Dyax Receives FDA Approval For Kalbitor
RCT licensee, Dyax has received approval from the FDA for Kalbitor (ecallantide) for the treatment of acute attacks of hereditary angioedema (HAE) in patients 16 years of age
The US Food and Drug Administration (FDA) has approved Pfizer’s Tukysa (tucatinib) along with pertuzumab and trastuzumab as a maintenance therapy for breast cancer.
Alethia Biotherapeutics (Alethia) has obtained the exclusive worldwide diagnostic rights to a peptide that specifically binds to tumor-associated clusterin from the National Research Council Biotechnology Research Institute (NRC-BRI)