Research use only. Not for human consumption. 18+ only.

Metabolic & Weight Loss / Subcutaneous

Cholecystokinin (CCK)

Also known as CCK-8, CCK-33, Cholecystokinin octapeptide

A satiety hormone that promotes fullness and reduces food intake by signaling through CCK receptors. Researched for appetite regulation and metabolic health.

What is Cholecystokinin (CCK) used for? Research has focused on promotes satiety and reduces food intake; stimulates pancreatic enzyme secretion; enhances gallbladder contraction.

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Evidence grade CResearch only

Cholecystokinin (CCK) injection at a glance

Figures from the published research literature. Research use only.

Dose range
0.5-2 mcg
Route
Subcutaneous

How often, when, and the dosing notes are in the dosing reference further down.

Work out your units in the free calculator

Research status

Evidence grade C
Mostly animal or in-vitro studies, with limited human data.
Research only
No regulatory approval in any major jurisdiction. Research use only.

Clinical trials

For research purposes only. Not approved for human use. Not medical advice.

Research areas

  • Promotes satiety and reduces food intake
  • Stimulates pancreatic enzyme secretion
  • Enhances gallbladder contraction
  • Regulates gastric emptying
  • Supports postprandial glucose control
  • Modulates appetite signaling pathways

Side effects

EffectHow oftenSeverity
NauseaOccurs in some subjects, particularly at higher doses or when injected on an empty stomach. Usually resolves within 30-60 minutes. May be reduced by injecting with or shortly after food.CommonMild
Abdominal discomfort or crampingRelated to enhanced gastric and pancreatic secretion. Typically mild and self-resolving. More common with higher doses.UncommonMild
DiarrheaMay occur due to increased pancreatic enzyme secretion and altered intestinal motility. Usually transient.UncommonMild
HeadacheReported in some research subjects. Mechanism unclear; may be related to systemic effects of CCK.UncommonMild
Injection site reactionsMild erythema, itching, or swelling at injection site. Minimize by rotating sites and using proper injection technique.UncommonMild
Anxiety or nervousnessReported rarely in research settings. CCK has been studied in anxiety models; mechanism in humans unclear.RareMild
PancreatitisExtremely rare but documented in animal models at very high doses. Seek immediate medical attention if severe abdominal pain, elevated amylase, or lipase occurs.RareSerious

Dosing reference

Dose scale from the research

Starting
0.5 mcg
Typical
1 mcg
Upper end
2 mcg
Cholecystokinin (CCK) dosing reference
ParameterValue
Dose range0.5-2 mcg
Frequency, timing and route are for members

Checked October 2026

Research disclaimer. Figures are drawn from published research literature and community logs. They are not clinical recommendations. Consult a qualified professional. Research use only.

Reconstitution guide

  • Do not use saline or bacteriostatic saline, use only bacteriostatic water for reconstitution
  • Do not shake the vial vigorously; gentle swirling prevents peptide degradation
  • Discard immediately if the solution appears cloudy, discolored, or contains visible particles
  • Use within 30 days of reconstitution when stored at 2-8°C
  • Do not freeze the reconstituted solution; freezing may denature the peptide
  • Use the PeptideVolt reconstitution calculator for your exact concentration

Worked example

With 1 mg in the vial, the water you add changes the draw. Mixed with 1 mL that is 1,000 mcg per mL, so on a U-100 syringe 0.5 mcg is 0.05 units and 2 mcg is 0.2 units. Mixed with 2 mL it is 500 mcg per mL, so 0.5 mcg is 0.1 units and 2 mcg is 0.4 units.

Work out your exact dose in the free peptide calculator

Molecular and pharmacological data

Molecular weight1143 Da (CCK-8); 3918 Da (CCK-33)
Half-life2-3 minutes (endogenous CCK in circulation)
SequenceMembers only

Cholecystokinin (CCK) is a gastrointestinal hormone that acts as a satiety signal by binding to CCK receptors (primarily CCKA and CCKB) on vagal afferent neurons and in the brain. This receptor activation triggers signals that promote feelings of fullness, reduce food intake, and regulate digestive processes including gallbladder contraction and pancreatic enzyme secretion. CCK's appetite-suppressing effects have been extensively studied as a potential mechanism for weight management and metabolic regulation.

Pathways and mechanism detail are for members

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Recent research

All results on PubMed

Source: PubMed / NCBI. Updated daily. Articles are listed for research reference only.

Research citations

5 sources
  • Gibbs J, Young RC, Smith GP. (1973). Cholecystokinin decreases food intake in rats. Journal of Comparative and Physiological Psychology. 84(3):488-495. PMID: 4745816

  • Moran TH, Katz LF, Plata-Salaman CR, Schwartz GJ. (1998). Disordered food intake and obesity in rats lacking cholecystokinin A receptors. American Journal of Physiology. 274(3):R618-625. PMID: 9530226

  • Beglinger C, Degen L. (2006). Gastrointestinal satiety signals in humans--physiologic roles for GLP-1 and peptide YY? Journal of Clinical Endocrinology & Metabolism. 91(12):4753-4761. PMID: 16968799

  • Rehfeld JF. (2017). Cholecystokinin - from local gut hormone to ubiquitous messenger. Frontiers in Endocrinology. 8:47. PMID: 28408889

  • Kissileff HR, Pi-Sunyer FX, Thornton J, Smith GP. (1981). C-terminal octapeptide of cholecystokinin decreases food intake in man. American Journal of Clinical Nutrition. 34(2):154-160. PMID: 7211734

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Research use only. All content on this page is provided for informational and educational purposes related to scientific research. Cholecystokinin (CCK) is not approved for human use by the FDA or any equivalent regulatory body. This is not medical advice. Do not use any substance discussed here for therapeutic, diagnostic, or preventative purposes. Consult a qualified healthcare professional before making any health-related decisions. The Peptide Volt does not endorse the use of any research chemicals. 18+ only.