FDA approves Roche’s Susvimo as the first and only continuous delivery treatment for the leading cause of diabetes-related blindness
Roche (RHHBY) has received FDA approval for Susvimo to treat diabetic macular edema (DME), marking its second indication after wet age-related macular degeneration. DME affects over 29 million adults worldwide and is a leading cause of vision loss in diabetic adults.
The treatment offers a groundbreaking continuous delivery system requiring only two treatments per year, compared to traditional monthly eye injections. The approval is based on the phase III Pagoda study results, where Susvimo demonstrated non-inferior vision improvements compared to monthly ranibizumab injections (9.6 vs 9.4 eye chart letters).
Susvimo's Port Delivery Platform provides continuous medication delivery, offering a more convenient alternative to current treatments that may require monthly injections. The product is now available to US retina specialists and their DME patients.
Roche (RHHBY) ha ricevuto l'approvazione della FDA per Susvimo nel trattamento dell'edema maculare diabetico (DME), segnando la sua seconda indicazione dopo la degenerazione maculare senile umida. Il DME colpisce oltre 29 milioni di adulti in tutto il mondo ed è una delle principali cause di perdita della vista negli adulti diabetici.
Il trattamento offre un innovativo sistema di somministrazione continua che richiede solo due trattamenti all'anno, rispetto alle tradizionali iniezioni mensili negli occhi. L'approvazione si basa sui risultati del studio di fase III Pagoda, in cui Susvimo ha dimostrato miglioramenti visivi non inferiori rispetto alle iniezioni mensili di ranibizumab (9,6 contro 9,4 lettere della tabella oculistica).
La Port Delivery Platform di Susvimo fornisce una somministrazione continua di medicazioni, offrendo un'alternativa più comoda rispetto ai trattamenti attuali che possono richiedere iniezioni mensili. Il prodotto è ora disponibile per gli specialisti della retina negli Stati Uniti e per i loro pazienti con DME.
Roche (RHHBY) ha recibido la aprobación de la FDA para Susvimo para tratar el edema macular diabético (DME), marcando su segunda indicación después de la degeneración macular relacionada con la edad húmeda. El DME afecta a más de 29 millones de adultos en todo el mundo y es una de las principales causas de pérdida de visión en adultos diabéticos.
El tratamiento ofrece un innovador sistema de entrega continua que solo requiere dos tratamientos al año, en comparación con las tradicionales inyecciones mensuales en el ojo. La aprobación se basa en los resultados del estudio de fase III Pagoda, donde Susvimo demostró mejoras visuales no inferiores en comparación con las inyecciones mensuales de ranibizumab (9.6 frente a 9.4 letras de la tabla ocular).
La Port Delivery Platform de Susvimo proporciona una entrega continua de medicamentos, ofreciendo una alternativa más conveniente a los tratamientos actuales que pueden requerir inyecciones mensuales. El producto ya está disponible para los especialistas en retina de EE.UU. y sus pacientes con DME.
로슈 (RHHBY)는 수스비모의 당뇨병성 황반부종(DME) 치료에 대한 FDA 승인을 받았으며, 이는 습성 노인성 황반변성에 이어 두 번째 적응증입니다. DME는 전 세계 2,900만 명 이상의 성인에게 영향을 미치며 당뇨병 환자의 시력 손실의 주요 원인입니다.
이 치료법은 전통적인 월 1회 안구 주사에 비해 연간 단 두 번의 치료만으로도 가능한 혁신적인 지속적 약물 전달 시스템을 제공합니다. 승인은 수스비모가 월별 라니비주맙 주사(9.6 대 9.4 시력 차트 문자)와 비교해 시력 개선을 비열등하게 입증한 3상 파고다 연구 결과를 기반으로 하고 있습니다.
