A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety and Efficacy of SPI-1005 in Severe COVID-19 Patients
et al., NCT04483973, NCT04483973, Jun 2026
RCT 25 severe 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, 125.0% higher, RR 2.25, p = 0.62, treatment 4 of 16 (25.0%), control 1 of 9 (11.1%).
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risk of no recovery, 13.3% higher, RR 1.13, p = 0.78, treatment mean 2.64 (±2.01) n=11, control mean 2.33 (±2.42) n=6, relative WHO score, day 30.
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| Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates |
Treggiari et al., 29 Jun 2026, Double Blind Randomized Controlled Trial, placebo-controlled, USA, preprint, 1 author, trial NCT04483973 (history).
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