Clinical TrialsBDTX-1535 elicited a 36% objective response rate in response evaluable patients, which improved to 42% after excluding patients without on-target resistance mutations.
Drug DevelopmentThe safety profile of BDTX-1535 is consistent with approved EGFR TKI class drugs, showing no severe side effects like G3/4 diarrhea or off-target effects.
EarningsBlack Diamond reported a net loss of $0.28 per share, which is narrower than the estimated net loss of $0.37 per share, due to lower-than-anticipated operating expenses.