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Tesamorelin

Clinical10 studies

Tesamorelin is a stabilized GHRH analogue investigated for its effects on growth hormone release and metabolic pathways.

Being studied for

  • GH secretion research
  • Metabolic signaling pathways

Published Research

Evidence profile

Human Phase 3 evidence

10 cited publications · 8 primary trials

Findings below belong to the studies that reported them. They describe the material and conditions those authors used, not this product, and not an outcome to expect.

Core evidence

The publications most central to understanding this compound.

ReviewSystematic review and meta-analysis

Body composition, hepatic fat, metabolic, and safety outcomes of Tesamorelin, a GHRH analogue, in HIV-associated lipodystrophy: A meta-analysis of randomized controlled trials

Badran AS et al. · Obesity research & clinical practice · 2026

Population: People with HIV-associated lipodystrophy

Pools the randomised evidence for tesamorelin across body composition, hepatic fat, metabolic and safety outcomes.

Context: Conducted entirely in an HIV-associated lipodystrophy population; it does not describe use for general body composition.

PMID 41545261DOI 10.1016/j.orcp.2026.01.002View on PubMed

Supporting evidence

ClinicalPrimary trial · Phase 2

Effects of Tesamorelin on Neurocognitive Impairment in Persons With HIV and Abdominal Obesity

Ellis RJ et al. · The Journal of infectious diseases · 2025

The study reportedWhile tesamorelin reduced WC, the cognitive benefits did not significantly differ between groups. Recognizing the limitations of insufficient power and no placebo arm, this study suggests no clear benefit of short-term AO reduction with tesamorelin on NCI.

PMID 39813152DOI 10.1093/infdis/jiaf012View on PubMed
ClinicalRandomised controlled trial

Efficacy and safety of tesamorelin in people with HIV on integrase inhibitors

Russo SC et al. · AIDS (London, England) · 2024

Population: People with HIV receiving integrase inhibitors

A randomised trial of tesamorelin in people with HIV taking integrase inhibitor regimens.

Context: A single population defined by its antiretroviral regimen.

PMID 38905488DOI 10.1097/QAD.0000000000003965View on PubMed
ClinicalPrimary trial

Effects of tesamorelin on hepatic transcriptomic signatures in HIV-associated NAFLD

Fourman LT et al. · JCI insight · 2020

The study reportedNotably, among tesamorelin-treated participants, these changes in hepatic expression correlated with improved fibrosis-related gene score. Our findings inform our knowledge of the biology of pulsatile growth hormone action and provide a mechanistic basis for the observed clinical effects of tesamorelin on the liver.

PMID 32701508DOI 10.1172/jci.insight.140134View on PubMed
ClinicalPrimary trial

Effects of tesamorelin on non-alcoholic fatty liver disease in HIV: a randomised, double-blind, multicentre trial

Stanley TL et al. · The lancet. HIV · 2019

The study reportedTesamorelin might be beneficial in people with HIV and NAFLD. Further studies are needed to determine the long-term effects of tesamorelin on liver histology.

PMID 31611038DOI 10.1016/S2352-3018(19)30338-8NCT02196831View on PubMed
ClinicalPrimary trial · Phase 1

Population pharmacokinetic analysis of tesamorelin in HIV-infected patients and healthy subjects

González-Sales M et al. · Clinical pharmacokinetics · 2015

The study reportedAn open one-compartment model with first and zero order absorption processes and linear elimination is suitable to characterize the pharmacokinetics of tesamorelin. The fraction of tesamorelin absorbed by a first-order process evolves with time.

PMID 25358450DOI 10.1007/s40262-014-0202-xView on PubMed
ClinicalPrimary trial

Predictors of Treatment Response to Tesamorelin, a Growth Hormone-Releasing Factor Analog, in HIV-Infected Patients with Excess Abdominal Fat

Mangili A et al. · PloS one · 2015

The study reportedIndividuals with baseline MetS-NCEP, elevated triglyceride levels, or white race were most likely to experience reductions in VAT after 6 months of tesamorelin treatment. The odds of response of VAT <140 cm2 was 3.9 times greater for tesamorelin-treated patients than that of patients receiving placebo.

PMID 26457580DOI 10.1371/journal.pone.0140358View on PubMed
ClinicalPrimary trial

The effects of tesamorelin on phosphocreatine recovery in obese subjects with reduced GH

Makimura H et al. · The Journal of clinical endocrinology and metabolism · 2014

The study reportedIncreases in IGF-I from 12 months of treatment with tesamorelin were significantly associated with improvements in PCr recovery parameters in obese men and women with reduced GH secretion, suggestive of improvements in mitochondrial function.

PMID 24178787DOI 10.1210/jc.2013-3436NCT00675506View on PubMed
ClinicalPrimary trial · Phase 3

Effects of tesamorelin on inflammatory markers in HIV patients with excess abdominal fat: relationship with visceral adipose reduction

Stanley TL et al. · AIDS (London, England) · 2011

The study reportedIn HIV patients with abdominal adiposity, tesamorelin may have a modest beneficial effect on adiponectin and fibrinolytic markers in association with changes in VAT. Further studies are needed to determine the clinical significance of these changes.

PMID 21516030DOI 10.1097/QAD.0b013e328347f3f1View on PubMed
ReviewMeta-analysis

Efficacy and Safety of Tesamorelin in People Living With HIV (PLWH) With Lipodystrophy: A Systematic Review and Meta-Analysis

Ditta AM et al. · Journal of the International Association of Providers of AIDS Care · 2026

The study reportedHowever, some side effects related to growth hormone were reported, and more people stopped treatment compared to those not receiving the drug. Overall, tesamorelin appeared quite useful as long as it is continued, but more research is needed to understand its long-term safety and benefits.

PMID 42538058DOI 10.1177/23259582261475549View on PubMed

Published studies summarised here concern the specific investigational or pharmaceutical materials and study conditions described by their authors. Their findings are not performance claims for Cobalt Peptides material. Citations verified against PubMed on 2026-08-09.

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