Welcome to our dedicated page for Precision Biosciences news (Ticker: DTIL), a resource for investors and traders seeking the latest updates and insights on Precision Biosciences stock.
Precision Biosciences, Inc. (DTIL) is a biotechnology innovator advancing the ARCUS genome editing platform for therapeutic and agricultural solutions. This page serves as the definitive source for verified company news, providing investors and industry professionals with timely updates on scientific milestones and corporate developments.
Access consolidated information on regulatory filings, research breakthroughs, and strategic partnerships directly impacting DTIL's position in the genome editing sector. Our curated feed includes earnings announcements, clinical trial updates, and technology licensing agreements, enabling informed analysis of the company's progress.
Key focus areas include ARCUS platform advancements in gene therapy programs, allogeneic CAR-T developments, and agricultural biotechnology applications. Users can track patent approvals, peer-reviewed study publications, and executive leadership updates through our chronologically organized news archive.
Bookmark this page for streamlined access to Precision Biosciences' official communications and third-party analysis. Check regularly for updates on how DTIL's precision gene editing technology continues to shape the future of genomic medicine and sustainable agriculture.
Precision BioSciences, Inc. (Nasdaq: DTIL) announced that its partner iECURE has received FDA Fast Track designation for ECUR-506 to treat Neonatal Onset Ornithine Transcarbamylase (OTC) Deficiency. The Fast Track designation expedites the review process for therapeutics addressing unmet medical needs. ECUR-506 also received Rare Pediatric Disease and Orphan Drug designations.
iECURE, Inc. has received Fast Track designation from the FDA for ECUR-506, an in vivo gene insertion program to treat neonatal onset Ornithine Transcarbamylase (OTC) deficiency. The designation helps expedite the review process for therapies addressing unmet medical needs. The company's OTC-HOPE study is open for enrollment in the UK, with sites in the US and Australia to follow, focusing on safety, efficacy, and other endpoints.
Precision BioSciences, Inc. announced a late-breaking poster presentation at the European Association for Study of the Liver Congress 2024, showcasing preclinical safety data for their clinical candidate PBGENE-HBV for the treatment of chronic hepatitis B. The data supports the progression of the gene editing program towards potential clinical trials and regulatory filings in 2024.
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