New Brunswick, NJ, United States · Est. 1886 · 132,000 employees
Diversified healthcare company with pharmaceutical, medical device, and consumer health segments.
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 11 drugs with upcoming expirations
Pipeline
By Phase
38 drugs in development
By Therapeutic Area
top 6
R&D Momentum
95/100
Pipeline Velocity
74/100
Trial Completion Rate
86/100
Pipeline Concentration
21/100
Pipeline Freshness
63/100
Strategic Signals
Activity
Last 14 days
A Randomized, Controlled, Multicenter, Open-label Study to Investigate the Efficacy and Safety of Adding Apalutamide to Radiotherapy and LHRH Agonist in High-Risk Patients With Hormone-Sensitive Prostate Cancer, Assessed by PSMA-PET With an Observational Cohort
A Randomized, Double-blind, Placebo-controlled, Phase 3 Study of Apalutamide in Subjects With High-risk, Localized or Locally Advanced Prostate Cancer Who Are Candidates for Radical Prostatectomy
A Phase 1, First-in-Human, Dose Escalation Study of JNJ-88998377 in Participants With Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma (NHL)
A Randomized, Open-label Phase 3 Study of Amivantamab + FOLFIRI Versus Cetuximab/Bevacizumab + FOLFIRI in Participants With KRAS/NRAS and BRAF Wild-type Recurrent, Unresectable or Metastatic Colorectal Cancer Who Have Received Prior Chemotherapy
A Phase 3 Randomized, Open-label Induction, Double-blind Maintenance, Parallel-group, Multicenter Protocol to Evaluate the Efficacy, Safety, and Pharmacokinetics of Guselkumab in Pediatric Participants With Moderately to Severely Active Ulcerative Colitis
A Phase 1b/2, Multicenter, Open-label, Study of JNJ-90014496, an Autologous CD19/CD20 Bi-specific CAR-T Cell Therapy in Adult Participants With B-cell Non-Hodgkin Lymphoma
An Open-label, Randomized Study to Assess the Relative Bioavailability (BA) and Bioequivalence (BE) of Comparative Formulations of Niraparib and Abiraterone Acetate (AA) in Men With Prostate Cancer
A Multicenter, Randomized, Placebo-Controlled, Double-Blind, Parallel-Group Study, to Assess Efficacy, Safety and Immunogenicity of JNJ-64042056, a Phosphorylated Tau Targeted Active Immunotherapy, in Participants With Preclinical Alzheimer's Disease
A Phase 3 Randomized, Placebo-Controlled, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of Nipocalimab in Pregnancies at Risk for Severe Hemolytic Disease of the Fetus and Newborn (HDFN)
A Phase 2, Open-Label, Randomized Trial Evaluating the Impact of Enhanced Versus Standard Dermatologic Management on Selected Dermatologic Adverse Events Among Patients With Locally Advanced or Metastatic EGFR-Mutated NSCLC Treated First-Line With Amivantamab + Lazertinib
A Phase 1 Study of JNJ-89402638 for Unresectable Metastatic Colorectal Cancer and Other Gastrointestinal Malignancies
Details
Company Overview
$425.0B
Mkt Cap
$85.2B
Revenue
$22.8B
Cash
Therapeutic Focus
Pipeline
Regulatory
Darzalex — DARZALEX FASPRO
Application BLA761145
Darzalex — DARZALEX FASPRO
Application BLA761145
Darzalex — DARZALEX FASPRO
Application BLA761145
Balversa — BALVERSA
Application NDA212018
Tecvayli — TECVAYLI
Application BLA761291
Tremfya — TREMFYA
Application BLA761061
Tremfya — TREMFYA
Application BLA761061
Tremfya — TREMFYA
Application BLA761061
Gemzar — INLEXZO
Application NDA219683 (NDA)
Gemzar — INLEXZO
Application NDA219683 (NDA)
Tecvayli — TECVAYLI
Application BLA761291
Gemzar — AVGEMSI
Application NDA219920 (NDA)
Gemzar — AVGEMSI
Application NDA219920 (NDA)
Tremfya — TREMFYA
Application BLA761061
Darzalex — DARZALEX
Application BLA761036
Tecvayli — TECVAYLI
Application BLA761291
Icotyde — ICOTYDE
Application NDA220149 (NDA)
Tecvayli — TECVAYLI
Application BLA761291
Darzalex — DARZALEX FASPRO
Application BLA761145
Darzalex — DARZALEX FASPRO
Application BLA761145
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)