Where is Cagrilintide being studied?

Find registered human studies, phases, products, recruitment status and reported research locations around the world. Registry search matches are separate from this profile’s reviewed evidence.

Scientific intelligence record

Experience 2.0

Amylin analog

Cagrilintide

Cagrilintide is an amylin analog investigated for weight management, both alone and in combinations such as CagriSema. Evidence for the single agent must be separated from evidence for the combination.

Record status

Traceability partial

Last meaningful update: 9/26/2026

Evidence searched through:
Not recorded
Assessment updated:
9/26/2026
Documented human review:
No documented human review recorded
Automated scientific assessment:
9/26/2026
AI source check:
9/26/2026

Published source links and profile text pass separate gates. Only a documented human review is labelled as human review; an automated scientific assessment applies deterministic checks, and an AI source check confirms only that a source exists and matches its identifiers. A source count alone does not establish a review.

Evidence coverage has three distinct layers. The corpus count is a transparent screening inventory, the featured set contains study-level tiering and interpretation, and the published-source count contains records promoted through the institutional publication workflow. Source validation, editorial publication, and scientific appraisal are separate decisions; these numbers must not be merged.

Ranked research corpus

118

Categorized publications with provisional ranking; scientific review remains separate.

Featured tiered studies

36

Cornerstone publications with study-level interpretation, limitations, and tier disclosure.

Research domains

12

Clinical and scientific questions synthesized independently across the evidence atlas.

Published source records

41

Database records promoted through the governed publication workflow—not the corpus total.

Corpus generated 2026-09-18. Counts remain separately labeled so screening is not represented as completed review.

Human experience · separate evidence stream

No community pattern is displayed yet

Eligible observations remain below the privacy and reliability threshold. WPF will not convert a handful of reports into a percentage, trend, or clinical claim.

Observation is valuable human context. It is not evidence of causation, efficacy, or safety.

Public display gate

n ≥ 20 eligible observations

Exact progress remains private before the threshold.

Intelligence snapshot

The state of the record

A compact view of what is represented, what remains unresolved, and how completely the record can be traced.

Ranked research corpus

118

Categorized screening records; proposed rankings remain pending human appraisal.

Featured tiered studies

36

Cornerstone studies with published study-level interpretation and tier disclosure.

Research domains

12

Independent evidence dossiers covering the major research questions.

Published source records

41

Source records published through the governed workflow; this count does not certify scientific conclusions.

Contradictions

0

Conflicting evidence relationships that remain visible.

Research gaps

1

Questions the current record identifies as unresolved.

Connected media

0

Media records explicitly linked to this scientific record.

What we know

Evidence, claims, and boundaries

The project separates represented evidence from qualification, contradiction, uncertainty, and what the evidence does not establish.

Reconciled domain conclusions

12 published domain syntheses connected to 36 featured studies

Cagrilintide no longer relies on the legacy “no public claim” state. Each research domain publishes a bounded synthesis, confidence level, evidence context, limitations, geographic applicability, regulatory interpretation, and research gaps. Publication of these syntheses is separate from the scientific review status shown above.

Inspect the reconciled evidence atlas
Inspect the published evidence record41 governed records · titles, provenance, and original-source linksOpen records ↓
2026Phase 3 human evidence

Cagrilintide-semaglutide (CagriSema) versus semaglutide or cagrilintide in people with type 2 diabetes (REIMAGINE 2): a double-blind, randomised, controlled, phase 3 study.

Content-verified record concerning Cagrilintide: "Cagrilintide-semaglutide (CagriSema) versus semaglutide or cagrilintide in people with type 2 diabetes (REIMAGINE 2): a double-blind, randomised, controlled, phase 3 study." Abstract excerpt: The amylin receptor agonist cagrilintide and the GLP-1 receptor agonist semaglutide have complementary effects on glycaemic control and bodyweight. We aimed to investigate the efficacy and safety of a fixed-dose combination of cagrilintide and semaglutide (cagrilintide-semaglutide; known as CagriSema) versus semaglutide or cagrilintide for glycaemic control in people with type 2 diabetes and overw

Source
peer_reviewed_research
DOI
10.1016/s2213-8587(26)00125-7
PubMed
42251859
Open original source
2026Phase 3 human evidence

Cagrilintide-semaglutide (CagriSema) as an add-on to basal insulin in adults with type 2 diabetes (REIMAGINE 3): a randomised, double-blind, placebo-controlled, multicentre, phase 3 study.

Content-verified record concerning Cagrilintide: "Cagrilintide-semaglutide (CagriSema) as an add-on to basal insulin in adults with type 2 diabetes (REIMAGINE 3): a randomised, double-blind, placebo-controlled, multicentre, phase 3 study." Abstract excerpt: Basal insulin treatment for type 2 diabetes often results in inadequate glycaemic control and is associated with weight gain and increased risk of hypoglycaemia. We aimed to compare the efficacy and safety of a once per week combination of cagrilintide with semaglutide (CagriSema) versus placebo as an add-on to basal insulin in individuals with type 2 diabetes. This double-blind, parallel-group, r

Source
peer_reviewed_research
DOI
10.1016/s0140-6736(26)01022-6
PubMed
42251856
Open original source
2021Phase 1–2 human evidence

Safety, tolerability, pharmacokinetics, and pharmacodynamics of concomitant administration of multiple doses of cagrilintide with semaglutide 2·4 mg for weight management: a randomised, controlled, phase 1b trial.

