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
110 drugs in development
By Therapeutic Area
top 6
R&D Momentum
98/100
Pipeline Velocity
79/100
Trial Completion Rate
90/100
Pipeline Concentration
19/100
Pipeline Freshness
67/100
Strategic Signals
Activity
Last 14 days
A Phase 1, Open-Label, Randomized, Parallel-Group Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Two GSK3862995B Formulations After a Single Dose in Healthy Participants
A Phase 3, Open-label Study to Assess the Pharmacokinetics, Pharmacodynamics and Safety of Depemokimab (GSK3511294) Administered Subcutaneously as Add on Maintenance Treatment of Asthma With Type 2 Inflammation Characterised by an Eosinophilic Phenotype in Participants Aged 6 to 11 Years Old
A Phase 1, Randomized, Double-Blind, Placebo Controlled, Single Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Target Engagement of GSK4528287 in Healthy Participants
A Phase 2, Multicenter, Open Label, Non-randomized Study to Evaluate the Efficacy and Safety of Extended Dosing of Belantamab Mafodotin in Different Combinations With Standard of Care Regimens in Participants With Relapsed-refractory Multiple Myeloma (DREAMM-15)
A Phase I, First-Time-in Human (FTiH), Open-label, Dose Escalation, Non-randomized Study to Assess Safety, Reactogenicity and Immune Response of a CoV-2 SAM (LNP) Vaccine When Administered Intramuscularly on a 0, 1 Month Schedule in Healthy Adults 18 to 50 Years of Age
A Multi-arm, Phase 3, Randomized, Placebo Controlled, Double Blind Clinical Trial to Investigate the Efficacy and Safety of Fostemsavir (BMS-663068/GSK3684934) in Heavily Treatment Experienced Subjects Infected With Multi-drug Resistant HIV-1 (BRIGHTE Study)
A Randomized, Non-inferiority, Double-blind, Controlled, Single-dose, 2-way Cross-over Study to Assess the Potential for Airway Sensitivity Reactions With Propellants HFA-152a (Test) and HFA-134a (Reference) Administered Via Pressurized Metered Dose Inhalers in Adults Aged 18-45 With Mild Asthma
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)