Lilly's Omvoh® (mirikizumab) recommended by CHMP for approval in the European Union for adults with moderately to severely active Crohn's disease
Eli Lilly's Omvoh® (mirikizumab) received a positive recommendation from EMA's CHMP for treating adults with moderately to severely active Crohn's disease. The recommendation is based on the Phase 3 VIVID-1 trial, which demonstrated significant improvements in endoscopic response, clinical remission, and bowel urgency symptoms. Omvoh would be the first Crohn's disease treatment showing improvements in histologic measures of inflammation in its label.
Already approved in 44 countries for ulcerative colitis, Omvoh awaits European Commission's final decision in the next 1-2 months. The drug is also under review in the U.S., with a decision expected in first half of 2025.
Omvoh® (mirikizumab) di Eli Lilly ha ricevuto una raccomandazione positiva dal CHMP dell'EMA per il trattamento degli adulti con malattia di Crohn attiva da moderata a grave. La raccomandazione si basa sullo studio di fase 3 VIVID-1, che ha dimostrato miglioramenti significativi nella risposta endoscopica, nella remissione clinica e nei sintomi di urgenza intestinale. Omvoh sarebbe il primo trattamento per la malattia di Crohn a mostrare miglioramenti nelle misure istologiche di infiammazione nel suo approvato.
Già approvato in 44 paesi per la colite ulcerosa, Omvoh attende la decisione finale della Commissione Europea nei prossimi 1-2 mesi. Il farmaco è anche sotto revisione negli Stati Uniti, con una decisione attesa nella prima metà del 2025.
Omvoh® (mirikizumab) de Eli Lilly recibió una recomendación positiva del CHMP de la EMA para el tratamiento de adultos con enfermedad de Crohn activa de moderada a grave. La recomendación se basa en el ensayo de fase 3 VIVID-1, que demostró mejoras significativas en la respuesta endoscópica, la remisión clínica y los síntomas de urgencia intestinal. Omvoh sería el primer tratamiento para la enfermedad de Crohn que muestra mejoras en las medidas histológicas de inflamación en su etiqueta.
Ya aprobado en 44 países para la colitis ulcerosa, Omvoh espera la decisión final de la Comisión Europea en los próximos 1-2 meses. El medicamento también está bajo revisión en EE. UU., con una decisión esperada en la primera mitad de 2025.
Omvoh® (mirikizumab)는 Eli Lilly가 제조한 약물로, EMA의 CHMP에서 중등도에서 중증 활동성 크론병 치료를 위한 긍정적인 권고를 받았습니다. 이 권고는 임상 3상 VIVID-1 시험을 기반으로 하며, 내시경 반응, 임상 관해, 장의 긴급 증상에서의 유의미한 개선이 있음을 보여주었습니다. Omvoh는 라벨에서 염증의 조직학적 조치에서 개선을 보인 첫 번째 크론병 치료제가 될 것입니다.
Omvoh는 이미 44개국에서 궤양성 대장염 치료제로 승인되었으며, 유럽연합 집행위원회의 최종 결정을 1-2개월 이내에 기다리고 있습니다. 이 약물은 또한 미국에서 검토 중이며, 2025년 상반기 중에 결정이 예상됩니다.
Omvoh® (mirikizumab) d'Eli Lilly a reçu une recommandation positive du CHMP de l'EMA pour le traitement des adultes atteints de maladie de Crohn active de modérée à sévère. Cette recommandation est basée sur l'essai clinique de phase 3 VIVID-1, qui a démontré des améliorations significatives dans la réponse endoscopique, la rémission clinique et les symptômes d'urgence intestinale. Omvoh serait le premier traitement pour la maladie de Crohn à montrer des améliorations dans les mesures histologiques de l'inflammation sur son étiquette.
Déjà approuvé dans 44 pays pour la colite ulcéreuse, Omvoh attend la décision finale de la Commission européenne dans les 1 à 2 mois à venir. Le médicament est également en cours d'examen aux États-Unis, avec une décision attendue dans la première moitié de 2025.
Omvoh® (mirikizumab) von Eli Lilly erhielt eine positive Empfehlung vom CHMP der EMA zur Behandlung von Erwachsenen mit gemäßigter bis schwerer aktiver Morbus Crohn. Die Empfehlung basiert auf der Phase-3-Studie VIVID-1, die signifikante Verbesserungen in der endoskopischen Antwort, klinischen Remission und den Symptomen der Stuhldrang zeigte. Omvoh wäre die erste Behandlung für Morbus Crohn, die Verbesserungen in histologischen Entzündungsmaßnahmen in ihrem Label zeigt.
Das Medikament ist bereits in 44 Ländern zur Behandlung von Colitis ulcerosa zugelassen und wartet auf die endgültige Entscheidung der Europäischen Kommission in den nächsten 1-2 Monaten. Das Medikament wird auch in den USA geprüft, mit einer Entscheidung, die für die erste Hälfte von 2025 erwartet wird.
