Basel, Switzerland · Est. 1896 · 100,000 employees
Global pioneer in pharmaceuticals and diagnostics.
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 9 drugs with upcoming expirations
Pipeline
By Phase
116 drugs in development
By Therapeutic Area
top 6
R&D Momentum
100/100
Pipeline Velocity
79/100
Trial Completion Rate
87/100
Pipeline Concentration
16/100
Pipeline Freshness
64/100
Strategic Signals
Activity
Last 14 days
A Study of the Clinical Utility of Point of Care Cobas® Liat CT/NG/MG Nucleic Acid Test Versus Current Standard Practice
A Randomized, Double-Blind, Placebo-Controlled, 52-Week Phase II Study to Evaluate the Efficacy of Intravenous RO7046015/Prasinezumab (PRX002) in Participants With Early Parkinson's Disease With a 11-Year All-Participants-on-Treatment Extension
A Phase I, Randomized, Double-Blind, Adaptive, Placebo-Controlled, Single- Ascending Dose and Multiple-Ascending Dose, Parallel Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Food Effect of RO7763505 Following Oral Administration in Healthy Participants and Patients With Stable Coronary Artery Disease
A Phase III Randomized Double-Blind Multi-Center Treat-Through Study to Evaluate the Pharmacokinetics, Safety and Efficacy of Induction and Maintenance Therapy With Afimkibart (RO7790121) in Children Aged 2-17 Years With Moderately to Severely Active Crohn's Disease
Clinical Study to Evaluate the Impact of the Accu-Chek SmartGuide CGM Solution on the Mean Change in Time in Range of 70 - 180 mg/dl Compared to SMBG
A Phase Ib, Open-Label, Multicenter Study Evaluating the Safety, Pharmacokinetics, and Efficacy of Mosunetuzumab or Glofitamab in Combination With CC-220 and/or CC-99282 in Patients With B-Cell Non-Hodgkin Lymphoma
A Phase Ib/II Multicenter, Open-Label, Randomized Study Evaluating the Safety, Pharmacokinetics, and Activity of GDC-4198 Alone and in Combination With Giredestrant in Comparison With Abemaciclib and Giredestrant in Participants With Locally Advanced or Metastatic Estrogen Receptor-Positive, HER2-Negative Breast Cancer Who Have Previously Progressed During or After a CDK4/6 Inhibitor
A Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of Inavolisib Plus Ribociclib Plus Fulvestrant Versus Placebo Plus Ribociclib Plus Fulvestrant in Patients With Endocrine- Resistant Hormone-Receptor-Positive, HER2-Negative Advanced Breast Cancer With Chromosome 8P Loss and Without a PIK3CA Mutation
An Open-label, Multicenter, Dose-escalation, Randomized, Phase I Study to Evaluate Safety, Pharmacokinetics, Pharmacodynamics and Anti-Tumor Activity of RO7567132, as a Single Agent and in Combination With Atezolizumab in Participants With Advanced and/or Metastatic Solid Tumors
A Phase Ib/II, Open-Label, Multicenter Study Evaluating the Safety, Activity, and Pharmacokinetics of Divarasib as a Single Agent or in Combination With Other Anti-Cancer Therapies in Patients With Previously Untreated Advanced Or Metastatic Non-Small Cell Lung Cancer With a KRAS G12C Mutation
A Phase II, Open-label, Multi-cohort, Multicenter Study in Patients With Unresectable Hepatocellular Carcinoma and Child-pugh B7 and B8 Cirrhosis
Details
Company Overview
$240.0B
Mkt Cap
$58.7B
Revenue
$8.4B
Cash
Therapeutic Focus
Pipeline
Regulatory
Xofluza — XOFLUZA
Application NDA210854 (NDA)
Rozlytrek — ROZLYTREK
Application NDA212725 (NDA)
Polivy — POLIVY
Application BLA761121 (BLA)
HERCEPTIN HYLECTA — HERCEPTIN HYLECTA
Application BLA761106 (BLA)
Xofluza — XOFLUZA
Application NDA214410 (NDA)
ENSPRYNG — ENSPRYNG
Application BLA761149 (BLA)
Evrysdi — EVRYSDI
Application NDA213535 (NDA)
PHESGO — PHESGO
Application BLA761170 (BLA)
Lucentis — SUSVIMO
Application BLA761197 (BLA)
LUNSUMIO — LUNSUMIO
Application BLA761263 (BLA)
Vabysmo — VABYSMO
Application BLA761235 (BLA)
Rozlytrek — ROZLYTREK
Application NDA218550 (NDA)
Actemra — TOFIDENCE
Application BLA761354 (BLA)
COLUMVI — COLUMVI
Application BLA761309 (BLA)
Fotivda — ITOVEBI
Application NDA219249 (NDA)
PIASKY — PIASKY
Application BLA761388 (BLA)
CellCept — MYHIBBIN
Application NDA216482 (NDA)
Evrysdi — EVRYSDI
Application NDA219285 (NDA)
Actemra — AVTOZMA
Application BLA761420 (BLA)
Actemra — AVTOZMA
Application BLA761498 (BLA)
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)