수스비모의 포트 전달 플랫폼은 지속적인 약물 전달을 제공하여 월별 주사를 필요로 할 수 있는 현재의 치료법에 대한 보다 편리한 대안을 제공합니다. 이 제품은 이제 미국의 망막 전문의와 DME 환자에게 제공됩니다.
Roche (RHHBY) a reçu l'approbation de la FDA pour Susvimo afin de traiter l'œdème maculaire diabétique (DME), marquant sa deuxième indication après la dégénérescence maculaire liée à l'âge humide. Le DME touche plus de 29 millions d'adultes dans le monde et est l'une des principales causes de perte de vision chez les adultes diabétiques.
Ce traitement propose un système de délivrance continue révolutionnaire nécessitant seulement deux traitements par an, par rapport aux injections oculaires mensuelles traditionnelles. L'approbation repose sur les résultats de l'étude de phase III Pagoda, où Susvimo a démontré des améliorations visuelles non inférieures par rapport aux injections mensuelles de ranibizumab (9,6 contre 9,4 lettres sur le tableau de vision).
La Port Delivery Platform de Susvimo permet une administration continue des médicaments, offrant une alternative plus pratique aux traitements actuels qui peuvent nécessiter des injections mensuelles. Le produit est désormais disponible pour les spécialistes de la rétine aux États-Unis et leurs patients atteints de DME.
Roche (RHHBY) hat die FDA-Zulassung für Susvimo zur Behandlung von diabetischem Makulaödem (DME) erhalten, was die zweite Indikation nach der feuchten altersbedingten Makuladegeneration darstellt. DME betrifft weltweit über 29 Millionen Erwachsene und ist eine der Hauptursachen für Sehverlust bei diabetischen Erwachsenen.
Die Behandlung bietet ein bahnbrechendes kontinuierliches Abgabesystem, das nur zwei Behandlungen pro Jahr erfordert, im Vergleich zu den herkömmlichen monatlichen Injektionen ins Auge. Die Zulassung basiert auf den Ergebnissen der Phase-III-Studie Pagoda, in der Susvimo keine minderwertigen Sehverbesserungen im Vergleich zu monatlichen Ranibizumab-Injektionen (9,6 vs. 9,4 Augen-Diagramm-Buchstaben) zeigte.
Die Port Delivery Platform von Susvimo bietet eine kontinuierliche Medikamentenabgabe und stellt eine bequemere Alternative zu aktuellen Behandlungen dar, die möglicherweise monatliche Injektionen erfordern. Das Produkt ist jetzt für Retina-Spezialisten in den USA und deren DME-Patienten verfügbar.
- First FDA-approved continuous delivery treatment for DME
- Requires only 2 treatments per year vs monthly injections
- Demonstrated equivalent efficacy to standard treatment (9.6 vs 9.4 letter improvement)
- Expands market reach with second FDA indication
- Addresses large market (29M+ adults affected worldwide)
- None.
- Susvimo is the first and only continuous delivery treatment that offers an alternative to regular eye injections to treat diabetic macular edema (DME)
- With as few as two treatments per year, Susvimo may help people with DME maintain their vision
- Approval marks the second indication for Susvimo in addition to neovascular or ‘wet’ age-related macular degeneration (nAMD)
Basel, 04 February 2025 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that the US Food and Drug Administration (FDA) has approved Susvimo® (ranibizumab injection) 100 mg/mL for the treatment of diabetic macular edema (DME), a leading cause of vision loss in adults with diabetes, affecting more than 29 million adults worldwide.1-3 Susvimo is the first and only FDA-approved treatment shown to maintain vision in people with DME with fewer treatments than standard-of-care eye injections.4-6 Susvimo is now available to US retina specialists and their patients with DME.
“Susvimo presents a unique, convenient treatment alternative to routine eye injections for people with a potentially blinding diabetic eye condition,” said Levi Garraway, MD, PhD, Roche's Chief Medical Officer and Head of Global Product Development. “As the global prevalence of diabetic macular edema continues to grow, today's FDA approval for Susvimo reflects our dedication to innovation and enhancing the patient experience.”
