PubMed
Kisspeptin signaling in reproductive biology
Pinilla et al., 2012
Kisspeptin-10
Neuropeptide signaling regulator of the GnRH axis, studied for reproductive endocrinology.
Overall check-ins
Trackers & reports
Overview
Neuropeptide signaling regulator of the GnRH axis, studied for reproductive endocrinology.
Community
From check-in ratings — separate from side effects logged below. Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.
Favorable 3% · Mixed 4% · Unfavorable overall 93%
Benefits users selected when logging a favorable or mixed check-in.
Median bucket: 200–400 mcg · Most common: 200–400 mcg
Reports span 100–1000 mcg
Anonymized self-reports from PeptIQ users — not prescribing guidance. Buckets group similar logged amounts; open-ended top buckets mean “at least” that dose.
Among repeat reporters, 78% said they felt similar to their last entry, 22% more positive, and 0% more negative.
Overall, repeat reporters leaned more positive than their previous entry.
Median gap between entries: 160 days · Based on 23 repeat reporters
Research
PubMed
Pinilla et al., 2012
PubMed
Skorupskaite et al., 2018
ClinicalTrials.gov
ClinicalTrials.gov, 2024
PubMed
Abreu et al., 2016
PubMed
Hameed et al., 2011
Tools
More ways to learn about Kisspeptin from observational PeptIQ data.
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This page summarizes 29 anonymized self-reports from PeptIQ users who track Kisspeptin, including commonly reported effects and co-tracked peptides. These are observational patterns, not clinical outcomes.
PeptIQ separates overall check-in ratings (favorable, mixed, or unfavorable) from logged side effects like nausea or fatigue. Users often report benefits and side effects in the same check-in — a high experience score does not mean zero side effects were noted.
5 sources are linked on this page, including PubMed articles, clinical trial registries, and FDA labels where applicable. Citations describe published research — not recommendations.
This wiki does not assess safety or recommend use. Kisspeptin is listed as Research Only. Consult a licensed clinician for personal medical decisions.
Research, primarily in animal models, suggests Kisspeptin may have a wide range of therapeutic potentials due to its ability to promote angiogenesis (formation of new blood vessels), stimulate collagen synthesis, and modulate inflammatory responses.
SourceKisspeptin is not approved by the FDA for any human use. There is no legal basis for selling it as a drug, food, or dietary supplement in the United States. The FDA has classified Kisspeptin as a Category 2 bulk drug substance, which explicitly prohibits licensed compounding pharmacies from using it in compounded medications.
SourceThe safety and effectiveness of Kisspeptin have not been thoroughly evaluated in humans through rigorous clinical trials. This lack of human data means that safe dosages, short-term side effects, and long-term health consequences are largely unknown.
SourceWhile there are over 200 published studies on Kisspeptin, the vast majority are animal or in vitro (cell) studies. These preclinical studies consistently show positive results across various tissue types. However, there is a significant lack of comprehensive human clinical trial data.
Source