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Tesamorelin Effects on Liver Fat and Histology in HIV

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ClinicalTrials.gov Identifier: NCT02196831
Recruitment Status : Active, not recruiting
First Posted : July 22, 2014
Last Update Posted : March 11, 2019
Sponsor:
Collaborator:
National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by (Responsible Party):
Steven K. Grinspoon, MD, Massachusetts General Hospital

Brief Summary:

Liver disease is one of the leading co-morbidities of human immunodeficiency virus (HIV) infection, and nonalcoholic fatty liver disease (NAFLD) is present in approximately 30-40% of patients with HIV infection. Nonalcoholic steatohepatitis (NASH) is a more severe form of NAFLD in which increased liver fat is also accompanied by inflammation, cellular damage, and fibrosis.

NAFLD is most prevalent in patients who also have increased visceral adiposity, and our group has previously shown that HIV-infected individuals with increased visceral adiposity generally have decreased growth hormone secretion. Tesamorelin is a growth hormone releasing hormone (GHRH) analogue that increases endogenous growth hormone secretion. Tesamorelin is FDA-approved for the reduction of visceral fat in HIV-infected individuals. In a previous study, treatment with tesamorelin in HIV-infected individuals selected for abdominal adiposity reduced liver fat. The current study is designed to test the effect of tesamorelin on liver fat and steatohepatitis in HIV-infected individuals who have NAFLD. The investigators hypothesize that tesamorelin will reduce liver fat and will also ameliorate the inflammation, fibrosis, and hepatocellular damage seen in conjunction with NASH.


Condition or disease Intervention/treatment Phase
Human Immunodeficiency Virus (HIV) Nonalcoholic Fatty Liver Disease (NAFLD) Nonalcoholic Steatohepatitis (NASH) Drug: tesamorelin Drug: Placebo Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 61 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Tesamorelin Effects on Liver Fat and Histology in HIV: A Collaborative UO1 Grant
Actual Study Start Date : July 1, 2015
Actual Primary Completion Date : January 16, 2019
Estimated Study Completion Date : July 2019


Arm Intervention/treatment
Experimental: Tesamorelin
tesamorelin 2mg subcutaneously daily x 12 months double-blind phase. At the end of 12 months, subjects enter open-label tesamorelin treatment phase for 6 months.
Drug: tesamorelin
Other Name: Egrifta

Placebo Comparator: Placebo
placebo subcutaneously daily x 12 months double-blind phase. At the end of 12 months, subjects enter open-label tesamorelin treatment phase for 6 months.
Drug: Placebo
inactive substance that looks like tesamorelin




Primary Outcome Measures :
  1. Liver fat as measured by 1-H Magnetic resonance spectroscopy [ Time Frame: 12 months ]

Secondary Outcome Measures :
  1. Nonalcoholic fatty liver disease activity score [ Time Frame: 12 months ]
  2. alanine aminotransferase (ALT) [ Time Frame: 12 months ]
  3. aspartate aminotransferase (AST) [ Time Frame: 12 months ]
  4. liver stiffness measured by FibroScan [ Time Frame: 12 months ]


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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  • Men and women 18-70yo
  • HIV-infection and treatment with a stable antiretroviral regimen for ≥ 6 months
  • Hepatic steatosis as demonstrated by liver fat fraction ≥5% on 1H-MRS
  • Hepatitis C antibody negative, or, if Hepatitis C antibody positive, either: a) known clinical disease, successful therapy ≥1 year prior to baseline and undetectable HCV RNA, or b) HCV resolved spontaneously and undetectable HCV RNA. Hepatitis B surface antigen negative at screen visit
  • For females ≥50yo, negative mammogram within 1 year of baseline visit
  • If use of Vitamin E ≥400 IU daily (in any formulation), stable dose for ≥6 months prior to study.

