GHRP-2

evidence score
peptide
Gray Market
Evidence Level B
Growth Hormone Releasing Peptide 2KP-102pralmorelin+1 more

GHRP-2 (pralmorelin) is a synthetic hexapeptide that potently stimulates growth hormone release by mimicking ghrelin at the GHS-R1a receptor on pituitary somatotrophs. It is the most potent GHRP in terms of peak GH release — producing larger GH pulses than ipamorelin, GHRP-6, or hexarelin — but with a less clean side effect profile. Unlike ipamorelin, GHRP-2 significantly increases cortisol (~20-40% transient elevation) and prolactin (~50-100% transient elevation), which limits its use in protocols where hormonal cleanliness matters. It also stimulates appetite via ghrelin pathway activation, though less than GHRP-6. GHRP-2 is approved in Japan as a diagnostic agent for GH deficiency (pralmorelin/GHRP Kaken). The synergy with GHRH analogs (CJC-1295, mod-GRF 1-29) is well-documented: GHRP-2 + GHRH produces 5-10x the GH release of either alone. Preferred by users who want maximum GH output and tolerate the cortisol/prolactin trade-off.

Evidence

No score yet

Safety

Unknown safety profile

Clinical Status

Phase II (diagnostic use approved in Japan as pralmorelin)

Last Sync

Not synced yet

Last Reviewed

Not reviewed yet

Dosing

Typical
200 mcg
100 mcgRange300 mcg
Frequency2-3x/day, fasted (pre-bed, AM, pre-workout)

Set height & weight in Settings to see your dose.

Pharmacology

Half-life~15-30 minutes (active peptide); GH pulse lasts 2-3 hours
OnsetGH release within 15-30 minutes post-injection
DurationGH pulse 2-3 hours; return to baseline by 4 hours
Routes
subcutaneous
intravenous

Evidence Score

0 studies indexed
Scoring Factors
Volume(24%)
Quality(24%)
Sample Size(12%)
Consistency(14%)
Replication(8%)
Recency(18%)
Evidence Levels
AScore ≥75 with at least 1 meta-analysis and 3+ RCTs
BScore ≥50 with at least 1 RCT or meta-analysis
CScore ≥25 — observational or animal evidence only
DScore <25 — very limited or preclinical data

Plain-English Snapshot

GHRP-2 is currently categorized as a peptide compound.

Evidence scoring has not been fully computed yet, so interpret this profile as preliminary.

Safety scoring is incomplete. Start conservatively and monitor carefully.

Core mechanism

Potent ghrelin mimetic at GHS-R1a; amplifies GH pulse via calcium-dependent exocytosis; also activates ACTH/cortisol and prolactin pathways (less selective than ipamorelin)

Practical Context

Strongest current signals

No indexed study summaries yet.

Compound Profile