Content-verified record concerning Cagrilintide: "Safety, tolerability, pharmacokinetics, and pharmacodynamics of concomitant administration of multiple doses of cagrilintide with semaglutide 2·4 mg for weight management: a randomised, controlled, phase 1b trial." Abstract excerpt: Cagrilintide, a long-acting amylin analogue, and semaglutide 2·4 mg, a glucagon-like peptide-1 analogue, are both being investigated as options for weight management. We aimed to determine the safety, tolerability, pharmacokinetics, and pharmacodynamics of this drug combination. In this randomised, placebo-controlled, multiple-ascending dose, phase 1b trial, individuals aged 18-55 years with

Source
peer_reviewed_research
DOI
10.1016/s0140-6736(21)00845-x
PubMed
33894838
Open original source
2021Phase 1–2 human evidence

Once-weekly cagrilintide for weight management in people with overweight and obesity: a multicentre, randomised, double-blind, placebo-controlled and active-controlled, dose-finding phase 2 trial.

Content-verified record concerning Cagrilintide: "Once-weekly cagrilintide for weight management in people with overweight and obesity: a multicentre, randomised, double-blind, placebo-controlled and active-controlled, dose-finding phase 2 trial." Abstract excerpt: Natural amylin is a pancreatic hormone that induces satiety. Cagrilintide is a long-acting amylin analogue under investigation for weight management. We assessed the dose-response relationship of cagrilintide regarding the effects on bodyweight, safety, and tolerability. We conducted a multicentre, randomised, double-blind, placebo-controlled and active-controlled, dose-finding phase 2 trial at 57

Source
peer_reviewed_research
DOI
10.1016/s0140-6736(21)01751-7
PubMed
34798060
Open original source
2026Phase 1–2 human evidence

Efficacy and safety of once-weekly cagrilintide-semaglutide (CagriSema) in adults with type 2 diabetes inadequately controlled on diet and exercise (REIMAGINE 1): a randomised, double-blind, placebo-controlled, phase 3a study.

Content-verified record concerning Cagrilintide: "Efficacy and safety of once-weekly cagrilintide-semaglutide (CagriSema) in adults with type 2 diabetes inadequately controlled on diet and exercise (REIMAGINE 1): a randomised, double-blind, placebo-controlled, phase 3a study." Abstract excerpt: Cagrilintide-semaglutide (CagriSema) is a novel, once-weekly combination of the amylin receptor agonist cagrilintide and the GLP-1 receptor agonist semaglutide. We aimed to assess the efficacy and safety of cagrilintide-semaglutide for people with type 2 diabetes inadequately controlled with diet and exercise. REIMAGINE 1 was a randomised, double-blind, parallel-group, phase 3a study carried out a

Source
peer_reviewed_research
DOI
10.1016/s2213-8587(26)00126-9
PubMed
42251860
Open original source
2026Phase 1–2 human evidence

Efficacy and safety of co-administered cagrilintide and semaglutide versus semaglutide alone in adults with overweight or obesity with or without type 2 diabetes in Japan and Taiwan (REDEFINE 5): a multicentre, randomised, active-controlled, phase 3a trial.

Content-verified record concerning Cagrilintide: "Efficacy and safety of co-administered cagrilintide and semaglutide versus semaglutide alone in adults with overweight or obesity with or without type 2 diabetes in Japan and Taiwan (REDEFINE 5): a multicentre, randomised, active-controlled, phase 3a trial." Abstract excerpt: The combination of cagrilintide and semaglutide has been shown in global studies to induce reductions in bodyweight. We assessed the efficacy and safety of a fixed-dose combination of cagrilintide 2·4 mg and semaglutide 2·4 mg versus semaglutide 2·4 mg for weight management in an east Asian population. This double-blind, parallel-group, phase 3a trial (REDEFINE 5) was conducted acro

Source
peer_reviewed_research
DOI
10.1016/s2213-8587(25)00402-4
PubMed
42009015
Open original source
2023Phase 1–2 human evidence

Efficacy and safety of co-administered once-weekly cagrilintide 2·4 mg with once-weekly semaglutide 2·4 mg in type 2 diabetes: a multicentre, randomised, double-blind, active-controlled, phase 2 trial.

Content-verified record concerning Cagrilintide: "Efficacy and safety of co-administered once-weekly cagrilintide 2·4 mg with once-weekly semaglutide 2·4 mg in type 2 diabetes: a multicentre, randomised, double-blind, active-controlled, phase 2 trial." Abstract excerpt: Combining the GLP-1 receptor agonist semaglutide with the long-acting amylin analogue cagrilintide has weight-loss benefits; the impact on glycated haemoglobin (HbA 1c ) is unknown. This trial assessed the efficacy and safety of co-administered semaglutide with cagrilintide (CagriSema) in participants with type 2 diabetes. This 32-week, multicentre, double-blind, phase 2 trial was conducted across

Source
peer_reviewed_research
DOI
10.1016/s0140-6736(23)01163-7
PubMed
37364590
Open original source
2025Animal research

Coadministered Cagrilintide and Semaglutide in Adults with Overweight or Obesity.

Directly concerns the combination in adults with overweight or obesity; does not isolate cagrilintide alone.

Source
peer_reviewed_research
DOI
10.1056/NEJMoa2502081
PubMed
40544433
Open original source
2025Animal research

In adults with overweight or obesity, weekly subcutaneous cagrilintide-semaglutide increased weight loss at 68 wk.

Content-verified record concerning Cagrilintide: "In adults with overweight or obesity, weekly subcutaneous cagrilintide-semaglutide increased weight loss at 68 wk." Abstract excerpt: GIM/FP/GP: [Formula: see text].

