MGI and SuperGen’s Dacogen accepted for review
The new drug application (NDA) for Dacogen (decitabine) injection was submitted to the FDA on November 1, 2004. The acceptance for review of the NDA represents the FDA’s
Harbour BioMed’s partner Solstice Oncology has raised $225m in funding to advance its lead candidate, porustobart, a neoadjuvant immuno-oncology therapy.
The formulation for Wellbutrin XL (bupropion hydrochloride extended-release tablets) was developed by Biovail, which licensed the product’s worldwide (excluding Canada) sales and distribution rights to GlaxoSmithKline in October