GSK Clinical Trials
GlaxoSmithKline · ViiV Healthcare · GSK Clinical Trials
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Trials
Studies that name GSK Clinical Trials as principal investigator, study chair or study director, newest first. Live from ClinicalTrials.gov, fetched 2026-11-12 10:43 UTC. Showing 200 of 3797. Open this list on ClinicalTrials.gov
- Ph4NCT07908459 · B-Ensure: Long-term Follow-up Study to Evaluate Durability of Treatment Response in Previous Bepirovirsen Study ParticipantsGlaxoSmithKline · not yet recruiting · Hepatitis B · study director
- Ph1NCT07905157 · A Study to Compare Blood Levels of Bepirovirsen and Safety Using Different Methods of Injecting in Healthy Adult ParticipantsGlaxoSmithKline · not yet recruiting · Hepatitis B · study director
- Ph1NCT07867171 · A Study to Investigate the Effects of Moderate or Severe Renal Impairment (RI) on VelzatinibGlaxoSmithKline · not yet recruiting · Healthy Participants, Gastrointestinal Neoplasms · study director
- Ph1NCT07862114 · A Study to Investigate the Effect of Omeprazole and Cyclosporine on Velzatinib in Healthy ParticipantsGlaxoSmithKline · not yet recruiting · Healthy Participants, Gastrointestinal Neoplasms · study director
- Ph3NCT07860450 · Two Part (Phase1b/ Phase3) Trial of Subcutaneous Dostarlimab Plus Carboplatin-Paclitaxel in Participants With Primary Advanced or Recurrent Endometrial CancerGlaxoSmithKline · not yet recruiting · Endometrial Carcinoma, Neoplasms, Endometrial · study director
- Ph1NCT07859735 · A Study to Investigate the Effects of Impaired Hepatic Function on VelzatinibGlaxoSmithKline · not yet recruiting · Healthy Participants, Gastrointestinal Neoplasms · study director
- N/ANCT07850141 · Prospective Registry of Exposure to Gepotidacin (PREG)GlaxoSmithKline · not yet recruiting · Sexually Transmitted Diseases · study director
- Ph1NCT07789899 · A Study to Evaluate Pharmacokinetics, Safety, and Tolerability of Two GSK3862995B Formulations in Healthy ParticipantsGlaxoSmithKline · recruiting · Pulmonary Disease, Chronic Obstructive · study director
- Ph2NCT07791043 · A Study to Investigate the Safety and Efficacy of Efimosfermin Alfa Compared With Placebo in Adult Participants With Alcohol-related Liver Disease (ALD)GlaxoSmithKline · recruiting · Liver Diseases, Alcoholic · study director
- Ph3NCT07782970 · A Study to Assess the Efficacy and Safety of GSK5784283 (Felcorekibart) in Participants With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)GlaxoSmithKline · recruiting · Nasal Polyps · study director
- Ph3NCT07782957 · A Study to Assess the Efficacy and Safety of GSK5784283 (Felcorekibart) Compared With Placebo in Participants With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)GlaxoSmithKline · recruiting · Nasal Polyps · study director
- Ph3NCT07782996 · A Study to Investigate the Efficacy and Safety of GSK5784283 Compared With Placebo in Participants With Uncontrolled Asthma (PERSIST ASTHMA-2)GlaxoSmithKline · recruiting · Asthma · study director
- Ph3NCT07780669 · A Study to Investigate the Efficacy and Safety of GSK5784283 (Felcorekibart) Compared With Placebo in Participants With Moderate to Very Severe COPD (PERSIST COPD-1)GlaxoSmithKline · recruiting · Pulmonary Disease, Chronic Obstructive · study director
- Ph3NCT07780643 · A Study to Investigate the Efficacy and Safety of GSK5784283 Compared With Placebo in Participants With Uncontrolled Asthma (PERSIST ASTHMA-1)GlaxoSmithKline · recruiting · Asthma · study director
- Ph3NCT07780656 · A Study to Investigate the Efficacy and Safety of GSK5784283 (Felcorekibart) Compared With Placebo in Participants With Moderate to Very Severe COPD (PERSIST COPD-2)GlaxoSmithKline · recruiting · Pulmonary Disease, Chronic Obstructive · study director
- Ph1NCT07747480 · A Sub Study to Investigate the Safety and Tolerability of Aletekitug in Participants With Moderate To Severe Ulcerative ColitisGlaxoSmithKline · recruiting · Colitis, Ulcerative · study director
- Ph1NCT07747467 · A Study to Investigate the Safety and Tolerability of Multiple Study Interventions in Participants With Moderate to Severe Ulcerative ColitisGlaxoSmithKline · recruiting · Colitis, Ulcerative · study director
- Ph1NCT07712393 · A Comparative Study to Investigate the Difference in Blood Levels of Two Different Formulations of GSK5784283GlaxoSmithKline · active not recruiting · Asthma · study director
- Ph3NCT07704892 · A Study to Investigate Safety and Efficacy of Efimosfermin Compared With Placebo in Adult Participants With Compensated Cirrhosis Due to Metabolic Dysfunction-associated Steatohepatitis (MASH)GlaxoSmithKline · recruiting · Metabolic Dysfunction-associated Steatohepatitis · study director
- Ph3NCT07701993 · A Pivotal Clinical Study to Investigate the Safety and Efficacy of Efimosfermin Compared With Placebo in Adult Participants With Compensated Cirrhosis Due to Metabolic Dysfunction-associated Steatohepatitis (MASH)GlaxoSmithKline · recruiting · Metabolic Dysfunction-associated Steatohepatitis · study director
- Ph4NCT07701967 · Efficacy and Safety of Depemokimab Monotherapy Without Concomitant Use of Intranasal Corticosteroids (INCS) in Japanese Participants With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)GlaxoSmithKline · recruiting · Nasal Polyps · study director
- Ph1NCT07684586 · A Study to Investigate the Difference In Blood Levels of Camlipixant Between Different Camlipixant Formulation PrototypesGlaxoSmithKline · withdrawn · Cough · study director
- Ph3NCT07671001 · A Study of Depemokimab in Participants of 6 to 11 Years of AgeGlaxoSmithKline · recruiting · Asthma · study director
