Aqumeldi® is an innovative paediatric formulation — a mini ODT that rapidly disperses in the mouth2
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Aqumeldi® is an innovative paediatric formulation — a mini ODT that rapidly disperses in the mouth2
Aqumeldi® is readily available in a low dose strength (0.25 mg) — enabling accurate titration and dose adjustments1,2
Aqumeldi® - dedicated paediatric clinical studies in HF establishing its safety profile over a duration of 1 year1,5
Aqumeldi® is an innovative formulation, learn more about its features here
Head to this section for guidance on the dosing and administration for Aqumeldi®
Read more about the LENA trials and clinical data supporting the development and licensing of Aqumeldi® here
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1. Aqumeldi Summary of Product Characteristics, (January 2024)
2. Bajcetic, M., et al., (2019). Orodispersible minitablets of enalapril for use in children with heart failure (LENA): Rationale and protocol for a multicentre pharmacokinetic bridging study and follow-up safety study Contemporary Clinical Trials Communications. Vol 15:100393
3. Klassen, T.P., et al. (2008). Children are not just small adults: the urgent need for high quality trial evidence in children. PLOS Medicine. Vol 5(8):e172.
4. British National Formulary for Children (BNFC). Enalapril maleate. Available from:https://bnfc.nice.org.uk/drugs/enalapril-maleate/
5. Data on file
UK-ENA-24-0039 | January 2025
Adverse Event Reporting Information
UK: Adverse events should be reported. Reporting forms and information can be found at: www.mhra.gov.uk/yellowcard.
Republic of Ireland: Adverse events should be reported. Reporting forms and information can be found at: www.hpra.ie.
Adverse events should also be reported to Proveca Limited. Phone: +44 333 200 1866 E-Mail: medinfo@proveca.com