Independent · non-commercial · publishes on a quarterly cycle|Current cycle 2026 Q3
Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Trial abstract · §3

GHRP6-PH1-GH — results

Primary endpoint, absolute and relative effect where derivable, and harms as reported.

Document identifier
CEI-TR-0107/3
Series
Trial abstract
Version
3.3
Published
29 Jan 2023
Last reviewed
29 May 2023
Next review
29 May 2025
Identifier
10.71829/cei.trial.107
Certainty
Low
Cycle
2023 Q1
Phase
Phase 1
Status
Reported

§3Results

§3.1Primary endpoint

Table 3. Primary endpoint as reported.

EndpointResult as reportedCertainty
Growth-hormone response and effect on appetiteDose-dependent growth-hormone release with a marked orexigenic effectLow
Reproduced from the published report. Where the report states a confidence interval the Institute reproduces it; where it does not, none is constructed.

§3.2Endpoint hierarchy

§3.3Harms as reported

Table 5. Adverse events for GHRP-6 from the safety tables the Institute holds for this compound. Where a row names a different trial as its source, the figure is from that trial and not from this one.

EventActive, %Comparator, %Source trial
Marked appetite stimulationThe most prominent effect and the one that distinguishes this compound from selective secretagogues
Cortisol elevationConsistent and larger than with GHRP-2
Prolactin elevationConsistent
FlushingReported
SomnolenceReported
Injection-site reactionReported
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