Experimental: Lopinavir/ritonavir plus Interferon ß-1a22 Apr 2020 10:16
it is been going on in France ,
using solution not in form of inhaler
https://clinicaltrials.gov/ct2/show/NCT04315948?id=NCT04251871+OR+NCT04276688+OR+NCT04315948+OR+NCT04320238+OR+NCT04293887+OR+NCT04275388&draw=2&rank=2&load=cart
Actual Study Start Date : March 22, 2020
Estimated Primary Completion Date : March 2023
Estimated Study Completion Date : March 2023
WHO Solidarity” clinical trial for COVID-19 treatments
Drug: Interferon Beta-1A
IFN-ß-1a is supplied as a STERILE SOLUTION containing no preservative available in a prefilled syringe. It will be provided as a single-dose prefilled graduated syringe with 44 µg per 0.5 mL. The liquid should be clear to slightly yellow. Do not use if the liquid is cloudy, discolored or contains particles. Use a different syringe
* Lopinavir/ritonavir (400 lopinavir mg/100 mg ritonavir) will be administered every 12 h for 14 days in tablet form. For patients who are unable to take medications by mouth, the lopinavir/ritonavir (400 lopinavir mg/100 mg ritonavir) will be administered as a 5-ml suspension every 12 h for 14 days via a pre-existing or newly placed nasogastric tube.
* Interferon ß1a will be administered subcutaneously at the dose of 44 µg for a total of 3 doses in 6 days (day 1, day 3, day 6).
n=620