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Peptide Database

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Peptides
5-Amino-1MQ
Weight Management
Abarelix
Hormone Support
Acetyl Hexapeptide-3 (Argireline)
Cosmetic
Adipotide
Weight Management
Adrenomedullin
Healing & Recovery
Alexamorelin
Growth Hormone
Angiotensin (1-7)
Healing & Recovery
AOD-9604
Weight Management
Apelin-13
Healing & Recovery
ARA-290 (Cibinetide)
Healing & Recovery
Bestatin (Ubenimex)
Immune
BPC-157
Healing & Recovery
Buserelin
Hormone Support
Cagrilintide
Weight Management
CagriSema
Weight Management
Capromorelin
Growth Hormone
Cartalax
Anti-Aging
Cathelicidin (hCAP-18 / Synthetic Derivatives)
Immune
Cerebrolysin
Cognitive
Cerluten
Cognitive
Cetrorelix
Hormone Support
Chonluten
Immune
CJC-1295 (No DAC)
Growth Hormone
CJC-1295 with DAC
Growth Hormone
Cortexin
Cognitive
Crystagen
Immune
Daptomycin
Immune
Defensin (HBD-2)
Immune
Defensin (HBD-3)
Immune
Degarelix
Hormone Support
Dihexa
Cognitive
DSIP (Delta Sleep-Inducing Peptide)
Sleep & Recovery
Dulaglutide
Weight Management
Enalapril
Healing & Recovery
Epithalon
Anti-Aging
Exenatide
Weight Management
Fertirelin
Hormone Support
FOXO4-DRI
Anti-Aging
Ganirelix
Hormone Support
GHK-Cu (Copper Peptide)
Cosmetic
GHRH (1-29)
Growth Hormone
GHRP-2
Growth Hormone
GHRP-6 (Growth Hormone Releasing Peptide-6)
Growth Hormone
Glutathione
Anti-Aging
Gonadorelin (GnRH)
Hormone Support
Gramicidin
Immune
Hexarelin
Growth Hormone
Human Chorionic Gonadotropin (HCG)
Hormone Support
Human Growth Hormone (HGH)
Growth Hormone
IGF-1 LR3
Growth Hormone
Immunoxel (Dzherelo)
Immune
Imunofan
Immune
Intermedin (Adrenomedullin-2)
Healing & Recovery
Ipamorelin
Growth Hormone
Kisspeptin-10
Sexual Health
KPV (Alpha-MSH Fragment)
Healing & Recovery
Lactoferricin B
Immune
Larazotide
Healing & Recovery
Lentinan
Immune
Leuphasyl
Cosmetic
Leuprolide
Hormone Support
Liraglutide
Weight Management
Livagen
Anti-Aging
Lixisenatide
Weight Management
LL-37
Immune
Macimorelin
Growth Hormone
Magainin-2
Immune
Mazdutide
Weight Management
Melanotan-2
Cosmetic
MK-677 (Ibutamoren)
Growth Hormone
MOTS-c
Metabolic
Myristoyl Pentapeptide-17
Cosmetic
N-Acetyl Selank
Cognitive
N-Acetyl Semax Amidate
Cognitive
NAD+
Mitochondrial
Nafarelin
Hormone Support
Natriuretic Peptide (ANP)
Healing & Recovery
Nesiritide (BNP)
Healing & Recovery
Nisin
Immune
Noopept (Omberacetam)
Cognitive
Orforglipron
Weight Management
Ovagen
Anti-Aging
Oxytocin Acetate
Hormone Support
P21 (P021)
Cognitive
PACAP-38
Healing & Recovery
Palmitoyl Oligopeptide
Cosmetic
Palmitoyl Pentapeptide-4 (Matrixyl)
Cosmetic
Palmitoyl Tetrapeptide-7
Cosmetic
Palmitoyl Tripeptide-1
Cosmetic
Pancragen
Metabolic
PEG-MGF
Healing & Recovery
Pemvidutide
Weight Management
Pentadecapeptide (BPC Analog)
Healing & Recovery
Pidotimod
Immune
Pinealon
Cognitive
PNC-27
Immune
Polymyxin B
Immune
Pralmorelin (GHRP-2)
Growth Hormone
Pramlintide
Weight Management
Prostamax
Hormone Support
PT-141 (Bremelanotide)
Sexual Health
Relaxin-2 (Serelaxin)
Healing & Recovery
Retatrutide
Weight Management
Selank
Cognitive
Semaglutide
Weight Management
Semax
Cognitive
Sermorelin
Growth Hormone
Setmelanotide
Weight Management
SLU-PP-332
Metabolic
SM-130686
Growth Hormone
Snap-8
Cosmetic
SS-31 (Elamipretide)
Mitochondrial
Substance P Antagonists
Healing & Recovery
Survodutide
Weight Management
SYN-AKE
Cosmetic
Tabimorelin
Growth Hormone
TB-500
Healing & Recovery
Tesamorelin
Growth Hormone
Testagen
Hormone Support
Thymalin
Immune
Thymopentin (TP-5)
Immune
Thymopoietin
Immune
Thymosin Alpha-1
Immune
Thymosin Beta-4
Healing & Recovery
Thymulin (FTS)
Immune
Thymulin Analog (PAT)
Healing & Recovery
Tirzepatide
Weight Management
Tripeptide-29
Cosmetic
Triptorelin
Hormone Support
Ularitide
Healing & Recovery
Urocortin
Healing & Recovery
Ventfort
Anti-Aging
Vesilute
Hormone Support
Vilon
Immune
VIP (Vasoactive Intestinal Peptide)
Healing & Recovery
Xenin-25
Metabolic
Ziconotide (Prialt)
Healing & Recovery
Total Peptides: 137
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Cagrilintide

