CytomX Therapeutics, Inc., a biopharmaceutical company developing therapeutics for the treatment of cancer, has appointed Dr. Rachel Humphrey chief medical officer. Humphrey formerly led immuno-oncology at Eli Lilly and AstraZeneca; oversaw clinical development of Yervoy (ipilmumab), the first FDA approved checkpoint inhibitor, at Bristol-Myers Squibb; and played a role in the development of Nexavar (sorafenib) at Bayer. She was also previously a member of CytomX's board of directors.
Immuno-Oncology Veteran Rachel Humphrey Joins CytomX
CytomX Therapeutics, Inc., a biopharmaceutical company developing therapeutics for the treatment of cancer, has appointed Dr. Rachel Humphrey chief medical officer. Humphrey formerly led immuno-oncology at Eli Lilly and AstraZeneca; oversaw clinical development of Yervoy (ipilmumab), the first FDA approved checkpoint inhibitor, at Bristol-Myers Squibb; and played a role in the development of Nexavar (sorafenib) at Bayer. She was also previously a member of CytomX's board of directors.
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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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