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AOD-9604 Dosage: What Human Trials Actually Tested

Review the 24-week oral AOD-9604 trial, its tested doses and result, and why it does not support the injection schedules and timing advice often...

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This article is part of our Peptide Therapy collection. See also: GLP-1 Guides | Provider Comparisons

What AOD-9604 dose has been tested in human obesity research?

The best-documented large human obesity trial tested oral AOD-9604 at 0.25 mg, 0.5 mg, or 1 mg once daily for 24 weeks, alongside diet and exercise support. It did not test the 250 to 500 microgram subcutaneous schedule, fasting timing, injection technique, reconstitution recipe, or cycling advice previously presented on this page.

What did the 24-week trial find?

The FDA Pharmacy Compounding Advisory Committee briefing describes the OPTIONS study as a randomized, double-blind, placebo-controlled study in adults with obesity. Among 502 randomized participants, oral AOD-9604 at 0.25, 0.5, or 1 mg daily did not produce a statistically significant weight-loss difference from placebo at the reported endpoints. This finding applies to that oral study design and does not answer every possible research question about AOD-9604.

Study detailWhat was tested or reported
RouteOral tablets, not subcutaneous injection
Daily study doses0.25 mg, 0.5 mg, or 1 mg
Duration24 weeks, with diet and exercise support
Participants502 randomized adults with obesity
Weight-loss resultNo statistically significant difference from placebo reported by FDA

What this study does not establish

An oral trial cannot be converted into a subcutaneous dose by matching the number of milligrams. The study also does not establish an empty-stomach rule, morning or bedtime timing, split dosing, an 8-to-12-week cycle, time off between cycles, dose adjustment by body size, combination protocols, or long-term use outcomes. The injection schedules and preparation directions previously shown here are not supported by this trial and have been removed.

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How to read the safety summary

Stier, Vos, and Kenley summarized six randomized, double-blind, placebo-controlled AOD-9604 studies, with a focus on selected safety measures including IGF-1, glucose tolerance, and detected antibodies. The paper is a safety summary, not evidence that the subcutaneous dose ranges or cycling protocols formerly listed here were tested. Its abstract reports no treatment-related withdrawals or serious adverse events in the summarized studies; that statement should be read within the studies and follow-up included in the review.

Sources

  1. FDA Pharmacy Compounding Advisory Committee briefing document, AOD-9604, December 2024.
  2. Stier H, Vos E, Kenley D. Safety and Tolerability of the Hexadecapeptide AOD9604 in Humans. J Endocrinol Metab. 2013;3(1-2):7-15. doi:10.4021/jem157w.

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Disclaimer: This article is for informational purposes only and doesn't constitute medical advice. AOD-9604 isn't FDA-approved for the treatment, cure, or prevention of any disease. Dosage information is based on clinical research and general practice guidelines. individual dosing must be determined by a licensed physician. Always consult with a qualified healthcare provider before starting any peptide therapy. FormBlends provides physician-supervised telehealth services. all treatment decisions are made by licensed medical professionals based on individual patient evaluations.

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AOD-9604

Fat-targeting fragment without growth hormone side effects · From $199/mo · compounded by a licensed 503A pharmacy, dispensed only after provider review.

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Medical Disclaimer: This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication or treatment. FormBlends articles are source-checked against medical and regulatory references, but they are not a substitute for a personal medical consultation.

Written by FormBlends Editorial Research

Prepared by FormBlends Editorial Research.

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