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Tiotropium+ SERETIDE 50/500

Phase 3

Pulmonary Disease, Chronic Obstructive | Small molecule | Respiratory |GSK plc|Last Updated: Feb 15, 2018

Success Probability

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials3
Total Enrollment477

FDA Designations

No designations recorded

Clinical trial landscape

Tiotropium+ SERETIDE 50/500 · 3 trials · 1 indication

Phase 3 1Phase 2 2
NCT01395888A Study to Compare the Impact of Fulticasone Furoate/Vilanterol vs. Tiotropium on Arterial Stiffness in COPDPulmonary Disease, Chronic Obstructive
COMPLETED260 Analytics
PHASE3COMPLETED
A Study to Compare the Impact of Fulticasone Furoate/Vilanterol vs. Tiotropium on Arterial Stiffness in COPD
Pulmonary Disease, Chronic ObstructiveUnlock trial analytics

Study Endpoints

Primary Endpoints

Mean Change From Baseline (BL) in Aortic Pulse Wave Velocity (aPWV) at the End of the 12-week Treatment Period (Day 84)
Baseline to Day 84 (Early Withdrawal)

PWV is defined as the speed of travel of the pressure pulse along an arterial segment and can be obtained for any arterial segment accessible to palpation. aPWV is measured with tonometers positioned transcutaneously at the base of the common carotid artery and over the femoral artery. PWV increases with arterial stiffness and is defined by the Moens-Korteweg equation: PWV=square root of Eh/2pR, where E is Young's modulus of the arterial wall, h is the wall thickness, R is the arterial radius at the end of diastole, and p is the blood density. Change from Baseline was calculated as the Day 84 value minus the Baseline value. The analysis was performed using a repeated measures model with covariates of treatment, visit, age, gender, smoking status at screening, geographical region, Baseline aPWV, and interaction terms of Baseline by visit and treatment by visit.

Change From Baseline in Trough Forced Expiratory Volume in One Second (FEV1) at Day 15 of Each Treatment Period
Baseline and Day 15 of each treatment period (up to Study Day 71)

FEV1 is a measure of lung function and is defined as the maximal amount of air that can be forcefully exhaled in one second. Trough FEV1 on Treatment Day 15 is defined as the value obtained 24 hours after the morning dose administered on Day 14. Analysis were performed using a mixed model with covariates of mean Baseline, period Baseline, treatment and period as fixed effects and participant as a random effect. Baseline is the FEV1 value recorded pre-dose on Day 1 of each treatment period; mean Baseline is the mean of the Baselines for each participant and period Baseline is the difference between the Baseline and the mean Baseline in each treatment period for each participant. Change from Baseline for each treatment period is the trough FEV1 at Day 15 minus the Baseline value for that treatment period.

AUC (0-4hrs, sGAW after morning dose of medication at day 14)

Secondary Endpoints

Change From Baseline (BL) in Weighted Mean FEV1 Over 0 to 24 Hours Obtained Post-dose on Day 14 of Each Treatment Period
Baseline and Day 14 of each treatment period (TP; up to Study Day 70)
Change From Baseline (BL) in Serial FEV1 Over 0-28 Hours After the Morning Dose at Day 14 of Each Treatment Period
Baseline and Day (D) 14 of each treatment period (TP; up to Study Day 70)
Effects of SERETIDE 50/500mcg twice daily plus tiotropium bromide 18mcg once daily compared with the individual treatments on further elements of lung function, dyspnoea, symptoms and a patient/physician assessment of treatment effect.
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
RelovairEXPERIMENTALInhaled long-acting bronchodilator and corticosteroid combination
TiotropiumACTIVE_COMPARATORInhaled long-acting anticholinergic
PlaceboPLACEBO_COMPARATORPlacebo
Arm 1EXPERIMENTALGSK573719 1000mcg once daily
Arm 2EXPERIMENTALGSK573719 500mcg once daily
Arm 3EXPERIMENTALGSK573719 250mcg once daily
Arm 4EXPERIMENTALGSK573719 125mcg once daily
Arm 5EXPERIMENTALGSK573719 62.5 mcg once daily
Arm 6EXPERIMENTALGSK573719 250mcg twice daily
Arm 7EXPERIMENTALGSK573719 125mcg twice daily
Arm 8EXPERIMENTALGSK573719 62.5mcg twice daily

Interventions

NameTypeDescription
fluticasone furoate (FF, GW685698)/vilanterol (VI, GW642444) 100/25 mcg Novel Dry Powder Inhaler (NDPI)DRUGfluticasone furoate (FF, GW685698)/vilanterol (VI, GW642444) 100/25 mcg Inhalation Powder delivered once daily via a Novel Dry Powder Inhaler (NDPI)
TiotropiumDRUG• Tiotropium (18 mcg) administered QD via a HandiHaler
PlaceboDRUGInactive/ excipients only
GSK573179DRUGGSK573179 investigational drug
Tiotropium + SERETIDE 50/500DRUG -
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Eligibility Criteria

Age Range40 Years to 80 Years
SexALL
Healthy VolunteersNo
Study Sites55

Inclusion Criteria: * Type of subject: Outpatient * Informed consent: Subjects must give their signed and dated written informed consent to participate. * Gender: Male or female subjects. * Age: greater then or equal to 40 years of age at Screening (Visit 1) * COPD diagnosis: Subjects with a clinic...

Countries:ArgentinaFranceGermanyItalyNorwayRussiaUkraineUnited StatesBelgiumUnited Kingdom
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Frequently asked questions about Tiotropium+ SERETIDE 50/500

What is Tiotropium + SERETIDE 50/500 used for?

Tiotropium + SERETIDE 50/500 is used for chronic obstructive pulmonary disease (COPD). It is a combination therapy being developed by GSK plc for the treatment of this respiratory condition. The drug is currently in Phase 3 clinical development.

Who makes Tiotropium + SERETIDE 50/500?

GSK plc (ticker: GSK) is developing Tiotropium + SERETIDE 50/500. The company is conducting clinical trials to evaluate this combination therapy for chronic obstructive pulmonary disease. GSK is the developer of this investigational drug.

What phase is Tiotropium + SERETIDE 50/500 in?

Tiotropium + SERETIDE 50/500 is in Phase 3 clinical development for chronic obstructive pulmonary disease. It is an investigational drug and has not been approved by regulatory authorities. The Phase 3 trial is completed, and the drug remains under clinical investigation.

What clinical trials is Tiotropium + SERETIDE 50/500 in?

Tiotropium + SERETIDE 50/500 has been studied in three completed clinical trials. These include NCT00325169, a Phase 2 study comparing SERETIDE plus tiotropium versus individual components; NCT00950807, a Phase 2 dose ranging study; and NCT01395888, a Phase 3 study comparing fluticasone furoate/vilanterol versus tiotropium on arterial stiffness in COPD.

Is Tiotropium + SERETIDE 50/500 a small molecule?

Yes, Tiotropium + SERETIDE 50/500 is a small molecule drug. It is being developed for chronic obstructive pulmonary disease, a respiratory condition. The drug is administered as a combination therapy and is currently in Phase 3 clinical trials.

What is the enrollment in Tiotropium + SERETIDE 50/500 clinical trials?

The clinical trials for Tiotropium + SERETIDE 50/500 have enrolled a total of 477 participants across three completed studies. The trials were randomized, double-blind, and placebo-controlled. The studies included patients aged 40 years and older with chronic obstructive pulmonary disease.