Novartis AG
Commercial
About
Novartis AG is a Swiss multinational pharmaceutical company listed on the SIX Swiss Exchange (NOVN) and, as American Depositary Shares, on the New York Stock Exchange (NVS). It was formed in 1996 from the merger of Ciba-Geigy and Sandoz and is headquartered in Basel. It is included here as a major industry player whose portfolio intersects with aging biology rather than as a dedicated longevity company. Two Novartis assets have probed core aging pathways in humans. The interleukin-1-beta antibody canakinumab (Ilaris) was tested in the CANTOS trial, which linked inhibition of this inflammaging pathway to fewer cardiovascular events and a dose-dependent reduction in cancer mortality. The mTOR inhibitor everolimus (RAD001) improved the immune response to influenza vaccination in older adults, providing early human evidence that mTOR inhibition can partially reverse immunosenescence. Discovery is led by Novartis Biomedical Research.
Rating breakdown
Aggregate 70/100 · rank #3 in the commercial table full ratings →
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Discovery69
Trials from ClinicalTrials.gov (this org as lead sponsor), matched to aging by their condition or intervention.
- Efficacy and Safety of Brolucizumab 6mg in a Treat and Extend Regimen in Patients With Neovascular Age-Related Macular Degeneration (nAMD) With Prior Anti-VEGF Exposure (PEREGRINE) ↗ PHASE3 · Age-related Macular Degeneration (AMD)
- Phase 3 Study of Pelabresib (CPI-0610) in Myelofibrosis (MF) (MANIFEST-2) ↗ PHASE3 · Myelofibrosis, Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis
- Study to Assess the Efficacy and Safety of Brolucizumab 6mg Compared to Aflibercept 2 mg in a Treat-to-control Regimen (TALON) ↗ PHASE3 · Age-related Macular Degeneration
- A Prospective, Two-arm, Non-interventional Study of JAKAVI® (Ruxolitinib) in Patients With Myelofibrosis ↗ Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia Myelofibrosis
- Efficacy and Safety of Vildagliptin 50mg Bid as an add-on Therapy to Insulin With or Without Metformin, in Patients With Type 2 Diabetes Mellitus ↗ PHASE3 · Type 2 Diabetes Mellitus
- Intravitreal LFG316 in Patients With Advanced Age-related Macular Degeneration ↗ PHASE1 · Advanced Age-related Macular Degeneration
- Canakinumab (Ilaris): interleukin-1-beta antibody; the CANTOS trial linked inhibition of the inflammaging pathway to fewer recurrent cardiovascular events and a dose-dependent reduction in cancer mortality ↗
- Everolimus (RAD001): mTOR inhibitor shown to enhance influenza-vaccine response in older adults, early human evidence that mTOR inhibition can partially reverse immunosenescence ↗
Development98
Clinical-phase depth of the same aging-relevant trials (later phase weighs more).
