FDA approves Nubeqa™ (darolutamide) for patients with advanced prostate cancer
“Patients with mHSPC want treatments that delay disease progression and extend life – without compromising their ability to stay active,” said Christine Roth, Executive Vice President, Global Product Strategy and Commercialization and Member of the Pharmaceuticals Leadership Team at Bayer. “This approval, supported by compelling clinical data, reaffirms Nubeqa’s potential to become a leading therapy across various stages of prostate cancer, underscoring our commitment to deliver meaningful outcomes for patients and their loved ones.”
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