Press releases
-
U.S. FDA Approves Label Update to Accelerate Thaw Time for ADSTILADRIN® (nadofaragene firadenovec-vncg)
-Accelerated water-bath thawing, completed in about 25 minutes, may help streamline clinical workflows and support efficient patient management Label update includes data showing that product stability is maintained with the 25-minute, 25° C water-bath method Label update reinforces Ferring’s commitment to improving patient and provider experience through continued innovation in the delivery and handling of ADSTILADRIN
-
Ferring Announces Update to NCCN Guidelines Expanding Category 2A Recommendation for Nadofaragene Firadenovec-vncg (ADSTILADRIN®) in Patients with BCG-Unresponsive NMIBC
-Nadofaragene firadenovec-vncg received an NCCN Category 2A recommendation for patients with papillary tumors (+Ta/T1) without carcinoma in situ (CIS), an upgrade from its 2B recommendation Nadofaragene firadenovec-vncg maintained its Category 2A recommendation for patients with CIS with or without papillary tumors (+Ta/T1)
-
Ferring Pharmaceuticals and Theralase® Technologies Announce Clinical Development Agreement to Investigate Combination Therapy in Bladder Cancer
-The collaborative clinical study will evaluate ADSTILADRIN® (nadofaragene firadenovec-vncg) in combination with the investigational drug Ruvidar® (TLD-1433) in patients with Bacillus Calmette-Guérin-unresponsive non-muscle invasive bladder cancer carcinoma in situ with or without papillary tumors (±Ta/T1)