“I am excited to offer Susvimo to my patients living with diabetic macular edema who want an option with longer intervals between treatments due to their busy personal and professional lives,” said vitreoretinal surgeon, Jordan Graff, MD, Barnet Dulaney Perkins Eye Center, Arizona, US. “Having completed dozens of Susvimo surgeries in my patients with wet, or neovascular, age-related macular degeneration (nAMD), I’ve seen first-hand how Susvimo, with its continuous delivery of medication, can help preserve vision with fewer treatments. I look forward to broadening Susvimo’s impact to even more patients in my clinic.”
The FDA decision was based on positive one-year results from the phase III Pagoda study, which showed that Susvimo demonstrated sustained vision improvements in people with DME, with safety consistent with the known safety profile for Susvimo.7 In Pagoda, people with DME who received Susvimo refilled every six months achieved non-inferior improvements in vision compared with those receiving monthly 0.5 mg ranibizumab intravitreal injections (9.6 eye chart letters, similar to gaining two more lines on an eye chart, compared to 9.4 letters, respectively).7
Susvimo provides continuous delivery of a customised formulation of ranibizumab via the Port Delivery Platform, while other currently approved treatments may require eye injections as often as once per month.6,8 Susvimo was first approved by the FDA for the treatment of nAMD in 2021.9 Discussions with other global regulatory agencies are ongoing.
Roche is focused on saving people’s eyesight from the leading causes of vision loss through pioneering therapies and has the broadest retina pipeline in ophthalmology, which is led by science and informed by insights from people with eye conditions.
About diabetic macular edema (DME)
Affecting around 29 million people globally, DME is a vision-threatening retinal condition associated with blindness and decreased quality of life when left untreated.1-3,10 DME occurs when damaged blood vessels leak into and cause swelling in the macula – the central area of the retina responsible for the sharp vision needed for reading and driving.11,12 The number of people with DME is expected to grow as the prevalence of diabetes increases.13
About the Pagoda study14
Pagoda (NCT04108156) is a multicentre, randomised, active treatment-controlled, non-inferiority US-based phase III study evaluating the efficacy, safety and pharmacokinetics of Susvimo® (Port Delivery Platform with ranibizumab) refilled every six months compared with monthly ranibizumab 0.5 mg intravitreal injections, in 634 people with diabetic macular edema. Participants were randomised 3:2 to receive either Susvimo refilled every six months or continued monthly intravitreal ranibizumab injections. In the Susvimo arm, participants received four loading doses of intravitreal ranibizumab, before Susvimo implantation at week 16. The primary endpoint of the study is a change in best-corrected visual acuity score (the best distance vision a person can achieve – including with correction such as glasses – when reading letters on an eye chart) from baseline at the average of week 60 and week 64. Following primary analyses, participants who were initially randomised to intravitreal injections received Susvimo, with refills every 24 weeks.
About Susvimo® (Port Delivery Platform with ranibizumab) in the US
Susvimo is a refillable eye implant surgically inserted into the eye during a one-time, outpatient procedure. Susvimo continuously delivers a customised formulation of ranibizumab over time.8 Ranibizumab is a vascular endothelial growth factor (VEGF) inhibitor designed to bind to and inhibit VEGF-A, a protein that has been shown to play a critical role in the formation of new blood vessels and the leakiness of the vessels.15
The customised formulation of ranibizumab delivered by Susvimo is different from the ranibizumab intravitreal injection, a medicine marketed as Lucentis® (ranibizumab injection)*, which is approved to treat neovascular or ‘wet’ age-related macular degeneration (nAMD) and other retinal diseases. Lucentis was first approved for nAMD by the US Food and Drug Administration in 2006.16 Roche is also developing DutaFabs – the next generation of bispecific antibodies designed for increased efficacy and durability – tailored for continuous delivery via the Port Delivery implant.
