RE: Section 3.11 and 3.1422 Feb 2021 08:13
What are you talking about. The document publishes the SNG001 lancet data which were very good. The below is taken straight from your link!
"Monk et al. 2020 published results from randomised, double-blind, placebo- controlled, phase 2 pilot trial at nine UK sites (NCT04385095) [106]. 101 COVId-19 hospitalized adult patients were randomly assigned (1:1) to receive inhaled nebulised interferon beta-1a (SNG001) (6 MIU) or placebo by inhalation via a mouthpiece daily for 14 days. 66 (67%) patients required oxygen
supplementation at baseline: 29 in the placebo group and 37 in the SNG001 group. Patients receiving SNG001 had greater odds of improvement on the OSCI scale (odds ratio 2·32 [95% CI 1·07–5·04]; p=0·033) on day 15 or 16 and were more likely than those receiving placebo to recover to an OSCI score of 1 (no limitation of activities) during treatment (hazard ratio 2·19 [95% CI 1·03– 4·69]; p=0·043). No significant difference was found between treatment groups in the odds of hospital discharge by day 28: 39 (81%) of 48 patients had been discharged in the nebulised interferon beta-1a group compared with 36 (75%) of 48 in the placebo group (OR 1·84 [95% CI 0·64–5·29]; p=0·26). There was no significant difference between treatment groups in the odds of intubation or the time to intubation or death. SNG001 was well tolerated: the most frequently reported treatment-emergent adverse event was headache (seven [15%] patients in the SNG001 group and five [10%] in the placebo group). There were three deaths in the placebo group and none in the SNG001 group."