Source
peer_reviewed_research
DOI
10.7326/annals-25-03745-jc
PubMed
41052437
Open original source
2026Animal research

Cagrilintide and retatrutide combination therapy enhances weight loss and metabolic outcomes in obese male rats.

Content-verified record concerning Cagrilintide: "Cagrilintide and retatrutide combination therapy enhances weight loss and metabolic outcomes in obese male rats." Abstract excerpt: Peptide multi-receptor agonists have advanced obesity treatment, yet challenges remain in achieving maximal weight loss and metabolic control, especially in patients with obesity and type 2 diabetes. Here we demonstrate enhanced metabolic benefits of a combination therapy with retatrutide, a unimolecular GLP-1R/GIPR/GCGR tri-agonist, and cagrilintide, an AMLNR/CALCR co-agonist, in diet-induced obe

Source
peer_reviewed_research
DOI
10.1038/s42255-026-01603-y
PubMed
42744908
Open original source
2026Animal research

A cross-species atlas of the dorsal vagal complex reveals neural mediators of the effects of cagrilintide on energy balance.

Content-verified record concerning Cagrilintide: "A cross-species atlas of the dorsal vagal complex reveals neural mediators of the effects of cagrilintide on energy balance." Abstract excerpt: Amylin receptor agonists such as cagrilintide represent emerging obesity therapies. To understand mediators of cagrilintide action, we generated a transcriptomics atlas of over 530,000 cells comprising 80 neuronal cell populations across rat, mouse and macaque caudal brainstem, with spatial profiling to map distribution in the rat dorsal vagal complex (DVC). Here we show that cagrilintide regulate

Source
peer_reviewed_research
DOI
10.1038/s42255-026-01539-3
PubMed
42260119
Open original source
2025Animal research

Cagrilintide-Semaglutide in Adults with Overweight or Obesity and Type 2 Diabetes.

Content-verified record concerning Cagrilintide: "Cagrilintide-Semaglutide in Adults with Overweight or Obesity and Type 2 Diabetes." Abstract excerpt: Cagrilintide and semaglutide have each been shown to induce weight loss as monotherapies. Data are needed on the coadministration of cagrilintide and semaglutide (called CagriSema) for weight management in adults with type 2 diabetes, including those in a subgroup who are undergoing continuous glucose monitoring. In this phase 3a, double-blind, randomized, placebo-controlled trial conducted in 12

Source
peer_reviewed_research
DOI
10.1056/NEJMoa2502082
PubMed
40544432
Open original source
2022Animal research

Does receptor balance matter? - Comparing the efficacies of the dual amylin and calcitonin receptor agonists cagrilintide and KBP-336 on metabolic parameters in preclinical models.

Content-verified record concerning Cagrilintide: "Does receptor balance matter? - Comparing the efficacies of the dual amylin and calcitonin receptor agonists cagrilintide and KBP-336 on metabolic parameters in preclinical models." Abstract excerpt: Cagrilintide is a novel long-acting amylin receptor agonist, which has shown a potent induction of weight loss. Interestingly, cagrilintide is a Dual Amylin and Calcitonin Receptor Agonist (DACRA) derived from an amylin backbone. Another class of long-acting DACRAs exists, namely the KBPs. These are salmon calcitonin-based and have shown preclinical potential; however, how and if they differentiat

Source
peer_reviewed_research
DOI
10.1016/j.biopha.2022.113842
PubMed
36242844
Open original source
2025Animal research

Characterization of 0839 - A tool compound for pre-clinical mode-of-action studies of amylin analogues such as cagrilintide.

Content-verified record concerning Cagrilintide: "Characterization of 0839 - A tool compound for pre-clinical mode-of-action studies of amylin analogues such as cagrilintide." Abstract excerpt: Cagrilintide (also known as 0833) is an amylin and calcitonin receptor agonist in clinical development for weight management and type-2-diabetes in a fixed-dose combination with semaglutide. Here, we introduce 0174-0839 (0839) as a tool compound for mouse and rat in vivo and in vitro studies of amylin analogues such as cagrilintide. Structurally, 0839 shares 95 % sequence homology with 0833 a

Source
peer_reviewed_research
DOI
10.1016/j.lfs.2025.123845
PubMed
40628316
Open original source
2024Laboratory research

Cagrilintide: A Long-Acting Amylin Analog for the Treatment of Obesity.

Content-verified record concerning Cagrilintide: "Cagrilintide: A Long-Acting Amylin Analog for the Treatment of Obesity." Abstract excerpt: Despite the worldwide epidemic of obesity, there remain few approved pharmacological treatment options to bridge the gap between lifestyle therapy and bariatric surgery. Cagrilintide is an amylin-analog, now being developed in combination with the GLP-1 agonist semaglutide to achieve sustained weight loss in persons with overweight and obesity. Amylin, released with insulin from beta cells in the

Source
peer_reviewed_research
DOI
10.1097/CRD.0000000000000513
PubMed
36883831
Open original source
Insufficient evidence

A Cross-Species Atlas of the Dorsal Vagal Complex Reveals Neural Mediators of Cagrilintide’s Effects on Energy Balance

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1101/2025.01.13.632726
Open original source
Insufficient evidence

A combined cryo_EM structure of Cagrilintide-CTR-Gs complex

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.2210/pdb9uwm/pdb
Open original source
Insufficient evidence

A combined Cryo_EM structure of Cagrilintide-AMY1R-Gs complex

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.2210/pdb9uwq/pdb
Open original source
Insufficient evidence

1969-LB: Effect of Combined Therapy with Once-Weekly Subcutaneous Cagrilintide 2.4 mg and Semaglutide 2.4 mg (CagriSema) on Energy Intake, Gastric Emptying, and Appetite in Adults with Overweight or Obesity

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.2337/db25-1969-lb
Open original source
2026Insufficient evidence

Cagrilintide-semaglutide: a new option for patients with type 2 diabetes.

