UCB announces U.S. availability of RYSTIGGO® (rozanolixizumab-noli) for the treatment of generalized myasthenia gravis (gMG) in adult patients who are anti-acetylcholine receptor (AChR) or anti-muscle-specific tyrosine kinase (MuSK) antibody positive.
- RYSTIGGO is now commercially available by prescription in
the United States for adult patients with gMG who are anti-acetylcholine receptor (AChR) or anti-muscle-specific tyrosine kinase (MuSK) antibody positive1 - RYSTIGGO is the first and only FDA-approved targeted treatment for both anti-AChR Ab+ and anti-MuSK Ab+ adults with gMG1
- ONWARD™, a personalized patient support program, is available to eligible patients and caregivers to provide support during treatment with UCB rare disease medicines, including RYSTIGGO.
RYSTIGGO is an HCP-administered injection, for subcutaneous use. RYSTIGGO can be ordered from a limited, defined specialty distribution network. UCB also offers the "UCB Infusion Finder", an online search tool providing a non-exhaustive listing of approximately 1,000 infusion locations nationwide. RYSTIGGO will have options for infusion at multiple sites of care, including physicians' offices, hospital outpatient clinics, and independent infusion centers. UCB is partnered with a limited network of specialty pharmacies with home infusion capabilities to support eligible patients with administration in the home setting.3
Myasthenia gravis is a rare, chronic, autoimmune neuromuscular disease, which is characterized by muscle weakness that worsens after periods of activity and improves after periods of rest.4,5 In the
"Now that RYSTIGGO is FDA-approved and commercially available, we are committed to advancing access to the care and support journey of eligible patients. This is so important because we know there is a high unmet need for personalized rare disease support," said Kimberly Moran, Ph.D., Head of
UCB is offering ONWARD to support eligible patients get started on their prescribed treatment. The patient will be paired with a dedicated Care Coordinator, who will help them understand their coverage and explain potential financial assistance options that could help. The program is currently open for enrollment for eligible patients living in the
"For many people, myasthenia gravis is a chronic illness that continues to be overwhelming to patients due to function loss and inadequate control of symptoms," said Samantha Masterson, CEO & President of Myasthenia Gravis Foundation of America."An additional FDA-approved targeted treatment that is now available provides a new option to eligible patients and their treating physicians who have not yet found an option that works for their needs."
Affordability and access are important when talking about rare disease treatment. If an eligible patient or caregiver is looking for support, please visit www.UCBONWARD.com or call 1-844-ONWARD.
About Generalized Myasthenia Gravis
Generalized myasthenia gravis is a rare disease with a global prevalence of 100–350 cases per every 1 million people.5,7 People living with generalized myasthenia gravis can experience a variety of symptoms, including muscle weakness, drooping eyelids, double vision, and difficulty with speech, swallowing or talking.6
About RYSTIGGO® (rozanolixizumab-noli)
RYSTIGGO is a prescription medicine used to treat adults with a disease called generalized myasthenia gravis (gMG) who are acetylcholine receptor (anti-AChR) antibody positive or muscle-specific tyrosine kinase (anti-MuSK) antibody positive.
IMPORTANT SAFETY INFORMATION
Infection: RYSTIGGO may increase the risk of infection. In clinical studies, the most common infections were upper respiratory tract infections, COVID-19, urinary tract infections, and herpes simplex infections. Your healthcare provider should check you for infections before starting and during treatment with RYSTIGGO. Tell your healthcare provider if you have any history of infections. Tell your healthcare provider right away if you have signs or symptoms of an infection during treatment with RYSTIGGO. Some of the signs and symptoms may include fever, chills, frequent and/or painful urination, cough, runny nose, wheezing, shortness of breath, fatigue, sore throat, excess phlegm, nasal discharge, back pain, and/or chest pain.
Aseptic Meningitis: RYSTIGGO could cause aseptic meningitis. Tell your healthcare provider right away if you develop any signs or symptoms of meningitis during treatment with RYSTIGGO such as severe headache, neck stiffness, drowsiness, fever, sensitivity to light, painful eye movements, nausea, and vomiting.
Hypersensitivity Reactions: RYSTIGGO can cause swelling and rash. Your healthcare provider should monitor you during and after treatment and discontinue RYSTIGGO if needed. Tell your healthcare provider immediately about any undesirable reactions you experience after administration.