- Ph4NCT07652515 · A Study to Evaluate the Safety of Dostarlimab in Adult Participants in India With Primary Advanced or Recurrent Endometrial CancerGlaxoSmithKline · not yet recruiting · Neoplasms, Endometrial · study director
- Ph3NCT07650084 · A 24-Week Study of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough - China ExtensionGlaxoSmithKline · recruiting · Refractory Chronic Cough · study director
- Ph3NCT07645248 · A Study to Compare Safety of 4 Weeks Exposure to Propellants Hydrofluoroalkane 1,1-difluoroethane (HFA-152a) and HFA-1,1,1,2-tetrafluoroethane (134a)GlaxoSmithKline · recruiting · Asthma · study director
- Ph2NCT07614360 · Study of Alternative and Approved Dosing Regimens of Belantamab Mafodotin, Bortezomib, and Dexamethasone (BVd) in Participants With Relapsed/Refractory Multiple MyelomaGlaxoSmithKline · not yet recruiting · Multiple Myeloma · study director
- Ph1NCT07600450 · A Study of GSK4771261 in Healthy Participants Aged 25 to 55 Years of Age InclusiveGlaxoSmithKline · recruiting · Kidney Disease · study director
- Ph2/Ph3NCT07569081 · A Study Evaluating the Efficacy and Safety of Momelotinib in Participants With Vacuoles, E1-enzyme, X-linked, Autoinflammatory, Somatic (VEXAS) SyndromeGlaxoSmithKline · not yet recruiting · VEXAS Syndrome · study director
- Ph2NCT07519395 · A Study to Investigate Abdominal Symptoms With Camlipixant Compared With Placebo in Adults With Irritable Bowel Syndrome - Diarrhea (IBS-D) and Irritable Bowel Syndrome - Mixed (IBS-M)GlaxoSmithKline · recruiting · Irritable Bowel Syndrome · study director
- Ph3NCT07456033 · A Study of Efficacy and Safety of Depemokimab Compared With Placebo in Adults and Adolescents With at Risk Type 2 AsthmaGlaxoSmithKline · recruiting · Asthma · study director
- Ph1NCT07371468 · A Study of GSK5926371 in Participants With B-cell Driven Autoimmune Rheumatic Diseases (ARD)GlaxoSmithKline · recruiting · Systemic Lupus Erythematosus · study director
- Ph1NCT07358546 · A Study of Efimosfermin Alfa in Adults With Hepatic ImpairmentGlaxoSmithKline · recruiting · Non-alcoholic Fatty Liver Disease · study director
- Ph1NCT07335198 · A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenicity of Efimosfermin Alfa Administered as a Single Dose to Healthy Participants of Chinese, Japanese, and White/European AncestryGlaxoSmithKline · completed · Non-alcoholic Fatty Liver Disease · study director
- Ph1/Ph2NCT07332455 · First-Time-in-Human Study of GSK5471713 in Adults With mCRPCGlaxoSmithKline · recruiting · Neoplasms, Prostate · study director
- Ph3NCT07221188 · A Clinical Study to Investigate the Safety and Tolerability of Efimosfermin Alfa Injection in Participants With Known or Suspected F2- or F3-stage MASHGlaxoSmithKline · recruiting · Non-alcoholic Fatty Liver Disease · study director
- Ph3NCT07221227 · A Pivotal Clinical Study to Investigate Efimosfermin Alfa in Participants With Biopsy-confirmed F2- or F3-stage MASHGlaxoSmithKline · recruiting · Non-alcoholic Fatty Liver Disease · study director
- Ph2NCT07201051 · A Study to Assess the Effectiveness and Safety of GSK3862995B in Adults With BronchiectasisGlaxoSmithKline · recruiting · Bronchiectasis · study director
- Ph3NCT07177339 · eValuating the Efficacy and Safety of InitiatinG depemokImab earLy therApy iN Chronic Obstructive Pulmonary Disorder (COPD) With Type 2 InflammationGlaxoSmithKline · recruiting · Pulmonary Disease, Chronic Obstructive · study director
- Ph1NCT07168356 · A Study to Evaluate Blood Levels of Bepirovirsen in Adult Participants With Severe or Moderate Kidney DiseaseGlaxoSmithKline · active not recruiting · Hepatitis B · study director
- Ph2NCT07105709 · Open-label Extension Study in Participants With Early Alzheimer's DiseaseGlaxoSmithKline · recruiting · Alzheimer's Disease · study director
- Ph1/Ph2NCT06990880 · A Study of GSK5458514 Administered Alone or In Combination With Other Anti-Cancer Agents in Participants With Prostate CancerGlaxoSmithKline · recruiting · Neoplasms, Prostate · study director
- Ph1NCT06979518 · A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of GSK3862995B Administered as a Single Dose to Healthy Participants of Chinese, Japanese, and European AncestryGlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- Ph3NCT06979323 · Depemokimab Asthma Imaging and Bronchoscopy Sub-StudyGlaxoSmithKline · recruiting · Asthma · study director
- Ph2NCT06964165 · A Study Comparing Niraparib Versus Platinum-Taxane Doublet Chemotherapy as Neoadjuvant Treatment in Participants With Homologous Recombination-Deficient Stage III/IV Ovarian Cancer (COHORT-C)Tesaro, Inc. · terminated · Ovarian Neoplasms · study director
- Ph3NCT06961214 · Depemokimab as an Extended Treatment Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA-2)GlaxoSmithKline · recruiting · Pulmonary Disease, Chronic Obstructive · study director
- Ph3NCT06959095 · Depemokimab as an Extended Treatment Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 InflammationGlaxoSmithKline · recruiting · Pulmonary Disease, Chronic Obstructive · study director
- Ph1NCT06734234 · A Study to Evaluate the Safety, Tolerability, and Effects on Blood and Urine Markers of Single Ascending Dose of GSK4771261 in Healthy Participants and Participants With Autosomal Dominant Polycystic Kidney DiseaseGlaxoSmithKline · active not recruiting · Kidney Disease · study director
- Ph3NCT06716606 · A Study to Investigate the Long-term Safety and Efficacy of Belimumab in Adults With Interstitial Lung Disease (ILD) Associated With Systemic Sclerosis (SSc) and Other Connective Tissue Diseases (CTD) (BLISSconneCTD-OLE)GlaxoSmithKline · recruiting · Connective Tissue Diseases · study director
