Cosentyx Becomes First Novartis Medicine Offered at 55% Discount Through New DTP Model

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(IN BRIEF) Novartis will launch a direct-to-patient (DTP) platform in the US on November 1, 2025, starting with Cosentyx, which will be offered at a 55% discount off list price for cash-paying patients. Cosentyx, a biologic approved for multiple immune-mediated inflammatory diseases, has been used globally by more than 1.8 million patients since its 2015 launch. Novartis President US Victor Bultó said the program is designed to provide patients with more direct access to net pricing while reducing systemic barriers. The DTP platform serves as proof-of-concept for a new distribution model, with potential expansion to other Novartis medicines and a direct-to-employer option. Existing patient support and assistance programs remain available, ensuring multiple pathways to affordability and access.

(PRESS RELEASE) BASEL, 29-Sep-2025 — /EuropaWire/ —  Novartis (SWX: NOVN), a Swiss multinational pharmaceutical company, has announced the launch of a new direct-to-patient (DTP) platform in the United States, beginning November 1, 2025, with its first offering focused on Cosentyx® (secukinumab). Through the initiative, select units of the company’s top-selling US medicine will be available to cash-paying patients at a 55% discount from the list price, making specialty care more affordable and accessible outside traditional distribution channels.

Cosentyx is a biologic treatment approved by the FDA for several immune-mediated inflammatory conditions, including psoriasis, hidradenitis suppurativa, and psoriatic arthritis. With more than 17 years of clinical research and real-world use among 1.8 million patients globally since 2015, it has become a trusted therapy for those managing chronic inflammatory diseases.

Victor Bultó, President of Novartis US, said the initiative reflects a broader shift in how the company aims to connect directly with patients: “Innovation at Novartis is not only about scientific breakthroughs—it’s also about how we deliver medicines. In the US, the complexity of the system can prevent patients from accessing therapies affordably. This platform is our first step toward providing patients with net prices more directly, removing barriers, and creating a healthcare system that works better for Americans.”

The DTP platform is intended as a proof-of-concept model for specialty medicines. By offering prices comparable to savings typically negotiated by insurers and pharmacy benefit managers, Novartis aims to demonstrate the potential for a more transparent and patient-centric approach. Looking ahead, the company plans to expand DTP access to other appropriate medicines in its portfolio and is also exploring a direct-to-employer model, which would enable large businesses to purchase Cosentyx—and potentially other therapies—on behalf of employees at reduced costs.

This new option complements existing Novartis patient support programs. US patients with commercial insurance may qualify for as little as $0 out-of-pocket costs through assistance programs, and those facing delays or coverage denials can access interim support for up to two years at no cost. For patients who are uninsured, underinsured, or covered by government insurance and meet eligibility requirements, the Novartis Patient Assistance Foundation, Inc., an independent nonprofit, continues to provide Cosentyx free of charge.

By broadening affordability pathways and testing new direct distribution models, Novartis is positioning itself at the forefront of efforts to redefine access to specialty medicines in the US healthcare system.

Disclaimer
This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements can generally be identified by words such as “potential,” “can,” “will,” “plan,” “may,” “could,” “would,” “expect,” “anticipate,” “look forward,” “believe,” “committed,” “investigational,” “pipeline,” “launch,” or similar terms, or by express or implied discussions regarding potential marketing approvals, new indications or labeling for the investigational or approved products described in this press release, or regarding potential future revenues from such products. You should not place undue reliance on these statements. Such forward-looking statements are based on our current beliefs and expectations regarding future events, and are subject to significant known and unknown risks and uncertainties. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those set forth in the 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 labeling in any market, or at any particular time. Nor can there be any guarantee that such products will be commercially successful in the future. In particular, our expectations regarding such products could be affected by, among other things, the uncertainties inherent in research and development, including clinical trial results and additional analysis of existing clinical data; regulatory actions or delays or government regulation generally; global trends toward health care cost containment, including government, payor and general public pricing and reimbursement pressures and requirements for increased pricing transparency; our ability to obtain or maintain proprietary intellectual property protection; the particular prescribing preferences of physicians and patients; general political, economic and business conditions, including the effects of and efforts to mitigate pandemic diseases; safety, quality, data integrity or manufacturing issues; potential or actual data security and data privacy breaches, or disruptions of our information technology systems, and other risks and factors referred to in Novartis AG’s current Form 20-F on file with the US Securities and Exchange Commission. Novartis is providing the information in this press release as of this date and does not undertake any obligation to update any forward-looking statements contained in this press release as a result of new information, future events or otherwise.

