For clinicians

IL-17 inhibitors

secukinumab, ixekizumab, bimekizumab, anti-IL-17

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Bottom lineBottom line: EULAR 2024 lists IL-17 inhibitors (secukinumab, ixekizumab) among non-TNFi biologics that may be used in pregnancy if needed to control maternal disease. Breastfeeding data are limited; paternal use compatible. Individualise.

By reproductive phase

PhasePositionDetailEvidence
Pre-conceptionUse if neededMay be continued to maintain control; shared decision.[2]●●○○low evidenceconditional
1st trimesterUse if neededUse if needed to control maternal disease.[2]●●○○low evidenceconditional
2nd/3rd trimesterUse if neededUse if needed; account for IgG transplacental transfer later in pregnancy.[2]●●○○low evidenceconditional
BreastfeedingUse if neededLimited lactation data; minimal milk transfer expected for large antibodies; individualise.[2]○○○very low evidenceconditional
PaternalContinueCompatible with paternal exposure.[2]●●○○low evidenceconditional

Guideline comparison

GuidelinePositionStrength
ACR 2020Conditionally recommend discontinuing at conception; conditionally recommend AGAINST continuing during pregnancy (grouped with the other biologics: limited transfer in early pregnancy but high transfer in the second half). Breastfeeding: conditionally compatible, expecting minimal transfer from the large molecular size, though there are no data. Paternal: unable to make a recommendation (limited data).[1]Conditional (discontinue at conception; against during pregnancy); no paternal recommendation
EULAR 2024Secukinumab and ixekizumab may be used in pregnancy if needed (both 4/C); limited lactation data (both 5/D) though minimal milk transfer is expected; continuable in men (both 4/C).[2]Oxford LoE/GoR as shown
BSR 2022/23Consider stopping at conception; use in either trimester only for severe maternal disease if no other pregnancy-compatible drugs are suitable. Breastfeeding and paternal exposure compatible (limited evidence). If used in the third trimester, avoid infant live vaccinations until 6 months of age.[3]Verified against BSR Table 1
=Guideline divergence. VERIFIED DIVERGENCE. EULAR 2024 (5b) permits secukinumab and ixekizumab in pregnancy if needed (both 4/C) and considers them continuable in men (4/C); BSR 2023 advises considering stopping at conception and reserving use for severe maternal disease. On lactation EULAR grades the IL-17 inhibitors 5/D (limited data) while BSR marks breastfeeding compatible on limited evidence.

Key points

PointEvidence
An option for active PsA/axSpA in pregnancy when TNF inhibitors are unsuitable; limited data.[2]●●○○low evidenceconditional

Monitoring

References

  1. Sammaritano LR, et al. 2020 ACR Guideline for the Management of Reproductive Health in RMD. Arthritis Rheumatol. 2020;72(3):529-556. https://acrjournals.onlinelibrary.wiley.com/doi/10.1002/art.41191
  2. Ruegg L, et al. EULAR recommendations for antirheumatic drugs in reproduction, pregnancy, and lactation: 2024 update. Ann Rheum Dis. 2025;84(6):910-926. https://ard.eular.org/article/S0003-4967(25)00818-0/fulltext
  3. Russell MD, et al. BSR guideline on prescribing drugs in pregnancy and breastfeeding: immunomodulatory drugs and corticosteroids. Rheumatology (Oxford). 2023;62(4):e48-e88. https://academic.oup.com/rheumatology/article/62/4/e48/6783012
  4. BIMZELX (bimekizumab injection) Product Monograph. UCB Canada Inc. Health Canada; 2025-12-12. https://pdf.hres.ca/dpd_pm/00082779.PDF
  5. COSENTYX (secukinumab) Product Monograph. Novartis Pharmaceuticals Canada Inc. Health Canada; 2022. https://pdf.hres.ca/dpd_pm/00066639.PDF
  6. TALTZ (ixekizumab) Product Monograph. Eli Lilly Canada Inc. Health Canada; 2024. https://pdf.hres.ca/dpd_pm/00080067.PDF