- Ph1/Ph2NCT06655818 · Sub-study of Belantamab Mafodotin (GSK2857916) as Monotherapy and in Combination With Dostarlimab (GSK4057190) in Participants With RRMMGlaxoSmithKline · terminated · Relapsed/Refractory Multiple Myeloma · study director
- Ph1NCT06597500 · A Study to Evaluate the Effect of Itraconazole on the Concentration of GSK3923868 in the Blood in Healthy ParticipantsGlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- Ph1NCT06577597 · Safety, Tolerability and Blood Sampling of GSK3923868 Administered Via Dry Powder Inhaler to Healthy Participants of Chinese, Japanese and European AncestryGlaxoSmithKline · completed · Respiratory Tract Infections · study director
- Ph1NCT06576271 · A Study of GSK4527363 in Healthy Participants, Systemic Lupus Erythematosus (SLE) Participants, Healthy Chinese, and Japanese Participants and CTD-ILD ParticipantsGlaxoSmithKline · recruiting · Systemic Lupus Erythematosus · study director
- Ph3NCT06572384 · A Study of the Efficacy and Safety of Belimumab in Adults With Interstitial Lung Disease Associated With Connective Tissue DiseaseGlaxoSmithKline · recruiting · Lung Diseases, Interstitial · study director
- Ph2NCT06537414 · A Study of Sequential Therapy With Daplusiran/Tomligisiran (DAP/TOM) Followed by Bepirovirsen in Participants Living With Chronic Hepatitis B (CHB)GlaxoSmithKline · active not recruiting · Chronic Hepatitis B Virus Infection, Hepatitis B · study director
- N/ANCT06527872 · Study to Assess Real-world Effectiveness of Belimumab for Treatment of Adults With LNGlaxoSmithKline · recruiting · Lupus Nephritis · study director
- Ph1/Ph2NCT06521567 · A Study of Cobolimab Plus Dostarlimab in Pediatric and Young Adult Participants With CancerGlaxoSmithKline · active not recruiting · Melanoma, Hodgkin Lymphoma, High and Low Grade Glioma · study director
- Ph2NCT06497504 · Study of Bepirovirsen in Participants Living With Human Immunodeficiency Virus and Chronic Hepatitis B Virus Infection (B-Focus)GlaxoSmithKline · active not recruiting · Hepatitis B · study director
- Ph1NCT06497517 · A Study to Investigate the Effect of Food on Camlipixant Concentrations in Healthy ParticipantsBellus Health Inc. - a GSK company · completed · Cough · study director
- N/ANCT06488703 · Retrospective Analysis of Systemic Glucocorticoid Mediated Long-term Effects, Patient Pathways and Economic Burden Across Multiple IndicationsGlaxoSmithKline · completed · Asthma · study director
- Ph2NCT06447506 · Long-Term Study (AtDvance) to Evaluate GSK1070806 in Atopic Dermatitis.GlaxoSmithKline · terminated · Dermatitis, Atopic · study director
- Ph1NCT06422767 · Study to Evaluate the Effect of Bepirovirsen on Cardiac Conduction as Assessed by 12-lead Electrocardiogram in Healthy VolunteersGlaxoSmithKline · completed · Hepatitis B · study director
- Ph1NCT06413511 · A Study to Investigate the Safety and Pharmacological Effect of a Single Intravenous Infusion of Belantamab in Male and Female Participants Aged 18 to 75 With Autoimmune DiseaseGlaxoSmithKline · withdrawn · Autoimmune Diseases · study director
- Ph4NCT06411249 · A Study Describing the Efficacy and Safety of Belimumab Administered in Adult Participants With Early Systemic Lupus Erythematosus (SLE)GlaxoSmithKline · active not recruiting · Systemic Lupus Erythematosus · study director
- Ph2NCT06317285 · A Study to Evaluate the Efficacy and Safety of GSK3915393 in Participants With Idiopathic Pulmonary Fibrosis (IPF)GlaxoSmithKline · terminated · Idiopathic Pulmonary Fibrosis · study director
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- Ph1NCT06222892 · A Study of Camlipixant in Male and Female Healthy Participants and Participants With Hepatic Impairment Aged 18-75 Years of AgeBellus Health Inc. - a GSK company · completed · Cough · study director
- Ph2NCT06213506 · A Study on the Safety, Reactogenicity, and Immune Response to the GVGH iNTS-GMMA Vaccine Against Invasive Nontyphoidal Salmonella in Adults, Children, and InfantsGlaxoSmithKline · completed · Salmonella Infections · study director
- Ph1NCT06188507 · A First Time in Human Study to Evaluate the Safety and Tolerability of GSK3996401 Following Dosing With GSK4347859 in Healthy ParticipantsGlaxoSmithKline · suspended · Systemic Lupus Erythematosus · study director
- Ph1/Ph2NCT06160609 · Platform Sub-study of Belantamab Mafodotin (GSK2857916) in Combination With aOX40 (GSK3174998) in Participants With RRMMGlaxoSmithKline · terminated · Relapsed/Refractory Multiple Myeloma · study director
- Ph1NCT06154837 · A Study for GSK3862995B in Healthy Participants and Participants With Chronic Obstructive Pulmonary DiseaseGlaxoSmithKline · active not recruiting · Pulmonary Disease, Chronic Obstructive · study director
- Ph2NCT06079190 · Efficacy and Safety of GSK4527226 [AL101] in Participants With Early Alzheimer's DiseaseGlaxoSmithKline · terminated · Alzheimer's Disease · study director
- Ph1/Ph2NCT06077877 · A Study to Investigate the Safety, Tolerability, Pharmacokinetics (PK), and Preliminary Anticancer Activity of GSK4524101 Alone or With Niraparib in Participants With Solid TumorsGlaxoSmithKline · active not recruiting · Neoplasms · study director
- Ph1NCT06065735 · Concentration-QT Study of Paroxetine in Healthy AdultsGlaxoSmithKline · completed · Anxiety Disorders · study director
- Ph2NCT06062420 · A Platform Study of Novel Immunotherapy Combinations as First-Line Treatment in Participants With PD-L1 Positive Recurrent/Metastatic Squamous Cell Carcinoma of the Head and Neck- GALAXIES H&N-202GlaxoSmithKline · active not recruiting · Neoplasms, Head and Neck · study director