Content-verified record concerning Cagrilintide: "Cagrilintide-semaglutide: a new option for patients with type 2 diabetes." (identity confirmed; no abstract text available to excerpt.)

Source
peer_reviewed_research
DOI
10.1016/s2213-8587(26)00129-4
PubMed
42251858
Open original source
2024Insufficient evidence

Cagrilintide is not associated with clinically relevant QTc prolongation: A thorough QT study in healthy participants.

Content-verified record concerning Cagrilintide: "Cagrilintide is not associated with clinically relevant QTc prolongation: A thorough QT study in healthy participants." Abstract excerpt: The combination of cagrilintide and semaglutide (CagriSema) is being developed for the treatment of obesity and type 2 diabetes. The objective of this thorough QT study was to confirm that cagrilintide does not result in a clinically relevant prolongation in cardiac repolarization compared with placebo. This was a double-blind study (NCT05804162) in which healthy participants were randomized to ca

Source
peer_reviewed_research
DOI
10.1111/dom.15951
PubMed
39279639
Open original source
2026Insufficient evidence

Cagrilintide and CagriSema for weight reduction and metabolic risk modification in overweight or obesity: a systematic review and meta-analysis.

Content-verified record concerning Cagrilintide: "Cagrilintide and CagriSema for weight reduction and metabolic risk modification in overweight or obesity: a systematic review and meta-analysis." Abstract excerpt: Obesity is a global health challenge associated with substantial cardiometabolic morbidity. Cagrilintide, a long-acting amylin analogue, alone or in combination with semaglutide (CagriSema), has emerged as a novel pharmacologic strategy for weight management. We conducted a systematic review and meta-analysis to evaluate the efficacy and safety of cagrilintide-based therapies in adults with overwe

Source
systematic_review_or_meta_analysis
DOI
10.1007/s40200-026-01942-3
PubMed
42180166
Open original source
2026Insufficient evidence

Efficacy and Safety of Cagrilintide and Cagrisema Versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression.

Content-verified record concerning Cagrilintide: "Efficacy and Safety of Cagrilintide and Cagrisema Versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression." Abstract excerpt: Obesity is a complex chronic disease requiring effective long-term management. We performed a systematic review and meta-analysis to evaluate the efficacy and safety of cagrisema and cagrilintide monotherapy compared with semaglutide in individuals with obesity. We searched MEDLINE, Embase, Scopus, Cochrane, and ClinicalTrials.gov for randomized controlled trials accessing cagrisema or cagrilintid

Source
systematic_review_or_meta_analysis
DOI
10.1111/dom.70667
PubMed
41834765
Open original source
2024Insufficient evidence

Efficacy and Safety of Cagrilintide Alone and in Combination with Semaglutide (Cagrisema) as Anti-Obesity Medications: A Systematic Review and Meta-Analysis.

Content-verified record concerning Cagrilintide: "Efficacy and Safety of Cagrilintide Alone and in Combination with Semaglutide (Cagrisema) as Anti-Obesity Medications: A Systematic Review and Meta-Analysis." Abstract excerpt: No meta-analysis has analysed role of cagrilintide as weight-loss medication in obese individuals. Electronic databases were searched for RCTs involving obese individuals receiving cagrilintide or cagrilintide-2.4 mg with semaglutide-2.4 mg combination (Cagrisema) compared to placebo/active comparator. Primary outcomes were changes in body weight; secondary outcomes were alterations in glycemia, l

Source
systematic_review_or_meta_analysis
DOI
10.4103/ijem.ijem_45_24
PubMed
39676787
Open original source
2026Insufficient evidence

Amylin-based obesity therapy: a meta-analysis of Cagrilintide and CagriSema versus placebo.

Content-verified record concerning Cagrilintide: "Amylin-based obesity therapy: a meta-analysis of Cagrilintide and CagriSema versus placebo." Abstract excerpt: Obesity remains a major global health challenge, driving demand for effective pharmacotherapies. Cagrilintide, a once-weekly amylin receptor agonist, and its fixed-dose combination with semaglutide (CagriSema) represent novel therapeutic approaches. This systematic review and meta-analysis evaluated their efficacy and safety in adults with overweight or obesity. Four databases were searched from i

Source
systematic_review_or_meta_analysis
DOI
10.1097/ms9.0000000000005353
PubMed
42583410
Open original source
2026Insufficient evidence

Renal or Hepatic Impairment Does Not Affect Pharmacokinetics, Safety, or Tolerability of Subcutaneous Cagrilintide.

Content-verified record concerning Cagrilintide: "Renal or Hepatic Impairment Does Not Affect Pharmacokinetics, Safety, or Tolerability of Subcutaneous Cagrilintide." Abstract excerpt: Cagrilintide is a long-acting amylin agonist under development as monotherapy for weight management and as a fixed-dose combination with the glucagon-like peptide-1 receptor agonist semaglutide (CagriSema) for weight management and treatment of type 2 diabetes. Two studies were conducted to assess the effects of renal or hepatic impairment on pharmacokinetics, safety and tolerability following sin

Source
peer_reviewed_research
DOI
10.1007/s40262-026-01654-0
PubMed
42228334
Open original source
2021Insufficient evidence

Development of Cagrilintide, a Long-Acting Amylin Analogue.

