Treatment of Abnormal Adipose Tissue Accumulation in Human Immunodeficiency Virus (HIV) Patients

Inclusion Criteria

• 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.

• 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.
• 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.
• Have parameter values less than the following limits (using results from the central laboratory):
• AST, ALT, and amylase = 36 kg (79.3 lb)
• Be between 18 and 60 years of age (inclusive) unless local law dictates different limits.
• Sufficiently literate in English to be able to comprehend and complete the Quality of Life Questionnaire.
• Willing and able to comply with the protocol for the duration of the study.
• 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.
• Female subjects must:
• Be post menopausal (>= 1 year) or surgically sterilized (i.e., have undergone tubal ligation or hysterectomy)

or

• 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

• Must be neither pregnant nor breast feeding.
• 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

• 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.
• 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.
• Have a CNS mass or active CNS process associated with neurological findings.
• 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.
• 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.
• Have a recent history of sleep apnea or intermittent upper respiratory obstruction.
• Have any condition, which interferes with informed consent or protocol compliance including, but not limited to, active substance abuse and/or dementia.
• Are unabl