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Two-part, double-blind, placebo-controlled, randomized, parallel-group study - (Part 1) in healthy male volunteers to assess safety and tolerability of ascending repeated oral doses of BAY 1817080 followed (Part 2), two-way crossover administration with four-step dose titration in patients with refractory chronic cough to assess safety, tolerability and efficacy for proof of concept and dose-finding

People Involved

Status Project Complete
Funder(s) Bayer Pharma AG
Value £61,101.00
Project Dates Jul 18, 2018 - Dec 31, 2019