Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Tiotropium+ SERETIDE 50/500 · 3 trials · 1 indication
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.
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.
| Arm | Type | Description |
|---|---|---|
| Relovair | EXPERIMENTAL | Inhaled long-acting bronchodilator and corticosteroid combination |
| Tiotropium | ACTIVE_COMPARATOR | Inhaled long-acting anticholinergic |
| Placebo | PLACEBO_COMPARATOR | Placebo |
| Arm 1 | EXPERIMENTAL | GSK573719 1000mcg once daily |
| Arm 2 | EXPERIMENTAL | GSK573719 500mcg once daily |
| Arm 3 | EXPERIMENTAL | GSK573719 250mcg once daily |
| Arm 4 | EXPERIMENTAL | GSK573719 125mcg once daily |
| Arm 5 | EXPERIMENTAL | GSK573719 62.5 mcg once daily |
| Arm 6 | EXPERIMENTAL | GSK573719 250mcg twice daily |
| Arm 7 | EXPERIMENTAL | GSK573719 125mcg twice daily |
| Arm 8 | EXPERIMENTAL | GSK573719 62.5mcg twice daily |
| Name | Type | Description |
|---|---|---|
| fluticasone furoate (FF, GW685698)/vilanterol (VI, GW642444) 100/25 mcg Novel Dry Powder Inhaler (NDPI) | DRUG | fluticasone furoate (FF, GW685698)/vilanterol (VI, GW642444) 100/25 mcg Inhalation Powder delivered once daily via a Novel Dry Powder Inhaler (NDPI) |
| Tiotropium | DRUG | • Tiotropium (18 mcg) administered QD via a HandiHaler |
| Placebo | DRUG | Inactive/ excipients only |
| GSK573179 | DRUG | GSK573179 investigational drug |
| Tiotropium + SERETIDE 50/500 | DRUG | - |
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...
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.
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.
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.
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.
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.
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.