About Roche in ophthalmology
Roche is focused on saving people’s eyesight from the leading causes of vision loss through pioneering therapies. Through our innovation in the scientific discovery of new potential drug targets, personalised healthcare, molecular engineering, biomarkers and continuous drug delivery, we strive to design the right therapies for the right patients.
We have the broadest retina pipeline in ophthalmology, which is led by science and informed by insights from people with eye conditions. Our pipeline includes innovative treatments across different modalities, such as antibodies, and gene and cell therapies targeting multiple vision-threatening conditions, including retinal vascular and diabetic eye diseases, geographic atrophy, and autoimmune conditions, such as thyroid eye disease and uveitic macular edema.
Applying our extensive experience, we have brought breakthrough ophthalmic treatments to people living with vision loss. Susvimo® (previously called Port Delivery Platform with ranibizumab) 100 mg/mL for intravitreal use via ocular implant is the first US Food and Drug Administration-approved refillable eye implant for neovascular or ‘wet’ age-related macular degeneration (nAMD) and diabetic macular edema (DME) that continuously delivers a customised formulation of ranibizumab over a period of months.4,8 Vabysmo® (faricimab) is the first bispecific antibody approved for the eye, which targets and inhibits two signalling pathways linked to a number of vision-threatening retinal conditions by neutralising angiopoietin-2 and vascular endothelial growth factor-A.17-19 Vabysmo is approved around the world for people living with nAMD, DME and macular edema following retinal vein occlusion.19-24 Lucentis® (ranibizumab injection)* was the first treatment approved to improve vision in people with certain retinal conditions.16
About Roche
Founded in 1896 in Basel, Switzerland, as one of the first industrial manufacturers of branded medicines, Roche has grown into the world’s largest biotechnology company and the global leader in in-vitro diagnostics. The company pursues scientific excellence to discover and develop medicines and diagnostics for improving and saving the lives of people around the world. We are a pioneer in personalised healthcare and want to further transform how healthcare is delivered to have an even greater impact. To provide the best care for each person we partner with many stakeholders and combine our strengths in Diagnostics and Pharma with data insights from the clinical practice.
For over 125 years, sustainability has been an integral part of Roche’s business. As a science-driven company, our greatest contribution to society is developing innovative medicines and diagnostics that help people live healthier lives. Roche is committed to the Science Based Targets initiative and the Sustainable Markets Initiative to achieve net zero by 2045.
Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan.
For more information, please visit www.roche.com.
*Lucentis® (ranibizumab injection) was developed by Genentech, a member of the Roche Group. Genentech retains commercial rights in the United States and Novartis has exclusive commercial rights for the rest of the world.
All trademarks used or mentioned in this release are protected by law.
References
[1] Diep TM, et al. Risk factors associated with diabetic macular edema (DME). Diabetes Res Clin Pract. 2013 Jun;100(3):298-305.
[2] The Lancet. Diabetes: A defining disease of the 21st century. Lancet. 2023;24;401(10394):2087.
[3] Im JHB, et al. Prevalence of DME based on optical coherence tomography in people with diabetes: a systematic review and meta-analysis. Survey of Ophthalmology. 2022;67(4):1244-1251.
[4] US Food and Drug Administration (FDA). Highlights of prescribing information, Susvimo. 2021. [Internet; cited February 2025]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761197s000lbl.pdf.
[5] Sakini ASA, et al. DME: dissecting pathogenesis, prognostication, diagnostic modalities along with current and futuristic therapeutic insights. Int J Retina Vitreous. 2024 Oct 28;10(1):83.
[6] National Eye Institute. Injections to treat eye conditions. [Internet; cited February 2025]. Available from: https://www.nei.nih.gov/learn-about-eye-health/eye-conditions-and-diseases/diabetic-retinopathy/injections-treat-eye-conditions.
