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Comparison

CJC-1295 vs Tirzepatide

Side-by-side of CJC-1295 and Tirzepatide. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

CJC-1295

  • GHRH analog that binds the GHRH receptor on pituitary somatotrophs to release endogenous GH
  • DAC variant has ~7 day half-life via albumin binding; non-DAC variant ~30 minutes
  • Teichman 2006 trial showed sustained 2 to 10 fold IGF-1 elevation at 60 to 250 mcg/kg DAC dosing
  • Anecdotal protocols pair non-DAC CJC-1295 with Ipamorelin to mimic pulsatile GH release
  • Side effects: water retention, numbness or tingling at injection site, vivid dreams, transient flushing
  • No completed phase III RCTs; research-use-only and not FDA approved

Tirzepatide

  • Dual GIP plus GLP-1 receptor agonist with a ~5-day half-life supporting once-weekly subcutaneous dosing
  • SURMOUNT-1 reported ~22.5% mean body-weight loss at 15 mg over 72 weeks versus 2.4% on placebo
  • Lowers HbA1c by ~1.9 to 2.6 percentage points in type 2 diabetes across SURPASS trials
  • Outperformed semaglutide 1.0 mg head-to-head on weight loss and HbA1c in SURPASS-2
  • GI effects (nausea, diarrhea, vomiting) drive most discontinuations and ease with slow titration
  • Lean-mass loss observed in body-composition substudies; resistance training and protein intake mitigate this

Side-by-side

Attribute CJC-1295 Tirzepatide
Category peptide pharmaceutical
Also known as CJC-1295 DAC, CJC-1295 no-DAC, Mod GRF 1-29, tesamorelin analog Mounjaro, Zepbound, LY3298176
Half-life (hr) 168 120
Typical dose (mg) 0.1 10
Dosing frequency weekly (DAC); 1-3x daily (non-DAC) weekly
Routes subcutaneous subcutaneous
Onset (hr) 1 24
Peak (hr) 3 72
Molecular weight 3367.83 4813.45
Molecular formula C152H252N44O42 C225H348N48O68
Mechanism Binds the GHRH receptor on pituitary somatotrophs, stimulating pulsatile growth-hormone release. The DAC modification extends plasma residence by tethering the peptide to serum albumin via a maleimide-cysteine bond. Synthetic 39-amino-acid peptide that activates both GIP and GLP-1 receptors. Potentiates glucose-dependent insulin secretion, suppresses glucagon, slows gastric emptying, and acts on hypothalamic and brainstem satiety circuits.
Legal status Not FDA approved; research-use-only grey market; banned by WADA Prescription only; FDA-approved 2022 (T2DM, Mounjaro) and 2023 (chronic weight management, Zepbound)
WADA status banned allowed
DEA / Rx Not FDA approved; not scheduled; research-chemical status Rx only (not a controlled substance)
Pregnancy Insufficient data; not recommended Not recommended; discontinue 2 months before planned pregnancy
CAS 446262-90-4 2023788-19-2
PubChem CID 91971820 156588324
Wikidata Q5012154 Q105099794

Safety profile

CJC-1295

Common side effects

  • injection-site reactions
  • water retention
  • numbness or tingling at injection site
  • vivid dreams
  • transient flushing
  • head pressure or mild headache

Contraindications

  • pregnancy
  • active malignancy
  • diabetic retinopathy (theoretical)
  • history of pituitary tumor

Interactions

  • Ipamorelin: synergistic GH release; commonly co-administered in anecdotal protocols(minor)
  • insulin: GH-induced insulin resistance can shift glycemic control over weeks(moderate)
  • corticosteroids: blunt GH-axis response; reduce expected efficacy(moderate)

Tirzepatide

Common side effects

  • nausea
  • diarrhea
  • vomiting
  • constipation
  • decreased appetite
  • injection-site reactions
  • fatigue
  • abdominal pain

Contraindications

  • personal or family history of medullary thyroid carcinoma
  • multiple endocrine neoplasia type 2
  • pregnancy
  • history of pancreatitis (use caution)
  • severe gastroparesis

Interactions

  • insulin: additive hypoglycemia risk; insulin dose typically reduced(major)
  • sulfonylureas (glipizide, glyburide): hypoglycemia risk, sulfonylurea dose often reduced(major)
  • oral medications (general): delayed gastric emptying can alter absorption kinetics(moderate)
  • oral contraceptives: reduced exposure after first dose; backup contraception recommended for 4 weeks after initiation and each dose escalation(moderate)
  • warfarin: monitor INR due to altered absorption(moderate)

Which Should You Take?

Tirzepatide comes out ahead for most readers on the criteria we weight: 3 catalogued goals, prescription-only, with a Tier-A outcome catalogued. CJC-1295 is the right call when one of the conditionals below applies.

  • If your priority is post-training recovery, pick CJC-1295.
  • If your priority is growth-hormone axis, pick CJC-1295.
  • If your priority is metabolic health and glucose control, pick Tirzepatide.
  • If your priority is fat loss, pick Tirzepatide.

Default choice: Tirzepatide. Wider use case, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for CJC-1295 only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between CJC-1295 and Tirzepatide?

CJC-1295 and Tirzepatide differ in category (peptide vs pharmaceutical), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, CJC-1295 or Tirzepatide?

CJC-1295 half-life is 168 hours; Tirzepatide half-life is 120 hours.

Can you stack CJC-1295 with Tirzepatide?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

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