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On April 14, Innovent announced that IBI310 (recombinant fully human anti-CTLA-4 monoclonal antibody) has been included in the breakthrough therapy drug category by CDE.
The breakthrough therapy designation of IBI310 is based on the results of an ongoing Phase 2 clinical study in patients with advanced cervical cancer (CDE registration number: CTR20202017) Phase 1 data
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