A long-acting amylin analogue given once weekly.

Alone it produced up to 10.8% weight loss over 26 weeks against 3.0% on placebo [1]; the 20.4% figure people quote is the CagriSema combination with semaglutide, not cagrilintide on its own [3]. Not approved anywhere — the combination is under FDA review.

Written by Michael Carroll — Owner, Director of Research · Reviewed by the Peptide Initiative Research Team · Editorial standards

Weight Management

Suggested dose

0.3 – 4.5 mg

Once weeklyOnset: Gradual (3-4 weeks)
159-195 hoursHalf-life(~7-8 days)
~100%Bioavailability(subcutaneous)
4409 g/molMolecular weight
Strong human trialsEvidence level

Compound profile

Cagrilintide scientific & efficacy data

Weight Management

Peptide profile

Appetite Control9.5
Weight Loss9.2
GLP-1 Synergy9.8

Strong human trials

Cagrilintide

0.3 mg · Once weekly

Molecular formula

C194H312N54O59S2

Mol. weight
4409 g/mol
CAS number
1415456-99-3
PubChem
171397054
Developed · 2021
Thomas Kruse
Novo Nordisk

Amino acid sequence

Lys-Cys-Asn-Thr-Ala-Thr-Cys-Ala-Thr-Gln-Arg-Leu-Ala-Asn-Phe-Leu-Val-Arg-Ser-Ser-Asn-Asn-Leu-Gly-Pro-Val-Leu-Pro-Pro-Thr-Asn-Val-Gly-Ser-Asn-Thr-Tyr-NH2 (acylated with C18 diacid via gamma-Glu linker)

Appetite Control

Amylin is a pancreatic hormone released with insulin that signals satiety; cagrilintide is a long-acting version of it, engineered with a half-life of 159-195 hours so a single weekly injection holds the signal [2]. The mechanism is independent of GLP-1, which is why the two add together rather than overlap [4].

Weight Loss

On its own: up to 10.8% of body weight (11.5 kg) at 26 weeks at the 4.5 mg dose, against 3.0% (3.3 kg) on placebo [1]. Combined with semaglutide 2.4 mg: 20.4% at 68 weeks against 3.0% on placebo in 3,417 adults [3]. The second number is the pair, not the peptide — quoting 20% for cagrilintide alone is wrong by roughly a factor of two.

