Healthcare nonprofit Open Medicine Foundation (OMF) on Wednesday launched a large-scale international collaborative study to investigate the potential conversion of Post-Acute Sequelae SARS-CoV-2 infection to Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), a chronic, life-altering disease with no known cause, diagnostic test or US FDA approved treatments available.
The company added that the Post-Acute Sequelae SARS-CoV-2 infection is also known as Long COVID or Post-COVID Syndrome. Up to 2.5m people in the US alone suffer from ME/CFS; the COVID-19 pandemic could at least double that number. The company's goal is to find targeted treatments for ME/CFS patients and ultimately prevent its onset in people infected with SARS-CoV-2 or other infections.
This USD5m, three-year study will be conducted across the globe at OMF funded Collaborative Research Centers, led by some of the world's top researchers and ME/CFS experts. The focus is to find the biological differences between persons returning to good health after COVID-19 and persons who remained ill more than six months after infection and developed ME/CFS.
Additionally, the federal government is now investing in Post-COVID research, with no focus on its connection to ME/CFS.
Biofrontera reports Phase 2b data for Ameluz photodynamic therapy in acne vulgaris treatment
Precision BioSciences receives FDA Fast Track designation for PBGENE-DMD
Egetis receives US notice of allowance for MCT8 deficiency composition patent
Ipsen withdraws tazverik across all markets following safety concerns in lymphoma trial
Foresee Pharmaceuticals receives positive CHMP opinion for CAMCEVI 21 mg
Great Novel Therapeutics' GNTbm-38 approved by US FDA for Phase I trial
Johnson & Johnson reports US FDA approval of TECVAYLI plus DARZALEX FASPRO for RRMM
Airiver Medical's Airiver Pulmonary DCB receives US FDA Breakthrough Device Designation
Sanaregen receives FDA clearance for retinal degeneration clinical trial
Esperion to acquire Corstasis, expanding cardiovascular portfolio
ReviR Therapeutics doses first participant in First-in-Human Phase 1 clinical trial of RTX-117
BD receives FDA clearance for Surgiphor 1000mL irrigation system
United Therapeutics' ralinepag reduces risk of clinical worsening in pivotal PAH study