- Ph2NCT06061081 · A Study to Investigate the Antiviral Effect, Safety, Tolerability and Pharmacokinetics of VH3739937 in in Treatment-Naive Adults Living With HIV-1ViiV Healthcare · terminated · HIV Infections · study director
- Ph1NCT06058390 · A Study to Evaluate the Relative Bioavailability of Subcutaneous Bepirovirsen When Delivered From a Vial or Prefilled Syringe Fitted With a Safety Syringe Device in Healthy Adult ParticipantsGlaxoSmithKline · completed · Hepatitis B · study director
- Ph4NCT06041386 · REIMAGINE - Real World EvaluatIon of Mepolizumab in Severe Asthma achievinG on Treatment clinIcal remissioN, a prospEctive StudyGlaxoSmithKline · active not recruiting · Asthma · study director
- Ph2NCT05999799 · A Dose Finding Study to Investigate the Safety and Effectiveness of GSK1070806 in Adult Participants With Moderate to Severe Atopic DermatitisGlaxoSmithKline · terminated · Dermatitis, Atopic · study director
- Ph1NCT05999708 · A First Time in Human Study to Evaluate the Safety and Tolerability of GSK4381406 in Healthy ParticipantsGlaxoSmithKline · withdrawn · Colitis, Ulcerative · study director
- Ph1NCT05917288 · A Study of Belimumab in Chinese Pediatric Participants With Systemic Lupus ErythematosusGlaxoSmithKline · completed · Systemic Lupus Erythematosus · study director
- Ph3NCT05896748 · Study to Assess the Effects of Cabotegravir (CAB) and Rilpivirine (RPV) Long-Acting (LA) Injections Following Sub-cutaneous (SC) Administration Compared With Intramuscular (IM) Administration in Adult Participants Living With Human Immunodeficiency Virus (HIV-1) Infection in the FLAIR StudyViiV Healthcare · completed · Human Immunodeficiency Virus Type 1 (HIV-1) · study director
- Ph3NCT05896761 · A Sub-study of Cabotegravir (CAB) and Rilpivirine (RPV) in Human Immunodeficiency Viruses (HIV)-Infected ParticipantsViiV Healthcare · completed · Human Immunodeficiency Virus Type 1 (HIV-1) · study director
- Ph3NCT05855200 · Study of Perioperative Dostarlimab in Participants With Untreated T4N0 or Stage III dMMR/MSI-H Resectable Colon CancerGlaxoSmithKline · recruiting · Colonic Neoplasms, Neoplasms, Colon · study director
- Ph2NCT05838755 · A Study to Evaluate Efficacy and Safety of GSK3858279 in Diabetic Peripheral Neuropathic PainGlaxoSmithKline · terminated · Pain · study director
- Ph2NCT05838742 · A Dose-Finding Study to Evaluate the Efficacy and Safety of GSK3858279 in Adults With Knee Osteoarthritis (OA) PainGlaxoSmithKline · terminated · Pain, Osteoarthritis, Knee · study director
- Ph1/Ph2NCT05823974 · A Study to Assess the Safety and Immune Response of a Vaccine Against Influenza in Healthy Younger and Older AdultsGlaxoSmithKline · completed · Influenza, Human · study director
- Ph1NCT05791565 · Green (Sustainable) VENTOLIN - Pharmacokinetics (PK) Study in Healthy ParticipantsGlaxoSmithKline · completed · Asthma · study director
- Ph1NCT05776108 · A Study to Assess the Food Effect and the Relative Bioavailability of the Cabotegravir (CAB) Pediatric Dispersible Tablet (DT) FormulationViiV Healthcare · completed · HIV Infections · study director
- Ph1NCT05760261 · Drug Interaction Assessment of GSK3882347 in Healthy Participants Aged 18 to 65 YearsGlaxoSmithKline · completed · Urinary Tract Infections · study director
- Ph3NCT05757102 · A Study to Compare the Efficacy, Safety and Tolerability of FF/UMEC/VI With FF/VI in 12-17-year-olds With AsthmaGlaxoSmithKline · active not recruiting · Asthma · study director
- Ph2NCT05751629 · Study to Evaluate the Safety and Efficacy of TSR-042, Bevacizumab, and Niraparib in Participants With Recurrent Ovarian CancerTesaro, Inc. · completed · Ovarian Neoplasm · study director
- Ph2NCT05723562 · A Study of Dostarlimab in Untreated dMMR/MSI-H Locally Advanced Rectal CancerGlaxoSmithKline · active not recruiting · Neoplasms, Rectal · study director
- Ph1/Ph2NCT05714839 · A Study to Investigate the Safety and Efficacy of Belantamab for the Treatment of Multiple Myeloma When Used as Monotherapy and in Combination TreatmentsGlaxoSmithKline · recruiting · Multiple Myeloma · study director
- Ph3NCT05705440 · A Follow-up Study to Describe the Safety of Study Participants Who Received RSVPreF3 Maternal Vaccination (Any Dose) or Controls From Previous RSV MAT Studies During Any Pregnancy Conceived Post Vaccination/ControlGlaxoSmithKline · completed · Respiratory Syncytial Virus Infections · study director
- Ph3NCT05682326 · Anemia Studies in CKD: Erythropoiesis Via a Novel PHI Daprodustat - Pediatric (ASCEND-P)GlaxoSmithKline · completed · Anaemia · study director
- Ph1/Ph2NCT05674656 · Pharmacokinetics, Safety, Tolerability of Dolutegravir/Rilpivirine in PediatricsViiV Healthcare · recruiting · HIV Infections · study director
- Ph1NCT05660265 · A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Oral GSK4172239D Compared With Placebo in Sickle Cell Disease Participants Aged 18 to 50 YearsGlaxoSmithKline · terminated · Hematologic Diseases, Anaemia, Sickle Cell · study director
- Ph4NCT05648357 · A Study to Assess the Safety and Immune Response of Quadrivalent Seasonal Influenza Vaccine (Fluarix Tetra) in Participants Aged 65 Years and Older in IndiaGlaxoSmithKline · completed · Influenza, Human · study director
- Ph2NCT05630846 · A Study on the Immune Response and Safety of a Combined Measles, Mumps, Rubella, Chickenpox Vaccine Compared to a Marketed Combined Vaccine, Given to Healthy Children 4 to 6 Years of AgeGlaxoSmithKline · completed · Measles; Mumps; Rubella; Chickenpox, Measles · study director