GLP-1 Synergy

The clearest demonstration is the phase 1b trial, where everyone received semaglutide 2.4 mg and only cagrilintide differed: 17.1% weight loss at 20 weeks with cagrilintide 2.4 mg against 9.8% with placebo added to the same semaglutide — about 7 percentage points attributable to cagrilintide [2]. In type 2 diabetes the combination also beat semaglutide alone on weight (-15.6% vs -5.1% at 32 weeks) though the HbA1c difference was small [5][7].

Dosing

How much Cagrilintide do I take?

0.3 – 4.5 mg · once weekly

0.3 – 4.5 mg

Once weekly

Covers all 5 documented dose levels · timing · dose-adjustment guidance.

Every documented dose level

PhaseDoseFrequency
26 weeks in the dose-finding trial0.3 mgOnce weekly
26 weeks in the dose-finding trial0.6 mgOnce weekly
26 weeks alone; 20 weeks in combination1.2 mgOnce weekly
26 to 68 weeks depending on the trial2.4 mgOnce weekly
26 weeks in the dose-finding trial4.5 mgOnce weekly
CagrilintideOnce weekly

How much peptide is in your bottle?

Look at the label on the vial. It’s the number next to the unit — like "5 mg". Labeled in IU? Switch the unit to IU.

Type a number to continue.
0

Suitability

Is Cagrilintide right for me?

Best for weight loss & appetite control

Best for

Weight loss and appetite control

Cagrilintide excels at reducing hunger by mimicking amylin, a hormone your pancreas naturally releases after meals. Phase 2 trials showed people losing up to 10.8% of body weight with cagrilintide alone - and that's without combining it with other medications.

Boosting GLP-1 medication results

When you hit a plateau with semaglutide or want even better results, cagrilintide adds a second satiety pathway. The CagriSema combination achieved over 20% weight loss in clinical trials - significantly more than either drug alone.

People who want once-weekly convenience

Unlike older amylin medications that required three daily injections, cagrilintide's extended half-life of about a week means you only inject once weekly. Set a reminder on your phone and you're done.

Those seeking natural-feeling appetite reduction

Cagrilintide works by enhancing your body's own fullness signals rather than forcing you to eat less. Many users report feeling genuinely satisfied with smaller meals rather than fighting willpower battles.

Metabolic health improvement

Beyond weight loss, cagrilintide helps with blood sugar control and metabolic markers. It slows stomach emptying and reduces post-meal glucose spikes, making it valuable for people with or at risk for type 2 diabetes.

Consider alternatives if

Similar weight loss without amylin mechanismSemaglutide, Tirzepatide, Liraglutide
Maximum possible weight lossCagriSema (cagrilintide + semaglutide), Retatrutide, Tirzepatide
Lower cost weight loss optionCompounded semaglutide, AOD-9604, Tesofensine
Non-injectable appetite controlOral semaglutide (Rybelsus), 5-Amino-1MQ, Dietary interventions

Do not use if

Pregnancy or breastfeedingActive eating disordersSevere gastroparesis

Use with caution if

You have a history of pancreatitisYou have gallbladder disease or history of gallstonesYou have diabetic retinopathyYou are taking insulin or sulfonylureas (increased hypoglycemia risk)You have significant kidney impairmentYou have difficulty maintaining adequate nutrition

Not sure?

Compare Cagrilintide with similar peptides to find the best fit for your goals.

Administration

How do I use Cagrilintide?

Subcutaneous injection

Route

Subcutaneous injection once weekly

Best sites

Abdomen (2 inches away from navel)Front of thigh (middle third)Upper arm (outer area)Lower back area (above buttocks)

Covers reconstitution · step-by-step technique · storage · a sample daily schedule.

Safety

Is Cagrilintide safe?

4 common side effects · 3 serious

Gastrointestinal effects are the dominant finding and they are common, not rare.

