Data edition of
Residue An evidence-graded reference for peptide science

AOD-9604 research

What PubMed holds on AOD-9604, sorted by study design: the papers this site relies on, every clinical-trial publication PubMed tags, and the newest additions.

PubMed records
22
Trial publications
00 randomized
Reviews
9
Human-subject tagged
18
Animal-only
3
  • Clinical-trial publications 0
  • Reviews 9
  • Animal-only studies 3
  • Other (in vitro, chemistry, commentary, unindexed) 10
Figure 1. Composition of the AOD-9604 literature by PubMed publication type and MeSH tags. Categories come from separate PubMed filters and can overlap; “animal-only” means tagged Animals and not Humans. Query: (AOD9604[tiab] OR AOD-9604[tiab]).
024 2000: 1 records 2000 2001: 2 records 2002: 0 records 2003: 2 records 2004: 1 records 2005: 1 records 2005 2006: 2 records 2007: 1 records 2008: 0 records 2009: 0 records 2010: 0 records 2010 2011: 0 records 2012: 1 records 2013: 1 records 2014: 4 records 2015: 3 records 2015 2016: 1 records 2017: 0 records 2018: 0 records 2019: 0 records 2020: 0 records 2020 2021: 0 records 2022: 0 records 2023: 0 records 2024: 0 records 2025: 0 records 2025 2026: 4 records (year to date) 2026
Figure 2. PubMed records per publication year matching (AOD9604[tiab] OR AOD-9604[tiab]) — 22 in total; peak 4 in 2014. The 2026 bar is year-to-date (hatched). Volume of literature is not evidence of efficacy. Run this query on PubMed.

Studies this site relies on

Ordered by strength of design. Conclusions are quoted verbatim from each abstract as indexed by PubMed; read the full paper before relying on any of them.

  1. Primary study Drug Test Anal · 2013 PMID 24124033

    AOD-9604 does not influence the WADA hGH isoform immunoassay

    Orlovius AK, Thomas A, Schänzer W, et al.

    No abstract is available in PubMed for this record.

  2. Primary study Endocrinology · 2001 PMID 11713213

    The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism following chronic treatment in obese mice and beta(3)-AR knock-out mice

    Heffernan M, Summers RJ, Thorburn A, et al.

    However, in an acute experiment, AOD9604 was capable of increasing energy expenditure and fat oxidation in the beta(3)-AR knock-out mice. In conclusion, this study demonstrates that the lipolytic actions of both hGH and AOD9604 are not mediated directly through the beta(3)-AR although both compounds increase beta(3)-AR expression, which …

  3. Primary study Int J Obes Relat Metab Disord · 2001 PMID 11673763

    Increase of fat oxidation and weight loss in obese mice caused by chronic treatment with human growth hormone or a modified C-terminal fragment

    Heffernan MA, Thorburn AW, Fam B, et al.

    Both hGH and its C-terminal fragment reduce body weight gain, increase fat oxidation, and stimulate lipolysis in obese mice, yet AOD9604 does not interact with the hGH receptor. Thus, the concept of hGH behaving as a pro-hormone is further confirmed. This data shows that fragments of hGH can act in a manner novel to traditional …

  4. Primary study Horm Res · 2000 PMID 11146367

    Metabolic studies of a synthetic lipolytic domain (AOD9604) of human growth hormone

    Ng FM, Sun J, Sharma L, et al.

    In contrast to chronic treatment with intact hGH, chronic treatment with AOD9604 showed no adverse effect on insulin sensitivity of the animals, as demonstrated with euglycemic clamp techniques. The results in the present study suggest that the analogue of the hGH lipolytic domain may have the potential to be developed into an orally …

  5. Review Curr Opin Investig Drugs · 2004 PMID 15134286

    AOD-9604 Metabolic

    Wilding J

    Metabolic is developing AOD-9604 for the potential treatment of obesity. By February 2002, phase IIa trials were underway.

Clinical-trial publications in PubMed

PubMed returns no publication tagged as a clinical trial for this query. That absence is itself a finding: claims about effects in people are not supported by trial reports indexed in PubMed.

Newest records

The most recent PubMed additions for this query at the data-edition date, regardless of design.

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