BridgeBio Pharma reported its Q1 2023 financial results, highlighting the positive results from the Phase 2 trial of infigratinib for achondroplasia and progress in other key programs. The company closed a public offering with gross proceeds of $150 million and ended the quarter with $467 million in cash and cash equivalents.
Phase 3 ATTRibute-CM trial of acoramidis completed last patient last visit, with topline data expected in late July 2023.
Positive results were announced in Cohort 5 of Phase 2 PROPEL 2 trial of low-dose infigratinib in children with achondroplasia, demonstrating a mean increase in annualized height velocity (AHV) of 3.03cm/year.
Preliminary findings were shared on a novel bioassay measuring glycosylated alpha-dystroglycan (αDG) in patients with limb-girdle muscular dystrophy type 2I (LGMD2I).
Closed underwritten public offering with gross proceeds of approximately $150 million, and ended the quarter with $467 million in cash, cash equivalents, marketable securities, and restricted cash.
BridgeBio is focused on advancing its key programs, including acoramidis, infigratinib, BBP-418, encaleret and BBP-631. The company expects to announce topline data for the month 30 primary endpoint in late July, 2023 and is continuing to evaluate restructuring alternatives to drive operational changes in business processes, efficiencies, and cost savings.