In the 26-week dose-finding trial, gastrointestinal adverse events occurred in 41% to 63% of cagrilintide participants across the dose groups against 32% on placebo, with nausea in 20% to 47% against 18%; 73 of 906 participants (10%) stopped treatment permanently and 30 (4%) did so because of adverse events [1].

In the 68-week phase 3 obesity trial the combination with semaglutide produced gastrointestinal adverse events in 79.6% against 39.9% on placebo, mainly transient and mild to moderate [3]; in the type 2 diabetes phase 3 the figures were 72.5% against 34.4% [6].

In the 2,713-person REIMAGINE 2 trial, adverse events were reported by 82.2% (125 of 152) of those on cagrilintide 2.4 mg alone against 70.5% (105 of 149) on placebo [7].

A dedicated cardiac study in 105 healthy participants found no clinically relevant QTc prolongation at the highest studied dose of 4.5 mg against placebo [8].

Cagrilintide is not approved anywhere, so none of this comes from a regulator-reviewed label — it comes from the trials, all of them funded and run by Novo Nordisk.

Monotherapy evidence is thinner than the phase 3 headline numbers suggest: about 100 participants per dose group for 26 weeks in the dose-finding trial [1], 302 in the REDEFINE 1 cagrilintide arm [3], and 152 in REIMAGINE 2 [7].

Most of the large-scale safety data describes the COMBINATION with semaglutide, where the two drugs cannot be separated. There is no data beyond 68 weeks, none in pregnancy, and none in people using cagrilintide without medical supervision.

Less common

VomitingHeadache

These typically resolve with continued use or dose adjustment.

Common side effects · experienced by some users

  • Nausea

    The most frequently reported side effect, affecting 20-47% of users depending on dose. Usually mild and improves over the first few weeks.

    Management: Start with lower doses and titrate slowly. Eat smaller, more frequent meals. Avoid greasy or heavy foods.

  • Constipation

    Occurs due to slowed gastric emptying and reduced food intake. Reported in 15-25% of users.

    Management: Increase fiber and water intake. Stay physically active. Consider a stool softener if needed.

  • Diarrhea

    May occur especially during dose adjustments. Usually temporary and mild to moderate.

    Management: Stay well hydrated. Avoid foods that trigger symptoms. Usually resolves within 1-2 weeks.

  • Injection site reactions

    Mild redness, swelling, or itching at injection sites. Generally resolves quickly.

    Management: Rotate injection sites regularly. Ensure proper injection technique. Apply ice if needed.

Stop and seek help if

  • Severe allergic reaction (rash, swelling, difficulty breathing)
  • Persistent severe nausea or vomiting not improving with dose reduction
  • Signs of pancreatitis (severe abdominal pain radiating to back)
  • Planned pregnancy or positive pregnancy test
  • Inability to maintain adequate nutrition despite dose adjustments
  • Any concerning symptoms your healthcare provider advises stopping for

Always consult your healthcare provider before stopping or modifying your dose. Do not stop abruptly without medical guidance, especially if you are also on diabetes medications.

With other peptides

  • Safe:Semaglutide — Designed to be combined - the CagriSema combination shows enhanced weight loss through complementary mechanisms
  • Safe:Tirzepatide — May be combined, but both affect appetite strongly - monitor for excessive appetite suppression
  • Safe:BPC-157 — Generally safe to combine for gut support during weight loss
  • Caution:Pramlintide — Do NOT combine - both are amylin analogs with overlapping mechanisms

With medications

  • Caution:Insulin — Increases hypoglycemia risk - insulin dose may need reduction, especially post-meal doses
  • Caution:Sulfonylureas — Increased hypoglycemia risk - may need dose adjustment with provider guidance
  • Safe:Metformin — Generally safe to combine - may provide complementary metabolic benefits
  • Safe:Oral medications — Slowed gastric emptying may affect absorption timing - take critical meds separately

With supplements

  • Safe:Protein supplements — Highly recommended to maintain muscle mass during weight loss
  • Safe:Fiber supplements — Can help with constipation - take with plenty of water
  • Safe:Multivitamins — Recommended as reduced food intake may limit nutrient intake
  • Safe:Electrolytes — Helpful if experiencing GI side effects to prevent dehydration

Effectiveness

How do I know Cagrilintide is working?

