Roche and its US subsidiary Genentech were given the go-ahead by the FDA on 14 November to market Avastin (bevacizumab) plus chemotherapy to treat women with platinum-resistant, recurrent ovarian cancer.
Roche and its US subsidiary Genentech were given the go-ahead by the FDA on 14 November to market Avastin (bevacizumab) plus chemotherapy to treat women with platinum-resistant, recurrent ovarian cancer.
Specifically, Avastin was approved in combination with paclitaxel, pegylated liposomal doxorubicin or topotecan chemotherapy as a treatment for women with...
Interim results from the Phase III REMARK study presented at WCLC showed the Chinese company’s second-generation ALK/ROS1 inhibitor met its primary endpoint as a first-line therapy in ALK-positive advanced NSCLC.
Pipelines in bioconjugates continue to develop, from ADCs to XDCs, with radionuclide drug conjugates (RDCs) and antibody-oligonucleotide conjugates (AOCs) leading the expansion.
Interim results from the Phase III REMARK study presented at WCLC showed the Chinese company’s second-generation ALK/ROS1 inhibitor met its primary endpoint as a first-line therapy in ALK-positive advanced NSCLC.
The US precision medicine company hopes its drug response predictor technology will enhance responses to the chemotherapy Ixempra on the basis of promising data from a handful of breast cancer patients in a Phase II trial, marking a positive turn in its journey to date.
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Pipelines in bioconjugates continue to develop, from ADCs to XDCs, with radionuclide drug conjugates (RDCs) and antibody-oligonucleotide conjugates (AOCs) leading the expansion.
Interim results from the Phase III REMARK study presented at WCLC showed the Chinese company’s second-generation ALK/ROS1 inhibitor met its primary endpoint as a first-line therapy in ALK-positive advanced NSCLC.
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