Precision BioSciences (DTIL) announced that it has received Clinical Trial Application, CTA, approval to expand the ongoing global Eliminate-B clinical trial of PBGENE-HBV. The regulatory authorization will allow Precision to initiate important hepatitis B clinical trial sites in France and Romania. This expansion broadens the trial’s global footprint deeper into Europe, adding to existing clinical trial sites in the United Kingdom, Moldova, New Zealand, Hong Kong and the United States. The Company expects the addition of clinical trial sites in France and Romania to support continued patient enrollment and clinical execution in Eliminate-B with the goal to treat as many clinical trial patients as possible with PBGENE-HBV. Site initiation activities are underway, with initial patient screening expected in Q2 2026.
Claim 55% Off TipRanks
- Unlock hedge fund-level data and powerful investing tools for smarter, sharper decisions
- Discover top-performing stock ideas and upgrade to a portfolio of market leaders with Smart Investor Picks
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on DTIL:
- Precision BioSciences Highlights PBGENE-DMD Program and Trial
- Precision BioSciences Advances PBGENE-DMD Trial, Putting New Focus on Duchenne Gene Therapy
- Precision BioSciences reports Q4 EPS $1.05, consensus (64c)
- Precision receives two notices of allowance from USPTO for PBGENE-HBV
- Precision BioSciences presents new PBGENE-DMD data at conference
