The company was awarded over USD2 m by the Department of Defense to accelerate testing of its Diocheck system and is expected to begin human clinical trials in December 2020.
The Diocheck SARS-CoV-2 Visual Immune Response Indicator provides a simple, universal way to continually monitor a person's immune response status to COVID-19 over an extended period of time, eliminating the need for more frequent testing.
Diomics' proprietary biopolymer material, Diomat, containing a COVID-19 antigen, will be injected under the skin with the PharmaJet Tropis device.
The skin reaction at the injection site will act as an indicator of an immune response against COVID-19 infection, showing whether a person has been exposed to the virus, and whether they need to get tested and take precautions to avoid infecting others.
This procedure is readily scalable and could provide consistent, accurate ongoing monitoring of the immunity status of essential front-line workers, including military, healthcare, transportation, and public safety personnel.
PharmaJet's mission is worldwide acceptance of PharmaJet Needle-free Injection Systems as a standard of care in the vaccine delivery market.
The PharmaJet Needle-free Systems are safe, fast, and easy-to-use. They eliminate needlestick injuries, needle reuse and cross contamination, and help reduce sharps waste disposal.
The Stratis System has US FDA 510(k) marketing clearance, CE Mark, and WHO PQS certification to deliver medications and vaccines either intramuscularly or subcutaneously. The Tropis System has CE Mark and WHO PQS certification for intradermal injections.
Diomics Corp. is a biotechnology company focused on science-based innovation and the development of life-improving products.
Their proprietary Diomat technology platform is optimized for the collection and delivery of compounds and proteins and can also be used for drug delivery, long-term monitoring, diagnostics and production of life-saving hormones and other bio-compounds.
Based in San Diego, California, Diomics has developed numerous products, tools and services for the molecular, diagnostic and forensic industries.
Futura Medical reports positive home user test results for Eroxon and Intense variant
GSK secures Japan Orphan Drug status for lung cancer ADC
Belief BioMed enters exclusive partnership with Grand Life Sciences for haemophilia A treatment
Glaukos launches Epioxa to advance incision-free treatment for keratoconus
Sanofi's venglustat receives FDA Breakthrough Therapy designation for type 3 Gaucher disease
Sentynl Therapeutics and PRG S&T enter licensing agreement for potential HGPS treatment
CMIC agrees agentic AI partnership with Bluenote
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