Content-verified record concerning Cagrilintide: "Development of Cagrilintide, a Long-Acting Amylin Analogue." Abstract excerpt: A hallmark of the pancreatic hormone amylin is its high propensity toward the formation of amyloid fibrils, which makes it a challenging drug design effort. The amylin analogue pramlintide is commercially available for diabetes treatment as an adjunct to insulin therapy but requires three daily injections due to its short half-life. We report here the development of the stable, lipidated long-acti

Source
peer_reviewed_research
DOI
10.1021/acs.jmedchem.1c00565
PubMed
34288673
Open original source
2025Insufficient evidence

Cagrilintide-Semaglutide in Adults with Overweight or Obesity.

Content-verified record concerning Cagrilintide: "Cagrilintide-Semaglutide in Adults with Overweight or Obesity." (identity confirmed; no abstract text available to excerpt.)

Source
peer_reviewed_research
DOI
10.1056/nejmc2513141
PubMed
41259764
Open original source
2026Insufficient evidence

Cellular loci for cagrilintide action identified.

Content-verified record concerning Cagrilintide: "Cellular loci for cagrilintide action identified." (identity confirmed; no abstract text available to excerpt.)

Source
peer_reviewed_research
DOI
10.1038/s42255-026-01541-9
PubMed
42260118
Open original source
2021Insufficient evidence

Cagrilintide plus semaglutide for obesity management.

Content-verified record concerning Cagrilintide: "Cagrilintide plus semaglutide for obesity management." (identity confirmed; no abstract text available to excerpt.)

Source
peer_reviewed_research
DOI
10.1016/s0140-6736(21)00944-2
PubMed
33894837
Open original source
Insufficient evidence

Comparative Effectiveness of CagriSegma, Semaglutide, Cagrilintide and Tirzepatide in the Management of Overweight and Obesity: A Network Meta-Analysis of Randomized Clinical Trials.

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1002/edm2.70248
PubMed
42207966
Open original source
Insufficient evidence

Decision letter for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1111/dom.70667/v1/decision1
Open original source
Insufficient evidence

26-A-15734-ACC CAGRILINTIDE-SEMAGLUTIDE (CAGRISEMA) VS SEMAGLUTIDE: SUPERIOR WEIGHT LOSS AND COMPARABLE SAFETY THROUGH SYNERGISTIC AMYLIN-GLP-1 CO-THERAPY: A META-ANALYSIS

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1016/j.jacc.2026.02.688
Open original source
Insufficient evidence

1713-P: AT7687, a Novel GIP-Receptor Antagonist, Combined with Cagrilintide, Leads to Robust Weight Loss and Substantial Improvements in Insulin Sensitivity and Body Composition in Obese Insulin-Resistant Monkeys

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.2337/db26-1713-p
Open original source
Insufficient evidence

Structural and mechanistic insights into dual activation of cagrilintide in amylin and calcitonin receptors.

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1038/s41401-025-01635-2
PubMed
40847076
Open original source
Insufficient evidence

Review for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1111/dom.70667/v2/review1
Open original source
Insufficient evidence

26-A-9711-ACC CAGRISEMA VERSUS CAGRILINTIDE OR SEMAGLUTIDE MONOTHERAPY AS ANTI-OBESITY MEDICATIONS: A SYSTEMATIC REVIEW AND BAYESIAN NETWORK META-ANALYSIS WITH TRIAL SEQUENTIAL ANALYSIS

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1016/j.jacc.2026.02.652
Open original source
Insufficient evidence

Author response for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1111/dom.70667/v2/response1
Open original source
Insufficient evidence

Decision letter for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1111/dom.70667/v2/decision1
Open original source
Insufficient evidence

2458-P: Arcuate Hypothalamic Circuits Mediate Acute Cagrilintide-Induced Feeding in Mice

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.2337/db26-2458-p
Open original source
Insufficient evidence

Review for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

Source reference associated with Cagrilintide. Source identity and peptide connection confirmed; scientific conclusions and evidence strength have not been assessed in this source-linking step.

Source
other
DOI
10.1111/dom.70667/v1/review3
Open original source

Scientific context

Chemistry and represented biological context

Existing reviewed chemistry is preserved as scientific context. Chemistry and mechanism information do not establish clinical efficacy or safety.

