Summary

for people ages 40 years and up (full criteria)
at UCSD
study started
estimated completion:
Ronald J Ellis (ucsd)

Description

Summary

The aim of this study is to test whether tesamorelin, in combination with a text-messaging application to help with motivation and adherence, will significantly improve memory and thinking in HIV.

Details

HIV infection can result in memory and thinking difficulties in some people, even those successfully treated with antiretroviral medications. Tesamorelin is an injectable medication already approved by the U.S. FDA to treat abdominal fat accumulation in HIV. Abdominal fat accumulation is linked to memory and thinking difficulties, and previous studies have suggested that tesamorelin also may be beneficial for memory and thinking, but this has not been tested in HIV. The aim of this study is to test whether tesamorelin, in combination with a text-messaging application to help with motivation and adherence, will significantly improve memory and thinking in HIV. We plan to enroll 100 volunteers with HIV infection at 2 sites - the University of California, San Diego and the University of Southern California and the satellite site, Borrego Health Stonewall Medical Center. Before entry, volunteers will be required to show evidence of abdominal obesity and a minimum level of memory and thinking difficulties on cognitive tests. This is a randomized trial in which each volunteer will have a 60% chance of initially receiving tesamorelin (the immediate group) and a 40% chance of initially receiving no treatment (the deferred group). Subsequently, the deferred group (those who initially received no treatment) will receive tesamorelin for 6 months and those who initially received tesamorelin will receive no treatment for 6 months. Volunteers will be trained in the use of a 2-way text-messaging system that will help the research team to support volunteers' ability to take the study medication as directed. We will measure volunteers' memory and thinking skills before and at the end of treatment. We will collect blood at various points during the study to check for safety of the treatment and to determine its effects on the body. Volunteers will also be asked to have magnetic resonance scans of the head and abdomen to monitor the effects of the study medication on brain chemistry and abdominal fat.

Keywords

Mild Cognitive Impairment Cognitive Dysfunction Growth Hormone-Releasing Hormone Tesamorelin

Eligibility

You can join if…

Open to people ages 40 years and up

  • HIV-1 infection documented by any FDA licensed clinical test including HIV enzyme/antigen test or chemiluminescence immunoassay (E/CIA) or plasma HIV-1 RNA viral load.
  • Antiretroviral therapy: Patient currently receiving a combination antiretroviral therapy (cART) regimen ≥24 weeks with no interruptions longer than 7 days and HIV<1000 copies/ml during that time.
  • Men or women 40 years of age and older
  • Abdominal minimal waist circumference ≥ 95cm for men and ≥94cm for women or minimal waist to hip ratio of ≥ 0.88 for women (each based on an average of three separate measurements)
  • Screening neuropsychological Global Deficit Score of ≥ 0.35
  • The following laboratory values obtained within 90 days prior to entry by any CLIA certified laboratory.
  • Absolute neutrophil count (ANC) ≥750/mm3
  • Hemoglobin ≥8.0 g/dL
  • Platelet count ≥50,000/mm3
  • HgbA1C <6.5%
  • Calculated creatinine clearance of ≥60 mL/min as estimated by the Cockroft-Gault formula
  • Aspartate aminotransferase (AST) (SGOT), alanine aminotransferase (ALT) (SGPT),and alkaline phosphatase ≤5 X upper limit of normal (ULN)
  • Total bilirubin ≤2.5 x ULN (if the participant is receiving atazanavir, a total bilirubin of ≤5 x ULN is acceptable).
  • For females of reproductive potential, negative serum or urine pregnancy test within 30 days prior to entry by any test performed by a CLIA certified laboratory or is using a point of care (POC)/ CLIA-waived test.
  • Contraception requirements: For females of reproductive potential, she or male partner is willing to use a contraceptive during sexual intercourse.
  • Ability and willingness of participant or legal guardian/representative to provide informed consent

You CAN'T join if...

  • Clinical contraindications
  • History of neurocognitive confounding conditions that explain current impairment including but not limited to stroke, head injury, psychotic disorder, active substance use disorder by DSM, or opportunistic CNS infection
  • Hepatitis C virus infection defined as HCV antibody positive requiring treatment and plans for treatment during study therapy
  • Active or relapsing autoimmune disorder that may require immunotherapy during this treatment trial
  • Active malignancy other than basal or squamous skin cancer.
  • Breastfeeding or pregnancy
  • Excluded medications used within the last 90 days: active or planned use of rhGH,anti-TNFa therapy or other biologic (tocilizumab, Xelijanz, etc.), systemic corticosteroids, need for prescription dosing of NSAIDs administered regularly one or more times daily, or investigational medication
  • Known allergy/sensitivity or any hypersensitivity to tesamorelin
  • Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements
  • Acute or serious illness requiring systemic treatment and/or hospitalization within 60 days prior to entry
  • Use of tesamorelin in the last 6 months

Locations

  • HIV Neurobehavioral Research Program (HNRP) accepting new patients
    San Diego California 92103 United States
  • Keck School of Medicine of the University of Southern California accepting new patients
    Los Angeles California 90033 United States

Lead Scientist

  • Ronald J Ellis (ucsd)
    Dr. Ellis’s clinical work and research are focused on the neurological manifestations of HIV infection and their pathogenesis and treatment, particularly dementia, neurocognitive disorders and sensory polyneuropathy.

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Diego
ID
NCT02572323
Phase
Phase 2
Study Type
Interventional
Last Updated