RESEARCH USE ONLY. Reference data for laboratory research. Not medical advice; not for human consumption.
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AOD-9604 vs Tesamorelin

A GH fragment developed as an obesity drug versus an approved GHRH analogue for HIV-associated belly fat.

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Research use only. A summary of published literature for educational reference — not medical advice and not a guide to human use.

The short version

AOD-9604 is a modified fragment of growth hormone developed for obesity; its published human data are a pooled safety report, without a demonstrated weight-loss result. Tesamorelin is FDA-approved for excess abdominal fat in HIV-associated lipodystrophy, based on randomized trials. The evidence behind them is not comparable.

At a glance

Class

Modified C-terminal GH fragment

GHRH analogue

Approval status

No approved drug indication

FDA-approved (Egrifta) for HIV-associated abdominal fat only

Headline human data

Pooled safety of 6 RCTs (893 adults); no published efficacy result

412-patient RCT: visceral fat −15.2% vs +5.0% at 26 weeks

Effect on IGF-I

No significant increase reported

Raises IGF-I (about +81% in the trial)

Research vial sizes

2 / 5 mg

10 / 20 mg

The details · tap a section to open it

01

How they work

AOD-9604 was designed to mimic the fat-metabolism part of growth hormone without raising IGF-I. Its clinical target and a meaningful weight effect have not been established in published human trials.

AOD-9604 was designed to mimic the fat-metabolism part of growth hormone without raising IGF-I. Its clinical target and a meaningful weight effect have not been established in published human trials.

Tesamorelin works upstream: it stimulates the pituitary to release the body's own GH, which raises IGF-I.

02

What studies measured

A published report pooling six randomized, double-blind, placebo-controlled trials (893 adults, mostly obese) looked at safety: it reported no significant IGF-I rise, no harm to glucose tolerance, no antibodies in those tested and no treatment-related serious adverse events. It describes a 502-person efficacy study but gives no verifiable weight-loss result.

A published report pooling six randomized, double-blind, placebo-controlled trials (893 adults, mostly obese) looked at safety: it reported no significant IGF-I rise, no harm to glucose tolerance, no antibodies in those tested and no treatment-related serious adverse events. It describes a 502-person efficacy study but gives no verifiable weight-loss result.

Tesamorelin's 412-patient trial in people with HIV measured visceral fat by CT: −15.2% versus +5.0% with placebo at 26 weeks.

03

Reported side effects

AOD-9604's safety report is sponsor-associated and does not establish long-term safety or the safety of every formulation.

AOD-9604's safety report is sponsor-associated and does not establish long-term safety or the safety of every formulation.

Tesamorelin's label warns about elevated IGF-I, glucose intolerance, fluid retention and injection-site reactions.

04

Evidence limits

No published primary report shows AOD-9604 causing clinically meaningful weight loss. Tesamorelin's results are specific to HIV-associated lipodystrophy and are not evidence for ordinary obesity.

No published primary report shows AOD-9604 causing clinically meaningful weight loss. Tesamorelin's results are specific to HIV-associated lipodystrophy and are not evidence for ordinary obesity.

Citations

Safety and Tolerability of the Hexadecapeptide AOD9604 in Humans

2 papers
  1. [1]Pooled safety report of six randomized controlled trials2013

    Safety and Tolerability of the Hexadecapeptide AOD9604 in Humans

    Stier H, et al. J Endocrinol Metab, 2013.

    Read paper ↗
  2. [2]Randomized controlled trial2007

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

    Falutz J, et al. N Engl J Med, 2007.

    Read paper ↗

Research use only. A summary of published literature for educational reference — not medical advice and not a guide to human use.

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