Open chemistry and biological context ↓
Chemical identity

Molecular and structural record

Structured record
Molecular formula
C194H312N54O59S2
Molecular weight (Da)
4409
InChI
InChI=1S/C194H312N54O59S2/c1-19-100(10)151(184(298)233-128(78-98(6)7)189(303)248-75-49-60-137(248)190(304)247-74-48-59-136(247)182(296)243-155(107(17)255)187(301)232-127(86-143(201)262)173(287)238-150(99(8)9)183(297)210-88-146(265)218-129(90-249)176(290)230-126(85-142(200)261)175(289)244-156(108(18)256)191(305)246-73-46-57-134(246)157(202)271)239-181(295)135-58-47-72-245(135)147(266)89-211-161(275)120(79-109-50-36-34-37-51-109)225-171(285)123(82-139(197)258)228-172(286)124(83-140(198)259)229-177(291)130(91-250)235-178(292)131(92-251)234-170(284)122(81-111-87-207-95-212-111)227-164(278)114(56-45-71-209-194(205)206)221-168(282)119(77-97(4)5)224-169(283)121(80-110-52-38-35-39-53-110)226-166(280)116(65-68-149(269)270)219-158(272)101(11)213-167(281)118(76-96(2)3)223-163(277)113(55-44-70-208-193(203)204)220-165(279)115(63-66-138(196)257)222-186(300)153(105(15)253)240-159(273)102(12)214-179(293)132-93-308-309-94-133(180(294)231-125(84-141(199)260)174(288)242-152(104(14)252)185(299)215-103(13)160(274)241-154(106(16)254)188(302)237-132)236-162(276)112(54-42-43-69-195)216-145(264)67-64-117(192(306)307)217-144(263)61-40-32-30-28-26-24-22-20-21-23-25-27-29-31-33-41-62-148(267)268/h34-39,50-53,87,95-108,112-137,150-156,249-256H,19-33,40-49,54-86,88-94,195H2,1-18H3,(H2,196,257)(H2,197,258)(H2,198,259)(H2,199,260)(H2,200,261)(H2,201,262)(H2,202,271)(H,207,212)(H,210,297)(H,211,275)(H,213,281)(H,214,293)(H,215,299)(H,216,264)(H,217,263)(H,218,265)(H,219,272)(H,220,279)(H,221,282)(H,222,300)(H,223,277)(H,224,283)(H,225,285)(H,226,280)(H,227,278)(H,228,286)(H,229,291)(H,230,290)(H,231,294)(H,232,301)(H,233,298)(H,234,284)(H,235,292)(H,236,276)(H,237,302)(H,238,287)(H,239,295)(H,240,273)(H,241,274)(H,242,288)(H,243,296)(H,244,289)(H,267,268)(H,269,270)(H,306,307)(H4,203,204,208)(H4,205,206,209)/t100-,101-,102-,103-,104+,105+,106+,107+,108+,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123+,124-,125-,126-,127-,128-,129-,130-,131-,132-,133-,134-,135-,136-,137-,150-,151-,152-,153-,154-,155-,156-/m0/s1
InChIKey
LDERDVMBIYGIOI-DDPFBLHVSA-N

Chemical identity describes the recorded molecular information. It does not establish biological activity, clinical efficacy, safety, or therapeutic suitability.

Research

How the scientific record is developing

Chronology, unresolved research questions, opportunities, and researcher activity remain descriptive rather than evaluative.

Research chronology

  1. 2021 · study · Temporal status not established

    Safety, tolerability, pharmacokinetics, and pharmacodynamics of concomitant administration of multiple doses of cagrilintide with semaglutide 2·4 mg for weight management: a randomised, controlled, phase 1b trial.

    peer_reviewed_research

  2. 2021 · study · Temporal status not established

    Once-weekly cagrilintide for weight management in people with overweight and obesity: a multicentre, randomised, double-blind, placebo-controlled and active-controlled, dose-finding phase 2 trial.

    peer_reviewed_research

  3. 2021 · study · Temporal status not established

    Development of Cagrilintide, a Long-Acting Amylin Analogue.

    peer_reviewed_research

  4. 2021 · study · Temporal status not established

    Cagrilintide plus semaglutide for obesity management.

    peer_reviewed_research

  5. 2022 · study · Temporal status not established

    Does receptor balance matter? - Comparing the efficacies of the dual amylin and calcitonin receptor agonists cagrilintide and KBP-336 on metabolic parameters in preclinical models.

    peer_reviewed_research

  6. 2023 · study · Temporal status not established

    Efficacy and safety of co-administered once-weekly cagrilintide 2·4 mg with once-weekly semaglutide 2·4 mg in type 2 diabetes: a multicentre, randomised, double-blind, active-controlled, phase 2 trial.

    peer_reviewed_research

  7. 2024 · study · Temporal status not established

    Cagrilintide: A Long-Acting Amylin Analog for the Treatment of Obesity.

    peer_reviewed_research

  8. 2024 · study · Temporal status not established

    Cagrilintide is not associated with clinically relevant QTc prolongation: A thorough QT study in healthy participants.

    peer_reviewed_research

  9. 2024 · study · Temporal status not established

    Efficacy and Safety of Cagrilintide Alone and in Combination with Semaglutide (Cagrisema) as Anti-Obesity Medications: A Systematic Review and Meta-Analysis.

    systematic_review_or_meta_analysis

  10. 2025 · study · Temporal status not established

    Coadministered Cagrilintide and Semaglutide in Adults with Overweight or Obesity.

    peer_reviewed_research

  11. 2025 · study · Temporal status not established

    In adults with overweight or obesity, weekly subcutaneous cagrilintide-semaglutide increased weight loss at 68 wk.

    peer_reviewed_research

  12. 2025 · study · Temporal status not established

    Cagrilintide-Semaglutide in Adults with Overweight or Obesity and Type 2 Diabetes.

    peer_reviewed_research

  13. 2025 · study · Temporal status not established

    Characterization of 0839 - A tool compound for pre-clinical mode-of-action studies of amylin analogues such as cagrilintide.

    peer_reviewed_research

  14. 2025 · study · Temporal status not established

    Cagrilintide-Semaglutide in Adults with Overweight or Obesity.

    peer_reviewed_research

  15. 2026 · study · Temporal status not established

    Cagrilintide-semaglutide (CagriSema) versus semaglutide or cagrilintide in people with type 2 diabetes (REIMAGINE 2): a double-blind, randomised, controlled, phase 3 study.

    peer_reviewed_research

  16. 2026 · study · Temporal status not established

    Cagrilintide-semaglutide (CagriSema) as an add-on to basal insulin in adults with type 2 diabetes (REIMAGINE 3): a randomised, double-blind, placebo-controlled, multicentre, phase 3 study.

