In conjunction with today’s press release, the company commented that patient recruitment in the coming months may be slowed down due to the COVID-19 pandemic, but that it still remains committed to the previously announced timeline at this stage; (1) Middle of 2021: Result of first phase (safety and selection of optimal dose), subject to number of cohorts; and (2) Second half of 2021: Efficacy result from the second phase, including estimation of the potential magnitude of benefit of FG001 in guiding surgery of patients with high grade glioma.
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