- Efficacy and Safety of Brolucizumab 6mg in a Treat and Extend Regimen in Patients With Neovascular Age-Related Macular Degeneration (nAMD) With Prior Anti-VEGF Exposure (PEREGRINE) ↗ PHASE3 · Age-related Macular Degeneration (AMD)
- Phase 3 Study of Pelabresib (CPI-0610) in Myelofibrosis (MF) (MANIFEST-2) ↗ PHASE3 · Myelofibrosis, Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis
- Study to Assess the Efficacy and Safety of Brolucizumab 6mg Compared to Aflibercept 2 mg in a Treat-to-control Regimen (TALON) ↗ PHASE3 · Age-related Macular Degeneration
- Efficacy and Safety of Vildagliptin 50mg Bid as an add-on Therapy to Insulin With or Without Metformin, in Patients With Type 2 Diabetes Mellitus ↗ PHASE3 · Type 2 Diabetes Mellitus
- Intravitreal LFG316 in Patients With Advanced Age-related Macular Degeneration ↗ PHASE1 · Advanced Age-related Macular Degeneration
- A Prospective, Two-arm, Non-interventional Study of JAKAVI® (Ruxolitinib) in Patients With Myelofibrosis ↗ Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia Myelofibrosis
Fundraising91
- Market cap USD 277.45B · NVS (2026-09-29) source ↗
Education60
- Elena Bonfiglioli ARDD speaker 2024;2025;2026 source ↗
- Collin Ewald ARDD speaker 2024;2025 source ↗
- Mara Fornaro ARDD speaker 2024 source ↗
- Fraser Hall ARDD speaker 2024 source ↗
- Jacob Hanna ARDD speaker 2024 source ↗
- Lisa Melton ARDD speaker 2024;2025;2026 source ↗
- Chris Reading ARDD speaker 2024 source ↗
- Xingli Wang ARDD speaker 2024;2025;2026 source ↗
- Jerome Feige ARDD speaker 2025 source ↗
- Avi D. Spier ARDD speaker 2025 source ↗
- Fiona H. Marshall ARDD speaker 2026 source ↗
- Sophie Lemire-Brachat ARDD speaker 2026 source ↗
Key outputs
- product Canakinumab (Ilaris): interleukin-1-beta antibody; the CANTOS trial linked inhibition of the inflammaging pathway to fewer recurrent cardiovascular events and a dose-dependent reduction in cancer mortality ↗ 2017
- product Everolimus (RAD001): mTOR inhibitor shown to enhance influenza-vaccine response in older adults, early human evidence that mTOR inhibition can partially reverse immunosenescence ↗ 2014
- publication Effect of interleukin-1-beta inhibition with canakinumab on incident lung cancer in patients with atherosclerosis: exploratory results from CANTOS (Lancet): inhibiting the inflammaging pathway reduced incident lung cancer and lung-cancer mortality ↗ 2017
Registered clinical trials
130 trials list this organisation as lead sponsor ClinicalTrials.gov ↗
- A Real-world Study of the Effectiveness of Angiotensin Receptor-Neprilysin Inhibitor Therapy in Hypertensive Patients in the United Arab Emirates ↗ NOT_YET_RECRUITING · 2026-09-15
- Brain Imaging and Immune Changes During Remibrutinib Treatment in Multiple Sclerosis. ↗ RECRUITING · 2026-08-15
- HJB647 Phase 1b Study in Japanese Healthy Participants With Elevated Blood Pressure and Patients With Hypertension ↗ PHASE1 · RECRUITING · 2026-07-02
- Integrating Point of Care Testing (POCT) For Newborn Screening and Early Care for Sickle Cell Disease in Yopougon, Côte d'Ivoire ↗ PHASE4 · NOT_YET_RECRUITING · 2026-04
- Platform Study to Evaluate the Efficacy and Safety of Anti-malarial Agents in Participants With Uncomplicated Plasmodium Falciparum Malaria (Cohort C2) ↗ PHASE2 · RECRUITING · 2026-02-12
- Long Term Observational Study to Collect in a Real-world populatIon Data on the Treatment Pattern of Secukinumab in Adult Patients With Moderate to Severe HS Within the Italian Population ↗ RECRUITING · 2025-12-17
- A Phase II Trial to Evaluate the Clinical Efficacy, Safety and Tolerability of MAS825 in Pediatric and Adult Participants With Still's Disease ↗ PHASE2 · RECRUITING · 2025-11-03
- Phase I Study of [177Lu]Lu-NNS309 in Patients With Pancreatic, Lung, Breast and Colorectal Cancers ↗ PHASE1 · RECRUITING · 2024-10-15
Showing 8 of 130 registered trials.
Financial
Key people
Research fields
Links
Sources
- https://www.novartis.com/
- https://www.novartis.com/about/executive-committee
- https://www.novartis.com/about/executive-committee/vasant-narasimhan
- https://www.novartis.com/our-science/novartis-institutes-biomedical-research
- https://en.wikipedia.org/wiki/Novartis
- https://www.sec.gov/Archives/edgar/data/1114448/000111444826000008/a260204-99_1.pdf
- https://www.nejm.org/doi/full/10.1056/NEJMoa1707914
- https://www.science.org/doi/10.1126/scitranslmed.3009892