Skip to content

A study to evaluate the safety and efficacy of Indacaterol, Mometasone, Glycopyrronium Dry powder inhaler in Asthma patients.

An open label single arm, multicentric, prospective, phase IV study to evaluate the safety and effectiveness of Indacaterol/ Mometasone/ Glycopyrronium DPI in the management of Asthma patients - OASIS Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060605
Enrollment
182
Registered
2023-12-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: J45- Asthma

Interventions

Intervention1: Indamet G®: Indacaterol (as acetate 150 mcg + Mometasone furoate 160 mcg+ Glycopyrronium 50 mcg) powder for inhalation Control Intervention1: Not Applicable: Not Applicable

Sponsors

Glenmark Pharmaceuticals Ltd
Lead Sponsor
Clinical Research Network India
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: a.Patients =18 years of age with a documented physician diagnosis of Asthma b. Symptomatic patients on ongoing maintenance therapy with ICS/LABA or ICS/FOR c. ACQ-5 score = 1.5 at baseline. d. History of one or more asthma exacerbations in last one year. e. Ability to use dry powder inhaler independently and correctly in view of the investigator. f. Patient is willing to sign a written informed consent form and agree to follow up on a regular basis as specified in the protocol.

Exclusion criteria

Exclusion criteria: a. History of current hospitalization with life threatening condition or patients with acute exacerbation of asthma (acute condition). b. Smoking history of more than 10 pack-years. c. Ongoing treatment with Triple therapy i.e. ICS/LABA/LAMA. d. Subjects with any life threatening condition. e. Women of childbearing potential are not restricted in this study, however it is expected that the investigator will assess the risks and benefits of the assigned treatment as per the product label(s) and discuss this with any women of childbearing potential prior to providing the patient with the prescription for the assigned treatment. f. Subjects with history of hypersensitivity to the active substance or to any of its excipients of study drug.

Design outcomes

Primary

MeasureTime frame
To evaluate the safety of IND/MF/GLY DPI in treatment of Asthma in Indian population Number of patients with any drug related treatment emergent adverse events (TEAEs). Number of patients with TEAEs Number of patients with serious TEAEs (STEAEs)Timepoint: At week 12

Secondary

MeasureTime frame
To evaluate the effectiveness of IND/MF/GLY DPI in treatment of Asthma in Indian population Mean change in Trough FEV1 from baseline Mean change in ACQ-5 score from baseline Percentage change in ACQ-5 score at week 4 and 12 from baseline.Timepoint: At week 12

Countries

India

Contacts

Public ContactDr Nidhi Singh

Glenmark Pharmaceuticals Ltd

Sumit.Bhushan@glenmarkpharma.com08800352225

Outcome results

None listed

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