- Ph3NCT05630807 · Study of Bepirovirsen in Nucleos(t)Ide Analogue-treated Participants With Chronic Hepatitis B (B-Well 1)GlaxoSmithKline · completed · Chronic Hepatitis B, Hepatitis B, Chronic · study director
- Ph3NCT05630833 · A Study to Investigate the Efficacy and Safety With Gepotidacin in Japanese Female Participants With Uncomplicated Urinary Tract Infection (Acute Cystitis)GlaxoSmithKline · completed · Urinary Tract Infections · study director
- Ph3NCT05630820 · Study of Bepirovirsen in Nucleos(t)Ide Analogue-treated Participants With Chronic Hepatitis B (B-Well 2)GlaxoSmithKline · completed · Chronic Hepatitis B, Hepatitis B, Chronic · study director
- Ph1NCT05631704 · A Study to Investigate Safety, Tolerability, and Pharmacokinetics (PK) of VH4524184 and the Potential for Changes in Cytochrome P450 3A (CYP3A) ActivityViiV Healthcare · completed · HIV Infections · study director
- Ph1NCT05613205 · Safety and Immunogenicity of a Novel Conjugate Vaccine Against Salmonella Typhi and Salmonella Paratyphi A in Healthy AdultsGlaxoSmithKline · completed · Typhoid Fever · study director
- Ph1NCT05602025 · A Study to Compare the Pharmacokinetics (PK) of Depemokimab When Delivered With a Safety Syringe Device (SSD) or an Autoinjector in Healthy Adult ParticipantsGlaxoSmithKline · completed · Asthma · study director
- Ph3NCT05599191 · A 52-Week Study of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic CoughBellus Health Inc. - a GSK company · completed · Cough, Refractory Chronic Cough · study director
- Ph3NCT05600777 · A 24-Week Study of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic CoughBellus Health Inc. - a GSK company · active not recruiting · Cough, Refractory Chronic Cough · study director
- Ph2NCT05583344 · Phase 2b Study of GSK4532990 in Adults With NASHGlaxoSmithKline · active not recruiting · Nonalcoholic Fatty Liver Disease, Non-alcoholic Fatty Liver Disease · study director
- N/ANCT05582083 · Managed Access Program for Momelotinib in MyelofibrosisGlaxoSmithKline · no longer available · Myelofibrosis, Primary Myelofibrosis · study director
- Ph1NCT05570539 · Assessment of the Pharmacokinetics of BLU-5937 Extended Release Prototypes and a BLU-5937 Immediate Release Reference FormulationBellus Health Inc. - a GSK company · completed · Cough, Healthy · study director
- Ph2NCT05565378 · A Platform Study of Novel Immunotherapy Combinations in Participants With Previously Untreated, Advanced/Metastatic Non-Small-Cell Lung CancerGlaxoSmithKline · active not recruiting · Lung Cancer, Non-Small Cell · study director
- Ph2NCT05553808 · Platform Trial of Novel Regimens Versus Standard of Care (SoC) in Participants With Non-small Cell Lung Cancer (NSCLC) - Sub-study 1GlaxoSmithKline · completed · Neoplasms · study director
- Ph4NCT05535972 · To Evaluate Real-World Effectiveness of Fluticasone Furoate/Umeclidinium Bromide/Vilanterol (FF/UMEC/VI) in a Single Inhaler (Trelegy Ellipta) in Participants With Symptomatic COPDGlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- Ph4NCT05514509 · A Study Evaluating Implementation Strategies for the Delivery of APRETUDE for Black cis-and Transgender Women in United States EHE TerritoriesViiV Healthcare · completed · HIV Infections · study director
- Ph1/Ph2NCT05480800 · A Study to Evaluate Safety, Reactogenicity, and Immune Response of GVGH iNTS-TCV Vaccine Against Invasive Nontyphoidal Salmonella and Typhoid FeverGlaxoSmithKline · completed · Salmonella Infections · study director
- N/ANCT05448170 · Linerixibat Compassionate Use for Cholestatic Pruritus Adult Patients With Primary Biliary Cholangitis (PBC)GlaxoSmithKline · available · Pruritus · study director
- Ph1NCT05446740 · A Study on the Safety, Reactogenicity and Immune Response of a Vaccine Against Influenza in Healthy Younger and Older AdultsGlaxoSmithKline · completed · Influenza, Human · study director
- Ph1NCT05418868 · A Study to Investigate Pharmacokinetics, Safety and Tolerability of Long-Acting Cabotegravir Plus Recombinant Human Hyaluronidase PH20 in Healthy Adult ParticipantsViiV Healthcare · recruiting · HIV Infections · study director
- Ph1NCT05398198 · Efficacy and Safety of GSK3923868 Inhalation Powder, During Experimental Human Rhinovirus Infection in Participants With Mild AsthmaGlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- Ph1NCT05393271 · First-Time-in-Human (FTIH) Study to Evaluate the Safety, Tolerability and Pharmacokinetics (PK) of VH4011499 in Healthy ParticipantsViiV Healthcare · completed · HIV Infections · study director
- Ph1NCT05393076 · Phase I Study of Linerixibat in Adults With Moderate Hepatic Impairment and Healthy ControlsGlaxoSmithKline · completed · Pruritus · study director
- Ph2NCT05382312 · Early Bactericidal Activity, Safety & Tolerability of Oral GSK3036656 in a Dual Combination With Novel and Established Antitubercular Agents, or Standard of Care in Adults With Rifampicin Susceptible Pulmonary TuberculosisGlaxoSmithKline · completed · Tuberculosis · study director
- Ph4NCT05374525 · A Study Evaluating Implementation Strategies for the Delivery of Cabotegravir in Low and High-Volume PrEP Site in the United StatesViiV Healthcare · completed · HIV Infections · study director
- Ph3NCT05371080 · A Study on the Long-term Efficacy, Safety and Persistence of Immune Response of a Vaccine Against Herpes Zoster in Older AdultsGlaxoSmithKline · active not recruiting · Herpes Zoster · study director
- Ph2NCT05340257 · A Pharmacokinetics and Safety Study of Augmentin ES-600 in Children With CAP and ABRSGlaxoSmithKline · withdrawn · Infections, Bacterial · study director
