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
109 drugs in development
By Therapeutic Area
top 6
R&D Momentum
95/100
Pipeline Velocity
70/100
Trial Completion Rate
86/100
Pipeline Concentration
23/100
Pipeline Freshness
62/100
Strategic Signals
Activity
Last 14 days
64007957MMY1001: A Phase 1/2, First-in-Human, Open-Label, Dose Escalation Study of Teclistamab, a Humanized BCMA x CD3 Bispecific Antibody, in Subjects With Relapsed or Refractory Multiple Myeloma
A Phase 1, First-in-Human Study of a Novel CD79bxCD20xCD3 Trispecific Antibody in B-Cell Non-Hodgkin Lymphoid Malignancies (NHLs)
Phase II Trial of Eflornithine (DFMO) and Etoposide for Relapsed/Refractory Neuroblastoma
A Phase 3 Multicenter, Randomized, Double-blind, Placebo-controlled and Deucravacitinib Active Comparator-controlled Study to Evaluate the Efficacy and Safety of JNJ-77242113 for the Treatment of Participants With Moderate to Severe Plaque Psoriasis
A Phase 3B, Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic Arthritis Who Had an Inadequate Response and/or Intolerance to One Prior Anti-Tumor Necrosis Factor Alpha Agent
A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of Guselkumab Subcutaneous Induction Therapy in Participants With Moderately to Severely Active Ulcerative Colitis
64407564MMY1001: A Phase 1/2, First-in-Human, Open-Label, Dose Escalation Study of Talquetamab, a Humanized GPRC5D x CD3 Bispecific Antibody, in Subjects With Relapsed or Refractory Multiple Myeloma
TECLIMMY1001-P3: A Phase 1/2, First-in-Human, Open-Label, Dose Escalation Study of Teclistamab, a Humanized BCMA x CD3 Bispecific Antibody, in Subjects With Relapsed or Refractory Multiple Myeloma
A Phase 3 Multicenter, Randomized, Double-blind, Placebo-controlled and Deucravacitinib Active Comparator-controlled Study to Evaluate the Efficacy and Safety of JNJ-77242113 for the Treatment of Participants With Moderate to Severe Plaque Psoriasis
RRA-18896: An Observational Study to Assess the Long-term Safety of Ustekinumab Versus Other Biologic Therapies Among Patients With Crohn's Disease: A New-User Cohort Study Using the Department of Defense Electronic Health Records Database
A Phase 2b Randomized, Double-blind, Active-and Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of Induction and Maintenance Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Ulcerative Colitis
A Phase 1b-2 Study of Niraparib Combination Therapies for the Treatment of Metastatic Castration-Resistant Prostate Cancer
Details
Company Overview
$425.0B
Mkt Cap
$85.2B
Revenue
$22.8B
Cash
Therapeutic Focus
Pipeline
Regulatory
Stelara — USTEKINUMAB
Application BLA761044 (BLA)
Tracleer — TRACLEER
Application NDA209279 (NDA)
Gemzar — GEMCITABINE HYDROCHLORIDE
Application NDA209604 (NDA)
Tremfya — TREMFYA
Application BLA761061 (BLA)
Gemzar — INFUGEM
Application NDA208313 (NDA)
Zytiga — YONSA
Application NDA210308 (NDA)
Erleada — ERLEADA
Application NDA210951 (NDA)
Balversa — BALVERSA
Application NDA212018 (NDA)
DARZALEX FASPRO — DARZALEX FASPRO
Application BLA761145 (BLA)
Uptravi — UPTRAVI
Application NDA214275 (NDA)
RYBREVANT — RYBREVANT
Application BLA761210 (BLA)
Tecvayli — TECVAYLI
Application BLA761291 (BLA)
Opfolda — OPFOLDA
Application NDA215211 (NDA)
TALVEY — TALVEY
Application BLA761342 (BLA)
Stelara — YESINTEK
Application BLA761406 (BLA)
Lazcluze — LAZCLUZE
Application NDA219008 (NDA)
Gemzar — INLEXZO
Application NDA219683 (NDA)
Gemzar — AVGEMSI
Application NDA219920 (NDA)
Fabhalta — IMAAVY
Application BLA761430 (BLA)
Icotyde — ICOTYDE
Application NDA220149 (NDA)
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)