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ARCA biopharma Inc (NASDAQ: ABIO) announced results from the ASPEN-COVID-19 Phase 2 trial evaluating rNAPc2, a specific inhibitor of tissue factor, as a potential treatment for patients hospitalized with COVID-19.
In the 160-patient trial, both doses of rNAPc2 demonstrated a treatment benefit; however, neither dose achieved statistical significance for the primary efficacy endpoint of change in D-dimer level from Baseline to Day 8 compared to standard of care heparin.
The pooled lower and higher rNAPc2 dose groups demonstrated a reduction in D-dimer levels of 16.8% versus 11.2% for the standard of care heparin.
The treatment effects of rNAPc2 and heparin were different in mild versus severe categories, with generally decreasing D-dimer levels from baseline in mild patients.
But in severe patients, D-dimer levels were increasing in the Heparin group with no change in the rNAPc2 groups.
On the secondary endpoint related to eligibility for hospital discharge, the rNAPc2 combined arms log-rank hazard ratio was 0.88 compared to heparin, representing a one-day reduction in time-to-recovery.
The thrombosis events component of the composite clinical outcome endpoint yielded nine events in the heparin group versus six in the combined rNAPc2 groups; neither results were statistically significant.
rNAPc2 was well-tolerated at both doses. There were no serious treatment-related adverse events, and no dose-dependent increase in adverse events was observed.
Price Action: ABIO shares are down 24.4% at $1.74 during the premarket session on the last check Friday.
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