- Ph3NCT05334368 · Depemokimab in Participants With Hypereosinophilic Syndrome, Efficacy, and Safety TrialGlaxoSmithKline · active not recruiting · Hypereosinophilic Syndrome · study director
- Ph1/Ph2NCT05330455 · Study of GSK3965193 in Healthy Participants and Participants Living With Chronic Hepatitis B InfectionGlaxoSmithKline · terminated · Hepatitis B · study director
- Ph4NCT05305651 · Study to Monitor the Occurrence of Viral Variants in Patients With Compromised Immune Systems Being Treated for COVID-19GlaxoSmithKline · completed · COVID-19 · study director
- Ph1NCT05304130 · A Study in Healthy Japanese Participants to Evaluate the Safety and Pharmacokinetics of OtilimabGlaxoSmithKline · withdrawn · Arthritis, Rheumatoid · study director
- Ph1/Ph2NCT05298254 · A Study on the Reactogenicity, Safety, Immune Response, and Efficacy of a Targeted Immunotherapy Against HSV in Healthy Participants Aged 18-40 Years or in Participants Aged 18-60 Years With Recurrent Genital HerpesGlaxoSmithKline · completed · Herpes Simplex · study director
- Ph1NCT05291520 · A Study to Investigate the Safety and Pharmacokinetics of a Single Dose of VH3810109 (Also Known as GSK3810109), Administered Either Subcutaneously (SC) With rHuPH20 or Intravenously (IV), in Healthy Adult ParticipantsViiV Healthcare · completed · HIV Infections · study director
- Ph3NCT05281523 · Efficacy and Safety of Depemokimab (GSK3511294) in Participants With Chronic Rhinosinusitis With Nasal Polyps (ANCHOR-2)GlaxoSmithKline · completed · Nasal Polyps · study director
- Ph1NCT05277051 · First-Time-in-Human Study of GSK4381562 in Participants With Advanced Solid TumorsGlaxoSmithKline · active not recruiting · Neoplasms · study director
- Ph2NCT05276297 · A Study on the Safety, Efficacy and Immune Response Following Sequential Treatment With an Anti-sense Oligonucleotide Against Chronic Hepatitis B (CHB) and Chronic Hepatitis B Targeted Immunotherapy (CHB-TI) in CHB Patients Receiving Nucleos(t)Ide Analogue (NA) TherapyGlaxoSmithKline · completed · Hepatitis B, Chronic · study director
- Ph3NCT05274750 · Efficacy and Safety of Depemokimab (GSK3511294) in Participants With Chronic Rhinosinusitis With Nasal PolypsGlaxoSmithKline · completed · Nasal Polyps · study director
- Ph1NCT05271799 · A Study to Evaluate Pharmacokinetic, Safety, Tolerability and Relative Bioavailability of Gepotidacin in Healthy Adult Male and Female ParticipantsGlaxoSmithKline · completed · Healthy Volunteers · study director
- Ph3NCT05263934 · Efficacy and Safety of Depemokimab Compared With Mepolizumab in Adults With Relapsing or Refractory Eosinophilic Granulomatosis With Polyangiitis (EGPA)GlaxoSmithKline · active not recruiting · Eosinophilic Granulomatosis With Polyangiitis · study director
- Ph3NCT05243680 · An Open-Label Extension Study of GSK3511294 (Depemokimab) in Participants Who Were Previously Enrolled in 206713 (NCT04719832) or 213744 (NCT04718103)GlaxoSmithKline · completed · Asthma · study director
- Ph3NCT05229068 · A Study of Safety, Reactogenicity and Immune Response of the Repeat Vaccination Against RSV When Given to Female Participants of 18-49 Years of Age During Their Subsequent Uncomplicated PregnancyGlaxoSmithKline · withdrawn · Respiratory Syncytial Virus Infections · study director
- Ph3NCT05219253 · A Study on the Immune Response and Safety of a Vaccine Against Herpes Zoster in Adults Aged 50 Years and Older in IndiaGlaxoSmithKline · completed · Herpes Zoster · study director
- Ph1NCT05174013 · Safety, Tolerability, Pharmacokinetics and Target Engagement of GSK3858279 in Healthy Caucasian, Chinese and Japanese ParticipantsGlaxoSmithKline · completed · Pain · study director
- Ph3NCT05169905 · A Study to Evaluate the Safety and Immune Response to an Unadjuvanted RSV Maternal Vaccine in Healthy Non-pregnant Females From 9 to 49 Years of AgeGlaxoSmithKline · completed · Respiratory Syncytial Virus Infections · study director
- Ph1NCT05163522 · First-Time-in-Human (FTIH) Study to Evaluate the Safety, Tolerability and Pharmacokinetics (PK) of VH4004280 in Healthy ParticipantsViiV Healthcare · completed · HIV Infections · study director
- Ph1NCT05140200 · Study of GSK3511294 in Healthy Chinese ParticipantsGlaxoSmithKline · completed · Asthma · study director
- Ph1NCT05138822 · Safety, Tolerability, Pharmacokinetic and Microbiological Investigation of GSK3882347 in Female Participants With Urinary Tract InfectionsGlaxoSmithKline · completed · Uncomplicated Urinary Tract Infections, Urinary Tract Infections · study director
- Ph1NCT05133830 · Linerixibat and Obeticholic Acid Drug Interaction Study in Healthy Adult ParticipantsGlaxoSmithKline · completed · Pruritus · study director
- Ph1NCT05131971 · A Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics (PD) of GSK3888130B in Healthy ParticipantsGlaxoSmithKline · completed · Multiple Sclerosis, Colitis, Ulcerative · study director
- Ph2NCT05124210 · Pharmacokinetics, Pharmacodynamics, and Safety of Single-dose Sotrovimab in High-risk Pediatric Participants With Mild to Moderate COVID-19GlaxoSmithKline · terminated · COVID-19 · study director
- Ph2NCT05100316 · Screening Protocol for Preliminary Eligibility Determination for Adoptive Cell Therapy TrialsGlaxoSmithKline · terminated · Neoplasms · study director
- Ph1/Ph2NCT05073003 · A Study on the Safety and Immune Responses to the GVGH altSonflex1-2-3 Vaccine Against Shigellosis in Adults, Children, and InfantsGlaxoSmithKline · completed · Diarrhoea · study director
- Ph2NCT05064358 · Study to Investigate Alternative Dosing Regimens of Belantamab Mafodotin in Participants With Relapsed or Refractory Multiple MyelomaGlaxoSmithKline · completed · Multiple Myeloma · study director
