Research use only.  Educational reference. Not medical advice. Not for human consumption.
📈 FAT LOSS + GH BLEND

AOD-9604 + CJC-1295 + Ipamorelin Triple Blend

This triple blend combines AOD-9604 (HGH fragment for lipolysis), CJC-1295 No DAC (pulsatile GHRH), and Ipamorelin (selective GHRP) in a single vial. The synergistic combination addresses GH pulsatility, GH-mediated lipolysis, and fat-specific receptor activity simultaneously — studied for body composition research.

⚡ QUICKSTART HIGHLIGHTS

VIAL SIZE
12 mg total
BAC WATER
3.0 mL
CONCENTRATION
4.0 mg/mL total (~1.33 mg/mL each)
FREQUENCY
Once daily, fasted

Dosing & Reconstitution Guide

VialBAC WaterTotal Conc.Per Componentmcg per Unit
12 mg blend3.0 mL4.0 mg/mL total~1.33 mg/mL each (4mg each)~13.3 mcg each per unit

Dosing Protocol

PhaseTotal Daily DoseUnitsVolumeNotes
Weeks 1–2 (titration)600 mcg total15 units0.15 mL200 mcg of each component
Weeks 3–4900 mcg total22.5 units0.225 mL300 mcg each
Weeks 5+1,200 mcg total30 units0.30 mL400 mcg each — standard research dose

Reconstitution Steps

  1. Wipe the vial stopper and BAC water vial with alcohol; let dry.
  2. Draw 3.0 mL of bacteriostatic water into a sterile syringe.
  3. Inject slowly down the inside glass wall of the blend vial. Do not aim at the powder.
  4. Gently swirl until fully dissolved. Do not shake.
  5. Label with reconstitution date. Refrigerate at 2–8°C; use within the window specified above.
Timing: Administer fasted (30+ min before eating or 2+ hours post-meal) to maximize GH pulse amplitude. Morning injection preferred. AOD-9604 component is particularly timing-sensitive to fasted state for lipolytic effect.

How This Works

This triple blend leverages three complementary GH-pathway mechanisms. AOD-9604 is fragment 176–191 of HGH — the C-terminal region responsible for HGH's fat-metabolizing activity without IGF-1 stimulation or glucose intolerance. It stimulates lipolysis via β3-adrenergic receptors and inhibits lipogenesis independently of the GH receptor.

CJC-1295 No DAC stimulates the GHRH receptor at the pituitary, amplifying the amplitude of GH pulses. Ipamorelin stimulates ghrelin receptors (GHS-R1a) at both pituitary and hypothalamus, increasing GH pulse frequency and amplitude. Combined, CJC+Ipamorelin produce synergistic GH release while AOD-9604 provides direct fat-specific lipolytic activity downstream.

Potential Benefits & Side Effects

Potential Benefits

  • Triple mechanism: GHRH amplification + ghrelin stimulation + direct lipolysis.
  • AOD-9604 provides fat-targeted lipolysis without insulin resistance or IGF-1 elevation.
  • Fasted state enhances all three components' effectiveness.
  • Convenient single-vial formulation vs three separate injections.
  • CJC + Ipamorelin synergy well-characterized in secretagogue literature.

Side Effect Profile

  • Mild water retention early (GH-mediated).
  • Fatigue or morning grogginess if dosed at night.
  • Injection-site reactions.
  • WADA prohibited — all three components.
  • Nausea at higher doses (rare).
  • Avoid with active malignancy.

Storage Instructions

StateTemperatureDuration
Lyophilized−20°C (−4°F)−20°C, up to 24 months
Reconstituted2–8°CUp to 14 days
⚠ Research Use Only: WADA prohibited. All three components are on the prohibited list. Administer fasted for maximum effect. Cycle 8–12 weeks then take a 4-week break.

References

1
Heffernan M et al. 'The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism' — J Endocrinol, 2001 View source ↗
2
Alba M et al. 'Once-monthly administration of CJC-1295 for stimulation of GH release' — J Clin Endocrinol Metab, 2006 View source ↗