There’s a new (?) study on secukinumab in ankylosing spondylitis in The Lancet.
I’ve seen similar, but not identical publications on secukinumab during the
past year. I think we get to know different details on one ongoing study. I
think that secukinumab isn’t working in rheumatoid arthritis, but it might work
in psoriatic arthritis and ankylosing spondylitis (AS). So I think it’s a good
idea to get ongoing information.
D. Baeten and colleagues published: “Anti-interleukin-17A monoclonal
antibody secukinumab in treatment of ankylosing spondylitis: a randomised,
double-blind, placebo-controlled trial”. The study looked at i.v. secukinumab (2×10 mg/kg) compared to placebo.
Results showed: “At week 6, ASAS20 response estimates were 59% on secukinumab
versus 24% on placebo (99·8% probability that secukinumab is superior to
placebo). One serious adverse event (subcutaneous abscess caused by Staphylococcus
aureus) occurred in the secukinumab-treated group.” Conclusion: “Secukinumab
rapidly reduced clinical or biological signs of active ankylosing spondylitis
and was well tolerated.” The drug needs to perform better than ASAS20 in larger
studies!
X. Baraliakos and colleagues presented a poster at the 2012 ACR Meeting [574]:
“Long Term Inhibition of Interleukin (IL)-17A with Secukinumab Improves
Clinical Symptoms and Reduces Spinal Inflammation As Assessed by Magnetic Resonance
Imaging in Patients with Ankylosing Spondylitis.” Conclusion: “This exploratory
MRI analysis shows that the IL-17 inhibitor secukinumab may reduce spinal
inflammation and this effect may be sustained for up to 24 months using a lower
dose in the maintenance compared to induction phase.”
Do these results warrant a phase 2 study? By all means – yes! Please go
ahead! We have patients suffering from ankylosing spondylitis, who are in
desperate need for another mode of action, as TNF-alpha inhibition isn’t
working. So, an IL-17A inhibitor would be most welcome.
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