- Ph3NCT05047770 · A Study on the Immune Response and Safety of the Shingles Vaccine and the Influenza Vaccine When Either is Given to Healthy Adults at the Same Time or Following a COVID-19 Booster VaccineGlaxoSmithKline · completed · Herpes Zoster · study director
- Ph3NCT05045144 · A Phase III Study to Assess the Lot-to-lot Consistency of GSK's Investigational RSV Maternal Vaccine and the Immune Response and Safety of RSV Maternal Vaccine When Given Alone or Co-administered With GSK's Influenza D-QIV Vaccine in Healthy Non-pregnant Women.GlaxoSmithKline · completed · Respiratory Syncytial Virus Infections · study director
- Ph1NCT05044325 · A First Time in Human (FTIH) Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Repeat Doses of GSK3884464 in Healthy ParticipantsGlaxoSmithKline · terminated · Heart Failure · study director
- Ph4NCT04982445 · Study Using CABENUVA™ for the Treatment of Human Immunodeficiency Virus (HIV)-1, Administered in Infusion Centers (IC) or Alternate Sites of Administration (ASA) in the United States (U.S.)ViiV Healthcare · completed · HIV Infections · study director
- Ph3NCT04980391 · A Study on the Safety and Immune Response to an Unadjuvanted RSV Maternal Vaccine, in High Risk Pregnant Women Aged 15 to 49 Years and Infants Born to the Vaccinated MothersGlaxoSmithKline · terminated · Respiratory Syncytial Virus Infections · study director
- Ph1NCT04975438 · Clinical Effect, Safety and Tolerability of GSK1070806 in Atopic DermatitisGlaxoSmithKline · completed · Dermatitis, Atopic · study director
- Ph1NCT04971928 · Phase 1 Study of GSK3228836 Pharmacokinetics in Participants With Hepatic ImpairmentGlaxoSmithKline · completed · Hepatitis B · study director
- N/ANCT04971590 · Study to Assess Demographic, Pharmacologic, Biomarker, Clinical Features and Quality of Life (QoL) of Participants With Lupus NephritisGlaxoSmithKline · completed · Systemic Lupus Erythematosus · study director
- Ph3NCT04965636 · Study in Pediatrics With HypEREosinophilic Syndrome (SPHERE)GlaxoSmithKline · completed · Hypereosinophilic Syndrome · study director
- N/ANCT04964063 · A Real-World Evidence Study to Evaluate Oral Health Related Quality of Life Using an Anti-Sensitivity ToothpasteHALEON · completed · Dentin Sensitivity · study director
- Ph1NCT04964050 · A Bioequivalence Study Between Capozide Versus ACE-Hemmer-ratiopharm in Healthy Adult Participants Under Fasting ConditionsGlaxoSmithKline · withdrawn · Healthy Volunteers · study director
- Ph2NCT04954859 · Long-term Follow-up Study to Evaluate Durability of Treatment Response in Previous Bepirovirsen Study Participants (B-Sure)GlaxoSmithKline · active not recruiting · Hepatitis B · study director
- N/ANCT04950465 · A Clinical Study to Evaluate the Efficacy of a Stannous Fluoride Dentifrice in the Relief of Dentinal Hypersensitivity in a Chinese PopulationHALEON · completed · Dentin Sensitivity · study director
- Ph3NCT04950127 · Global Linerixibat Itch Study of Efficacy and Safety in Primary Biliary Cholangitis (PBC) (GLISTEN)GlaxoSmithKline · completed · Pruritus · study director
- N/ANCT04950712 · An Epidemiological Study to Assess Performance of Using Healthcare Tools to Understand Genital Herpes Simplex Virus-2 (HSV-2) in Patients ≥ 18 Years of Age in the United States and Europe.GlaxoSmithKline · completed · Herpes Genitalis · study director
- Ph3NCT04937387 · Efficacy and Safety of Fluticasone Furoate/Umeclidinium/Vilanterol (FF/UMEC/VI) in Chinese Participants With Inadequately Controlled AsthmaGlaxoSmithKline · completed · Asthma · study director
- Ph4NCT04923347 · A Study to Evaluate the Safety and Efficacy of Fluticasone Furoate (FF)/Umeclidinium(UMEC)/Vilanterol (VI) in Participants With Chronic Obstructive Pulmonary Disease (COPD)GlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- Ph3NCT04915755 · Efficacy and Safety Comparison of Niraparib to Placebo in Participants With Human Epidermal Growth Factor 2 Negative (HER2-) Breast Cancer Susceptibility Gene Mutation (BRCAmut) or Triple-Negative Breast Cancer (TNBC) With Molecular DiseaseGlaxoSmithKline · active not recruiting · Neoplasms, Breast · study director
- Ph4NCT04908865 · Open-label Study of Belimumab Plus Standard Therapy in Chinese Pediatric Participants With Active Systemic Lupus Erythematosus (SLE)GlaxoSmithKline · completed · Systemic Lupus Erythematosus · study director
- Ph2NCT04900038 · A Clinical Trial of GSK3640254 + Dolutegravir (DTG) in Human Immunodeficiency Virus-1 Infected Treatment-naive AdultsViiV Healthcare · terminated · HIV Infections · study director
- Ph1/Ph2NCT04886154 · A Study on the Safety, Effectiveness and Immune Response of Meningococcal Combined ABCWY Vaccine in Healthy Adolescents and AdultsGlaxoSmithKline · completed · Infections, Meningococcal · study director
- Ph1NCT04878315 · Bioequivalence Study Between Capoten Versus Captopril Reference Product in Healthy Adult Participants Under Fasting ConditionsGlaxoSmithKline · withdrawn · Healthy Volunteers · study director
- Ph2NCT04871113 · A Study to Evaluate the Antiviral Effect, Safety and Tolerability of GSK3810109A in Viremic Human Immunodeficiency Virus (HIV)-1 Infected AdultsViiV Healthcare · completed · HIV Infections · study director
- Ph1NCT04857892 · A Relative Bioavailability and Food-Effect Study of the Fixed Dose Combination of GSK3640254 and Dolutegravir (DTG) in Healthy ParticipantsViiV Healthcare · completed · HIV Infections · study director