- First Crohn's disease treatment to demonstrate histologic healing improvements
- Achieved statistically significant improvement in all primary and secondary endpoints in Phase 3 VIVID-1 trial
- Already approved in 44 countries for ulcerative colitis treatment
- Demonstrated improvements in hard-to-treat bowel urgency symptoms
- None.
Insights
The Phase 3 VIVID-1 trial evaluated the safety and efficacy of Omvoh in patients with or without prior biologic failure and was the basis for the positive opinion
VIVID-1 was the first pivotal Crohn's disease trial to show benefits in hard-to-treat symptom of bowel urgency using a patient-centric scale
Omvoh will be the first treatment for Crohn's disease with results demonstrating improvements of histologic measures of inflammation included in its label, if approved by the European Commission
Lilly has also submitted Omvoh in the
"I am excited for the potential of Omvoh as a novel treatment option for patients suffering from moderately to severely active Crohn's disease, since the majority of patients do not achieve remission on current therapies or cannot maintain it long term," said Stefan Schreiber, M.D., Ph.D., director of the Clinic for Internal Medicine I at Kiel Campus of the University Hospital Schleswig-Holstein, Kiel,
Omvoh was previously approved in the European Union,
The positive CHMP opinion is supported by data from the Phase 3 VIVID-1 study evaluating the safety and efficacy of mirikizumab compared with placebo and an active control (ustekinumab) in adults with moderately to severely active Crohn's disease. In VIVID-1, patients treated with mirikizumab achieved statistically significant improvement compared to placebo-treated patients on both co-primary endpoints, composite endoscopic response and composite clinical remission, and all major secondary endpoints, including composite steroid-free clinical remission and endoscopic outcomes, at Week 12 and Week 52. Additionally, improvements in bowel urgency severity were achieved, as measured by a patient-centric, 11-point scale developed by Lilly. VIVID-1 is the first pivotal Crohn's disease trial to report improvements in histologic outcomes with strict definitions that were aligned with the European Crohn's and Colitis (ECCO) position statement on mucosal histopathology. Histologic healing, as evaluated by these histologic measures of inflammation, is associated with better long-term outcomes for patients with Crohn's disease. Mirikizumab's overall safety profile in patients with moderately to severely active Crohn's disease was consistent with its known safety profile in patients with UC. Results from the VIVID-1 study were recently published in The Lancet.
In addition, long-term, multi-year, sustained efficacy and safety data for both UC and Crohn's disease were also recently presented at the American College of Gastroenterology (ACG) Annual Meeting in October.
"Disruptive symptoms of Crohn's disease, such as bowel urgency, can interfere with all aspects of life, leaving many people searching for treatments that can help them fully participate in the things that they enjoy," said Mark Genovese, M.D., senior vice president of Lilly Immunology development. "Given the efficacy we saw on clinical remission and endoscopic response, combined with the improvements in bowel urgency and histological inflammation, this positive CHMP opinion for Omvoh brings us a step closer to advancing care for more people with inflammatory bowel disease around the world."
Lilly has submitted marketing applications for Omvoh in Crohn's disease around the globe, including the
About Crohn's Disease
Crohn's disease is a chronic, inflammatory bowel disease associated with progressive bowel damage, disability and decreased health-related quality of life. If not adequately controlled, it may lead to complications that require hospitalization and surgical intervention. A substantial proportion of patients do not experience adequate treatment outcomes, have secondary loss of response to maintenance therapy or do not tolerate existing therapies, including biologic agents. Patients with previous biologic failure may be more difficult to treat.
About VIVID-1
VIVID-1 was a Phase 3, randomized, double-blind, treat-through study that evaluated the safety and efficacy of mirikizumab compared with placebo and an active control (ustekinumab) in adults with moderately to severely active Crohn's disease. Patients randomized to mirikizumab were administered 900 mg of mirikizumab intravenously at Week 0, 4 and 8, then 300 mg subcutaneously every four weeks from Weeks 12-52. In this study,
Indications and Usage for Omvoh® (mirikizumab-mrkz) (in
Omvoh® is indicated for the treatment of moderately to severely active ulcerative colitis in adults.
Important Safety Information for Omvoh (mirikizumab-mrkz)
CONTRAINDICATIONS - Omvoh is contraindicated in patients with a history of serious hypersensitivity reaction to mirikizumab-mrkz or any of the excipients.
WARNINGS AND PRECAUTIONS
Hypersensitivity Reactions
Serious hypersensitivity reactions, including anaphylaxis during intravenous infusion, have been reported with Omvoh administration. Infusion-related hypersensitivity reactions, including mucocutaneous erythema and pruritus, were reported during induction. If a severe hypersensitivity reaction occurs, discontinue Omvoh immediately and initiate appropriate treatment.
