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suPAR-Guided Anakinra Treatment for Validation of the Risk and Early Management of Severe Respiratory Failure by COVID-19: The SAVE-MORE Double-blind, Randomized, Phase III Confirmatory Trial
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT04680949-Jul 28, 2026
NCT ID
NCT04680949
Status
COMPLETED
Phase
Phase 3
Sponsor
Hellenic Institute for the Study of Sepsis
Executive brief
Investment-Ready Snapshot
The SAVE-MORE trial, sponsored by the Hellenic Institute for the Study of Sepsis, evaluates the efficacy and safety of anakinra, an IL-1 receptor antagonist, in patients with severe respiratory failure due to COVID-19. Given the significant reduction in severe respiratory failure incidence and mortality rates observed in the trial, anakinra may position itself as a critical therapeutic option in the COVID-19 treatment landscape. The market for COVID-19 therapeutics remains competitive, with various agents under investigation; however, the unique biomarker-guided approach using suPAR may provide a differentiated value proposition. Companies should consider potential partnerships or licensing opportunities to leverage the findings and expedite market entry.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04680949
Indication
Covid19
Modality
small molecule
Target
suPAR (soluble urokinase plasminogen activator receptor) as a biomarker for guiding anakinra treatment in COVID-19 patients.
Intervention
Anakinra, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.