- N/ANCT04853238 · Chronic Obstructive Pulmonary Disease (COPD) Maintenance Treatment Patterns in ChinaGlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- N/ANCT04853225 · Investigation of Chronic Obstructive Pulmonary Disease (COPD) Phenotypes and Endotypes in ChinaGlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- Ph1NCT04827134 · A Food-effect Study of the Pediatric Dispersible Tablet Formulations of TRIUMEQ® and DOVATO® in Healthy Adult ParticipantsViiV Healthcare · completed · HIV Infections · study director
- Ph4NCT04813354 · A Comparison of Critical Errors, Overall Errors, Training/Teaching Time, and Preference Attributes of the ELLIPTA Versus BREEZHALER Dry Powder Inhalers (DPIs) in Adult Participants With AsthmaGlaxoSmithKline · completed · Asthma · study director
- Ph2NCT04789577 · A Study to Evaluate the Safety and Immunogenicity of GlaxoSmithKline Biologicals' Influenza Vaccine GSK3206641A Administered in Adults 18 to 64 Years of Age and 65 Years of Age and OlderGlaxoSmithKline · completed · Influenza, Human · study director
- Ph2NCT04772053 · Molecular Disease Characterization Initiative (MDCI)GlaxoSmithKline · terminated · Lung Cancer, Non-Small Cell, Neoplasms · study director
- Ph1NCT04762511 · A Study on the Reactogenicity, Safety and Immune Response of a Vaccine Against Herpes Simplex Virus (HSV)-2 in Healthy Participants Aged 18-40 YearsGlaxoSmithKline · terminated · Herpes Simplex · study director
- Ph1NCT04757974 · Low-dose Fostemsavir Extended Release Relative Bioavailability StudyViiV Healthcare · completed · HIV Infections · study director
- Ph2NCT04737538 · A Proof-of-principle Clinical Study Investigating the Efficacy of an Experimental Dentifrice Containing Sodium Bicarbonate and Sodium Hyaluronate on GingivitisGlaxoSmithKline · completed · Gingivitis · study director
- Ph3NCT04718389 · A Study of GSK3511294 (Depemokimab) Compared With Mepolizumab or Benralizumab in Participants With Severe Asthma With an Eosinophilic PhenotypeGlaxoSmithKline · completed · Asthma · study director
- Ph3NCT04719832 · Placebo-controlled Efficacy and Safety Study of GSK3511294 (Depemokimab) in Participants With Severe Asthma With an Eosinophilic PhenotypeGlaxoSmithKline · completed · Asthma · study director
- Ph3NCT04718103 · A Study of GSK3511294 (Depemokimab) in Participants With Severe Asthma With an Eosinophilic PhenotypeGlaxoSmithKline · completed · Asthma · study director
- Ph2NCT04676724 · Study of Sequential GSK3228836 and Peginterferon Treatment in Participants With Chronic Hepatitis B (CHB)GlaxoSmithKline · completed · Hepatitis B · study director
- N/ANCT04657211 · Triple Therapy in Chronic Obstructive Pulmonary Disease (COPD) ParticipantsGlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- Ph2/Ph3NCT04655976 · Efficacy Comparison of Cobolimab + Dostarlimab + Docetaxel to Dostarlimab + Docetaxel to Docetaxel Alone in Participants With Advanced Non-small Cell Lung Cancer Who Have Progressed on Prior Anti-PD-(L)1 Therapy and ChemotherapyGlaxoSmithKline · active not recruiting · Lung Cancer, Non-Small Cell · study director
- Ph1NCT04640311 · Comparison of Daprodustat Formulations Produced by Two Methods of Manufacture for Bioequivalence and Dissolution in Healthy ParticipantsGlaxoSmithKline · completed · Anaemia · study director
- Ph2NCT04641247 · A Long-term Treatment Extension Study of Niraparib in Participants Who Completed a Prior GlaxoSmithKline/TESARO-sponsored Niraparib StudyGlaxoSmithKline · recruiting · Ovarian Neoplasms, Breast Neoplasms · study director
- Ph1NCT04630002 · Drug-drug Interaction (DDI) Study of GSK3640254 With Darunavir/Ritonavir (DRV/RTV) and Etravirine (ETR)ViiV Healthcare · completed · HIV Infections · study director
- Ph3NCT04607005 · Efficacy and Safety of Mepolizumab in Adults With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)/ Eosinophilic Chronic Rhinosinusitis (ECRS)GlaxoSmithKline · completed · Nasal Polyps · study director
- Ph3NCT04605159 · A Phase III, Double-blind Study to Assess Safety and Efficacy of an RSV Maternal Unadjuvanted Vaccine, in Pregnant Women and Infants Born to Vaccinated MothersGlaxoSmithKline · terminated · Respiratory Syncytial Virus Infections · study director
- Ph1NCT04604795 · Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of GSK3915393 in Healthy Participants and to Evaluate the Interaction Between GSK3915393 and Grapefruit Juice and ItraconazoleGlaxoSmithKline · completed · Celiac Disease, Coeliac Disease · study director
- Ph4NCT04600752 · Study to Evaluate the Safety and Clinical Efficacy of Augmentin® Extra Strength-600 in Children With Acute Otitis Media in IndiaGlaxoSmithKline · completed · Otitis Media, Infections, Respiratory Tract, Respiratory Tract Infections · study director
- Ph1NCT04585009 · Safety, Tolerability and Pharmacokinetics of GSK3923868 Inhalation Powder in Healthy Participants and Stable AsthmaticsGlaxoSmithKline · completed · Pulmonary Disease, Chronic Obstructive · study director
- Ph2NCT04581824 · Efficacy Comparison of Dostarlimab Plus Chemotherapy Versus Pembrolizumab Plus Chemotherapy in Participants With Metastatic Non-squamous Non-small Cell Lung Cancer (NSCLC)GlaxoSmithKline · terminated · Lung Cancer, Non-Small Cell · study director
Grants
NIH projects from RePORTER, fetched 2026-11-12 10:43 UTC. A project is listed only when its grant number is on one of the trials above, or when the awardee institution matches an affiliation the registry gives for this name. Coverage is US federal funding only; UK and EU funders are not searched yet.
No NIH project could be tied to this name by a shared trial or a matching institution.
Most cited trial papers
PubMed returned no clinical-trial papers for this author name in diffuse midline glioma (dipg).