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The safety profile in patients with post-transplant recurrence appeared consistent with that of the overall population2

Treatment-emergent adverse events at Week 26 in post-kidney transplant patients1
Aspaveli - post transplant AEs at 26 weeks

No cases of encapsulated meningococcal infections reported1

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EMA indication:

ASPAVELI® is indicated for the treatment of adult and adolescent patients aged 12 to 17 years with C3 glomerulopathy (C3G) or primary immune-complex membranoproliferative glomerulonephritis (IC-MPGN) in combination with a renin-angiotensin system (RAS) inhibitor, unless RAS inhibitor treatment is not tolerated or contraindicated.2

For the full EMA Aspaveli SmPC, please click here

▼This medicine is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions via their national pharmacovigilance reporting system. Suspected adverse reactions should also be reported to Sobi via email at [email protected].

Abbreviations

C3, complement 3; C3G, C3 glomerulopathy; IC-MPGN, immune complex-mediated membranoproliferative glomerulonephritis; RAS, renin-angiotensin system; TEAE, treatment-emergent adverse event. 

Footnotes

*Influenza (moderate), nasopharyngitis (mild), and viral infection (moderate), 1 each. † Nasopharyngitis (mild).1 ‡ Proteinuria and tubulointerstitial nephritis, 1 each.1 

References

  1. Oosterveld M, et al. Poster presented at ERA Congress 2025, Vienna, Austria; 4–7 June 2025. Abstract 3482..

  2. Aspaveli EMA Summary of product characteristics. Swedish Orphan Biovitrum AB (publ) January 2026. 

This website contains information based on the ASPAVELI® Summary of Product Characteristics as approved by European Commission. License conditions vary between countries. Please consult your local Summary of Product Characteristics or Prescribing Information.
 

PP-32966