth Israel Med. Ctr., ACTU
  • Case CRS
  • MetroHealth CRS
  • Univ. of Texas Southwestern Med. Ctr., Amelia Court Continuity Clinic

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
December 30, 2002
Last Updated
October 28, 2021
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00050921
Brief Title
Administration of Growth Hormone to Increase CD4+ Count in Patients Taking Anti-HIV Drugs
Official Title
Improving Immune Reconstitution With Growth Hormone in HIV-infected Subjects With Incomplete CD4+ Lymphocyte Restoration on Highly Active Antiretroviral Therapy (HAART)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2005 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
This study is designed to evaluate the ability of growth hormone (GH, also known as somatropin) to increase CD4+ cell counts in patients taking anti-HIV drugs. The study is targeted toward patients with low levels of HIV who continue to have low CD4+ cell counts.
Detailed Description
After initiation of HAART, many HIV infected patients have significant improvement in CD4+ levels. However, some patients continue to have low CD4+ counts (< 350 cells/mm3) despite adequate viral suppression. The purpose of this study is to determine whether administration of GH will increase naïve CD4+ production. Further, the study will assess whether an increase in naïve CD4+ production will lead to increases in antigen-specific CD4+ and CD8+ T cells. Patients enrolled in this study will be randomized to one of two groups. Patients in both groups will continue their present HAART regimen for the duration of the study. Group A patients will receive daily subcutaneous injections of GH for 48 weeks. Group B participants will receive no additional therapy for 24 weeks, and will then receive daily subcutaneous GH injections during Weeks 24-28 of the study. Both groups will receive immunocyanin (keyhole-limpet hemocyanin) injections at Weeks 16 and 20 and hepatitis A vaccination at Weeks 40 and 44. At the conclusion of Week 48, all patients will discontinue GH therapy while maintaining their HAART regimen. Patients will then be followed for an additional 24 weeks. Patients may be asked to participate in a substudy to measure the size of the thymus in people taking GH. Patients in the substudy will have a noncontrast CT scan of the chest before beginning GH therapy and again after 24 weeks of GH therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
HIV Infections, CD4 Lymphocyte Count, Antiretroviral Therapy, Highly Active, Growth Hormone, Cell Division, CD4-Positive T-Lymphocytes, Treatment Experienced

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
somatropin
Intervention Type
Biological
Intervention Name(s)
Hepatitis A virus, inactivated
Intervention Type
Drug
Intervention Name(s)
Keyhole-Limpet Hemocyanin

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria HIV positive Minimum of 1 year of treatment with HAART CD4+ cell count <350 cells/mm3 HIV-1 RNA <400 copies/ml for 6 months prior to study entry Acceptable methods of contraception Exclusion Criteria Serious medical illness requiring hospitalization within 14 days prior to study entry Pregnant or breast-feeding Taking certain medications Allergy to r-hGH, hepatitis A vaccine, KLH, or their formulations, including allergies to shellfish Active drug or alcohol dependence Diabetes or uncontrolled hyperglycemia Uncontrolled hypertension History of carpal tunnel syndrome Active neoplasm requiring treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kimberly Smith, M.D., MPH
Organizational Affiliation
Rush Medical College of Rush University
Official's Role
Study Chair
Facility Information:
Facility Name
Alabama Therapeutics CRS
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35924
Country
United States
Facility Name
UCLA CARE Center CRS
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Facility Name
UC Davis Medical Center
City
Sacramento
State/Province
California
ZIP/Postal Code
95814
Country
United States
Facility Name
Univ. of California Davis Med. Ctr., ACTU
City
Sacramento
State/Province
California
ZIP/Postal Code
95814
Country
United States
Facility Name
Ucsf Aids Crs
City
San Francisco
State/Province
California
ZIP/Postal Code
94110
Country
United States
Facility Name
University of Colorado Hospital CRS
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80262
Country
United States
Facility Name
Northwestern University CRS
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Rush Univ. Med. Ctr. ACTG CRS
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
Univ. of Iowa Healthcare, Div. of Infectious Diseases
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Beth Israel Med. Ctr., ACTU
City
New York
State/Province
New York
ZIP/Postal Code
10003
Country
United States
Facility Name
Case CRS
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
MetroHealth CRS
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44109
Country
United States
Facility Name
Univ. of Texas Southwestern Med. Ctr., Amelia Court Continuity Clinic
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
10608789
Citation
Connick E, Lederman MM, Kotzin BL, Spritzler J, Kuritzkes DR, St Clair M, Sevin AD, Fox L, Chiozzi MH, Leonard JM, Rousseau F, D'Arc Roe J, Martinez A, Kessler H, Landay A. Immune reconstitution in the first year of potent antiretroviral therapy and its relationship to virologic response. J Infect Dis. 2000 Jan;181(1):358-63. doi: 10.1086/315171.
Results Reference
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PubMed Identifier
10608760
Citation
Smith KY, Valdez H, Landay A, Spritzler J, Kessler HA, Connick E, Kuritzkes D, Gross B, Francis I, McCune JM, Lederman MM. Thymic size and lymphocyte restoration in patients with human immunodeficiency virus infection after 48 weeks of zidovudine, lamivudine, and ritonavir therapy. J Infect Dis. 2000 Jan;181(1):141-7. doi: 10.1086/315169.
Results Reference
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PubMed Identifier
10716501
Citation
Vigano A, Vella S, Saresella M, Vanzulli A, Bricalli D, Di Fabio S, Ferrante P, Andreotti M, Pirillo M, Dally LG, Clerici M, Principi N. Early immune reconstitution after potent antiretroviral therapy in HIV-infected children correlates with the increase in thymus volume. AIDS. 2000 Feb 18;14(3):251-61. doi: 10.1097/00002030-200002180-00007.
Results Reference
background
PubMed Identifier
8967667
Citation
Schambelan M, Mulligan K, Grunfeld C, Daar ES, LaMarca A, Kotler DP, Wang J, Bozzette SA, Breitmeyer JB. Recombinant human growth hormone in patients with HIV-associated wasting. A randomized, placebo-controlled trial. Serostim Study Group. Ann Intern Med. 1996 Dec 1;125(11):873-82. doi: 10.7326/0003-4819-125-11-199612010-00002.
Results Reference
background
PubMed Identifier
12004268
Citation
Napolitano LA, Lo JC, Gotway MB, Mulligan K, Barbour JD, Schmidt D, Grant RM, Halvorsen RA, Schambelan M, McCune JM. Increased thymic mass and circulating naive CD4 T cells in HIV-1-infected adults treated with growth hormone. AIDS. 2002 May 24;16(8):1103-11. doi: 10.1097/00002030-200205240-00003.
Results Reference
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Administration of Growth Hormone to Increase CD4+ Count in Patients Taking Anti-HIV Drugs

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