L-alanyl-l-glutamine 10g/50ml solution for infusion bottles
Alanyl Glutamine is under investigation in clinical trial NCT00338221 (Clinical Trial of Alanyl-Glutamine or Glycine in Children With Persistent Diarrhea or Malnutrition).
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Yellow Card reports
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1 branded products available
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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NHS UK identifiers
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0.
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 4 · Randomised trials: 13 · 1988–2026
Showing the 50 most relevant studies, sorted by most relevant.
Hajimohammadebrahim-Ketabforoush M, Meybodi TE, Mehmandoost M, et al.
2025
- Inflammation
- Brain Injuries, Traumatic
- Immunonutrition Diet
BACKGROUND: Traumatic brain injury (TBI) induces a severe hypermetabolic state with elevated energy expenditure and progressive systemic inflammation. Nutritional optimization in this setting is challenging, particularly in severe TBI (Glasgow Coma Scale [GCS] = 3–8). Its clinical role in these hospitalized TBI patients remains unclear. This systematic review and meta-analysis aimed to evaluate the impact of immunonutrition on neuroinflammation and neurosurgical outcomes in TBI patients, with a focus on omega-3 fatty acids, arginine, and glutamine. METHODS: Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines, we systematically reviewed the available evidence from PubMed, Scopus, and Web of Science. The inclusion criteria focused on severely hospitalized TBI patients with a GCS score of 3 to 8 who were receiving immunonutrition components. The quality and certainty of the evidence were assessed using the Cochrane Risk of Bias tool and the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) approach, respectively. RESULTS: A total of 12 studies were eligible and included in our comprehensive full-text review. However, only 5 articles were included in the meta-analysis. Systematic review findings indicated that immunonutrition was associated with reductions in inflammatory markers, decreased rates of nosocomial infections, and improvements in CO₂ reactivity, blood–brain barrier integrity, and cerebral edema. The meta-analysis results showed non-significant trends toward a lower mortality rate (p = 0.06), shorter hospital length of stay (LOS) (p = 0.09), and reduced ICU LOS (p = 0.12). Considerable heterogeneity was observed across some outcomes; however, due to the limited number of studies, formal meta-regression was not statistically justified. Instead, leave-one-out sensitivity analyses were performed to confirm the stability and robustness of the pooled estimates, alongside efforts to reduce heterogeneity. CONCLUSIONS: Despite heterogeneity and a limited number of studies, consistent trends support the beneficial role of immunonutrition in severe TBI. These findings highlight the physiological plausibility and clinical safety of such interventions, warranting larger, standardized trials to confirm these effects.
Abstract licence: CC BY-NC-ND
Chen L, Wang D, Meng C, et al.
2025
- Colorectal Neoplasms
- Diarrhea
- Glutamine
ObjectiveTo assess the efficacy of glutamine in preventing diarrhea associated with chemotherapy or chemoradiotherapy in colorectal cancer.MethodsRandomized controlled trials of glutamine in the prevention of chemotherapy-associated diarrhea of colorectal cancer were retrieved from the Cochrane Library, Pubmed, EMBASE, CNKI, and Wanfang by computer up to August 1, 2024. Results were presented using relative risk (RR) or mean difference (MD) with a 95% confidence interval (CI). Publications were reviewed in accordance with the Cochrane Handbook and the guidelines of the Preferred Reporting Project for Systematic Review and Meta-Analysis (PRISMA2020). This study has been registered with INPLASY (registration number: INPLASY202490057).ResultsA total of 5 studies were included, and the total number of patients was 311. Meta-analysis showed that compared with the control group, glutamine supplementation significantly reduced the incidence of chemoradiation-induced diarrhea in colorectal cancer patients (RR = 0.72, 95%CI: 0.60-0.87, P 0.05). D-xylose levels were significantly higher in the glutamine group (MD = 0.32, 95%CI: 0.14-0.51, P ConclusionGlutamine supplementation is associated with a reduced incidence of diarrhea in patients with colorectal cancer, with a more pronounced efficacy observed in those receiving chemotherapy alone.
Abstract licence: CC BY-NC-ND
C. Fuentes-Orozco, R. Anaya-Prado, A. González-Ojeda, et al.
Clinical nutrition, 2004
- Parenteral Nutrition, Total
- Peritonitis
- Nitrogen
C. Fuentes-Orozco, G. Cervantes-Guevara, Ivette Muciño-Hernández, et al.
JPEN. Journal of parenteral and enteral nutrition, 2008
- Nutritional Status
- Pancreatitis
- Nitrogen
Ahmad AHM, Kamal Eldin F, Rashed MM
2023
- Diabetes Mellitus
- Diabetes Mellitus, Type 2
- Insulin
Adebola Obayan
Surgery International Open Access Journal, 2024
Herzog R, Daniel-Fischer L, Eibensteiner F, et al.
2026
P. Déchelotte, M. Hasselmann, L. Cynober, et al.
Critical Care Medicine, 2006
- Cross Infection
- Glucose Intolerance
- Glutamine
C. Goeters, A. Wenn, N. Mertes, et al.
Critical Care Medicine, 2002
- Parenteral Nutrition, Total
- Critical Care
- Glutamine
O. Y. Bushen, J. A. Davenport, A. B. Lima, et al.
Clinical Infectious Diseases, 2004
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Investigational
Major interactions
None known
Half-life
Not available
Mechanism
Not available
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
ATC B05XB02
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72