Strong human trials · first signs weeks 1-6

Evidence level

Strong human trials

(Phase 3 or FDA approved)

100/100

Regulatory status

Not approved anywhere

Cagrilintide alone is not in any regulatory filing; the fixed-dose CagriSema combination with semaglutide was submitted to the FDA on 18 December 2025 and is under review.

Onset of effects

Gradual

(3-4 weeks)

How it works

Cagrilintide is a lab-made version of amylin, a hormone your pancreas releases right after you eat.

Think of amylin as your body's natural 'I'm full' signal - it tells your brain to stop eating and slows down how fast food leaves your stomach so you feel satisfied longer. The problem with natural amylin is it only lasts about 15-20 minutes.

Cagrilintide is specially designed to last about a week, so you only need one injection and the fullness signals keep working day after day.

The deeper mechanism

Cagrilintide is a lipidated 37-amino acid amylin analog with dual agonist activity at both amylin receptors (AMY1-3) and calcitonin receptors (CTR).

The C18 diacid fatty acid chain attached via a gamma-glutamate linker enables non-covalent albumin binding, extending the half-life to 159-195 hours and permitting once-weekly dosing.

The peptide activates receptors in the area postrema and nucleus of the solitary tract, promoting meal-ending satiation through descending neural pathways to hypothalamic feeding centers.

Secondary mechanisms include delayed gastric emptying, suppression of postprandial glucagon secretion, and potential effects on energy expenditure through preventing compensatory metabolic adaptation.

When combined with GLP-1 receptor agonists like semaglutide, the complementary receptor activation produces synergistic effects on weight loss through independent but convergent satiety pathways.

What to expect

  1. Weeks 1-6

    What you might notice

    • This is the escalation window — trials took up to 6 weeks to reach the assigned dose [1], or 16 weeks when co-escalated with semaglutide [2]
    • Gastrointestinal effects are most likely here and are common, not rare: 41-63% across the cagrilintide groups against 32% on placebo [1]

    What's normal

    • Nausea, reported by 20-47% of cagrilintide participants against 18% on placebo [1]
    • Constipation and diarrhoea, the other two most frequent effects [1]

    What's next

    • 4% of the 906 phase 2 participants stopped because of adverse events — if effects are severe, that is a conversation with a prescriber, not something to push through [1]
  2. Week 26

    What you might notice

    • The endpoint of the monotherapy trial. Weight loss ranged 6.0% to 10.8% (6.4-11.5 kg) across the 0.3-4.5 mg dose groups against 3.0% (3.3 kg) on placebo [1]
    • At the top dose that was 10.8% against 9.0% for liraglutide 3.0 mg — better, by 1.8 percentage points (p=0.03) [1]

    What's normal

    • Loss below the headline figure: the range starts at 6.0%, and the 10.8% is the highest dose in the best case [1]

    What's next

    • No monotherapy trial has run past 26 weeks, so nothing beyond this point is established for cagrilintide alone [1]
  3. Week 68 (combination only)

    What you might notice

    • The phase 3 endpoint, and it belongs to the COMBINATION with semaglutide, not to cagrilintide alone: 20.4% against 3.0% on placebo in 3,417 adults [3], and 13.7% against 3.4% in 1,206 adults with type 2 diabetes [6]
    • Gastrointestinal effects persisted at that scale — 79.6% against 39.9% on placebo [3]

    What's normal

    • Nothing established past 68 weeks — no trial has run longer [3][6]

    What's next

    • The combination is under FDA review; cagrilintide alone is in no regulatory filing [3]

Signs it's working

Weight loss indicators

  • Clothes fitting more loosely
  • Scale showing consistent weekly weight reduction
  • Reduced waist circumference
  • Visible changes in body composition
  • Need to tighten belt or buy smaller sizes

