Peptide profile
GHRP-2 and GHRP-6: FDA Status, Research and Uses
Key takeaway
GHRP-2 and GHRP-6 are lab-made 6 amino acid peptides that trigger growth hormone release from the pituitary. Neither is FDA approved. They were studied in the 1980s and 1990s, mostly as growth hormone tests and in children of short stature. FDA lists both as compounding safety risks, and WADA bans both [1, 4, 6, 10].
At a glance
Where it stands
Checked
- FDA approvedNoNo approved product
- Pharmacy compounding (503A)Category 3Both GHRP-2 and GHRP-6 are in 503A category 3 (nominated without adequate support) on FDA's list updated May 14, 2026.
- Outsourcing facilities (503B)Category 2Status differs by route: GHRP-6, and GHRP-2 for injectable and nasal routes, are in 503B category 2 (significant safety risks, added September 29, 2023); GHRP-2 for other routes is in 503B category 1 (under evaluation). List updated March 21, 2025.
- WADA (sport)ProhibitedS2.2.4 GH-releasing peptides (GHRPs)
Same data as the Status Tracker. Checked against 7 sources
- FDA: Bulk drug substances nominated for use in compounding under section 503A (updated May 14, 2026)
- FDA: Bulk drug substances nominated for use in compounding under section 503B (updated March 21, 2025)
- FDA: Certain bulk drug substances for use in compounding that may present significant safety risks
- WADA: 2026 Prohibited List
- openFDA Drugs@FDA query: GHRP (no matches)
- openFDA drug shortages query: GHRP
- DEA Diversion: Controlled Substances - Alphabetical Order
Key facts
- Class
- Growth hormone-releasing peptides (GHRPs), a type of growth hormone secretagogue [10, 6]
- Half-life
- GHRP-2: about 0.55 hours after an IV dose (10 children). GHRP-6: no human half-life found in the sources reviewed [8]
- Route in studies
- IV in most human studies; intranasal GHRP-2 also tested in children [5, 6, 7]
- First studied
- 1984 (GHRP-6, in lab and animal studies) [4]
How it works
GHRP-2 and GHRP-6 are small peptides of 6 amino acids that act on the pituitary gland to release growth hormone. GHRP-6 has the sequence His-DTrp-Ala-Trp-DPhe-Lys-NH2. In early animal studies it released growth hormone without releasing LH, FSH, TSH or prolactin [4].
These peptides do not act like growth hormone-releasing hormone (GHRH). GHRP-2 shares no structural likeness with GHRH, but its effects on pituitary growth hormone release are similar in clinical studies [7]. In 18 healthy men, GHRP-6 and GHRH given together released more growth hormone than expected from each alone, which suggests they act through separate pathways [5].
GHRPs are less selective than some newer peptides. In healthy men, the highest tested dose of GHRP-6 roughly doubled prolactin and cortisol [5]. In pigs, both GHRP-6 and GHRP-2 raised ACTH and cortisol, while the related peptide ipamorelin did not [11].
GHRP-2 was the most studied of the pair in people. It raised growth hormone in children of short stature when given by IV or nasal spray [6]. It also reactivated growth hormone secretion in men with prolonged critical illness [9]. WADA lists GHRP-2 under the name pralmorelin [10].
What the research shows
5 human trials1 animal study
2002Human trial Van den Berghe et al., critical illness
33 men with prolonged critical illness Randomized to 5 days of placebo, GHRP-2, GHRP-2 plus TRH, or GHRP-2 plus TRH and GnRH
GHRP-2 infusion restarted GH secretion and brought IGF-1 to normal. Some metabolic changes were seen only with the combined hormones [9]
Read the study1998Human trial Pihoker et al., GHRP-2 phase 1 PK study
10 prepubertal children Phase 1, single 1 mcg/kg IV dose
GHRP-2 half-life was about 0.55 hours. GH rose in a predictable way [8]
Read the study1997Human trial Pihoker et al., intranasal GHRP-2 treatment
Studied for growth
15 children with short stature Single group, intranasal GHRP-2 for 6 months (6 children for 18 to 24 months)
Height velocity rose from 3.7 to 6.1 cm/yr at 6 months. IGF-1 did not change [7]
Read the study1995Human trial Pihoker et al., GHRP-2 diagnostic study
24 children of short stature Diagnostic comparison of IV and intranasal GHRP-2 with standard growth hormone tests
GH responses to GHRP-2 and GHRH were similar in each child. All 15 children given intranasal GHRP-2 had a significant GH response [6]
Read the study1990Human trial Bowers et al., GHRP-6 in healthy men
18 healthy men IV bolus doses of 0.1, 0.3 and 1.0 mcg/kg, alone and with GHRH, vs placebo
Mean peak GH was 68.7 mcg/L at 1.0 mcg/kg vs 1.2 on placebo. GHRP-6 and GHRH together had a synergistic effect [5]
Read the study1984Animal study Bowers et al., GHRP-6 discovery
Rat pituitary cells; rats, monkeys, lambs and calves Lab and animal tests
GHRP-6 released GH in a dose-related way without releasing LH, FSH, TSH or prolactin [4]
Read the study
Doses used in studies
In healthy men, GHRP-6 was given as a single IV bolus of 0.1, 0.3 or 1.0 mcg/kg [5].
