Treatment of Abnormal Adipose Tissue Accumulation in HIV Patients

• Register: ClinicalTrials.gov
• Last refreshed on: 19 February 2015
• Main ID: NCT00082628
• Date of registration: 13/05/2004
• Prospective Registration: No
• Primary sponsor: EMD Serono
• Public title: Treatment of Abnormal Adipose Tissue Accumulation in HIV Patients
• Scientific title: A Phase III, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study of the Safety and Efficacy of Serostim®, r-hGH in the Treatment and Maintenance of Human Immunodeficiency HIV-Associated Adipose Redistribution Syndrome, or HARS
• Date of first enrolment: May 2004
• Target sample size: 569
• Recruitment status: Completed
• URL: http://clinicaltrials.gov/show/NCT00082628
• Study type: Interventional
• Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
• Phase: Phase 3

Countries of recruitment

Canada, United States

Contacts

• Name: Norma Muurahainen, MD
• Affiliation: Sponsor GmbH

Key inclusion & exclusion criteria

Inclusion Criteria:

1. Have written laboratory documentation of an HIV infection by one of the following
methods:

- Detectable viral load measured by polymerase chain reaction (PCR) amplification,
branched chain DNA (bDNA) signal amplification or the presence of p24 antigen.

- Presence of HIV antibodies confirmed by either Western blot or
immunofluorescence assay.

Written laboratory documentation of an HIV infection must be obtained prior to
randomization. In the absence of documented historical confirmation, an assay of HIV
antibodies will be included in the Screening Laboratory Panel. Results will be
confirmed with a Western Blot.

2. Have evidence of excess abdominal adipose deposition when measured by the
anthropometric methodology, using the following cut off values:

- Men: Waist circumference >88.2 cm AND waist: hip ratio >= 0.95.

- Women: Waist circumference >75.3 cm AND waist: hip ratio >= 0.9.

3. Are taking antiretroviral medication(s) which is (are) approved or is (are) available
under a Treatment IND. The regimen must have remained stable for 30 days prior to
study entry. Subjects must also agree not to discontinue or to change their regimen
for the duration of the study except as judged medically necessary.

4. Have parameter values less than the following limits (using results from the central
laboratory):

- AST, ALT, and amylase <= 3 times the upper limit of normal (Screening).

- Fasting triglycerides <= 1,000 mg/dL (Screening).

- Fasting glucose <110 mg/dL (Screening).

- Two-hour (120 minute) glucose <140 mg/dL (Screening).

5. Weight >= 36 kg (79.3 lb)

6. Be between 18 and 60 years of age (inclusive) unless local law dictates different
limits.

7. Sufficiently literate in English to be able to comprehend and complete the Quality of
Life Questionnaire.

8. Willing and able to comply with the protocol for the duration of the study.

9. Have voluntarily provided written informed consent (with subject authorization under
HIPAA), prior to performing any study-related procedure that is not part of normal
medical care, and with the understanding that the subject may withdraw consent at any
time without prejudice to future medical care.

10. Female subjects must:

1. Be post menopausal (>= 1 year) or surgically sterilized (i.e., have undergone
tubal ligation or hysterectomy)

or

2. Use a contraceptive method for the duration of the study such as:

- Hormonal contraceptive

- Intra uterine device

- Diaphragm with spermicide, or condom with spermicide.

And

3. Must be neither pregnant nor breast feeding.

4. Confirmation that female subjects of childbearing potential are not pregnant
must be established by a negative beta-hCG serum pregnancy test during the
14-day screening period prior to Study Day 1. If the beta-hCG serum pregnancy
test is performed more than 7 days prior to Study Day 1, a urine pregnancy test
must be performed by the site laboratory on Study Day 1 to confirm a negative
test result.

Exclusion Criteria:

1. Have an active AIDS-defining opportunistic complication (OC) as defined by the CDC or
have had an untreated or suspected serious systemic infection, or have had a
persistent fever >= 101°F (38.3°C) during the 30 days prior to study entry.

2. Any active or past history of malignancy, except for localized cutaneous Kaposi's
sarcoma (fewer than 10 lesions, none of which are larger than 2 cm, and not on active
therapy). Such exceptions must be confirmed in writing by the Serono Study Director.

3. Have a CNS mass or active CNS process associated with neurological findings.

4. Have unstable or untreated hypertension, defined as >= 140/90 mm Hg at the time of
the Screening Visit, and/or have initiated or changed antihypertensive therapy in the
30 days prior to Study Day 1.

5. Have an acute critical illness treated in an intensive care unit, e.g., due to
complications following open heart or abdominal surgery, multiple accidental trauma,
or acute respiratory failure.

6. Have a recent history of sleep apnea or intermittent upper respiratory obstruction.

7. Have any condition, which interferes with informed consent or protocol compliance
including, but not limited to, active substance abuse and/or dementia.

8. Are unable to comply with the Concomitant Therapy restrictions including:

- therapy for obesity including therapy with anorexigenic or fat reducing drugs

- anti-diabetic or insulin sensitizing medications

- systemic glucocorticoids

- systemic chemotherapy, interferon or radiation therapy treatment

- androgenic agents including, but not limited to testosterone, nandrolone,
oxandrolone, oxymetholone, etc. (testosterone replacement therapy for
hypogonadism is the exception to this exclusion and will be allowed if started >
30 days prior to Study Day 1)

- progestational agents, unless used for oral contraception or post-menopausal
hormone replacement therapy

- appetite stimulants

- investigational agents, unless approved in advance by the study medical
director. Specifically, experimental antiretroviral agents are disallowed,
unless available under a treatment IND or expanded access program (30 days).

- Liposuction or other elective plastic surgery

- AIDS wasting therapy or prior growth hormone treatment other than study drug
(for 12 months prior to the screening visit)

9. Have ever been diagnosed with any of the following conditions:

- Pancreatitis

- Carpal tunnel syndrome (unless resolved by surgical release)

- Diabetes mellitus

- Angina pectoris

- Coronary artery disease

- Any disorder associated with moderate to severe edema (e.g., ascites, nephrotic
syndrome, congestive heart failure, lymphedema).

10. Allergy or hypersensitivity to growth hormone.

11. Are participating in any other clinical studies.

In order to participate in this trial a subject must meet all of the inclusion and
exclusion criteria specified above. Requests for protocol exceptions/exemptions must come
from a participating, fully i


Age minimum: 18 Years
Age maximum: 60 Years
Gender: Both

Health Condition(s) or Problem(s) studied

HIV Infections

Lipodystrophy

Intervention(s)

Drug: Serostim®[somatropin (rDNA origin) for injection]

Secondary ID(s)

24380

Source(s) of Monetary Support

Please refer to primary and secondary sponsors