Lixisenatide: indexed trial records
Records checked
Compiled and citation-checked by GLP-1 Receptor Agonists editorial desk
Qualified clinical review None on record
This page carries 12 of the 698 records the literature query returned for Lixisenatide, selected by citation count and preferring records that name the compound in their title. It is a selection, not a complete index.
Every row below resolves to a real identifier and names the study model the indexer assigned. The record class is read from the publication type on the record itself. Nothing here states what a record found.
At a glance
- Class
- Incretin receptor agonists
- Receptor targets as recorded
- GLP-1 receptor
- Records indexed here
- 12
- Records returned by the query
- 698
- Publication years covered
- 2015–2024
- Query retrieved
- 2026-10-12
Shape of the indexed record set
| Record class | Records |
|---|---|
| Phase 3 | 1 |
| Phase 2 | 2 |
| Trial, no phase assigned | 4 |
| Not a registered trial record | 5 |
| Study model as assigned | Records |
|---|---|
| human trial | 9 |
| rodent | 2 |
| other | 1 |
Study model is the indexer’s own assignment, taken from the MeSH population headings and the publication type. It is not a judgement about how well a record was conducted.
Endpoint coverage
| Endpoint | Records for this compound | Records across all compounds in scope |
|---|---|---|
| Body weight and adiposity | 5 | 108 |
| Glycaemic control | 10 | 117 |
| Cardiovascular | 4 | 30 |
| Renal | 2 | 10 |
| Hepatic | 0 | 9 |
| Neurological | 2 | 18 |
Derived record-set tier
Human trial evidence
(INFERRED, derived from record counts)
Basis: 9 of 12 indexed records are interventional human trials by their own assigned publication type.
This label counts record types. It is not an assessment of clinical efficacy, of safety, of
study quality or of consensus, and it does not rank one compound above another.
What the corpus does not carry for this compound
- Identity fields with no source retrieved: uniprot_id, sequence.
- Reported half-life: no source retrieved, so the value reads Unknown.
- Amounts reported in the cited literature: no row recorded.
- Adverse effects reported in the cited literature: no row recorded.
- Long-form mechanism: not written, because no source was read in full.
- Records the query returned that this corpus does not carry: 686.
An absent row records the absence of a retrieved report, never the absence of the thing itself.
Application register
A query of the FDA Drugs@FDA application register on 2026-10-09 returned 1 application record(s) for this compound name (including BLA208673, marketed as SOLIQUA 100/33). Material supplied as a research chemical is not the subject of those applications and is not an FDA-approved product.[2]
Scope statement: this records the result of a single automated query against the openFDA drugsfda endpoint on the stated date. It is not legal advice and is not a jurisdiction-by-jurisdiction legality assessment.
The records
Phase 3 — 1 record
| No. | Identifier | Year | Record | Model | Subject headings |
|---|---|---|---|---|---|
| 10 | pmid:27527848 | 2016 | Benefits of LixiLan, a Titratable Fixed-Ratio Combination of Insulin Glargine Plus Lixisenatide, Versus Insulin Glargine and Lixisenatide Monocomponents in Type 2 Diabetes Inadequately Controlled on Oral Agents: The LixiLan-O Randomized Trial Diabetes care · Clinical Trial, Phase III, Multicenter Study | human trial | Humans; Diabetes Mellitus, Type 2; Hypoglycemia; Metformin; Blood Glucose; Peptides; Drug Combinations; Hypoglycemic Agents |
Phase 2 — 2 records
| No. | Identifier | Year | Record | Model | Subject headings |
|---|---|---|---|---|---|
| 1 | pmid:38598572 | 2024 | Trial of Lixisenatide in Early Parkinson's Disease The New England journal of medicine · Clinical Trial, Phase II, Research Support, Non-U.S. Gov't | human trial | Humans; Parkinson Disease; Disease Progression; Peptides; Antiparkinson Agents; Neuroprotective Agents; Treatment Outcome; Injections, Subcutaneous |