    peer_reviewed_research

  17. 2026 · study · Temporal status not established

    Efficacy and safety of once-weekly cagrilintide-semaglutide (CagriSema) in adults with type 2 diabetes inadequately controlled on diet and exercise (REIMAGINE 1): a randomised, double-blind, placebo-controlled, phase 3a study.

    peer_reviewed_research

  18. 2026 · study · Temporal status not established

    Efficacy and safety of co-administered cagrilintide and semaglutide versus semaglutide alone in adults with overweight or obesity with or without type 2 diabetes in Japan and Taiwan (REDEFINE 5): a multicentre, randomised, active-controlled, phase 3a trial.

    peer_reviewed_research

  19. 2026 · study · Temporal status not established

    Cagrilintide and retatrutide combination therapy enhances weight loss and metabolic outcomes in obese male rats.

    peer_reviewed_research

  20. 2026 · study · Temporal status not established

    A cross-species atlas of the dorsal vagal complex reveals neural mediators of the effects of cagrilintide on energy balance.

    peer_reviewed_research

  21. 2026 · study · Temporal status not established

    Cagrilintide-semaglutide: a new option for patients with type 2 diabetes.

    peer_reviewed_research

  22. 2026 · study · Temporal status not established

    Cagrilintide and CagriSema for weight reduction and metabolic risk modification in overweight or obesity: a systematic review and meta-analysis.

    systematic_review_or_meta_analysis

  23. 2026 · study · Temporal status not established

    Efficacy and Safety of Cagrilintide and Cagrisema Versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression.

    systematic_review_or_meta_analysis

  24. 2026 · study · Temporal status not established

    Amylin-based obesity therapy: a meta-analysis of Cagrilintide and CagriSema versus placebo.

    systematic_review_or_meta_analysis

  25. 2026 · study · Temporal status not established

    Renal or Hepatic Impairment Does Not Affect Pharmacokinetics, Safety, or Tolerability of Subcutaneous Cagrilintide.

    peer_reviewed_research

  26. 2026 · study · Temporal status not established

    Cellular loci for cagrilintide action identified.

    peer_reviewed_research

  27. 2026 · regulatory · Temporal status not established

    Regulatory review: not_approved

    European Union — EMA

  28. 2026 · regulatory · Temporal status not established

    Regulatory review: not_approved

    United States — FDA

  29. Date unavailable · study · Temporal status not established

    A Cross-Species Atlas of the Dorsal Vagal Complex Reveals Neural Mediators of Cagrilintide’s Effects on Energy Balance

    other

  30. Date unavailable · study · Temporal status not established

    A combined cryo_EM structure of Cagrilintide-CTR-Gs complex

    other

  31. Date unavailable · study · Temporal status not established

    A combined Cryo_EM structure of Cagrilintide-AMY1R-Gs complex

    other

  32. Date unavailable · study · Temporal status not established

    1969-LB: Effect of Combined Therapy with Once-Weekly Subcutaneous Cagrilintide 2.4 mg and Semaglutide 2.4 mg (CagriSema) on Energy Intake, Gastric Emptying, and Appetite in Adults with Overweight or Obesity

    other

  33. Date unavailable · study · Temporal status not established

    Comparative Effectiveness of CagriSegma, Semaglutide, Cagrilintide and Tirzepatide in the Management of Overweight and Obesity: A Network Meta-Analysis of Randomized Clinical Trials.

    other

  34. Date unavailable · study · Temporal status not established

    Decision letter for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

    other

  35. Date unavailable · study · Temporal status not established

    26-A-15734-ACC CAGRILINTIDE-SEMAGLUTIDE (CAGRISEMA) VS SEMAGLUTIDE: SUPERIOR WEIGHT LOSS AND COMPARABLE SAFETY THROUGH SYNERGISTIC AMYLIN-GLP-1 CO-THERAPY: A META-ANALYSIS

    other

  36. Date unavailable · study · Temporal status not established

    1713-P: AT7687, a Novel GIP-Receptor Antagonist, Combined with Cagrilintide, Leads to Robust Weight Loss and Substantial Improvements in Insulin Sensitivity and Body Composition in Obese Insulin-Resistant Monkeys

    other

  37. Date unavailable · study · Temporal status not established

    Structural and mechanistic insights into dual activation of cagrilintide in amylin and calcitonin receptors.

    other

  38. Date unavailable · study · Temporal status not established

    Review for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

    other

  39. Date unavailable · study · Temporal status not established

    26-A-9711-ACC CAGRISEMA VERSUS CAGRILINTIDE OR SEMAGLUTIDE MONOTHERAPY AS ANTI-OBESITY MEDICATIONS: A SYSTEMATIC REVIEW AND BAYESIAN NETWORK META-ANALYSIS WITH TRIAL SEQUENTIAL ANALYSIS

    other

  40. Date unavailable · study · Temporal status not established

    Author response for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

    other

  41. Date unavailable · study · Temporal status not established

    Decision letter for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

    other

  42. Date unavailable · study · Temporal status not established

    2458-P: Arcuate Hypothalamic Circuits Mediate Acute Cagrilintide-Induced Feeding in Mice

    other

  43. Date unavailable · study · Temporal status not established

    Review for "Efficacy and Safety of Cagrilintide and Cagrisema versus Semaglutide as Anti-Obesity Medications: A Systematic Review, Meta-Analysis and Meta-Regression"

    other

The represented chronology reflects records currently included in the governed dataset and does not claim to represent the entire scientific literature.

What still needs investigation

Claim traceability

No institutional claim record is currently represented for this peptide.

Evidence is missing or not represented as studied; this is not a conclusion that the intervention does not work.