Appetite and eating changes

  • Feeling satisfied with smaller portions
  • Reduced interest in snacking between meals
  • Less food noise and obsessive food thoughts
  • Natural preference for lighter, smaller meals
  • Ability to stop eating when full

Metabolic improvements

  • Better blood sugar readings (if monitored)
  • Improved fasting glucose on lab work
  • More stable energy throughout the day
  • Reduced post-meal sluggishness
  • Better cholesterol and triglyceride levels

Not seeing results? Common reasons

  • Dose too low - may need to increase to therapeutic levels (2.4mg or higher)
  • Not enough time - meaningful results typically take 8-12 weeks at adequate doses
  • Calorie-dense liquid calories bypassing satiety signals - watch smoothies, alcohol, sugary drinks
  • Eating through fullness signals - pay attention to your body's cues
  • Inconsistent dosing schedule - must be same day each week for optimal levels
  • Unrealistic expectations - 1-2 lbs per week is healthy, sustainable weight loss

Key research

2021[1]
“Once-weekly cagrilintide for weight management in people with overweight and obesity”Lau DCW et al.Finding: The dose-finding trial, and the source of every cagrilintide monotherapy dose. 906 adults without diabetes at 57 sites in ten countries were randomised 6:1 to once-weekly subcutaneous cagrilintide at 0.3, 0.6, 1.2, 2.4 or 4.5 mg (100-102 per dose group), once-daily liraglutide 3.0 mg (99), or placebo (101), for 26 weeks after a dose-escalation period of up to 6 weeks. These were PARALLEL dose groups, not a ladder anyone climbed. Weight fell 6.0% to 10.8% (6.4-11.5 kg) across the cagrilintide groups against 3.0% (3.3 kg) on placebo — a treatment difference of 3.0 to 7.8 percentage points, p<0.001. The top dose beat liraglutide 3.0 mg: 10.8% (11.5 kg) against 9.0% (9.6 kg), difference 1.8 percentage points, p=0.03. Gastrointestinal adverse events occurred in 41-63% of cagrilintide participants against 32% on placebo, nausea in 20-47% against 18%. 73 participants (10%) stopped treatment permanently, 30 (4%) because of adverse events.View study
2021[2]
“Safety, tolerability, pharmacokinetics, and pharmacodynamics of cagrilintide with semaglutide”Enebo LB et al.Finding: The phase 1b combination trial, 95 adults exposed. Six sequential cohorts with a BMI of 27.0-39.9 were randomised 3:1 to once-weekly cagrilintide at 0.16, 0.30, 0.60, 1.2, 2.4 or 4.5 mg (n=11-12 each) or matched placebo (24), all on top of semaglutide 2.4 mg, with both drugs co-escalated in 4-week intervals over 16 weeks and no lifestyle intervention. At week 20, weight fell 15.7% on cagrilintide 1.2 mg and 17.1% on 2.4 mg against 9.8% on pooled placebo plus semaglutide — treatment differences of -6.0 (95% CI -9.9 to -2.0) and -7.4 (-11.2 to -3.5) percentage points. The 4.5 mg cohort fell 15.4% against 8.0% on its matched placebo. Note what the placebo arm here is: everyone received semaglutide 2.4 mg, so the 9.8% is semaglutide's own effect and cagrilintide added roughly 6-7 points on top. Of 566 adverse events in 92 participants, 207 (37%) were gastrointestinal. Cagrilintide's half-life was 159-195 hours, which is what makes weekly dosing possible.View study
2025[3]
“Coadministered Cagrilintide and Semaglutide in Adults with Overweight or Obesity”Garvey WT et al.Finding: REDEFINE 1, the phase 3a obesity trial. 3,417 adults without diabetes with a BMI of 30 or more, or 27 or more with an obesity-related complication, were randomised 21:3:3:7 to once-weekly cagrilintide-semaglutide 2.4 mg each (2,108), semaglutide 2.4 mg alone (302), cagrilintide 2.4 mg alone (302), or placebo (705), with lifestyle intervention, for 68 weeks. Body weight fell 20.4% on the combination against 3.0% on placebo (difference -17.3 percentage points, 95% CI -18.1 to -16.6, p<0.001), with more participants reaching 5%, 20%, 25% and 30% loss. Gastrointestinal adverse events affected 79.6% on the combination against 39.9% on placebo, mainly transient and mild to moderate. The 20.4% belongs to the combination; the cagrilintide-alone arm's own figure is not reported in the abstract.View study
