Mod-GRF 1-29

Growth Hormone Releasing Hormone AnalogRx: ResearchCompound: Investigational

Also known as: CJC-1295 no DAC, CJC-1295 without DAC, Modified GRF, Modified GRF 1-29, Sermorelin analog, Tesamorelin analog

Educational Only — Not medical advice. Consult a qualified clinician before using any peptide.

Source Mod-GRF 1-29 at Peptiology

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Summary

Modified growth hormone-releasing factor (1-29) with enhanced stability and bioactivity; truncated GHRH analog used in research settings for growth hormone stimulation

Mechanism of Action

Selective GHRH receptor agonist stimulating pulsatile growth hormone release from anterior pituitary

Routes of Administration

IntravenousSubcutaneous

Goals & Uses

  • fat lossBody CompositionLow
  • anti-agingLongevityLow
  • Growth hormone deficiencyEndocrineModerate
  • Body composition improvementMetabolicLow

Contraindications

  • Active malignancyOncologyHighUse caution or avoid depending on agent and context
  • hypersensitivity to GHRH analogsImmunologicHigh
  • PregnancyPopulationModeratePotential fetal risk or insufficient safety data
  • diabetes mellitusMetabolicModerate

Adverse Effects

  • HypoglycemiaMetabolicRareAbnormally low blood glucose
  • Carpal tunnel syndromeMusculoskeletalRare
  • HeadacheNeurologicUncommonPain in the head or upper neck
  • Antibody FormationImmunologicalRare
  • fluid retentionMetabolicUncommon
  • Injection site reactionLocalCommonRedness, swelling, itching, bruising, or pain at the injection site

Drug Interactions

  • GlucocorticoidsModerate
  • IGF-1Low
  • insulin/oral hypoglycemicsModerate
  • somatostatin analogsModerate

Population Constraints

  • patients with intracranial lesionsNeurologicAbsolute
  • Pediatric patientsAgeRelative
  • patients with diabetic retinopathyOphthalmologicRelative
  • Elderly patientsAgeRelative
  • Patients with history of cancerOncologyRelative

Regulatory Status

  • European UnionUnapprovedNot EMA approved; regulated as research chemical
  • United StatesUnapprovedNot FDA approved; DEA Schedule III controlled substance in some states; research use only
  • United KingdomUnapprovedNot MHRA approved; controlled under Psychoactive Substances Act in some contexts

Not approved for human therapeutic use; available as research chemical; regulatory status varies by jurisdiction

Evidence & Sources

No sources recorded yet.

Frequently Asked Questions

What is Mod-GRF 1-29?

Modified growth hormone-releasing factor (1-29) with enhanced stability and bioactivity; truncated GHRH analog used in research settings for growth hormone stimulation

What is Mod-GRF 1-29 used for?

Mod-GRF 1-29 is educationally associated with: fat loss, anti-aging, Growth hormone deficiency, Body composition improvement. Educational only — not medical advice.

How is Mod-GRF 1-29 administered?

Recorded routes of administration: Intravenous, Subcutaneous.

What are the potential side effects of Mod-GRF 1-29?

Reported adverse effects include: Hypoglycemia, Carpal tunnel syndrome, Headache, Antibody Formation, fluid retention, Injection site reaction. This list is not exhaustive — consult a qualified clinician.

Who should avoid Mod-GRF 1-29?

Recorded contraindications: Active malignancy, hypersensitivity to GHRH analogs, Pregnancy, diabetes mellitus. Consult a qualified clinician before use.