EpicGenetics developed and offers the FM/a Test, an FDA-compliant diagnostic blood test that identifies the immune system biomarkers of fibromyalgia.
According to the company, the new facility is 50,000 square feet and located at 11801 West Olympic in Los Angeles.
The move enables the company to expand its lab, support employee growth and facilitate new research initiatives.
In August, the company announced an FDA approved clinical trial that will be held at Massachusetts General Hospital.
The trial will evaluate the potential for BCG (an inexpensive generic vaccine used globally to prevent tuberculosis) to reverse fibromyalgia.
EpicGenetics is a privately held biomedical company based in Los Angeles, California that developed and manufactures the FM/a Test.
The company is dedicated to improving the diagnosis and treatment of fibromyalgia by offering the first conclusive diagnostic test for fibromyalgia, and by investing in and developing further comprehensive clinical studies at leading medical research centers.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval