preclinical-level evidence

Humanin

What the research and the regulators actually say, sourced to primary documents.

Studies indexed
0
Clinical trials
0
Last updated
July 23, 2026

Updated · sourced to primary documents

Research information only, not medical advice. Humanin is a 24-amino-acid mitochondrial-derived peptide encoded within the mitochondrial 16S rRNA (MT-RNR2) region, and was the first identified of a class of mitochondrial-derived peptides that also includes MOTS-c and the SHLP peptides (Lee et al., PMC3641182). It is not an approved drug for any indication; the literature treats it as an endogenous cytoprotective factor and candidate biomarker, with therapeutic work confined to cell and animal models (PMC3641182; PMC7778388). No human adverse-effect profile is established, because humanin and its analogs have not been administered as therapeutics in controlled clinical trials.

Humanin at a glance

The evidence base is preclinical (cell and animal models) together with human biomarker associations; humanin has not been administered as a therapeutic in controlled clinical trials (Lee et al., PMC3641182). Humanin was first described as neuroprotective against amyloid-beta toxicity in vitro and exerts anti-apoptotic effects by binding the pro-apoptotic protein Bax and by interacting with IGFBP3 (reviewed in PMC3641182). Mechanistically, it signals through the gp130/IL-6ST receptor complex to activate STAT3, ERK1/2, and AKT pathways (Cohen et al., 2017, PMC5216912). In humans, plasma humanin correlates positively with age in healthy subjects and is reported lower in Alzheimer's disease, but these are observational biomarker associations, not evidence of therapeutic benefit (Conte et al., PMC8110619). The potent analog S14G-humanin (HNG) reduces infarct size and improves outcomes in rodent models of stroke, diabetes, and ischemia/reperfusion, but has not entered human clinical trials (PMC8806847; PMC10692773).

See how we grade evidence for the methodology behind this page.

Evidence profile

173 studies
  • Human RCT 1 · 1%
  • Human trial 6 · 3%
  • Review 17 · 10%
  • Animal 29 · 17%
  • In-vitro 34 · 20%
  • Unknown 86 · 50%

The longer the green, the stronger the human evidence. For most research peptides the bar is dominated by animal and in-vitro work, which is a signal to read every claim carefully.

Regulatory status

Clinical trials

  • NCT03431844 COMPLETED

    Humanin Isoforms in Cardiac Muscle and Blood Plasma and Major Complications After Cardiac Operation

  • Clinical Value of Plasma Humanin in Acute Kidney Injury

  • NCT07678073 NA RECRUITING

    Comparison of the Effects of General Anesthesia and Combined Spinal-Epidural Anesthesia on Ferroptosis, Humanin and MOTS-c Levels in Renal Transplantation

Indexed research

Sorted by evidence level, strongest first.

+ 163 more studies indexed for Humanin.

Frequently asked questions

Is Humanin approved for human use?
Humanin is a 24-amino-acid mitochondrial-derived peptide encoded within the mitochondrial 16S rRNA (MT-RNR2) region, and was the first identified of a class of mitochondrial-derived peptides that also includes MOTS-c and the SHLP peptides (Lee et al., PMC3641182). It is not an approved drug for any indication; the literature treats it as an endogenous cytoprotective factor and candidate biomarker, with therapeutic work confined to cell and animal models (PMC3641182; PMC7778388). No human adverse-effect profile is established, because humanin and its analogs have not been administered as therapeutics in controlled clinical trials.
What does the research on Humanin show?
The evidence base is preclinical (cell and animal models) together with human biomarker associations; humanin has not been administered as a therapeutic in controlled clinical trials (Lee et al., PMC3641182). Humanin was first described as neuroprotective against amyloid-beta toxicity in vitro and exerts anti-apoptotic effects by binding the pro-apoptotic protein Bax and by interacting with IGFBP3 (reviewed in PMC3641182). Mechanistically, it signals through the gp130/IL-6ST receptor complex to activate STAT3, ERK1/2, and AKT pathways (Cohen et al., 2017, PMC5216912). In humans, plasma humanin correlates positively with age in healthy subjects and is reported lower in Alzheimer's disease, but these are observational biomarker associations, not evidence of therapeutic benefit (Conte et al., PMC8110619). The potent analog S14G-humanin (HNG) reduces infarct size and improves outcomes in rodent models of stroke, diabetes, and ischemia/reperfusion, but has not entered human clinical trials (PMC8806847; PMC10692773).