Benitec Biopharma reports Q2 EPS (33c) vs ($2.64) last year

“In 2024 the interim clinical study data demonstrated durable, clinically meaningful improvements in swallowing function for the first Subjects safely treated with BB-301, and we remain highly optimistic about the potential for continued benefit in Subjects enrolled in the ongoing clinical study,” said Jerel Banks, M.D., Ph.D., Executive Chairman and Chief Executive Officer of Benitec. “We continue to be extremely grateful for the strong support of the Subjects and their families and for their continued participation in the BB-301 clinical development program, and we look forward to enrolling additional Subjects at the low dose and, this year, at the next, higher dose of BB-301.”