Connections

Follow the scientific relationships

Connections appear only when they are represented by the project’s underlying records.

Open 3 represented connections ↓

institution

peer_reviewed_research

represented evidence source

institution

other

represented evidence source

institution

systematic_review_or_meta_analysis

represented evidence source

Traceability

Follow the record back to its source

The experience makes incomplete links visible instead of presenting a false impression of perfect provenance.

Source publication state

A governed source may be verified and approved for publication while its claim-to-evidence link is still incomplete.

Reviewer provenance state

“Human scientist reviewed: no” means that specific source-path attribution is not recorded. It does not silently negate the separate publication-review state.

Domain conclusion → Evidence

Connected

Evidence → Source

Connected

Source → Original record

Connected

Traceability documents how the project connects statements to records. It does not establish that a source is scientifically valid or that a claim is clinically true.

Reconciled for 12 domain conclusions and 36 featured studies.

Detailed study-to-domain mappings and original-source paths appear in the Cagrilintide evidence-governance section.

Inspect the ranked source records

Observational archive

What contributors reported

Observational archive data is intentionally separated from published scientific evidence.

Observational boundary

Insufficient eligible observations are available for display under the current filters.

Insufficient eligible observations are currently represented to display aggregated findings for this peptide.

Regulatory context

Published jurisdictional records

Regulatory status is jurisdiction-specific and time-dependent. It is presented as context, not as a recommendation for use or a substitute for scientific evidence evaluation.

United States — FDA

Regulator: FDA

not_approved

As of: 9/23/2026 · Temporal status not established

FDA Drugs@FDA database

Research + media

Media connected to this scientific record

Only media explicitly linked through the project’s relationship system appears here.

No scientifically connected media is currently represented for this peptide.

Sources + provenance

Read the scientific record with its boundaries intact

The public record organizes reviewed evidence; it does not establish scientific truth by itself.
Association, mechanism, observation and regulatory status must not be represented as proof of clinical efficacy or safety.
Observational reports describe contributor experiences and cannot establish causation, effectiveness, safety or clinical benefit.
Contradictory and qualifying evidence must remain visible rather than being silently discarded.
Absence of represented evidence is not evidence that research does not exist.
Research gaps identify unresolved questions; they are not negative conclusions.
Regulatory status is distinct from scientific evidence quality.
Media relationships provide context and explanation; they do not increase the strength of scientific evidence.
A section with no represented records is an incomplete project record, not a scientific conclusion.
Researcher and institutional relationships are shown only when supported by represented records and must not be interpreted as rankings or endorsements.

Generated: 11/8/2026, 5:28:48 PM

global evidence atlas

Cagrilintide research, ranked and separated by purpose

This is a deduplicated literature screening registry—not a claim that every mention directly proves efficacy or safety. Machine proposals remain visibly separate from governed human appraisal.

Investigational boundary: Cagrilintide is not presented here as FDA-approved, and screening records must not be interpreted as established clinical benefit.

118Discoverable source universe
118Ranked screening records
12Research domains
2Governed published sources

118 matching records · ranked 2026-09-18

Page 1 of 5

#16Proposed tier Arandomized trialAwaiting human appraisal

Efficacy and safety of co-administered cagrilintide and semaglutide versus semaglutide alone in adults with overweight or obesity with or without type 2 diabetes in Japan and Taiwan (REDEFINE 5): a multicentre, randomised, active-controlled, phase 3a trial.

The lancet. Diabetes & endocrinology · 2026 Jun · PMID 42009015 · DOI 10.1016/S2213-8587(25)00402-4

Weight loss and obesity · CagriSema combination evidence · Monotherapy evidence · Type 2 diabetes and glycemia · Safety and tolerability · Comparative effectiveness · Ongoing development

Count reconciliation: 118 discoverable source records match the peptide identity query; 118 are retained in this bounded, ranked screening view; 2 belong to the separate governed layer labeled “Governed published sources.” Domain totals overlap because one publication may inform several questions.

Cagrilintide evidence · ranking key

How evidence is ranked

A tier describes the evidentiary role and design strength of a source. It is not a popularity score, proof that every conclusion is correct, or a substitute for claim-level review.

A

Practice-defining evidence

Large, well-conducted randomized trials; prespecified major outcomes; rigorous systematic reviews or meta-analyses; and major regulatory assessments.

B

Strong supporting evidence

Smaller randomized trials, strong prospective cohorts, prespecified secondary analyses, and high-quality comparative-effectiveness studies.

C

Contextual evidence

Retrospective cohorts, claims-database studies, pharmacovigilance analyses, mechanistic human research, and well-documented case series.

D

Signal-generating evidence

Case reports, conference abstracts, preclinical research, hypothesis-generating analyses, and expert commentary.

Tier and confidence answer different questions

Tier classifies source design and evidentiary role. Confidence reflects risk of bias, sample size, comparator quality, outcome relevance, follow-up, missing data, directness, replication, reporting quality, and whether conclusions stay within the measured results.

Funding and conflicts are disclosed and considered, but sponsorship never automatically changes a tier. Corrections, retractions, and expressions of concern override the original rating.

Suggested citation

  • APA

    World Peptide Foundation. (n.d.). Cagrilintide — Peptide Scientific Intelligence. World Peptide Foundation. (Updated September 26, 2026.) https://www.worldpeptidefoundation.org/directory/cagrilintide

  • AMA / Vancouver

    World Peptide Foundation. Cagrilintide — Peptide Scientific Intelligence. World Peptide Foundation website. Updated September 26, 2026. https://www.worldpeptidefoundation.org/directory/cagrilintide