| 8 | pmid:27284114 | 2016 | Efficacy and Safety of LixiLan, a Titratable Fixed-Ratio Combination of Lixisenatide and Insulin Glargine, Versus Insulin Glargine in Type 2 Diabetes Inadequately Controlled on Metformin Monotherapy: The LixiLan Proof-of-Concept Randomized Trial Diabetes care · Clinical Trial, Phase II, Comparative Study | human trial | Humans; Diabetes Mellitus, Type 2; Hypoglycemia; Body Weight; Metformin; Blood Glucose; Peptides; Drug Combinations |
Trial, no phase assigned — 4 records
| No. | Identifier | Year | Record | Model | Subject headings |
|---|---|---|---|---|---|
| 2 | pmid:30623563 | 2019 | Effects of lixisenatide on postprandial blood pressure, gastric emptying and glycaemia in healthy people and people with type 2 diabetes Diabetes, obesity & metabolism · Research Support, Non-U.S. Gov't, Randomized Controlled Trial | human trial | Humans; Diabetes Mellitus, Type 2; Blood Glucose; Peptides; Placebos; Cross-Over Studies; Double-Blind Method; Blood Pressure |
| 7 | pmid:27222510 | 2016 | Prandial Options to Advance Basal Insulin Glargine Therapy: Testing Lixisenatide Plus Basal Insulin Versus Insulin Glulisine Either as Basal-Plus or Basal-Bolus in Type 2 Diabetes: The GetGoal Duo-2 Trial Diabetes care · Randomized Controlled Trial | human trial | Humans; Diabetes Mellitus, Type 2; Hypoglycemia; Body Weight; Metformin; Blood Glucose; Peptides; Hypoglycemic Agents |
| 9 | pmid:27311491 | 2016 | Once-Daily Liraglutide Versus Lixisenatide as Add-on to Metformin in Type 2 Diabetes: A 26-Week Randomized Controlled Clinical Trial Diabetes care · Randomized Controlled Trial | human trial | Humans; Diabetes Mellitus, Type 2; Hypoglycemia; Body Weight; Metformin; Blood Glucose; Peptides; Hypoglycemic Agents |
| 11 | pmid:27650977 | 2016 | Efficacy and Safety of LixiLan, a Titratable Fixed-Ratio Combination of Insulin Glargine Plus Lixisenatide in Type 2 Diabetes Inadequately Controlled on Basal Insulin and Metformin: The LixiLan-L Randomized Trial Diabetes care · Multicenter Study, Randomized Controlled Trial | human trial | Humans; Diabetes Mellitus, Type 2; Body Weight; Metformin; Insulin; Blood Glucose; Peptides; Drug Combinations |
Not a registered trial record — 5 records
| No. | Identifier | Year | Record | Model | Subject headings |
|---|---|---|---|---|---|
| 3 | pmid:29175324 | 2018 | Lixisenatide reduces amyloid plaques, neurofibrillary tangles and neuroinflammation in an APP/PS1/tau mouse model of Alzheimer's disease Biochemical and biophysical research communications · Research Support, Non-U.S. Gov't | rodent | Neurofibrillary Tangles; Animals; Mice, Inbred C57BL; Mice, Transgenic; Mice; Encephalitis; Alzheimer Disease; Peptides |
| 4 | pmid:30292589 | 2018 | Lixisenatide and renal outcomes in patients with type 2 diabetes and acute coronary syndrome: an exploratory analysis of the ELIXA randomised, placebo-controlled trial The lancet. Diabetes & endocrinology · Research Support, Non-U.S. Gov't | other | Humans; Kidney Diseases; Albuminuria; Diabetes Mellitus, Type 2; Peptides; Glomerular Filtration Rate; Treatment Outcome; Middle Aged |
| 5 | pmid:28449402 | 2017 | Postprandial renal haemodynamic effect of lixisenatide vs once-daily insulin-glulisine in patients with type 2 diabetes on insulin-glargine: An 8-week, randomised, open-label trial Diabetes, obesity & metabolism · Comparative Study, Research Support, Non-U.S. Gov't | human trial | Kidney; Humans; Diabetic Nephropathies; Diabetes Mellitus, Type 2; Insulin; Peptides; Hypoglycemic Agents; Glomerular Filtration Rate |
| 6 | pmid:28608285 | 2017 | The GLP-1 analogue lixisenatide decreases atherosclerosis in insulin-resistant mice by modulating macrophage phenotype Diabetologia · Research Support, Non-U.S. Gov't | rodent | Macrophages; Animals; Mice; Diabetes Mellitus, Type 2; Insulin Resistance; Inflammation; Peptides; Atherosclerosis |
| 12 | pmid:26630143 | 2015 | Lixisenatide in Patients with Type 2 Diabetes and Acute Coronary Syndrome The New England journal of medicine · Research Support, Non-U.S. Gov't, Multicenter Study | human trial | Humans; Cardiovascular Diseases; Angina, Unstable; Myocardial Infarction; Diabetes Mellitus, Type 2; Peptides; Hypoglycemic Agents; Treatment Failure |
Where this page sits
Receptor targets
All compounds in scope: the trial index. Coverage by endpoint: the endpoint index.
