IPAMORELIN
Peptide Data Sheet for Pharmacists and Compounding Professionals
BASIC INFORMATION
Name: Ipamorelin
Class: Growth hormone secretagogue, synthetic ghrelin analog
Structure: Pentapeptide (5-amino acid peptide)
Molecular Weight: 711.85 g/mol
Sequence: Aib-His-D-2-Nal-D-Phe-Lys-NH₂
Chemical Modifications:
- Contains non-natural amino acids (D-2-Nal, D-Phe)
- C-terminal amidation
- Aminoisobutyric acid (Aib) at position 1
Available Forms:
- Research peptide
- Compounded formulations (subject to regulatory requirements)
- Not available as an FDA-approved medication
REGULATORY STATUS
FDA Status
- Not FDA-approved for any medical condition
- Classified as a research compound
- FDA has clarified it is among peptides unlawful to use in making compounded medications
- Included on FDA’s list of substances nominated for the 503B bulks list that raised significant safety concerns
Legal Considerations
- Not approved for human use or consumption
- Often marketed “for research purposes only”
- Compounding pharmacies should be aware that FDA has specifically identified Ipamorelin as a substance that should not be used in compounding
MECHANISM OF ACTION
Ipamorelin is a selective growth hormone secretagogue that:
- Binds to the ghrelin/growth hormone secretagogue receptor (GHS-R) in the pituitary gland
- Stimulates the pulsatile release of growth hormone (GH)
- Does not significantly affect other pituitary hormones (ACTH, cortisol, prolactin, LH, FSH, TSH)
- Increases insulin-like growth factor 1 (IGF-1) production as a secondary effect
- Unlike GHRP-2 and GHRP-6, does not stimulate appetite or significantly increase prolactin or cortisol
The selective nature of Ipamorelin distinguishes it from other growth hormone secretagogues, potentially offering a more targeted effect profile.
PHARMACOKINETICS
| Parameter | Value | Notes | |———–|——-|——-| | Absorption | Rapid after subcutaneous injection | Complete bioavailability | | Distribution | Limited data available | Primarily studied in animal models | | Metabolism | Likely enzymatic degradation | Specific pathways not well characterized | | Elimination | Half-life: ~2 hours | Limited human data available |
Note: Pharmacokinetic data is primarily derived from animal studies; human data is extremely limited.
POTENTIAL APPLICATIONS (INVESTIGATIONAL)
Note: All applications are investigational and not FDA-approved. This information is provided for educational purposes only.
Endocrine
- Growth hormone deficiency (investigational)
- Age-related decline in growth hormone
Metabolic
- Body composition improvement
- Lean muscle mass preservation
- Fat reduction
Other Investigational Areas
- Recovery from injury
- Sleep quality improvement
- Bone mineral density enhancement
- Anti-aging research
ADMINISTRATION (INVESTIGATIONAL)
Routes
- Subcutaneous injection (most common)
- Intramuscular injection (less common)
Investigational Dosing
Note: No established safe or effective dosing regimen exists. The following information is based on research protocols and is not a recommendation for clinical use.
| Purpose | Investigational Dose Range | Frequency | |———|—————————-|———–| | Research protocols | 200-300 mcg | 1-3 times daily | | Typically administered | Evening or before sleep | To align with natural GH pulses |
SAFETY PROFILE
Reported Adverse Effects
Note: Safety data is limited and primarily from small studies and anecdotal reports.
- Injection site reactions (redness, pain, swelling)
- Headache
- Dizziness
- Water retention
- Numbness or tingling in extremities
- Increased insulin resistance
- Fatigue
Potential Risks and Concerns
- Potential for growth promotion in pre-existing cancers
- Glucose metabolism alterations
- Fluid retention
- Carpal tunnel syndrome
- Gynecomastia
- Unknown long-term effects
- Lack of quality control in commercially available products
Contraindications (Theoretical)
- Active malignancy
- History of pituitary disorders
- Uncontrolled diabetes
- Pregnancy and lactation
- Children and adolescents
- Intracranial hypertension
SPECIAL POPULATIONS
Pregnancy and Lactation
- No human data available
- Avoid use due to unknown risks
Pediatric
- No human data available
- Not recommended for use in pediatric populations
- Theoretical risk of affecting growth plates and development
Geriatric
- No specific data available
- Potentially higher risk of adverse effects
- May have different response due to age-related changes in GH/IGF-1 axis
PHARMACIST GUIDANCE
Compounding Considerations
- FDA has clarified that Ipamorelin is among peptides unlawful to use in making compounded medications
- Pharmacists should be aware of regulatory restrictions
- If compounding is legally permitted in specific circumstances:
- Requires aseptic technique and sterile compounding environment
- Stability affected by temperature and mechanical agitation
- Adhere to USP <797> standards for sterile compounding
Storage and Handling (Research Settings)
- Store lyophilized peptide at -20°C
- Reconstituted solutions typically stored at 2-8°C
- Use within 30 days of reconstitution
- Avoid repeated freeze-thaw cycles
- Protect from light
Patient Counseling Points
- Not FDA-approved for any indication
- Limited safety and efficacy data in humans
- Unknown long-term effects
- Potential for serious adverse effects
- Importance of discussing all supplements and medications with healthcare providers
- FDA has warned against its use in compounded medications
COMPARISON TO OTHER GROWTH HORMONE SECRETAGOGUES
| Feature | Ipamorelin | GHRP-2 | GHRP-6 | |———|————|——–|——–| | Selectivity | Highly selective for GH release | Less selective | Less selective | | Effect on Cortisol | Minimal | Significant increase | Significant increase | | Effect on Prolactin | Minimal | Moderate increase | Moderate increase | | Effect on Appetite | Minimal | Moderate increase | Significant increase | | Side Effect Profile | Generally milder | More pronounced | More pronounced |
ETHICAL AND PROFESSIONAL CONSIDERATIONS
For Pharmacists
- Be aware of FDA position on Ipamorelin in compounding
- Understand legal and ethical implications of dispensing non-FDA approved peptides
- Maintain professional standards when discussing investigational compounds
- Provide evidence-based information when consulted about Ipamorelin
- Consider liability issues related to non-FDA approved compounds
For Researchers
- Ensure proper informed consent in research settings
- Follow institutional and regulatory guidelines for research peptides
- Document and report adverse events
- Maintain scientific integrity in research protocols
REFERENCES
- FDA. Certain Bulk Drug Substances for Use in Compounding May Present Significant Safety Risks. https://www.fda.gov/drugs/human-drug-compounding/certain-bulk-drug-substances-use-compounding-may-present-significant-safety-risks
- Raun K, et al. Ipamorelin, the first selective growth hormone secretagogue. Eur J Endocrinol. 1998;139(5):552-61.
- Gobburu JV, et al. Pharmacokinetics-pharmacodynamics of ipamorelin, a growth hormone releasing peptide, in human volunteers. J Clin Pharmacol. 1999;39(11):1150-6.
- Johansen PB, et al. The effects of growth hormone secretagogues on bone. Growth Horm IGF Res. 1999;9(Suppl A):18-22.
- FDA. Pharmacy Compounding of Human Drug Products Under Section 503A of the Federal Food, Drug, and Cosmetic Act. https://www.fda.gov/media/94393/download