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Trial · Interventional

CompletedPhase 3Registry data

TH9507 in Patients With HIV-Associated Lipodystrophy

Overview

Status
Completed
Phase
Phase 3
Enrollment
412 participants (actual)
Sponsor
Theratechnologies · Industry
Design
Randomized · Double masking
Countries
2 countries

United States, Canada

Start
Jun 2005
Primary completion
Nov 2006
Completion
Apr 2007
First posted
22 Jul 2005 (estimated)
Last update posted
27 Nov 2013 (estimated)
Conditions
HIV Infections · Lipodystrophy

Timeline

1 trial · 1 completed

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
2005200620072008
  1. Ph 3

    TH9507 in Patients With HIV-Associated Lipodystrophy

    NCT00123253

    Jun 2005 to Apr 2007

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

HIV lipodystrophy affects a significant proportion of patients treated with combination antiretroviral therapy (ART) and is characterized by excess visceral fat accumulation and loss of extremity and subcutaneous fat, in association with dyslipidemia and insulin resistance. Data from a previous randomized, placebo-controlled trial demonstrated that daily administration of 2mg TH9507, a growth hormone releasing factor (GRF), to HIV patients with an excess of abdominal fat accumulation for 12 weeks resulted in decreases in visceral adipose tissue (VAT) and trunk fat, with no significant changes in limb fat and subcutaneous adipose tissue (SAT). This study is aimed at further assessing the efficacy and safety of 2 mg TH9507 in a larger population of HIV patients treated with ART and experiencing an excess of abdominal fat accumulation.

Interventions

  • TH9507Drug

Arms0

The registry lists no arms for this trial.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Visceral adipose tissue (VAT)

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

Completed trials do not always post results.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies5

Studies that cite this trial.

Studies with results

5 studies on this page

PubMed tag: none · 2017

3 results

Visceral fat reduction with tesamorelin is associated with improved liver enzymes in HIV.

Fourman et al. 2017AIDS (London, England)cited by 10

PMID 28832410PMC5633509DOI 10.1097/qad.0000000000001614PUB-28832410

Rights unknown3 results

Indexing hint: Randomized controlled trial · 2012

5 results

Reduction in visceral adiposity is associated with an improved metabolic profile in HIV-infected patients receiving tesamorelin.

Stanley et al. 2012Clinical infectious diseases : an official publication of the Infectious Diseases Society of Americacited by 23

PMID 22495074PMC3348954DOI 10.1093/cid/cis251PUB-22495074

Rights unknown5 results

Indexing hint: Randomized controlled trial · 2010

13 results

Effects of tesamorelin, a growth hormone-releasing factor, in HIV-infected patients with abdominal fat accumulation: a randomized placebo-controlled trial with a safety extension.

Falutz et al. 2010Journal of acquired immune deficiency syndromes (1999)cited by 51

PMID 20101189DOI 10.1097/qai.0b013e3181cbdaffPUB-20101189

Rights unknown13 results

PubMed tag: none · 2010

15 results

Effects of tesamorelin (TH9507), a growth hormone-releasing factor analog, in human immunodeficiency virus-infected patients with excess abdominal fat: a pooled analysis of two multicenter, double-blind placebo-controlled phase 3 trials with safety extension data.

Falutz et al. 2010The Journal of clinical endocrinology and metabolismcited by 78

PMID 20554713DOI 10.1210/jc.2010-0490PUB-20554713

Full text at the publisher15 results

Indexing hint: Randomized controlled trial · 2007

9 results

Metabolic effects of a growth hormone-releasing factor in patients with HIV.

Falutz et al. 2007The New England journal of medicinecited by 139

PMID 18057338DOI 10.1056/nejmoa072375PUB-18057338

Full text at the publisher9 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years up to 65 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Ages 18 to 65 years inclusive * HIV positive; CD4 cell counts \>100 cells/mm3; viral load \<10,000 copies/mL (stable for 8 weeks) * On stable ART regimen for at least 8 weeks prior to randomization * Have evidence of abdominal fat accumulation defined by the following anthropometric cut off values: * For males: waist circumference \> 95 cm and waist to hip ratio \> 0.94; * For females: waist circumference \> 94 cm and waist to hip ratio \> 0.88. * Females of childbearing potential not pregnant or lactating; normal mammography within 6 months of study. * Signed informed consent Exclusion Criteria: * Body mass index \< 20 kg/m2 * Opportunistic infection; HIV-related disease within 3 months of study. * History of malignancy; active neoplasm. * Prostate-specific antigen (PSA) \>5 ng/mL at screening * Hypopituitarism; history of pituitary tumor/surgery; head irradiation; head trauma that has affected the somatotropic axis. * Untreated hypothyroidism * Type 1 diabetics and type 2 diabetics on oral hypoglycemic or insulin sensitizing agent within 6 months of study * ALT or AST \> 3 x ULN; serum creatinine \> 133 mmol/L (1.5 mg/dL); hemoglobin more than 20 g/L below LLN; fasting blood glucose \> 8.33 mmol/L (150 mg/dL); fasting triglycerides \> 11.3 mmol/L (0.99 g/dL). * Untreated hypertension * Change in anti-hyperlipemic regimen within 3 months prior to study * Change in testosterone regimen and/or supraphysiological dose of testosterone * Estrogen therapy * Anoretics/anorexigenics or anti-obesity agents within 3 months of study * Growth hormone (GH); GH secretagogues; growth hormone releasing factor (GRF) products; IGF-1; or IGFBP-3 within 6 months of study. * Drug or alcohol dependence or use of methadone within 6 months of study entry * Participation in a clinical trial with any investigational drug/device within 30 days of screening.

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