Infections
Omvoh may increase the risk of infection. Do not initiate treatment with Omvoh in patients with a clinically important active infection until the infection resolves or is adequately treated. In patients with a chronic infection or a history of recurrent infection, consider the risks and benefits prior to prescribing Omvoh. Instruct patients to seek medical advice if signs or symptoms of clinically important acute or chronic infection occur. If a serious infection develops or an infection is not responding to standard therapy, monitor the patient closely and do not administer Omvoh until the infection resolves.
Tuberculosis
Evaluate patients for tuberculosis (TB) infection prior to initiating treatment with Omvoh. Do not administer Omvoh to patients with active TB infection. Initiate treatment of latent TB prior to administering Omvoh. Consider anti-TB therapy prior to initiation of Omvoh in patients with a history of latent or active TB in whom an adequate course of treatment cannot be confirmed. Monitor patients for signs and symptoms of active TB during and after Omvoh treatment. In clinical trials, subjects were excluded if they had evidence of active TB, a history of active TB, or were diagnosed with latent TB at screening.
Hepatotoxicity
Drug-induced liver injury in conjunction with pruritus was reported in a clinical trial patient following a longer than recommended induction regimen. Omvoh was discontinued. Liver test abnormalities eventually returned to baseline. Evaluate liver enzymes and bilirubin at baseline and for at least 24 weeks of treatment. Monitor thereafter according to routine patient management. Consider other treatment options in patients with evidence of liver cirrhosis. Prompt investigation of the cause of liver enzyme elevation is recommended to identify potential cases of drug-induced liver injury. Interrupt treatment if drug-induced liver injury is suspected, until this diagnosis is excluded. Instruct patients to seek immediate medical attention if they experience symptoms suggestive of hepatic dysfunction.
Immunizations
Avoid use of live vaccines in patients treated with Omvoh. Medications that interact with the immune system may increase the risk of infection following administration of live vaccines. Prior to initiating therapy, complete all age-appropriate vaccinations according to current immunization guidelines. No data are available on the response to live or non-live vaccines in patients treated with Omvoh.
ADVERSE REACTIONS
Most common adverse reactions (≥
During induction, Omvoh is available as a single dose vial for intravenous infusion containing 300 mg/15 mL that is administered in a healthcare facility. During maintenance, Omvoh is available as a one-time use prefilled pen or syringe with 100 mg/mL for subcutaneous injections. See Prescribing Information for dosing information.
MR HCP ISI 31JUL2024
Please click for Prescribing Information and Medication Guide for Omvoh. Please click for Instructions for Use included with the device.
About Omvoh®
Omvoh® (mirikizumab) is an interleukin-23p19 antagonist indicated for the treatment of moderately to severely active ulcerative colitis in adults. Omvoh selectively targets the p19 subunit of IL-23 and inhibits the IL-23 pathway. Inflammation due to over-activation of the IL-23 pathway plays a critical role in the pathogenesis of ulcerative colitis. Treatment of ulcerative colitis with Omvoh starts with 300-mg IV infusions, once every four weeks for a total of three infusions, and transitions to two, 100-mg subcutaneous injections every four weeks during maintenance treatment.
Omvoh® and its delivery device base are trademarks owned by Eli Lilly and Company.
About Lilly
Lilly is a medicine company turning science into healing to make life better for people around the world. We've been pioneering life-changing discoveries for nearly 150 years, and today our medicines help tens of millions of people across the globe. Harnessing the power of biotechnology, chemistry and genetic medicine, our scientists are urgently advancing new discoveries to solve some of the world's most significant health challenges: redefining diabetes care; treating obesity and curtailing its most devastating long-term effects; advancing the fight against Alzheimer's disease; providing solutions to some of the most debilitating immune system disorders; and transforming the most difficult-to-treat cancers into manageable diseases. With each step toward a healthier world, we're motivated by one thing: making life better for millions more people. That includes delivering innovative clinical trials that reflect the diversity of our world and working to ensure our medicines are accessible and affordable. To learn more, visit Lilly.com and Lilly.com/news, or follow us on Facebook, Instagram and LinkedIn. P-LLY
Cautionary Statement Regarding Forward-Looking Statements
This press release contains forward-looking statements (as that term is defined in the Private Securities Litigation Reform Act of 1995) about Omvoh (mirikizumab-mrkz) as a potential treatment for people with moderate to severe Crohn's disease and reflects Lilly's current beliefs and expectations. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of drug research, development, and commercialization. Among other things, there is no guarantee that planned or ongoing studies will be completed as planned, that future study results will be consistent with study results to date, that Omvoh will receive additional regulatory approvals, or that Omvoh will be commercially successful. For further discussion of these and other risks and uncertainties that could cause actual results to differ from Lilly's expectations, see Lilly's Form 10-K and Form 10-Q filings with the United States Securities and Exchange Commission. Except as required by law, Lilly undertakes no duty to update forward-looking statements to reflect events after the date of this release.
Refer to: | Kathleen Ritchie; kathleen.ritchie@lilly.com; 562-323-1667 (Lilly media) |
Michael Czapar; czapar_michael_c@lilly.com; 317-617-0983 (Investors) |
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