Medical diagnostics company Know Labs Inc (OTCQB: KNWN) on Wednesday confirmed the efficacy of a light bulb in inactivating multiple variants of SARS-CoV-2, the virus that causes COVID-19, based on Texas Biomedical Research Institute's new independent test data.
The light bulb is reportedly produced by the company's wholly owned subsidiary Particle Inc.
Earlier in 2021, Know Labs confirmed that Particle bulbs were effective against the Washington SARS-CoV-2 strain.
Additionally, the multiple tests performed by Texas Biomed demonstrated a 95% reduction in the SARS-CoV-2 virus after five hours of exposure to the Particle bulb, a 99% reduction in six hours and 99.9% reduction in 8 hours.
Texas Biomed's additional tests confirmed that Particle bulbs were equally efficient against the Alpha and Delta variants.
In conjunction, Know Labs Inc has received product and packaging samples from its contract manufacturer in Asia, a final step before commercial production can begin. It is exploring potential strategic and channel partner opportunities.
Tyra Biosciences to announce TYRA-300 preclinical results at ENDO 2025
Centivax raises USD45m to commercialise universal flu vaccine
Adcentrx Therapeutics' ADRX-0405 granted US FDA orphan drug designation
Avenzo Therapeutics doses first patient in AVZO-1418/DB-1418 Phase 1/2 clinical study
SCG Cell's SCG101V therapy Investigational New Drug Application receives Chinese regulatory approval
KalVista secures FDA approval for EKTERLY, first oral on-demand HAE treatment
BioDlink convenes peer advisory event on innovation and collaboration strategies
CyanVac's nasal COVID vaccine shows promise in phase 1 trial
Imfinzi approved in EU as first perioperative immunotherapy for muscle-invasive bladder cancer
Akeso's bispecific ADC (Trop2/Nectin4 ADC) enters clinical trials
Brii Biosciences enters BRII-693 licensing agreement with Joincare Group in Greater China
Neurizon enters global license agreement with Elanco to commercialise NUZ-001
Ascletis doses first US participants in ASC30 Phase IIa study for obesity treatment
Jacobio's JAB-8263 Phase I/II Clinical Trial IND application receives Chinese regulatory approval