Overview

Testosterone and Physical Function in HIV+ Men

Status:
Completed
Trial end date:
2006-06-01
Target enrollment:
0
Participant gender:
Male
Summary
Men infected with the HIV virus (the virus that causes AIDS) often lose weight even though they may try to eat more food to gain weight. The reasons for this weight loss are not clear. Many men with HIV have low levels of testosterone in their blood. Testosterone is a hormone that is naturally produced in the bodies of both men and women and has important effects on building muscle and bone mass. The purpose of this study is to find out if providing additional testosterone to HIV infected men who have low testosterone can help them gain weight, increase their muscle mass, and feel better. The study will also help see if testosterone improves the efficiency with which your body produces and uses energy including fat. The dose of testosterone being used in this study will raise testosterone levels in the blood to higher than normal levels (2-3 times normal level).
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborator:
Charles Drew University of Medicine and Science
Treatments:
Methyltestosterone
Testosterone
Testosterone 17 beta-cypionate
Testosterone enanthate
Testosterone undecanoate
Criteria
Inclusion Criteria:

- HIV positive men, 18-60 years of age, with objective evidence of HIV-infection with
low to low-normal testosterone levels (<400 ng/dL). In boys before the age of 18, the
hormonal and body composition changes of puberty can confound the data. We will
exclude men over 60 because of age-related changes in testosterone levels and body
composition, and increased risk of prostate disease.

- Documented weight loss within the previous 6 months of between 5-15% of body weight,
or an actual body mass index (BMI) at screening of between 17 and 20 (= 85-95% of the
lower limit of ideal weight).

- An energy intake of at least 80% of the estimated requirements. On stable and potent
antiretroviral therapy for at least 12 weeks, and in whom, in the opinion of the
primary care provider, a change in antiretroviral therapy is unlikely in the next 4
months. Stable therapy may include those not on any antiretroviral therapies and whom,
in the opinion of the primary care provider, will not be starting antiretroviral
therapy in the next 4 months CD4 cell count >50 /mm3, and HIV-copy number less than
10,000 copies/ml Testosterone levels <400ng/dL Able and willing to provide informed
consent and comply with the protocol

Exclusion Criteria:

- Concurrent severe lipodystrophy* according to the patient and the investigator,
defined as "the new appearance of thin extremities due to loss of subcutaneous fat
(especially the medial compartment of the thigh) along with the new appearance of
prominent veins. Loss of tissue in the buccal fat pad and subgluteal region provides
further evidence that thin extremities may be in large part due to loss of fat and not
just muscles."

- History of prostatic or mammary cancer

- Significant diarrhea defined as 6 or more stools per day with recent change in bowel
habits towards more frequent stools, especially if associated with weight loss and
fever

- Use of any androgen, growth hormone, or other anabolic or orexigenic agents within the
past 6 months

- Use of systemic corticosteroids, except for topical application

- Significant cardiac, renal, hepatic or other diseases that, in the opinion of the
Investigator, may put the subject at risk if entered onto the trial or prevent
successful completion of the trial.

- AIDS defining illness (CDC HIV Classification, 1993: Clinical Category C) within the
previous 3 months (except HIV wasting syndrome)

- Malignancy, other than Kaposi's Sarcoma localized to the skin

- Involvement in (vigorous) resistance exercise training programs (body building) in the
past 3 months

- Diabetes mellitus Limiting neuromuscular, joint or bone disease, or history of stroke
with residual neurological defect that would preclude measurements of muscle strength
or physical function

- Severe symptoms of BPH (American Urological Association [AUA] symptom index score of
>14), prostate nodule or induration on digital rectal examination (DRE) unless there
has been a negative transrectal biopsy within 3 months, and prostate specific antigen
(PSA) > 4

- Untreated severe obstructive sleep apnea, as assessed by Berlin's symptom score.

- Current alcohol or drug dependence which would interfere with compliance for the study

- Subject receive investigational treatment except stable antiretroviral investigational
drug in the last 12 weeks

- Subject have a history of hypersensitivity to anabolic steroids or to growth hormone

- Any of the following blood test results:

- Liver function test (ALT, AST) 5x the upper limit of the normal range (ULN)

- Alkaline Phosphotase > 5x ULN or > 3x ULN if bilirubin is above normal

- Cholesterol total (> 5 x ULN) or triglycerides 700 mg/dL

- Serum Creatinine 2x ULN

- Hemoglobin 8.0 g/dl or >18 g/dL

- Platelet count < 50x109/L

- HCT >48%

- PSA 4 ng/ml.

- Concomitant Medications: Men who have received in the preceding 6 months or are
currently using androgenic steroids, rhGH, IGF-I or other anabolic agents or appetite
stimulants will be excluded. Also, excluded are drugs that affect testosterone
secretion or metabolism such as ketoconazole, dilantin, and phenobarbital. Patients
who have been on a stable dose of erythropoietin for at least 3 months will be allowed
to continue the drug. The changes in antiretroviral therapy except for changes within
the same class of drugs are not allowed. The use of corticosteroids, except for
topical application, is not allowed. The food supplements that might affect body
composition such as creatine, high dose amino-acid supplements, whey protein
supplements, androstenedione, DHEA, and marinol, are also not allowed.

- On the Exclusion of Women. Women are not being included in this study because
testosterone administration in these doses will inevitably cause virilization, and is
ethically unacceptable.