COM701 was well-tolerated with no dose-limiting toxicities when
administered alone and in combination with Bristol-Myers
Squibb's cancer drug Opdivo (nivolumab), Compugen said.
Furthermore, COM701 demonstrated "encouraging signals of anti-tumour
activity" with high disease control rate both as a monotherapy
and in combination with Opdivo -- 69% and 75%, respectively, it
said.
"I am highly encouraged by the safety profile and preliminary
anti-tumour activity observed with COM701 both as a monotherapy
and in combination with nivolumab," said Ryan Sullivan,
assistant professor of medicine at Harvard Medical School and
presenting author of the data at the virtual annual meeting of
the American Association for Cancer Research.
The Phase 1 clinical trial is designed to assess the safety and
tolerability of administering escalating doses of COM701
monotherapy as well as combined with Opdivo.
Secondary endpoints include preliminary anti-tumour activity in
patients with selected tumour types, including non-small cell
lung cancer, ovarian cancer, breast cancer, endometrial cancer
and colorectal cancer.
COM701 is a humanized antibody that binds to PVRIG, a novel
immune checkpoint discovered computationally by Compugen.
(Reporting by Tova Cohen; Editing by Steven Scheer)
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