• Obtained U.S. FDA Fast Track designation for BDTX-189 for the treatment of adult patients with a solid tumor harboring an allosteric HER2 mutation or an EGFR or HER2 Exon 20 insertion mutation • Continued to enroll and dose patients in Phase 1/2 clinical trial of BDTX-189, with Phase 1 portion on track to complete by first half of 2021 • Strengthened executive team with the appointment of Fang Ni, Pharm.D., as Chief Business Officer • Cash, cash equivalents, and in
August 11, 2020
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