About Novartis
Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach nearly 300 million people worldwide.

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References

  1. Novartis Europharm Limited. Cosentyx® (secukinumab): Summary of Product Characteristics. Available at: https://www.ema.europa.eu/en/documents/product-information/cosentyx-epar-product-information_en.pdf [Last accessed: Sept 2025].
  2. Girolomoni G, Mrowietz U and Paul C. Psoriasis: rationale for targeting interleukin-17. Br J Dermatol 2012; 167: 717-724.
  3. Novartis AG. 2022. shows clinically meaningful symptom improvements in patients with hidradenitis suppurativa in pivotal Phase III trials. [Press release]. Available at: https://www.novartis.com/news/media-releases/novartis-cosentyx-shows-clinically-meaningful-symptom-improvements-patients-hidradenitis-suppurativa-pivotal-phase-iii-trials [Last accessed: Sept 2025].
  4. Novartis AG. 2021. Novartis Cosentyx® receives FDA approval for the treatment of children and adolescents with enthesitis-related arthritis and psoriatic arthritis. [Press release]. Available at: https://www.novartis.com/news/media-releases/novartis-cosentyx-receives-fda-approval-treatment-children-and-adolescents-enthesitis-related-arthritis-and-psoriatic-arthritis [Last accessed: Sept 2025].
  5. Novartis AG. 2022. Novartis Cosentyx® (secukinumab) receives positive CHMP opinion for expanded use in childhood arthritic conditions. [Press release]. Available at: https://www.novartis.com/news/media-releases/novartis-cosentyx-secukinumab-receives-positive-chmp-opinion-expanded-use-childhood-arthritic-conditions [Last accessed: Sept 2025].
  6. Data on file_Cosentyx WW LTD patients Q1’25
  7. Uta Kiltz et al. Secukinumab Retention and Effectiveness in Patients with PsA and Radiographic Axial Spondyloarthritis: 5-year Final Results of a Prospective Real-world Study. Abstract no:2344. ACR 2024 [Link]
  8. Ippoliti et al. Long-Term Real-World Safety Profile of Secukinumab Assessed Through a 9-Year Experience in Patients Affected by Psoriasis, Psoriatic Arthritis and Ankylosing Spondylitis: Results From a Multicentric Retrospective Study. Dermatologic Therapy. 2025. Article Number: 9618241 [Link]
  9. Mease PJ, Kavanaugh A, Reimold A, Tahir H, Rech J, Hall S, Geusens P, Pascale P, Delicha EM, Pricop L, Mpofu S. “Secukinumab Provides Sustained Improvements in the Signs and Symptoms in Psoriatic Arthritis: Final 5‑Year Efficacy and Safety Results from a Phase 3 Trial”. ACR/ARHP 2020 Annual Meeting Abstract. Presented in ACR Open Rheumatology (2020); CONCL‑00511 (Secukinumab Provides Sustained Improvements in the Signs and Symptoms of Psoriatic Arthritis: Final 5-year Results from the Phase 3 FUTURE 1 Study – PubMed)
  10. McInnes IB, Mease PJ, Kivitz AJ, Nash P, Rahman P, Rech J, Conaghan PG, Kirkham B, Navarra S, Belsare AD, Delicha EM, Pricop L, Mpofu S; FUTURE 2 Study Group. “Long‑term efficacy and safety of secukinumab in patients with psoriatic arthritis: 5‑year (end‑of‑study) results from the phase III FUTURE 2 study.” Lancet Rheumatology. 2020; 2(4): e227–e235. (Long-term efficacy and safety of secukinumab in patients with psoriatic arthritis: 5-year (end-of-study) results from the phase 3 FUTURE 2 study)
  11. Bissonnette R, Luger T, Thaçi D, Toth D, Lacombe A, Xia S, Mazur R, Patekar M, Charef P, Milutinovic M, Leonardi C, Mrowietz U.Secukinumab demonstrates high sustained efficacy and a favourable safety profile in patients with moderate-to-severe psoriasis through 5 years of treatment (SCULPTURE Extension Study). J Eur Acad Dermatol Venereol. 2018 Sep;32(9):1507–1514. (Secukinumab demonstrates high sustained efficacy and a favourable safety profile in patients with moderate-to-severe psoriasis through 5 years of treatment (SCULPTURE Extension Study) – PubMed)

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