Before taking RYSTIGGO, tell your healthcare provider about all of your medical conditions, including if you have a history of infection or think you have an active infection or have received or are scheduled to receive a vaccine (immunization). The use of vaccines during RYSTIGGO treatment has not been studied, and the safety with live or live-attenuated vaccines is unknown. Administration of live or live-attenuated vaccines is not recommended during treatment with RYSTIGGO. Completion of age-appropriate vaccines according to vaccination guidelines before starting a new treatment cycle with RYSTIGGO is recommended.
Before taking RYSTIGGO, tell your healthcare provider if you are pregnant or plan to become pregnant, or are breastfeeding or plan to breastfeed.
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
The most common side effects of RYSTIGGO include headache, infections, diarrhea, fever, hypersensitivity reactions, and nausea.
These are not all of the possible side effects of RYSTIGGO. For more information, ask your healthcare provider or pharmacist. Tell your healthcare provider about any side effect that bothers you or that does not go away. Call your healthcare provider for medical advice about side effects. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. You may also report side effects to UCB, Inc. by calling 1-844-599-CARE [2273].
Please see the full Prescribing Information and talk to your healthcare provider about your condition or your treatment. For more information, go to www.RYSTIGGO.com or call 1-844-599-2273.
For further information, contact UCB:
Daphne Teo
+1-770-880-7655
daphne.teo@ucb.com
Global Rare Disease Communications
Jim Baxter
T+32.2.473.78.85.01
jim.baxter@ucb.com
Corporate Communications, Media Relations
Laurent Schots
T+32.2.559.92.64
laurent.schots@ucb.com
Investor Relations
Antje Witte
T +32.2.559.94.14
antje.witte@ucb.com
About UCB
UCB,
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Given these uncertainties, you should not place undue reliance on any of such forward-looking statements. There can be no guarantee that the investigational or approved products described in this press release will be submitted or approved for sale or for any additional indications or labelling in any market, or at any particular time, nor can there be any guarantee that such products will be or will continue to be commercially successful in the future.
UCB is providing this information, including forward-looking statements, only as of the date of this press release and it does not reflect any potential impact from the evolving COVID-19 pandemic, unless indicated otherwise. UCB is following the worldwide developments diligently to assess the financial significance of this pandemic to UCB. UCB expressly disclaims any duty to update any information contained in this press release, either to confirm the actual results or to report or reflect any change in its forward-looking statements with regard thereto or any change in events, conditions or circumstances on which any such statement is based, unless such statement is required pursuant to applicable laws and regulations.
Additionally, information contained in this document shall not constitute an offer to sell or the solicitation of an offer to buy any securities, nor shall there be any offer, solicitation or sale of securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of such jurisdiction.
RYSTIGGO® is a registered trademark, and ONWARD™ is a trademark, of the UCB Group of Companies.
©2023 UCB, Inc., Smyrna, GA 30080. All rights reserved. US-P-RZ-MG-2300152
References
1 RYSTIGGO. [Prescribing Information]
2 UCB press release. www.ucb-usa.com/stories-media/UCB-U-S-News/detail/article/ucb-announces-us-fda-approval-of-rystiggo-rozanolixizumab-noli-for-the-treatment-of-adults-with-generalized-myasthenia-gravis. Accessed June 27, 2023; and www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761286
3 UCB data on file
4 National Institute of Neurological Disorders and Stroke. What is Myasthenia Gravis. www.ninds.nih.gov/health-information/disorders/myasthenia-gravis. Accessed July 2023.
5 Punga AR, Maddison P, Heckmann JM, Guptill JT, Evoli A. Epidemiology, diagnostics, and biomarkers of autoimmune neuromuscular junction disorders. Lancet Neurol. 2022;21(2):176-188. doi:10.1016/S1474-4422(21)00297-0
6 Howard, James F. Myasthenia Gravis Foundation of America. Clinical Overview of MG. https://myasthenia.org/Professionals/Clinical-Overview-of-MG. Accessed July 2023
7 Bril V. Efficacy and safety of rozanolixizumab in patients with generalised myasthenia gravis: a randomised, double-blind, placebo-controlled, adaptive Phase 3 study MyCarinG study. Lancet Neurol. 2023;22(5):383-94.
8 ONWARD is provided as a service of UCB and is intended to support the appropriate use of UCB medicines. Some program and eligibility restrictions may apply.
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