What is the recommended dosing regimen for CJC‑1295 (with drug‑affinity complex) and Ipamorelin in an otherwise healthy adult?

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Last updated: February 28, 2026View editorial policy

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CJC-1295/Ipamorelin Dosing Information

There are no FDA-approved dosing guidelines, clinical practice guidelines, or high-quality evidence supporting the use of CJC-1295 or Ipamorelin in clinical practice. These peptides remain investigational compounds without established safety or efficacy data for routine therapeutic use.

Research-Based Dosing from Clinical Trials

CJC-1295 Dosing from Human Studies

Single-dose administration:

  • Research trials used subcutaneous doses ranging from 30 to 60 mcg/kg as single injections in healthy adults 1
  • These doses produced sustained GH elevation for 6+ days and IGF-I elevation for 9-11 days 1
  • The estimated half-life was 5.8-8.1 days 1

Multiple-dose administration:

  • Weekly or biweekly dosing schedules were studied, with doses of 30-60 mcg/kg administered subcutaneously 1
  • IGF-I levels remained elevated for up to 28 days after multiple doses 1
  • For a 70 kg adult, this translates to approximately 2.1-4.2 mg per injection (30-60 mcg/kg × 70 kg)

Normalization of growth in animal models:

  • Daily administration of 2 mcg per dose was required to normalize growth in GHRH-deficient mice 2
  • Dosing every 48-72 hours was less effective than daily administration 2

Ipamorelin Dosing from Research Studies

Animal studies only:

  • In conscious swine, the effective dose (ED50) was 2.3 nmol/kg subcutaneously 3
  • Maximum efficacy (Emax) occurred at doses producing 65 ng GH/ml plasma 3
  • Ipamorelin demonstrated selectivity for GH release without affecting ACTH or cortisol, even at doses 200-fold higher than the ED50 3

Critical Safety and Regulatory Warnings

Regulatory status:

  • CJC-1295 is classified as a Prohibited Substance under Section S2 of the WADA Prohibited List as a growth hormone-releasing factor 4
  • These compounds are being manufactured and distributed illicitly, often before completing clinical trials 4
  • CJC-1295 has been identified in unknown pharmaceutical preparations submitted to law enforcement 4

Clinical trial limitations:

  • The longest human trial duration was only 49 days 1
  • No serious adverse reactions were reported in short-term studies, but long-term safety is completely unknown 1
  • There are no data on morbidity, mortality, or quality-of-life outcomes in any patient population

Detection and abuse potential:

  • CJC-1295 covalently binds to plasma proteins (particularly albumin), making detection difficult 5
  • The compound is being used within bodybuilding communities despite lack of approval 4
  • Specialized LC-MS/MS methods are required for detection in biological samples 5

Why These Compounds Should Not Be Used Clinically

No established therapeutic indication:

  • Neither compound has completed Phase III clinical trials or received FDA approval
  • No comparative effectiveness data exist versus approved GH therapies
  • No data on patient-centered outcomes (morbidity, mortality, quality of life)

Unknown long-term risks:

  • Chronic GH/IGF-I elevation carries theoretical risks of malignancy, metabolic dysfunction, and cardiovascular disease
  • The 28-day sustained IGF-I elevation seen with CJC-1295 has unknown clinical consequences 1
  • No post-marketing surveillance data exist

Legal and ethical concerns:

  • Use outside of approved clinical trials may violate federal regulations
  • Patients obtaining these compounds are likely receiving products of unknown purity and potency
  • No quality control or pharmaceutical-grade manufacturing standards apply to illicit preparations

If a patient presents having used these compounds, document the exposure, monitor for adverse effects (particularly cardiovascular and metabolic), and strongly advise discontinuation pending completion of legitimate clinical trials.

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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