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Recovery & Performance PeptidesRecovery research and practical context
Source comparison

CJC-1295 No DAC: Formulation Comparison

Plasma Half-Life 26–30 minutes 6–8 days 6–7 minutes No-DAC balances extended activity beyond native GHRH without the multi-day suppression of pulsatile feedback that DAC variants cause Peak GH Response Time 15–30 minutes 4–6 hours 10–15 minutes Rapid onset mat

This comparison does not assign a generated winner or score.

  • Plasma Half-Life
  • 26–30 minutes
  • 6–8 days
  • 6–7 minutes
  • No-DAC balances extended activity beyond native GHRH without the multi-day suppression of pulsatile feedback that DAC variants cause
  • Peak GH Response Time
  • 15–30 minutes
  • 4–6 hours
  • 10–15 minutes
  • Rapid onset matches endogenous pulse timing, allowing alignment with physiological GH release windows (sleep, fasted training)
  • GH Pulse Amplitude Increase
  • 200–300% above baseline
  • 150–200% sustained elevation
  • 100% (baseline reference)
  • Higher amplitude per pulse than DAC, but requires repeated dosing to match cumulative AUC. Trade-off is feedback preservation vs convenience
  • Receptor Occupancy Duration
  • <2 hours
  • 5–7 days continuous
  • <30 minutes
  • Short occupancy prevents receptor downregulation and maintains hypothalamic responsiveness to physiological GHRH stimuli
  • Albumin Binding
  • None (direct renal clearance)
  • Covalent via maleimidopropionic acid
  • None
  • Absence of albumin binding accelerates clearance, limiting off-target effects but requiring more frequent administration for sustained protocols
  • Administration Frequency (Research Protocols)
  • 2–3× daily for multi-day studies
  • Once every 5–7 days
  • Continuous IV infusion required
  • No-DAC suits pulsatile protocols; DAC suits long-term steady-state studies. Choice depends on research question, not 'better or worse'
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