Core Insights - Novartis is set to present data from 27 abstracts related to its Immunology portfolio at the 2025 ACR Convergence, including pivotal Phase III results for ianalumab in Sjögren's disease and biomarker data for rapcabtagene autoleucel in systemic lupus erythematosus [1][7] Group 1: Ianalumab and Sjögren's Disease - Ianalumab is an investigational therapy that may become the first targeted treatment for Sjögren's disease, which currently lacks FDA-approved options [2] - The NEPTUNUS-1 and NEPTUNUS-2 trials demonstrated significant reductions in disease activity for patients with Sjögren's disease [5][7] - Presentations will include insights into the dual mode of action of ianalumab, focusing on B cell depletion and blockade of B cell activating factor receptor signaling [3][5] Group 2: Rapcabtagene Autoleucel - Rapcabtagene autoleucel is a novel CAR-T cell therapy being evaluated for its potential to reset the immune system in severe refractory systemic lupus erythematosus [3][7] - Biomarker data from an ongoing Phase 1/2 study will be presented, suggesting a reset of the B cell compartment in patients with severe refractory SLE [8] Group 3: Cosentyx Data - Real-world data on Cosentyx (secukinumab) will be shared, particularly in relation to its use in psoriatic arthritis [3][8] - The data will compare the incidence of psoriatic arthritis in patients treated with different interleukin inhibitors [8] Group 4: Investor Engagement - Following the ACR event, Novartis will host a conference call for investors to discuss updates on its Immunology pipeline [4]

Core Insights - Novartis is set to present data from 27 abstracts related to its Immunology portfolio at the 2025 ACR Convergence, including pivotal Phase III results for ianalumab in Sjögren's disease and biomarker data for rapcabtagene autoleucel in systemic lupus erythematosus [1][6] Group 1: Ianalumab and Sjögren's Disease - Ianalumab is an investigational therapy that may become the first targeted treatment for Sjögren's disease, which currently has no FDA-approved therapies [2][5] - The NEPTUNUS-1 and NEPTUNUS-2 trials demonstrated significant reductions in disease activity for patients with Sjögren's disease [5][6] - The dual mode of action of ianalumab involves targeting B cells and blocking B cell activating factor receptor signaling [7] Group 2: Rapcabtagene Autoleucel - Rapcabtagene autoleucel is a novel CAR-T cell therapy being evaluated for its potential to reset the immune system in several refractory autoimmune diseases [3][6] - Biomarker data from a Phase 1/2 study suggests a reset of the B cell compartment in severe refractory systemic lupus erythematosus [6][7] Group 3: Cosentyx Data - Real-world data on Cosentyx (secukinumab) will be presented, focusing on its use in psoriatic arthritis [3][6] - A retrospective study comparing the incidence of psoriatic arthritis in patients treated with different interleukin inhibitors will also be discussed [7] Group 4: Investor Engagement - Following the ACR event, Novartis will host a conference call on October 30, 2025, to update investors on its Immunology pipeline [4][6]

Core Insights - Novartis is launching a direct-to-patient (DTP) platform in the US on November 1, 2025, allowing cash-paying patients to purchase Cosentyx at a 55% discount off the list price [1][7] - Cosentyx is Novartis' top-selling product in the US, approved for multiple immune-mediated inflammatory diseases, and has treated over 1.8 million patients globally since its launch in 2015 [1][5] Company Strategy - The DTP platform aims to remove barriers in the healthcare system and provide net prices directly to patients, enhancing affordability [2] - Novartis plans to expand the DTP model to additional medicines in its portfolio and is exploring a direct-to-business model to sell Cosentyx to large employers [2][7] Patient Assistance Programs - Novartis offers various programs to assist patients in accessing Cosentyx, including options for eligible patients with commercial insurance to pay as little as $0 for their prescriptions [3] - The Novartis Patient Assistance Foundation provides Cosentyx at no cost to uninsured patients or those with government insurance who meet specific income guidelines [4] Product Information - Cosentyx (secukinumab) is a fully human biologic that inhibits interleukin-17A, approved for several inflammatory diseases, and supported by extensive clinical data demonstrating long-term safety and efficacy [5] - Since its launch, Cosentyx has been approved in over 100 countries and has a strong real-world data backing its effectiveness [5]

Core Insights - Oruka Therapeutics is developing ORKA-002, a novel monoclonal antibody with an extended half-life targeting IL-17A/F, which shows potential for less frequent dosing compared to existing therapies [1][3][6] - The half-life of ORKA-002 in non-human primates (NHP) exceeds 30 days, which is over three times longer than bimekizumab, suggesting a dosing interval of two to three times per year [1][6] - ORKA-002 demonstrates equivalent potency to bimekizumab with similar binding affinity, indicating a promising profile for treating chronic skin diseases like plaque psoriasis and psoriatic arthritis [2][3][6] Company Overview - Oruka Therapeutics aims to set a new standard for treating chronic skin diseases, focusing on achieving high rates of complete disease clearance with infrequent dosing [4] - The company is advancing a proprietary portfolio of antibodies engineered to target the core mechanisms of plaque psoriasis and other dermatologic conditions [4] Product Details - ORKA-002 is administered subcutaneously and has shown superior efficacy in preclinical studies compared to existing therapies that require monthly maintenance dosing [3][6] - Projections indicate that ORKA-002 could have a human half-life of approximately 50 to 75 days, allowing for dosing intervals of once every four months or twice a year [6]