Basel, Switzerland · Est. 1996 · 78,000 employees
Global healthcare company focused on innovative medicines across multiple therapeutic areas.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Orange Book Patents
Across 31 drugs with upcoming expirations
Pipeline
By Phase
131 drugs in development
By Therapeutic Area
top 6
R&D Momentum
100/100
Pipeline Velocity
84/100
Trial Completion Rate
84/100
Pipeline Concentration
17/100
Pipeline Freshness
71/100
Strategic Signals
Activity
Last 14 days
Double-blind, Randomized, Active-controlled, Two-way Cross-over Study, With 12-week Treatment Duration Per Period, to Evaluate the Efficacy and Safety of QMF149 (Indacaterol Acetate / Mometasone Furoate) Compared to Budesonide in Children From 6 to Less Than 12 Years of Age With Asthma
A Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel-group Phase IIIb Study Evaluating the Effect of Inclisiran on Atherosclerotic Plaque Progression Assessed by Coronary Computed Tomography Angiography (CCTA) in Participants With a Diagnosis of Non-obstructive Coronary Artery Disease Without Previous Cardiovascular Events (VICTORION-PLAQUE)
A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 2 Study to Investigate the Efficacy, Safety and Tolerability of Remibrutinib (LOU064) in Adult Patients With Papulopustular Rosacea (PPR)
Fabhalta Capsules Specified Drug-use Survey(C3 Glomerulopathy, CLNP023B11401)
An Open-label, Multi-center, Phase I/II Study of ECI830 as a Single Agent and in Combination With Ribociclib and Endocrine Therapy in Patients With Advanced Hormone Receptor Positive, HER2-negative Breast Cancer and Advanced Solid Tumors
A Phase II, Single-arm Study of De-escalation and Treatment-free Remission in Patients With Chronic Myeloid Leukemia Treated With Nilotinib in First-line Therapy Followed by a Second Attempt After Nilotinib and Asciminib Combination: DANTE Study
KontRASt-R: An Open-label, Multi-center, Rollover Study for Participants Who Have Been Previously Enrolled Into a Novartis-sponsored Opnurasib (JDQ443) Study and Are Continuing to Benefit From Opnurasib as a Single Agent or in Combination With Other Study Treatments
A Multicenter, Randomized, Double-blind, Parallel Group, Placebo-controlled Study to Evaluate the Efficacy and Safety of Iptacopan (LNP023) in Complement 3 Glomerulopathy.
Real-world Evaluation of Patient Outcomes and Experiences With Ribociclib Early Adopters: A Hybrid Study With Prospective Patient-reported Outcomes and Retrospective Clinical Chart Review.
A Multicenter, Randomized, Double-blind, Parallel Group, Placebo-controlled Study to Evaluate the Efficacy and Safety of Iptacopan (LNP023) in Idiopathic Immune-complex-mediated Membranoproliferative Glomerulonephritis (IC-MPGN)
Details
Company Overview
$230.0B
Mkt Cap
$50.3B
Revenue
$13.2B
Cash
Therapeutic Focus
Pipeline
Regulatory
Tabrecta — TABRECTA
Application NDA213591 (NDA)
Leqvio — LEQVIO
Application NDA214012 (NDA)
Lioresal — LYVISPAH
Application NDA215422 (NDA)
Scemblix — SCEMBLIX
Application NDA215358 (NDA)
Neoral — VERKAZIA
Application NDA214965 (NDA)
Ritalin — RELEXXII
Application NDA216117 (NDA)
Piqray — VIJOICE
Application NDA215039 (NDA)
Lioresal — FLEQSUVY
Application NDA215602 (NDA)
Travatan — IDOSE TR
Application NDA218010 (NDA)
Fabhalta — FABHALTA
Application NDA218276 (NDA)
Cosentyx — COSENTYX
Application BLA761349 (BLA)
Klor-Con — POKONZA
Application NDA208019 (NDA)
Neoral — VEVYE
Application NDA217469 (NDA)
Tafinlar — TAFINLAR
Application NDA217514 (NDA)
Gleevec — IMKELDI
Application NDA219097 (NDA)
Piqray — VIJOICE
Application NDA218466 (NDA)
Alphagan — LUMIFY PRESERVATIVE FREE
Application NDA218424 (NDA)
Klor-Con — POKONZA
Application NDA206814 (NDA)
Rhapsido — RHAPSIDO
Application NDA218436 (NDA)
Vanrafia — VANRAFIA
Application NDA219208 (NDA)
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)