2021[4]
“Development of Cagrilintide, a Long-Acting Amylin Analogue”Kruse T et al.Finding: Describes the medicinal chemistry development of cagrilintide, explaining how lipidation extended the half-life from minutes (pramlintide) to approximately one week while maintaining receptor activity.View study
2023[5]
“Efficacy and safety of CagriSema in type 2 diabetes”Frias JP et al.Finding: In people with type 2 diabetes, CagriSema achieved 15.6% weight loss versus 5.1% with semaglutide alone over 32 weeks, with comparable HbA1c reductions and good tolerability.View study
2025[6]
“Cagrilintide-Semaglutide in Adults with Overweight or Obesity and Type 2 Diabetes (REDEFINE 2)”Davies MJ, Bajaj HS, Broholm C, et al.Finding: Phase 3a across 12 countries. 1,206 adults with type 2 diabetes and a BMI of 27 or more were randomised 3:1 to once-weekly cagrilintide-semaglutide, 2.4 mg of each (904), or placebo (302), with lifestyle intervention, for 68 weeks. Body weight fell 13.7% against 3.4% on placebo (difference -10.4 percentage points, 95% CI -11.2 to -9.5, p<0.001). HbA1c reached 6.5% or lower in 73.5% against 15.9% on placebo. Gastrointestinal adverse events were reported by 72.5% against 34.4% on placebo, most transient and mild to moderate.View study
2026[7]
“Cagrilintide-semaglutide (CagriSema) versus semaglutide or cagrilintide in people with type 2 diabetes (REIMAGINE 2)”Buse JB, Bajaj HS, Dalskov SM, et al.Finding: The largest trial to carry a cagrilintide monotherapy arm. 2,713 people with type 2 diabetes in 30 countries were randomised across six groups for 68 weeks, including cagrilintide 2.4 mg alone (n=152) alongside cagrilintide-semaglutide 2.4 mg each (n=603), semaglutide 2.4 mg (n=605), the 1.0 mg combination (n=595), semaglutide 1.0 mg (n=609) and placebo (n=149). On the primary endpoint the 2.4 mg combination beat semaglutide 2.4 mg on HbA1c (-1.91 vs -1.75 percentage points; difference -0.16, 95% CI -0.27 to -0.05, p=0.0035) — a real but small separation. Adverse events: 86.9% (524/603) on the 2.4 mg combination, 82.2% (125/152) on cagrilintide alone, 81.2% (491/605) on semaglutide 2.4 mg, and 70.5% (105/149) on placebo, most commonly gastrointestinal.View study
2024[8]
“Cagrilintide is not associated with clinically relevant QTc prolongation: a thorough QT study in healthy participants”Gabe MBN, Fuhr R, Sinn A, et al.Finding: A dedicated cardiac-safety study in 105 healthy participants randomised to once-weekly subcutaneous cagrilintide escalated to 4.5 mg (n=53) or placebo (n=52), with oral moxifloxacin 400 mg as a positive control to prove the assay could detect a real signal. After the final 4.5 mg dose the upper limit of the two-sided 90% confidence interval for the placebo-adjusted QTcF change was below 10 ms at every timepoint, so the highest dose ever studied does not prolong cardiac repolarisation to a clinically relevant degree.View study

Clinical trials

Cagrilintide tested in people

68 registered studies, 11 still enrolling.

68registered studies
11recruiting now
21phase 3 or 4
9with published results

By phase

Phase 321
Phase 117
Phase 25
No phase25

A trial spanning two phases is counted in both, so these can sum above the total. Observational studies carry no phase.