Exclusion criteria:

  • Heavy alcohol use defined as consumption of more than 20g daily for women or more than 30g daily for men for at least 3 consecutive months over the past 5 years
  • Use of insulin or thiazoledinediones (TZDs), or HbA1c ≥7%. Individuals with mild diabetes that is well-controlled with diet and/or oral anti-diabetic agents besides TZDs will be included. Use of oral anti-diabetics must have been stable for ≥6 months prior to study entry.
  • Known diabetic retinopathy.
  • Known cirrhosis, or Child-Pugh score ≥7, stage 4 fibrosis on biopsy, or clinical evidence of cirrhosis or portal hypertension on imaging or exam.
  • Chronic corticosteroid use except intermittent use of topical steroid creams and/or prior short-term physiologic corticosteroid use in the ≤ 6 months prior to baseline visit
  • Chronic use of methotrexate, amiodarone, or tamoxifen
  • Known diagnosis of Alpha-1 antitrypsin deficiency, Wilson's disease, hemochromatosis, or autoimmune hepatitis
  • Use of GH or GHRH within the past 1 year
  • Change in lipid lowering or anti-hypertensive regimen within 3 months of screening
  • HgB < 11.0 g/dL, CD4 < 100 th/mm3, or HIV viral load > 400 copies/mL
  • Active malignancy
  • For men, history of prostate cancer or evidence of prostate malignancy by PSA > 5 ng/mL
  • Severe chronic illness judged by the investigator to present a contraindication to participation
  • History of hypopituitarism, head irradiation or any other condition known to affect the GH axis
  • Use of physiologic testosterone (men) or estrogen or progesterone (women) unless stable use for a year or more prior to study entry
  • Routine MRI exclusion criteria such as the presence of a pacemaker or cerebral aneurysm clip
  • Previous weight loss surgery
  • For women, positive pregnancy test performed in a CLIA certified laboratory using a test with a sensitivity of at least 25mIU/mL, or breastfeeding.
  • Known hypersensitivity to tesamorelin or mannitol
  • Unwillingness to abstain from the conception process during the study (i.e., must agree not to participate in an active attempt to become pregnant or impregnate, donate sperm, or participate in in vitro fertilization)
  • Unwillingness to use one (for males) or two (for females) reliable methods of contraception while engaging in heterosexual intercourse during the study. Acceptable methods for women include hormonal contraception (estrogen/progesterone or progesterone-only formulations) if stable for a year or more prior to study entry, intrauterine device, or barrier methods (condom, or diaphragm with spermicide). Acceptable methods for males include condom use. This requirement does not apply to women who have been post-menopausal for at least 24 consecutive months or have undergone surgical sterilization, or to men who have undergone surgical sterilization or have documented azoospermia.
  • Not willing or able to adhere to dose schedules and required procedures per protocol

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02196831


Locations
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United States, Maryland
National Institutes of Health
Bethesda, Maryland, United States, 20892
United States, Massachusetts
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
Sponsors and Collaborators
Massachusetts General Hospital
National Institute of Allergy and Infectious Diseases (NIAID)
Investigators
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Principal Investigator: Steven K Grinspoon, MD MGH

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Responsible Party: Steven K. Grinspoon, MD, Professor of Medicine, Massachusetts General Hospital
ClinicalTrials.gov Identifier: NCT02196831     History of Changes
Other Study ID Numbers: 1U01AI115711 ( U.S. NIH Grant/Contract )
U01AI115711 ( U.S. NIH Grant/Contract )
First Posted: July 22, 2014    Key Record Dates
Last Update Posted: March 11, 2019
Last Verified: March 2019

Keywords provided by Steven K. Grinspoon, MD, Massachusetts General Hospital:
Human immunodeficiency virus (HIV)
Nonalcoholic fatty liver disease (NAFLD)
Nonalcoholic steatohepatitis (NASH)
Growth hormone releasing hormone
tesamorelin

Additional relevant MeSH terms:
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Fatty Liver
Non-alcoholic Fatty Liver Disease
Immunologic Deficiency Syndromes
Liver Diseases
Acquired Immunodeficiency Syndrome
HIV Infections
Immune System Diseases
Digestive System Diseases
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Slow Virus Diseases
Tesamorelin
Growth Hormone-Releasing Hormone
Growth Substances
Physiological Effects of Drugs
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists