CJC-1295 with DAC - Growth Hormone
Contraindications: This peptide has 5 known contraindication(s). See Safety section
Growth HormoneModerate

CJC-1295 with DAC

Also known as: CJC-1295 DAC, Modified GRF 1-29 with DAC, Drug Affinity Complex CJC-1295, DAC:GRF

Research Only
Preclinical
MW: 3647.28 g/mol • 125 amino acids

CJC-1295 with Drug Affinity Complex (DAC) is a long-acting GHRH analog with an extended half-life of 6-8 days. The DAC modification allows for sustained GH elevation with less frequent dosing compared to non-DAC variants.

Half-Life

6-8 days

Typical Dose

1-2 mg

Frequency

1-2x weekly

Routes

Subcutaneous

Half-Life Visualization

Comparing 2 peptides. CJC-1295 with DAC has a half-life of 7d, reaching 50% concentration at 7d and 25% at 14d. Ipamorelin has a half-life of 2h, reaching 50% concentration at 2h and 25% at 4h.

Half-Life Decay Curve

Concentration over time assuming initial dose = 100%

CJC-1295 with DAC(t1/2: 7d +/- 1d)
Ipamorelin(t1/2: 2h +/- 0.5h)
Peptide Half-Life Comparison ChartVisualization showing how peptide concentrations decay over time. CJC-1295 with DAC has a half-life of 7d. Ipamorelin has a half-life of 2h.

Use arrow keys to navigate: Left/Right for time, Up/Down for peptides

Shaded areas represent reported half-life variability from published studies.

PeptideHalf-Life50% at25% at12.5% atRedose Window
CJC-1295 with DAC
7d7d14d21d7d - 14d
Ipamorelin
2h2h4h6h2h - 4h

Comparing CJC-1295 with DAC with Ipamorelin

Open Full Comparison Tool

Mechanism of Action

CJC-1295 with DAC is a synthetic analog of growth hormone-releasing hormone (GHRH) that stimulates the pituitary gland to release growth hormone. The key distinguishing feature is the Drug Affinity Complex (DAC), a lysine-linked maleimidopropionic acid group that binds to serum albumin.

How the DAC Modification Works

Albumin Binding

The DAC moiety covalently binds to circulating albumin after injection:

  • Creates a depot effect extending half-life dramatically
  • Prevents rapid proteolytic degradation
  • Results in sustained, elevated GH levels rather than pulsatile release

GHRH Receptor Activation

CJC-1295 binds to GHRH receptors on pituitary somatotrophs:

  • Stimulates cAMP pathway activation
  • Increases GH synthesis and secretion
  • Maintains feedback sensitivity (unlike exogenous GH)

Physiological Effects

Growth Hormone Elevation

  • Sustained 2-3x elevation of baseline GH levels
  • IGF-1 levels increase correspondingly
  • Effects persist for 6-8 days post-injection

Metabolic Effects

  • Enhanced lipolysis and fat oxidation
  • Increased protein synthesis
  • Improved nitrogen retention

Tissue Effects

  • Supports muscle protein synthesis
  • May enhance connective tissue repair
  • Potential benefits for bone density

Comparison with Non-DAC Variant

FeatureCJC-1295 with DACCJC-1295 without DAC
Half-life6-8 days30 minutes
Dosing1-2x weekly2-3x daily
GH release patternSustained elevationPulsatile
IGF-1 elevationProlongedTransient

Research & Evidence

Research Status: CJC-1295 with DAC has limited human clinical data. Most evidence comes from animal studies and early-phase human trials conducted for potential therapeutic applications.

Human Studies

Phase I/II Trials

Early clinical trials examined CJC-1295 DAC for GH deficiency:

  • Single-dose studies showed sustained GH elevation for up to 14 days
  • IGF-1 levels increased by 40-100% above baseline
  • Generally well-tolerated in healthy subjects

Pharmacokinetic Studies

Human PK data confirmed the extended half-life:

  • Terminal half-life of 5.8-8.1 days
  • Peak GH levels at 24-48 hours post-injection
  • Dose-dependent IGF-1 response

Animal Studies

GH Secretion Studies

Research in various animal models demonstrated:

  • Robust and sustained GH elevation
  • Preserved pulsatile GH secretion pattern (blunted but not eliminated)
  • No desensitization with repeated dosing over 6 weeks

Metabolic Effects

Animal studies showed metabolic benefits:

  • Reduced adipose tissue mass
  • Improved lean body mass
  • Enhanced glucose disposal (acute) but impaired tolerance (chronic)

Limitations of Current Evidence

  • No Phase III trials completed
  • Development discontinued for undisclosed reasons
  • Long-term safety data lacking
  • Most research is 10+ years old

Dosing

Disclaimer: Dosing information is provided for research reference only. CJC-1295 with DAC is not approved for human use. Consult a healthcare provider before considering any peptide protocol.

Research Protocols

Administration Guidelines

Injection Technique

  • Subcutaneous injection in abdomen, thigh, or deltoid area
  • Rotate injection sites
  • Evening administration may better align with natural GH rhythm

Reconstitution

  • Use bacteriostatic water for reconstitution
  • Typical: 2mg vial + 1ml BAC water = 2mg/ml
  • Gently swirl, do not shake
  • Store refrigerated after reconstitution

Important Considerations

Continuous vs Pulsatile GH

The DAC version produces sustained GH elevation rather than natural pulsatile release:

  • May be less physiological than non-DAC variant
  • Some researchers prefer non-DAC for more natural GH pattern
  • Long-term implications of sustained elevation unknown

Cycling Recommendations

Due to the sustained nature:

  • Consider 8-12 week cycles
  • Allow washout periods between cycles
  • Monitor IGF-1 levels to guide cycling

Pharmacokinetics

Absorption

  • Subcutaneous: Well absorbed; bioavailability approximately 90%
  • Peak peptide levels: 2-4 hours post-injection
  • Peak GH response: 24-48 hours post-injection

Distribution

  • Extensive albumin binding (the DAC mechanism)
  • Large apparent volume of distribution due to albumin complex
  • Tissue distribution follows albumin kinetics

Metabolism

  • Gradual release from albumin complex
  • Peptide portion subject to proteolytic degradation
  • Hepatic metabolism of fragments

Elimination

  • Terminal half-life: 6-8 days
  • Primarily renal elimination of metabolites
  • No significant accumulation with weekly dosing
  • Steady state achieved by 3-4 weeks

Synergy & Stacking

GHRH + GHRP Combinations

With Ipamorelin

The classic combination of GHRH + GHRP:

  • CJC-1295 DAC provides sustained GHRH stimulation
  • Ipamorelin adds pulsatile GHRP stimulus
  • Combined effect greater than either alone
  • Note: Many prefer non-DAC CJC-1295 for this combination

With GHRP-6 or GHRP-2

Alternative GHRP options:

  • Greater GH release than ipamorelin
  • More side effects (hunger with GHRP-6)
  • Consider goals and tolerance

With MK-677

Oral GHS Addition

  • MK-677 provides daily oral GH stimulation
  • CJC-1295 DAC adds weekly injectable boost
  • May be redundant for some users
  • Monitor for excessive IGF-1 elevation

With Healing Peptides

BPC-157 or TB-500

  • No direct pharmacological interaction
  • Enhanced GH environment may support healing
  • Popular combination for recovery protocols

Illustration: Synergy & Stacking
Illustration: Synergy & Stacking

Timing Considerations

  • CJC-1295 DAC: Evening injection preferred
  • If combining with GHRP: Some inject simultaneously
  • MK-677: Typically taken at bedtime
  • Healing peptides: Timing based on their protocols

Safety & Side Effects

Common Side Effects

Injection Site Reactions (frequent)

  • Redness, swelling at injection site
  • Usually mild and transient
  • Rotate injection sites

Water Retention (common)

  • Mild edema, particularly in extremities
  • Usually resolves with continued use
  • May indicate excessive GH elevation

Flushing/Warmth (common)

  • Facial flushing post-injection
  • Sensation of warmth
  • Generally transient

Less Common Side Effects

Metabolic Effects

  • Increased hunger
  • Transient hyperglycemia
  • Insulin resistance with prolonged use

Musculoskeletal

  • Joint stiffness or mild pain
  • Carpal tunnel-like symptoms
  • Typically dose-related

Serious Concerns

Sustained GH Elevation Risks

  • Unlike pulsatile release, continuous elevation may carry additional risks
  • Potential for accelerated tumor growth in those with occult malignancy
  • Long-term cardiovascular effects unknown

Glucose Dysregulation

  • Can worsen or unmask diabetes
  • Monitor fasting glucose regularly
  • May require diabetes medication adjustment

Cancer Risk Warning: Sustained GH/IGF-1 elevation may promote growth of existing tumors. Those with personal or family history of cancer should avoid use. Regular cancer screening is advised for any long-term use.

Monitoring

Baseline Assessments

Before initiating any protocol:

  • IGF-1 level (primary marker)
  • Fasting glucose and HbA1c
  • Lipid panel
  • Complete blood count
  • Liver and kidney function
  • Consider baseline imaging if clinically indicated

During Protocol

Monthly Monitoring

  • IGF-1 levels (target: upper normal range)
  • Fasting glucose
  • Symptom assessment

Periodic Monitoring (every 3 months)

  • HbA1c if glucose elevated
  • Lipid panel
  • Liver function

Target Ranges

MarkerTargetConcern Level
IGF-1Upper normal for ageAbove 1.5x upper limit
Fasting glucoseBelow 100 mg/dLAbove 126 mg/dL
HbA1cBelow 5.7%Above 6.5%

Post-Protocol

  • Allow 4 weeks for complete washout
  • Recheck IGF-1 to confirm return to baseline
  • Assess for any persistent effects

Regulatory Status

Current Status by Region

RegionStatusNotes
United StatesResearch chemical onlyNot FDA approved
CanadaNot approvedAvailable for research
United KingdomPrescription onlyGrey area enforcement
European UnionNot approvedResearch use only
AustraliaSchedule 4Requires prescription
WADAProhibitedBanned in and out of competition

Anti-Doping Considerations

CJC-1295 (with or without DAC) is explicitly prohibited by WADA:

  • Listed under S2: Peptide Hormones, Growth Factors
  • Prohibited at all times (in and out of competition)
  • Detectable in urine for extended periods due to long half-life

Quality and Sourcing

  • No pharmaceutical-grade product available
  • Research chemical quality varies significantly
  • Third-party testing recommended
  • Counterfeit and underdosed products common

References

[] Teichman SL, et al.. Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults. Journal of Clinical Endocrinology & Metabolism () doi:10.1210/jc.2005-1528
[] Ionescu M, Bhopale VM. Pharmacokinetic studies of a long-acting growth hormone-releasing hormone analog. Journal of Clinical Pharmacology () doi:10.1177/0091270005283285
[] Alba M, et al.. Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse. American Journal of Physiology - Endocrinology and Metabolism () doi:10.1152/ajpendo.00201.2006
[] Jetté L, et al.. Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats. Journal of Endocrinology () doi:10.1677/joe.1.06670
[] Van Hout MC, Hearne E. Netnography of female use of the synthetic growth hormone CJC-1295: Pulses and Potions. Substance Use & Misuse () doi:10.3109/10826084.2015.1082595

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