London, United Kingdom · Est. 2000 · 70,000 employees
Global biopharma company uniting science, technology, and talent.
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 3 drugs with upcoming expirations
Pipeline
By Phase
91 drugs in development
By Therapeutic Area
top 6
R&D Momentum
94/100
Pipeline Velocity
74/100
Trial Completion Rate
90/100
Pipeline Concentration
19/100
Pipeline Freshness
65/100
Strategic Signals
Activity
Last 14 days
A Multi-part, Phase 1, First-Time-in-Human Study to Investigate Safety, Tolerability, and PK of VH4770359 in Healthy Participants
A Phase 1/2 Open-label, Multicentre, Dose Escalation and Expansion Study to Investigate the Safety, Tolerability, and Clinical Activity of Belantamab as Monotherapy and in Combination With Other Treatments in Participants With Multiple Myeloma
A Phase 1, Randomized, Double-Blinded, Placebo-Controlled, Parallel Group Study to Evaluate the Effect of Bepirovirsen on Cardiac Conduction as Assessed by 12-lead Electrocardiogram in Healthy Volunteers
A Phase 3b, Multicenter, Single-arm, Open-label Study Evaluating the Efficacy, Safety, and Tolerability of Switching to DTG/3TC Single Tablet Regimen Administered Once Daily From a Bictegravir/Emtricitabine/Tenofovir Alafenamide Single Tablet Regimen in People Living With HIV of at Least 50 Years of Age Who Are Virologically Suppressed
A Phase 3, Non-randomized, Single-arm, Open-label Study to Assess the Immunogenicity, Safety and Reactogenicity of Combined Reduced-antigen-content Diphtheria, Tetanus and Acellular Pertussis (dTpa) Vaccine, Administered as a Booster Dose in Healthy Japanese Adolescents Aged 11 Years to <13 Years
Phase 3 Multicenter, Randomized, Double-Blind, Study to Assess the Efficacy and Safety of Treatment With Bepirovirsen in Nucleos(t)Ide Analogue-treated Participants With Chronic Hepatitis B Virus (B-Well 1)
A Phase 2 Randomized, Double-blind, Placebo-controlled Study to Investigate Efficacy, Safety, Immunogenicity, and Pharmacokinetics, of GSK3862995B in Participants With Bronchiectasis
A Randomized, Open-label, Multicenter, Phase 3 Study to Investigate Mocertatug Rezetecan Compared With Standard of Care in Participants With Platinum-resistant Ovarian Cancer
A Phase 2a, Randomized, Blinded, Placebo-controlled Study of BOS-580 in Obese Subjects at Risk for, or With Biopsy-confirmed, Nonalcoholic Steatohepatitis (NASH) With a Single Arm Open-label Extension
A Phase 1/2, Randomized, Controlled, Observer-blind, Multicentre Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of GSK Biologicals' Investigational Respiratory Syncytial Virus (RSV)/Human Metapneumovirus (hMPV) Combination and Investigational hMPV Vaccines When Administered Intramuscularly According to a Single Dose Schedule in Younger Adults ≥18 to ≤49 Years and Older Adults Aged ≥60 to ≤80 Years
Details
Company Overview
$80.0B
Mkt Cap
$30.3B
Revenue
$4.2B
Cash
Therapeutic Focus
Pipeline
Regulatory
Potassium Chloride 0.037% In Sodium Chloride 0.9% In Plastic Container — SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER
Application NDA018722 (NDA)
Potassium Chloride 0.037% In Sodium Chloride 0.9% In Plastic Container — POTASSIUM CHLORIDE 20MEQ IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Application NDA019686 (NDA)
Potassium Chloride 0.037% In Sodium Chloride 0.9% In Plastic Container — POTASSIUM CHLORIDE 0.037% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Application NDA019708 (NDA)
Soriatane — SORIATANE
Application NDA019821 (NDA)
Rescriptor — RESCRIPTOR
Application NDA020705 (NDA)
Ziagen — ZIAGEN
Application NDA020977 (NDA)
Ziagen — ZIAGEN
Application NDA020978 (NDA)
Potassium Chloride 0.037% In Sodium Chloride 0.9% In Plastic Container — POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%
Application NDA017648 (NDA)
Lexiva — LEXIVA
Application NDA021548 (NDA)
Lexiva — LEXIVA
Application NDA022116 (NDA)
Selzentry — SELZENTRY
Application NDA208984 (NDA)
Selzentry — SELZENTRY
Application NDA022128 (NDA)
Tivicay — TIVICAY
Application NDA204790 (NDA)
Tivicay — TIVICAY PD
Application NDA213983 (NDA)
Bafiertam — BAFIERTAM
Application NDA210296 (NDA)
Cabenuva — APRETUDE
Application NDA215499 (NDA)
Cabenuva — VOCABRIA
Application NDA212887 (NDA)
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)