What kind of research

Gave the drug68
Records only0

About 35,373 people took part in the studies that actually administered Cagrilintide. Observational studies analyse the records of people already taking it — nobody was given anything for the study, so they are counted separately and cannot show cause and effect.

Most recent

  • NCT07357740Phase 2Withdrawn

    A Research Study to Compare Two Different Versions of Injectable CagriSema in People With Type 2 Diabetes

    Novo Nordisk A/S

  • 2023-509176-42-00Ongoing157 enrolled

    NN9838-4968

    Novo Nordisk A/S

  • NCT07282613Phase 3Not Yet Recruiting80 enrolled

    A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Placebo in Children and Adolescents With Type 2 Diabetes

    Novo Nordisk A/S

See all 68 trials for Cagrilintide

Sources: ClinicalTrials.gov, the EU Clinical Trials Information System and ISRCTN, deduplicated so a study registered twice is counted once. A study is counted when Cagrilintide is named as an intervention; studies that only mention it in passing are not.

Questions

Frequently asked about Cagrilintide

How is cagrilintide different from semaglutide?

They work through completely different mechanisms. Semaglutide mimics GLP-1, while cagrilintide mimics amylin - both are natural satiety hormones but they activate different receptors in your brain. Think of them as two different volume knobs for your hunger signals. That's why combining them (CagriSema) works so well - you're turning down appetite through two separate pathways.

When will cagrilintide be FDA approved?

Novo Nordisk submitted CagriSema (the combination of cagrilintide and semaglutide) to the FDA in 2025 based on successful Phase 3 trials. Approval is anticipated, but exact timing depends on the FDA review process. Cagrilintide alone is currently being studied for its own dedicated approval pathway.

Can I use cagrilintide by itself or does it need to be combined with semaglutide?

Cagrilintide works effectively on its own - the Phase 2 trial showed 10.8% weight loss with cagrilintide alone at the highest dose. However, the combination with semaglutide (CagriSema) produces even better results - around 20% weight loss. Your provider can help determine which approach is right for your goals.

What if I'm already on semaglutide - can I add cagrilintide?

Yes, that's actually the strategy behind CagriSema. If you've plateaued on semaglutide or want enhanced results, adding cagrilintide targets a complementary satiety pathway. Clinical trials show the combination significantly outperforms either drug alone for weight loss.

How long until I notice results with cagrilintide?

Most people notice reduced appetite within the first 1-2 weeks. Meaningful weight loss typically becomes apparent by weeks 4-8 as doses are titrated up. Maximum results are seen over 6-12 months of consistent use. Remember, healthy weight loss of 1-2 pounds per week is both safe and sustainable.

Are the side effects better or worse than GLP-1 medications?

The side effect profiles are similar - both primarily cause GI symptoms like nausea and constipation. Some data suggests cagrilintide may be slightly better tolerated, with lower rates of nausea in head-to-head comparisons. Most side effects improve within the first few weeks and can be minimized with gradual dose increases.

Will I regain weight if I stop taking cagrilintide?

Like other weight loss medications, stopping cagrilintide typically leads to weight regain because the underlying biology driving weight gain remains. These medications are designed for long-term use. Maintaining weight loss usually requires ongoing treatment combined with sustained lifestyle changes.

Is cagrilintide safe for people with diabetes?

Yes, cagrilintide has been studied specifically in people with type 2 diabetes. It can improve blood sugar control in addition to promoting weight loss. However, if you're on insulin or sulfonylureas, doses may need adjustment to prevent low blood sugar. Always work with your healthcare provider.

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Every dosing tier, administration route, timing note, and dose-adjustment rule for Cagrilintide, on one page.

Medical disclaimer

Cagrilintide is an investigational research compound not approved by the FDA for human therapeutic use. This information is for educational purposes only and should not be construed as medical advice. Always consult with a qualified healthcare provider before starting any new supplement or treatment protocol.

Last updated: Oct 12, 2026