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Home›Research›Compare›CJC-1295 (without DAC) vs Tesamorelin

Peptide Comparison

CJC-1295 (without DAC) vs Tesamorelin

Both are GH / IGF Axis peptides.

CJC-1295 (without DAC)

CJC 1295

Fat LossResearch Only

Half-life: ~30 minutes

501 providers listed

Full CJC-1295 (without DAC) profile →
vs

Tesamorelin

Egrifta

Fat LossFDA ApprovedPrescription

Half-life: 26–38 minutes

296 providers listed

Full Tesamorelin profile →
Bottom line

Tesamorelin is FDA-approved, while CJC-1295 (without DAC) is nomination withdrawn — the clearest structural difference between them.

Quick Verdict

CJC-1295 (without DAC)

Half-life

~30 minutes

Tesamorelin

Half-life

26–38 minutes

Which One Should You Choose?
Your goalBetter option
Stronger clinical evidenceTesamorelin
Further along in FDA reviewTesamorelin
More provider options (501 vs 296)CJC-1295 (without DAC)

Research summary only — not medical advice. Consult a qualified provider before making any decisions.

Side-by-Side Comparison
CJC-1295 (without DAC)
Tesamorelin
Mechanism Family
GH / IGF Axis
GH / IGF Axis
Half-life
~30 minutes
26–38 minutes
FDA Status
nomination withdrawn
approved
Admin Routes
subcutaneous
subcutaneous
Availability
Research Only
Prescription
Providers
501 listed
296 listed
FDA Update
—
Nov 2010
Avail. Notes
GHRH analog — the truncated 1-29 form (Mod GRF 1-29), WITHOUT the Drug Affinity Complex (DAC). No FDA approval; not on the FDA 503A bulks list. WADA prohibited (S2) as a growth-hormone-releasing factor. Sold as a research chemical only.
FDA-approved GHRH analog. Brand: Egrifta SV (NDA 022505, Nov 2010). Indicated for excess abdominal fat in HIV lipodystrophy. Prescription only. Daily subcutaneous injection.
Research Evidence

CJC-1295 (without DAC)

RCT · 3 key studies · most recent 2026

Tesamorelin

RCT · 7 key studies · most recent 2026
Research Citations

About CJC-1295 (without DAC)

CJC-1295 without DAC (Mod GRF 1-29) is a short-acting GHRH analog that binds and activates pituitary GHRH receptors to stimulate brief, pulsatile growth hormone release. Lacking the Drug Affinity Complex, it is not albumin-bound and clears within roughly half an hour, producing discrete GH pulses rather than the sustained elevation of the DAC form.

Research Areas
GH and IGF-1 elevationsustained GHRH receptor agonismbody composition supportrecovery enhancementGH axis restoration

About Tesamorelin

Tesamorelin stimulates pulsatile GH secretion from the anterior pituitary by binding GHRH receptors. Its stabilisation protects it from rapid enzymatic cleavage by dipeptidyl peptidase IV, extending the effective half-life compared to unmodified GHRH. Downstream effects on visceral adiposity are mediated through elevated IGF-1 and direct lipolytic signalling.

Research Areas
FDA-approved GHRH analog for HIV-associated lipodystrophy (Egrifta / Egrifta SV)visceral fat reduction via GH/IGF-1 axis — strongest clinical evidence of any fat-targeted peptide2 mg/day subcutaneous injection — structured monthly dosing in approved indicationIGF-1 elevation monitoring relevant — considered in metabolic syndrome and diabetes contexts
Safety Profile

Information below reflects published research data only — not medical advice. Consult a qualified provider before use.

CJC-1295 (without DAC)

Warnings & Cautions
Active malignancy — caution (GH/IGF-1 is mitogenic)Pregnancy — cautionKnown hypersensitivityGlucose intolerance / insulin resistance

Class-based (investigational)

Suggested Monitoring
IGF-1Fasting glucoseHbA1cInsulin

Research protocols routinely measure IGF-1 to track GH axis activity before and during use. Fasting glucose and insulin are monitored because GH elevation can reduce insulin sensitivity over time.

Regulatory Notes

global — WADA

This compound falls under WADA Prohibited List category S2 (Peptide Hormones, Growth Factors, Related Substances and Mimetics), prohibited at all times for competing athletes.

source

Tesamorelin

Absolute Contraindications
Disruption of the hypothalamic-pituitary axis (hypophysectomy, hypopituitarism, pituitary tumor/surgery, head irradiation, or head trauma)Active malignancy (any prior cancer must be inactive and treatment complete)PregnancyKnown hypersensitivity to tesamorelin or mannitol
Warnings & Cautions
Elevated IGF-1Glucose intolerance / new or worsening diabetesFluid retentionNot for use in children with open epiphyses

Source: FDA label

Suggested Monitoring

Under clinical review

Being verified by our medical team before we display monitoring guidance for this peptide.

Regulatory Notes

global — WADA

This compound falls under WADA Prohibited List category S2 (Peptide Hormones, Growth Factors, Related Substances and Mimetics), prohibited at all times for competing athletes.

source
Used Together?

CJC-1295 (without DAC)

  • Ipamorelin

    Research suggests Ipamorelin and CJC-1295 may produce enhanced growth hormone release effects when combined. CJC-1295 provides sustained GHRH receptor stimulation while Ipamorelin provides pulsatile ghrelin receptor stimulation — complementary pathways studied in GH secretion research.

  • GLP-1 agonists

    Research notes metabolic pathway overlap between growth hormone-releasing peptides and GLP-1 agonists. Both compound classes influence metabolic signaling; limited research has studied their combined effects. Consult your prescriber before combining.

Price (per mg)

CJC-1295 (without DAC)

$7.80/mg

$6.60 – $10.88 range

63 vendors

Tesamorelin

$7.86/mg

$6.32 – $10.57 range

73 vendors

Find Providers

Where to source these peptides

PeptideBase lists providers for educational research purposes only. Always consult a qualified healthcare professional before obtaining or using any peptide.

More GH / IGF Axis Comparisons

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Educational research tools — not medical advice.

Cite this page

Data last updated October 26, 2026

Free to reference and republish with attribution to PeptideBase. Choose a format:

PeptideBase. (2026). CJC-1295 (without DAC) vs Tesamorelin — Per-mg Price Comparison. Retrieved October 26, 2026, from https://peptidebase.io/peptides/compare/cjc-1295/tesamorelin

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