Cellectis Gains FDA Orphan Drug Status for ALL Therapy
Company Announcements

Cellectis Gains FDA Orphan Drug Status for ALL Therapy

Cellectis SA (CLLS) has released an update.

Cellectis SA, a clinical-stage biotech company, has been granted Orphan Drug Designation by the FDA for its investigational drug CLLS52, intended for the treatment of B-cell acute lymphoblastic leukemia (ALL). This designation could accelerate the drug’s development and commercialization, and highlights Cellectis’ innovation in combining gene-edited CAR T-cells with a lymphodepleting regimen to enhance clinical effectiveness. The company specializes in gene-editing technologies and CAR-T immunotherapies, aiming to deliver off-the-shelf solutions for cancer patients.

For further insights into CLLS stock, check out TipRanks’ Stock Analysis page.

Related Articles
TipRanks Auto-Generated NewsdeskCellectis Reveals Promising Cancer Therapy Breakthrough
GlobeNewswireCellectis Publishes a Molecular Therapy Article on a SMART DUAL CAR T-cell Approach for Treating Recalcitrant Solid Tumors
TipRanks Auto-Generated NewsdeskCellectis Boosts Leadership with New CMO
Looking for investment ideas? Subscribe to our Smart Investor newsletter for weekly expert stock picks!
Optimize your mobile reading experience. Download the TipRanks App today!