Review status
- Review tier
- High impact
- State
- Pending qualified review
- Compiled by
- automated pipeline
- Qualified clinical review
- None on record
Why this tier was assigned
- the name carries 1 Drugs@FDA application record(s), so readers may conflate it with an approved medicine
- 9 indexed record(s) are interventional human trials
- the class covers weight-management and metabolic prescribing, the highest-risk consumer subject in this corpus
Checks the pipeline performed
- every cited source id resolves to a sources[] row on the entity
- every identifier is a well-formed PMID or DOI
- study model derived only from assigned MeSH headings and publication types
- banned-phrase lint over rendered HTML including title, meta, alt and JSON-LD
- unknown values render as the literal word Unknown
Checks the pipeline did not perform
- no full text was read
- no clinical appraisal of any study
- no assessment of whether the indexed set is representative of the literature
A high_impact profile with qualified_review null must not be published as indexable. Compilation and linting are not clinical validation.
Sources
- PubChem Compound Summary for CID 90472060, Lixisenatide. PubChem, National Library of Medicine (2026). pubchem:90472060
- Drugs@FDA application register query for this compound, 1 application(s) returned: BLA208673. U.S. Food and Drug Administration, openFDA drugsfda endpoint (2026). fda:lixisenatide
- Randomized, double-blind, placebo-controlled trial of the once-daily GLP-1 receptor agonist lixisenatide in Asian patients with type 2 diabetes insufficiently controlled on basal insulin with or without a sulfonylurea (GetGoal-L-Asia). Diabetes, obesity & metabolism (2012). pmid:22564709
- Adding once-daily lixisenatide for type 2 diabetes inadequately controlled by established basal insulin: a 24-week, randomized, placebo-controlled comparison (GetGoal-L). Diabetes care (2013). pmid:23628617
- Adding once-daily lixisenatide for type 2 diabetes inadequately controlled with newly initiated and continuously titrated basal insulin glargine: a 24-week, randomized, placebo-controlled study (GetGoal-Duo 1). Diabetes care (2013). pmid:23564915
- Contrasting Effects of Lixisenatide and Liraglutide on Postprandial Glycemic Control, Gastric Emptying, and Safety Parameters in Patients With Type 2 Diabetes on Optimized Insulin Glargine With or Without Metformin: A Randomized, Open-Label Trial. Diabetes care (2015). pmid:25887358
- Benefits of LixiLan, a Titratable Fixed-Ratio Combination of Insulin Glargine Plus Lixisenatide, Versus Insulin Glargine and Lixisenatide Monocomponents in Type 2 Diabetes Inadequately Controlled on Oral Agents: The LixiLan-O Randomized Trial. Diabetes care (2016). pmid:27527848
- Efficacy and Safety of LixiLan, a Titratable Fixed-Ratio Combination of Insulin Glargine Plus Lixisenatide in Type 2 Diabetes Inadequately Controlled on Basal Insulin and Metformin: The LixiLan-L Randomized Trial. Diabetes care (2016). pmid:27650977
- Lixisenatide in Patients with Type 2 Diabetes and Acute Coronary Syndrome. The New England journal of medicine (2015). pmid:26630143
- Lixisenatide and renal outcomes in patients with type 2 diabetes and acute coronary syndrome: an exploratory analysis of the ELIXA randomised, placebo-controlled trial. The lancet. Diabetes & endocrinology (2018). pmid:30292589
- Drugs developed to treat diabetes, liraglutide and lixisenatide, cross the blood brain barrier and enhance neurogenesis. BMC neuroscience (2012). pmid:22443187
- Neuroprotective effects of lixisenatide and liraglutide in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mouse model of Parkinson's disease. Neuroscience (2015). pmid:26141845
- Trial of Lixisenatide in Early Parkinson's Disease. The New England journal of medicine (2024). pmid:38598572