jRCT2041210004.
Study name | A clinical phase III study of favipiravir in patients with early onset COVID‐19 with risk factors for severe illness ‐ a placebo‐controlled, stratified randomised, multicenter, double‐blind study |
Methods | Multicentre, randomized controlled study |
Participants | COVID‐19 patients with risk factors for progression to severe disease onset within 72 hours prior to the start of study drug administration |
Interventions | T‐705a tablets 200 mg administrated orally, 9 tablets twice daily for Day 1, and 4 tablets twice daily for Days 2 to 10. |
Outcomes | Percentage of participants with severe disease from randomization to Day 28 |
Starting date | 20 April 2021 |
Contact information | Name: Clinical Trial Information Officer Address: 2‐14‐1,Kyoubashi,Chuo‐ku,Tokyo, Japan Tokyo Japan 104‐0031 Telephone: +81‐3‐6228‐3129 E‐mail: fftc‐clinicaltrial‐info1@fujifilm.com |
Notes |