Academic medical centre Hospital for Special Surgery (HSS) stated on Tuesday that the approved immunosuppressive drug anakinra used to treat rheumatoid arthritis and neonatal-onset multisystem inflammatory disease may allow certain people with COVID-19 to avoid mechanical ventilation.
Based on a case study from investigators at HSS, anakinra appears to reduce the effects of systemic inflammation in people with COVID-19 who are in severe respiratory distress. The study, published online-first in Arthritis & Rheumatology, was led by Iris Navarro-Millán, MD, MSPH. Dr Navarro-Millán is now developing a controlled study of anakinra in patients with COVID-19 who fit into the criteria.
The patients with acute hypoxic respiratory failure (AHRF) and cytokine storm syndrome (CSS) are the two criteria identified as signals that a patient would soon require mechanical ventilation. CSS is the most dangerous consequence leading to fatality in people with COVID-19. AHRF is defined as an increased need for supplemental oxygen. Since the COVID-19 pandemic began, a number of immunosuppressive drugs have been evaluated in patients experiencing CSS. Some of these drugs, including anakinra, inhibit a protein called interleukin-1.
Roivant to announce Q3 2026 financial results
Avacta secures FDA clearance for second pre|CISION oncology programme
OncoHost receives BIG Innovation Award in Health category
Summit Therapeutics and GSK form collaboration to study ivonescimab combination therapy
Summit Therapeutics submits FDA application for ivonescimab in EGFR-mutated lung cancer
Antin to acquire clinical trial equipment provider Emsere
Merck completes acquisition of Cidara Therapeutics for USD9.2bn
Bambusa Therapeutics reports first patient dosed in proof-of-concept COPD trial
Kelun-Biotech lung cancer drug granted Breakthrough Therapy Designation in China
INOVIO's INO-3107 Biologics License Application accepted by US FDA
Sanofi and Regeneron's Dupixent gains Japan approval for paediatric asthma patients aged 6 to 11
Aqualung Therapeutics' Phase 2a lung fibrosis study approved by US FDA