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 33 drugs with upcoming expirations
Pipeline
By Phase
101 drugs in development
By Therapeutic Area
top 6
R&D Momentum
100/100
Pipeline Velocity
91/100
Trial Completion Rate
84/100
Pipeline Concentration
18/100
Pipeline Freshness
72/100
Strategic Signals
Activity
Last 14 days
Study Assessing the Efficacy, Safety and Pharmacokinetics of Alpelisib in Pediatric and Adult Patients With PIK3CA-related Overgrowth Spectrum (PROS)
A Phase 1b, Open Label, 2-Part Study to Evaluate the Effect of Pelabresib (DAK539/CPI-0610) on the Pharmacokinetics of Repaglinide, Midazolam, and Combined Drospirenone/Ethinyl Estradiol Oral Contraceptive in Patients With Advanced Malignancies
A Phase 3, Randomized, Double-blind, Active-control Study of Pelabresib (DAK539) and Ruxolitinib vs. Placebo and Ruxolitinib in Adult Patients With Myelofibrosis Who Are JAK Inhibitor Naive
TulmiSTAR-01: A Two-part, Phase I Dose Escalation and Expansion Followed by a Randomized, Open-label Multicenter, Phase II Study to Assess the Safety and Efficacy of the Combination of Tulmimetostat (DZR123) and JSB462 (Luxdegalutamide) vs Standard of Care in Patients With Progressive Metastatic Castrate Resistant Prostate Cancer
A Phase IIIb Study to Characterize the Efficacy and Safety of Adjuvant Ribociclib Plus Endocrine Therapy in a Close-to-clinical Practice Patient Population With HR+ HER2- Early Breast Cancer (Adjuvant WIDER)
A Post-trial Access Roll-over Study to Allow Access to Ribociclib (LEE011) for Patients Who Are on Ribociclib Treatment in Novartis-sponsored Study
An Open-label, Multi-center, Phase I/II Study of GVV858 as a Single Agent and in Combination With Endocrine Therapy in Patients With Advanced Hormone Receptor Positive, HER2- Negative Breast Cancer and Other Advanced Solid Tumors
A Phase III Multi-center, Randomized, Open-label Trial to Evaluate Efficacy and Safety of Ribociclib With Endocrine Therapy as an Adjuvant Treatment in Patients With Hormone Receptor-positive, HER2-negative Early Breast Cancer (New Adjuvant TriAl With Ribociclib [LEE011]: NATALEE)
An Open-label, Multi-center, Phase I/Ib Study of IEV407 as a Single Agent and in Combination With Endocrine Therapy in Patients With Advanced Hormone Receptor Positive, HER2- Negative Breast Cancer
A Phase II, Randomized, Open-label, Multi-center Study of JSB462 (Luxdegalutamide) in Combination With Abiraterone in Adult Male Patients With Metastatic Hormone-sensitive Prostate Cancer (mHSPC)
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
Open Label, Multi-center Roll-over Study to Assess Long Term Safety in Patients Who Have Completed a Global Novartis or GSK Sponsored Dabrafenib and/or Trametinib Study
Details
Company Overview
$230.0B
Mkt Cap
$50.3B
Revenue
$13.2B
Cash
Therapeutic Focus
Pipeline
Regulatory
Klor-Con — POKONZA
Application NDA206814 (NDA)
Rhapsido — RHAPSIDO
Application NDA218436 (NDA)
Leqvio — LEQVIO
Application NDA214012
Fabhalta — FABHALTA
Application NDA218276
Afinitor — AFINITOR DISPERZ
Application NDA203985
Afinitor — AFINITOR
Application NDA022334
Mekinist — MEKINIST
Application NDA204114
Cosentyx — COSENTYX
Application BLA125504
Cosentyx — COSENTYX
Application BLA761349
Cosentyx — COSENTYX
Application BLA125504
Cosentyx — COSENTYX
Application BLA761349
Kesimpta — KESIMPTA, ARZERRA
Application BLA125326
Mekinist — MEKINIST
Application NDA217513
Mekinist — MEKINIST
Application NDA204114
Tafinlar — TAFINLAR
Application NDA217514
Tafinlar — TAFINLAR
Application NDA202806
Cosentyx — COSENTYX
Application BLA125504
Cosentyx — COSENTYX
Application BLA761349
Leqvio — LEQVIO
Application NDA214012
Leqvio — LEQVIO
Application NDA214012
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)