MedPath

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:162
Completed:3202

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
  • Prev
  • 1
  • 2
  • 3
  • 4
  • 5
  • 13
  • Next

Clinical Trials

Distribution across different clinical trial phases (3327 trials with phase data)β€’ Click on a phase to view related trials

Phase 1
1096 (32.9%)
Phase 3
937 (28.2%)
Phase 2
827 (24.9%)
Phase 4
339 (10.2%)
Not Applicable
128 (3.8%)

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

Sub-study of Belantamab Mafodotin (GSK2857916) as Monotherapy and in Combination With Nirogacestat, Pomalidomide, 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
14
Registration Number
NCT07150104
Locations
πŸ‡ΈπŸ‡ͺ

GSK Investigational Site, Falun, Sweden

A Study to Assess the Immune Response and Safety of a Vaccine Against Influenza in Adults 18 Years of Age and Older

Not Applicable
Not yet recruiting
Conditions
Influenza, Human
Interventions
Biological: Flu mRNA (Formulation A)
Biological: Flu mRNA (Formulation B)
Combination Product: Comparator 2
Combination Product: Comparator 1
Combination Product: Comparator 3
First Posted Date
2025-08-13
Last Posted Date
2025-08-13
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
770
Registration Number
NCT07121192

A Study of Dostarlimab in Combination With Carboplatin-paclitaxel in Chinese Participants With Primary Advanced or Recurrent Endometrial Cancer (EC)

Not Applicable
Not yet recruiting
Conditions
Neoplasms, Endometrial
Interventions
First Posted Date
2025-08-07
Last Posted Date
2025-08-07
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
30
Registration Number
NCT07108270
  • Prev
  • 1
  • 2
  • 3
  • 4
  • 5
  • 712
  • Next

News

ALX Oncology Appoints Barbara Klencke as Interim Chief Medical Officer to Advance Cancer Pipeline

ALX Oncology has appointed Dr. Barbara Klencke as Interim Chief Medical Officer, replacing Dr. Alan Sandler who will return to the company's Board of Directors.

Hengrui Licenses Heart Disease Drug HRS-1893 to Braveheart Bio for $65M Upfront, Potential $1B+ Total

Jiangsu Hengrui Pharmaceuticals has licensed its selective myosin blocker HRS-1893 to Delaware-based startup Braveheart Bio for $65 million upfront plus potential milestone payments exceeding $1 billion.

SCYNEXIS Presents Promising Data on SCY-247 Against Drug-Resistant Fungal Infections at TIMM-12 Congress

SCYNEXIS will present six studies at TIMM-12 demonstrating SCY-247's broad-spectrum antifungal activity against drug-resistant Candida auris, C. glabrata, and Aspergillus species.

ArcaScience Secures $7M to Accelerate AI-Driven Drug Safety Evaluation Platform

ArcaScience raised $7 million in seed funding to expand its AI platform that transforms drug benefit-risk assessments from months-long processes to seconds-long computations.

GSK Receives FDA Orphan Drug Designation for Autosomal Dominant Polycystic Kidney Disease Treatment

GSK received FDA Orphan Drug Designation for its investigational treatment of autosomal dominant polycystic kidney disease (ADPKD), a rare genetic disorder affecting approximately 600,000 people in the U.S.

BioVersys Receives EMA Orphan Designation for Novel Tuberculosis Combination Therapy

BioVersys AG received European Medicines Agency orphan designation for alpibectir combined with ethionamide to treat tuberculosis, following successful Phase 2a proof of concept trials.

Comprehensive Clinical Trials Review Reveals Global Lennox-Gastaut Syndrome Research Landscape

A new comprehensive report analyzes the global clinical trials landscape for Lennox-Gastaut Syndrome, providing critical data on trial numbers, enrollment figures, and regional distribution across G7 and E7 nations.

GSK Launches First PD-1 Immunotherapy and PARP Inhibitor for Gynecological Cancers in India

GlaxoSmithKline has introduced Jemperli and Zejula therapies in India, marking the company's entry into the oncology segment with treatments for gynecological cancers.

Invivyd Raises $57.5 Million to Advance Monoclonal Antibody Pipeline Targeting RSV, Measles, and Long COVID

Invivyd completed a $57.5 million public offering in August 2025 to accelerate development of monoclonal antibody candidates for respiratory syncytial virus, measles, and Long COVID treatments.

Dynavax's Z-1018 Shingles Vaccine Matches GSK's Shingrix Efficacy with Superior Tolerability in Phase I/II Trial

Dynavax's investigational shingles vaccine Z-1018 demonstrated comparable immune responses to GSK's Shingrix, achieving a 100% humoral vaccine response rate versus 96.9% for Shingrix in adults aged 50-69 years.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

Β© 2025 MedPath, Inc. All rights reserved.