
CRSP
CRISPR Therapeutics AG develops gene editing product candidates using CRISPR/Cas9 technology to treat human diseases. The company is in the early stages of clinical development, with only a limited number of clinical trials underway for its gene editing-based therapies. CRISPR Therapeutics has not yet achieved regulatory approval for any products and expects to incur significant operating losses for the foreseeable future while advancing its pipeline toward commercialization.
Pipeline
Next-generation allogeneic CD19-directed CAR-T therapy (CRISPR Therapeutics) with multiple gene edits to improve persistence and reduce rejection. Phase 1/2 in B-cell malignancies and lupus.
Catalyst Calendar
“An update is now expected in the first half of 2026, reflecting a strategic decision to incorporate emerging insights from the evolving Lp(a) landscape.”