A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety and Efficacy of SPI-1005 in Moderate COVID-19 Patients
et al., NCT04484025, NCT04484025, Jun 2026
RCT 31 moderate COVID-19 patients showing no significant differences with SPI-1005 (ebselen).
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.
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risk of death, 140.9% higher, RR 2.41, p = 1.00, treatment 1 of 22 (4.5%), control 0 of 9 (0.0%), continuity correction due to zero event (with reciprocal of the contrasting arm).
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risk of no recovery, 20.5% higher, RR 1.21, p = 0.67, treatment mean 0.94 (±0.93) n=16, control mean 0.78 (±0.83) n=9, relative WHO score, day 30.
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| Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates |
Treggiari et al., 25 Jun 2026, Double Blind Randomized Controlled Trial, placebo-controlled, USA, preprint, 1 author, trial NCT04484025 (history).