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A clinical study to evaluate the efficacy and safety of Vilanterol and Glycopyrronium metered dose inhalation in patients with Chronic Obstructive Pulmonary Disease.

"A prospective, randomized, double-blind, parallel, active-controlled, multicentre, phase III clinical trial to assess the efficacy and safety of Vilanterol and Glycopyrronium metered dose inhalation as compared to Glycopyrrolate and Formoterol fumarate metered dose inhalation in the patients with Chronic Obstructive Pulmonary Disease".

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050167
Enrollment
288
Registered
2023-03-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J449- Chronic obstructive pulmonary disease, unspecified

Interventions

Intervention1: Vilanterol and Glycopyrronium inhalation 12.5 mcg and 25 mcg: Enrolled patients will be dispensed separate MDIs for morning dose and evening dose. The patients will be instructed to ta

Sponsors

Zydus Healthcare Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either gender between 40-65 years of age (both inclusive) 2. Patients who are current/ex-smokers 3. Patients diagnosed with moderate to severe COPD as per the GOLD guidelines classification at screening visit: a. Post-bronchodilator FEV1/FVC ratio b. Post-bronchodilator FEV1, = 30% to 4. Clinically stable COPD within 4 weeks prior to the screening visit and during the screening period 5. COPD Assessment Test (CAT) score = 10 at screening 6. Patients willing to provide written informed consent and comply with the protocol requirements 7. Patients literate enough to fill the diary card

Exclusion criteria

Exclusion criteria: 1. Patients suffering from other lung disorders such as but not limited to asthma, active tuberculosis, bronchiectasis, interstitial lung disease, lung cancer etc. 2. Patients with known hypersensitivity to formoterol, vilanterol, glycopyrronium, salbutamol, other beta-2 agonists or other anti-muscarinic agents 3. Patients diagnosed with COVID-19 within 3 months prior to screening 4. Patients with known a1 antitrypsin deficiency 5. COPD exacerbation that requires treatment with systemic corticosteroids or antibiotics within 4 weeks prior to screening or during the screening period 6. Patients hospitalized for COPD exacerbation within 3 months prior to the screening visit or during the screening period 7. Respiratory tract infections that required antibiotics within 4 weeks prior to the screening or during the screening period 8. Patients who required long-term oxygen therapy (=12 hours/day) within 4 weeks prior to the screening or during the screening period 9. Patients with known diagnosis of narrow angle glaucoma, prostatic hyperplasia, bladder-neck obstruction or urinary retention 10. Patients with clinically significant uncontrolled systemic diseases such as cardiovascular, renal, neurological, psychiatric, endocrine, immunological or hematological disorders or malignancy 11. Patients with hepatic dysfunction (serum transaminases = 3 x Upper Normal Limit) or renal dysfunction (serum creatinine = 2.5 mg/dl) at screening 12. Patients who have used prohibited medications 13. Patients with continuing history of alcohol and/or drug abuse 14. Pregnant or Lactating females; or female patients of childbearing potential unwilling to use effective contraception 15. Participation in another clinical trial in the past 3 months 16. Any other reason for which the investigator feels that the patient should not participate

Design outcomes

Primary

MeasureTime frame
Change from baseline in trough FEV1 at the end of the studyTimepoint: At baseline and Week 12

Secondary

MeasureTime frame
Adverse events / Serious adverse events reported during the studyTimepoint: At Week 4, Week 8 and Week 12;Change from baseline in CAT™ score at week 4, week 8 and at the end of the studyTimepoint: At baseline, Week 4, Week 8 and Week 12;Change from baseline in post-bronchodilator FEV1 and FVC at week 4 and at the end of the studyTimepoint: At baseline, Week 4 and Week 12;Change from baseline in trough FEV1 at week 4Timepoint: At baseline and Week 4;Change from baseline in trough FVC at week 4 and at the end of the studyTimepoint: At baseline, Week 4 and Week 12;COPD exacerbations reported during the studyTimepoint: At Week 4, Week 8 and Week 12;Rescue medication use during the treatment period as compared to the baseline (screening period)Timepoint: At Screening period, Week 4, Week 8 and Week 12;Responder rate at week 4 and at the end of the studyTimepoint: At Week 4 and Week 12

Countries

India

Contacts

Public ContactDr Pavankumar M Daultani

Zydus Healthcare Limited

pavankumar.daultani@zyduslife.com079-48041435

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026