At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 23 enrolled
Drug / intervention
Gefapixant 45 mg +1 moredrug
Likely dose
Gefapixant 45 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Phase II Study, Randomized, Double-Blind, Placebo-Controlled 4-Week Clinical Study, to Evaluate the Efficacy and Safety of MK-7264 in Adult Japanese Participants With Unexplained or Refractory Chronic Cough
In Brief
A Phase 2 clinical trial evaluating Gefapixant 45 mg and Placebo for Chronic Cough. Completed, enrolled 23 participants across 16 sites.
Detailed Summary
This estimation study (no hypotheses) will evaluate the safety, tolerability, and efficacy of gefapixant (MK-7264) in Japanese adult participants with unexplained or refractory chronic cough.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Cough
CountriesJapan
Collaborators--
Timeline
Phase 2CompletedFinished
201820192020202120222023202420252026
Enrollment StartMar 2018
First PostedMar 2018
Primary CompletionJun 2018
TodayJul 2026
First PostedMar 29, 2018
Enrollment StartMar 16, 2018
Primary CompletionJun 7, 2018
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 8.3 years ago
Interventions
Gefapixant 45 mgdrug
Gefapixant 45 mg (film-coated tablet) to be administered orally BID
Placebodrug
Placebo (film-coated tablet) matching gefapixant to be administered orally BID