A Phase 2, Randomized, Double-blind, Placebo-controlled, Multi-center Study to Evaluate the Efficacy and Safety of Brilacidin in Hospitalized Participants With COVID-19
, NCT04784897, NCT04784897, Jul 2021
RCT 120 hospitalized COVID-19 patients showing no significant differences in pre-defined outcomes with brilacidin.
Standard of Care (SOC) for COVID-19 in the study country,
the USA, is very poor with very low average efficacy for approved treatments1.
Only expensive, high-profit treatments were approved for early treatment. Low-cost treatments were excluded, reducing the probability of early treatment due to access and cost barriers, and eliminating complementary and synergistic benefits seen with many low-cost treatments.
|
risk of death, no change, RR 1.00, p = 1.00, treatment 4 of 60 (6.7%), control 4 of 60 (6.7%), day 60.
|
|
risk of death, 33.3% higher, RR 1.33, p = 1.00, treatment 4 of 60 (6.7%), control 3 of 60 (5.0%), day 28.
|
|
risk of death/intubation, 33.3% higher, RR 1.33, p = 1.00, treatment 4 of 60 (6.7%), control 3 of 60 (5.0%), day 29.
|
|
risk of no recovery, 20.0% higher, RR 1.20, p = 1.00, treatment 6 of 60 (10.0%), control 5 of 60 (8.3%), day 29.
|
|
recovery time, 8.3% higher, relative time 1.08, p = 0.54, treatment mean 13.0 (±5.08) n=44, control mean 12.0 (±9.88) n=60.
|
| Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates |
Innovation Pharmaceuticals et al., 30 Jul 2021, Double Blind Randomized Controlled Trial, placebo-controlled, USA, preprint, 1 author, trial NCT04784897 (history).
Contact: info@ipharminc.com.