[7] Khanani AM. Port Delivery System (PDS) with ranibizumab in patients with DME: Primary analysis results of the phase III Pagoda trial. Presented at: The Bascom Palmer Eye Institute Angiogenesis, Exudation, and Degeneration Annual Meeting; 2023 Feb 10-11; virtual.
[8] Holekamp N, et al. Archway randomised phase III trial of the PDS with ranibizumab for neovascular age-related macular degeneration (nAMD). Ophthalmology. 2021.
[9] FDA. 2021 Calendar year approvals. [Internet; cited February 2025]. Available from: https://www.fda.gov/media/150966/download.
[10] Khorrami-Nejad M, et al. The Impact of Visual Impairment on Quality of Life. Med Hypothesis Discov Innov Ophthalmol. 2016 Fall;5(3):96-103.
[11] All About Vision. Macula lutea. [Internet; cited February 2025]. Available from: https://www.allaboutvision.com/resources/macula.
[12] National Eye Institute. Diabetic Retinopathy (DR). [Internet; cited February 2025]. Available from: https://www.nei.nih.gov/learn-about-eye-health/eye-conditions-and-diseases/diabetic-retinopathy.
[13] Liu E, et al. DME: Clinical risk factors and emerging genetic influences. Clinical and Experimental Optometry. 2017;100:569–76.
[14] Clinical Trials.gov. A study to evaluate the efficacy, safety and pharmacokinetics of the PDS with ranibizumab in participants with DME compared with intravitreal ranibizumab (Pagoda). [Internet; cited February 2025]. Available from: https://clinicaltrials.gov/study/NCT04108156.
[15] Heier JS, et al. The angiopoietin/tie pathway in retinal vascular diseases: A review. The Journal of Retinal and Vitreous Diseases. 2021;41:1-19.
[16] US FDA. Highlights of prescribing information, Lucentis. 2014. [Internet; cited February 2025]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/125156s0069s0076lbl.pdf.
[17] Wykoff C, et al. Efficacy, durability and safety of intravitreal faricimab with extended dosing up to every 16 weeks in patients with DME (YOSEMITE and RHINE): Two randomised, double-masked, phase III trials. The Lancet. 2022; 399:741-755.
[18] Heier JS, et al. Efficacy, durability, and safety of intravitreal faricimab up to every 16 weeks for nAMD (TENAYA and LUCERNE): Two randomised, double-masked, phase III, non-inferiority trials. The Lancet. 2022;399:729-40.
[19] US FDA. Highlights of prescribing information, Vabysmo. 2024. [Internet; cited February 2025]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/761235s005lbl.pdf.
[20] Roche data on file.
[21] Medicines and Healthcare products Regulatory Agency approves faricimab through international work-sharing initiative. [Internet; cited February 2025]. Available from: https://www.gov.uk/government/news/mhra-approves-faricimab-through-international-work-sharing-initiative.
[22] Chugai obtains regulatory approval for Vabysmo, the first bispecific antibody in ophthalmology, for nAMD and DME. [Internet; cited February 2025]. Available from: https://www.chugai-pharm.co.jp/english/news/detail/20220328160002_909.html.
[23] European Medicines Agency. Summary of product characteristics, Vabysmo. 2022. [Internet; cited February 2025]. Available from: https://www.ema.europa.eu/en/documents/product-information/vabysmo-epar-product-information_en.pdf.
[24] Chugai obtains regulatory approval for Vabysmo, the only bispecific antibody in the ophthalmology field, for additional indication of macular edema associated with retinal vein occlusion. [Internet; cited February 2025]. Available from: https://www.chugai-pharm.co.jp/english/news/detail/20240326160000_1054.html.
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FAQ
What is the new FDA approval for Roche (RHHBY) Susvimo in February 2025?
How many treatments per year does Susvimo require for DME patients?
What were the efficacy results of Susvimo in the Pagoda trial for RHHBY?
What conditions is Roche's Susvimo now approved to treat?
How many people are affected by DME globally?
