With over 4 decades of experience UCB has a strong heritage in neurology.
With over 4 decades of experience UCB has a strong heritage in neurology.

In April 2026, RYSTIGGO® (rozanolixizumab) achieved a significant milestone as the first and only targeted therapy for myasthenia gravis (MG) to be reimbursed by NICE. This reflects our ongoing commitment to advancing innovative, patient-focused treatments.
![[UCBCares Pro][Rystiggo][Section 1][Image Text] [Image] In April 2026 we celebrated!](/_next/image/?url=https%3A%2F%2Fimages.eu.ctfassets.net%2Ffq4x32bitsfk%2F7ei71kbNEl0xJfgJU1YmeO%2Fdd082377648fe11541f255ef1b4a6d19%2F3c5e38a2a9cc453d2590eb82ee8882a6227815dc.png&w=3840&q=75)
Proudly driven by our commitment to science and innovation
RYSTIGGO delivered rapid, significant, clinically meaningful improvements in daily living*1
RYSTIGGO targets FcRn to reduce IgG levels, including pathogenic gMG autoantibodies1-4
Rystiggo® Administration Guide
Rystiggo® Summary
How to Prescribe Rystiggo®
With over 4 decades of experience UCB has a strong heritage in neurology.


Fintepla®▼ (fenfluramine) is indicated for the treatment of seizures associated with Dravet syndrome and Lennox-Gastaut syndrome as an add-on therapy to other antiepileptic medicines for patients 2 years of age and older.1
Rystiggo®▼ (rozanolixizumab) is indicated as an add-on to standard therapy for the treatment of generalised myasthenia gravis (gMG) in adult patients who are anti-acetylcholine receptor (AChR) or anti-muscle-specific tyrosine kinase (MuSK) antibody positive.
Rystiggo currently not reimbursed on the NHS in Scotland.
Zilbrysq®▼ (zilucoplan) is indicated as an add-on to standard therapy for the treatment of generalised myasthenia gravis (gMG) in adult patients who are anti-acetylcholine receptor (AChR) antibody positive.
References:
1. RYSTIGGO® (rozanolixizumab) Summary of Product Characteristics.
2. Bril V, et al. Lancet Neurol. 2023;22(5):383–394.
3. Wolfe GI, et al. J Neurol Sci. 2021;430:118074.
4. Bril V, et al. J Neuromuscul Dis. 2025;12(2):218–230
*MycarinG was a randomised, double-blind, placebo-controlled, parallel-group, two-stage adaptive, phase 3 study that evaluated the safety and efficacy of RYSTIGGO in adults with anti-AChR or anti-MuSK antibody-positive gMG (N=200).2
GB-RZ-2600004 | September 2026