In children, GHRP-2 was tested as a single 1 mcg/kg IV dose and as intranasal doses of 5 to 20 mcg/kg [6, 8]. In the treatment study, children used intranasal GHRP-2 at 5 to 15 mcg/kg twice a day for 3 months, then three times a day [7]. In critically ill men, GHRP-2 was infused at 1 mcg/kg per hour for 5 days [9].
Dosing is set by a licensed provider.
Side effects and safety
FDA lists both peptides on its compounding safety risks page. For GHRP-2, FDA cites a risk of immune reactions and reports of serious adverse events, including a higher insulin need to control blood sugar, deaths of critically ill study subjects, infection and pancreatitis, though causality was not established [1].
For GHRP-6, FDA cites a risk of immune reactions and limited safety data showing possible effects on cortisol and a rise in blood sugar from lower insulin sensitivity [1].
In the 1990 study in healthy men, no adverse clinical effects or lab abnormalities were seen with GHRP-6 [5]. Intranasal GHRP-2 was well tolerated in children [7]. In critically ill men, blood lactate and white blood cell counts rose by day 5 on GHRP-2 alone [9].
Legal and regulatory history
FDA's 503A nominations list, updated May 14, 2026, places both GHRP-2 and GHRP-6 in category 3 (nominated without adequate support) [2]. Source
FDA's compounding safety risks page (current as of April 22, 2026) lists GHRP-2 (injectable and nasal routes) and GHRP-6 in 503B category 2 [1]. Source
The WADA 2026 Prohibited List took effect. It names GHRP-2 (pralmorelin) and GHRP-6 under S2.2.4 (GH-releasing peptides), banned at all times [10]. Source
FDA's 503B list, updated March 21, 2025, places GHRP-2 for routes other than injection and nasal in category 1, while injectable and nasal GHRP-2 and all GHRP-6 are in category 2 [3]. Source
FDA added GHRP-2 (injectable and nasal routes) and GHRP-6 to 503B category 2 (significant safety risks) [1]. Source
Common questions
Are GHRP-2 and GHRP-6 FDA approved?
No. A 1995 study called GHRP-2 an investigational drug [6], and FDA's 503B list does not mark either as a component of an FDA-approved drug [3].
Can pharmacies compound GHRP-2 or GHRP-6?
What is the difference between GHRP-2 and GHRP-6?
Is GHRP-6 banned in sports?
Yes. The WADA 2026 Prohibited List names GHRP-2 and GHRP-6 under S2.2.4, banned in and out of competition [10].
Do GHRP-2 and GHRP-6 raise cortisol?
Do GHRP-2 and GHRP-6 affect blood sugar?
FDA cites a higher insulin need with GHRP-2 and a rise in blood sugar with GHRP-6 among its safety concerns [1].
Were GHRPs tested in children?
How is GHRP-6 different from ipamorelin?
In pig studies, GHRP-6 raised ACTH and cortisol while ipamorelin did not, at similar growth hormone release [11].
Sources
- FDA: Certain bulk drug substances for use in compounding that may present significant safety risks
- FDA: Bulk drug substances nominated under section 503A (categories, updated May 14, 2026)
- FDA: Bulk drug substances nominated under section 503B (categories, updated March 21, 2025)
- Bowers et al. 1984, Endocrinology (PubMed)
- Bowers et al. 1990, J Clin Endocrinol Metab (PubMed)
- Pihoker et al. 1995, J Clin Endocrinol Metab (PubMed)
- Pihoker et al. 1997, J Endocrinol (PubMed)
- Pihoker et al. 1998, J Clin Endocrinol Metab (PubMed)
- Van den Berghe et al. 2002, Clin Endocrinol (PubMed)
- WADA: 2026 Prohibited List
- Raun et al. 1998, Eur J Endocrinol (PubMed)
