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GlaxoSmithKline

GlaxoSmithKline logo
πŸ‡¬πŸ‡§United Kingdom
Ownership
Public
Established
1929-01-01
Employees
70.2K
Market Cap
$90B
Website
http://www.gsk.com
Introduction

GSK Plc is a healthcare company, which engages in the research, development, and manufacture of pharmaceutical medicines, vaccines, and consumer healthcare products. It operates through the Commercial Operations, and Research and Development segments. The Commercial Operations segment has three product groups of specialty medicines, vaccines, and general medicines. The company was founded in 1715 and is headquartered in Middlesex, the United Kingdom.

Clinical Trials

3.8k

Active:161
Completed:3203

Trial Phases

5 Phases

Phase 1:1096
Phase 2:827
Phase 3:937
+2 more phases

Drug Approvals

126

PPB:126

Drug Approvals

OMJJARA TABLETS 100MG

Approval Date
Dec 13, 2024
PPB

OMJJARA TABLETS 150MG

Approval Date
Dec 13, 2024
PPB

OMJJARA TABLETS 200MG

Approval Date
Dec 13, 2024
PPB

DERMOVATE CREAM 0.05% W/W

Approval Date
Oct 12, 2023
PPB

DERMOVATE OINTMENT 0.05% W/W

Approval Date
Oct 12, 2023
PPB
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Clinical Trials

Distribution across different clinical trial phases (3330 trials with phase data)β€’ Click on a phase to view related trials

Phase 1
1096 (32.9%)
Phase 3
937 (28.1%)
Phase 2
827 (24.8%)
Phase 4
339 (10.2%)
Not Applicable
131 (3.9%)

A Study to Evaluate the Immune Response and Safety of an Influenza Vaccine in Adults 18 Years of Age and Above

Not Applicable
Not yet recruiting
Conditions
Influenza, Human
Interventions
Biological: Flu mRNA (Formulation B1)
Biological: Flu mRNA (Formulation B3)
Biological: Flu mRNA(Formulation A)
Combination Product: Comparator 1
Combination Product: Comparator 2
Combination Product: Comparator 3
First Posted Date
2025-10-03
Last Posted Date
2025-10-03
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
960
Registration Number
NCT07204964

A Study to Assess the Effectiveness and Safety of GSK3862995B in Adults With Bronchiectasis

Not Applicable
Not yet recruiting
Conditions
Bronchiectasis
Interventions
Drug: GSK3862995B
Drug: Placebo
First Posted Date
2025-10-01
Last Posted Date
2025-10-01
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
400
Registration Number
NCT07201051

eValuating the Efficacy and Safety of InitiatinG depemokImab earLy therApy iN Chronic Obstructive Pulmonary Disorder (COPD) With Type 2 Inflammation

Not Applicable
Not yet recruiting
Conditions
Pulmonary Disease, Chronic Obstructive
Interventions
Drug: Placebo
First Posted Date
2025-09-17
Last Posted Date
2025-09-26
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
1196
Registration Number
NCT07177339

A Study to Evaluate Blood Levels of Bepirovirsen in Adult Participants With Severe or Moderate Kidney Disease

Not Applicable
Not yet recruiting
Conditions
Hepatitis B
Interventions
First Posted Date
2025-09-11
Last Posted Date
2025-09-11
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
32
Registration Number
NCT07168356

Sub-study of Belantamab Mafodotin (GSK2857916) in Combination With Nirogacestat, Lenalidomide, and Dexamethasone in Participants With RRMM

Not Applicable
Active, not recruiting
Conditions
Multiple Myeloma
Interventions
First Posted Date
2025-09-02
Last Posted Date
2025-09-02
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
20
Registration Number
NCT07150091
Locations
πŸ‡°πŸ‡·

GSK Investigational Site, Ulsan, South Korea

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News

Bioxodes Appoints Industry Veteran Philippe Monteyne as Chairman to Advance Breakthrough Stroke Therapy BIOX-101

Bioxodes has appointed Philippe Monteyne, MD, PhD, a former GSK and Sanofi executive with extensive neurological expertise, as chairman of its Board of Directors to guide development of breakthrough stroke candidate BIOX-101.

Sitryx Receives FDA Clearance for First-in-Class PKM2 Modulator SYX-5219 in Atopic Dermatitis

Sitryx Therapeutics received FDA clearance for its IND application for SYX-5219, a first-in-class oral PKM2 modulator targeting atopic dermatitis.

AnaptysBio Plans Corporate Split to Separate Royalty Assets from Drug Development Operations

AnaptysBio announced plans to separate into two independent public companies by year-end 2026, creating distinct investment opportunities for royalty management and drug development operations.

Cue Biopharma Appoints Dr. Usman Azam as CEO, Pivots to Autoimmune Disease Focus with CUE-401

Cue Biopharma has appointed Dr. Usman Azam as President and CEO, effective September 29, 2025, bringing over 25 years of drug development experience including CAR-T cell therapy leadership at Novartis.

GSK CEO Emma Walmsley to Step Down, Luke Miels Named Successor

Emma Walmsley, the first woman to lead a major pharmaceutical company, will step down as GSK CEO on December 31 after more than eight years at the helm.

Pi Health Partners with GSK to Accelerate Phase 2 Oncology Trial Using AI-Powered Platform

Pi Health has entered a Master Clinical Services Outsourcing Agreement with GSK to provide fully outsourced clinical research services for a global Phase 2 oncology clinical trial.

FDA Breaks Precedent with Literature-Based Approval for Leucovorin in Cerebral Folate Deficiency

The FDA is initiating approval of leucovorin calcium tablets for cerebral folate deficiency based on systematic literature analysis rather than traditional clinical trials, marking a departure from the agency's standard evidence requirements.

Transpire Bio Achieves FDA Filing Acceptance for Generic Breo Ellipta, Positioning for Market Exclusivity

Transpire Bio's abbreviated new drug application (ANDA) for a generic version of Breo Ellipta has been accepted for filing by the U.S. FDA, marking a significant milestone for the company's complex generic franchise.

GSK to Submit Label Update for Leucovorin Following FDA Request for Cerebral Folate Deficiency Treatment

GSK will submit a supplemental New Drug Application to update Wellcovorin (leucovorin) labeling to include cerebral folate deficiency treatment at FDA's request as part of the agency's initiative to repurpose older medications.

CDC Advisory Panel Votes to Limit Combined MMRV Vaccine Use in Young Children Due to Seizure Risk

The CDC's Advisory Committee on Immunization Practices voted 8-3 to recommend against using Merck's combined MMRV vaccine for first doses in children age 4 and younger, citing double the rate of febrile seizures compared to separate shots.

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