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NCT04124510: SWIFT

Efficacy and Safety of Flutiform K-haler in Patients With Uncontrolled Asthma Following Mid-dose ICS/LABA DPI Therapy

Terminated Phase 3 Last updated 25 January 2021
What this trial tests

Phase 3 trial testing Brand Name: Flutiform K-haler in Asthma in 20 participants. Terminated before completion.

Timeline
26 November 2019
Primary endpoint
14 September 2020
14 September 2020

Quick facts

Lead sponsorMundipharma Korea Ltd
PhasePhase 3
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date26 November 2019
Primary completion14 September 2020
Estimated completion14 September 2020
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Mundipharma Korea Ltd — full company profile →

Who can join

19 and older, any sex, with Asthma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the efficacy of the Asthma improvement of Flutiform K-haler after 12 weeks of treatment in patients with moderate to severe uncontrolled\* asthma following mid-dose ICS/LABA DPI therapy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Asthma

Currently open trials in the same condition.

Other Mundipharma Korea Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04124510.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing