BridgeBio reported first quarter results, highlighted by the FDA approval of NULIBRY, proof-of-concept data for encaleret in ADH1, a strategic collaboration with Helsinn Group for infigratinib, the completion of the Eidos Therapeutics acquisition, and nearly $750 million raised through convertible senior notes. The company ended the quarter with $1,001.3 million in cash, cash equivalents and marketable securities.
Received FDA approval for NULIBRY™ for injection for MoCD Type A.
Reported proof-of-concept data of encaleret in Autosomal Dominant Hypocalcemia Type 1 (ADH1).
Launched strategic collaboration with Helsinn Group to co-develop and commercialize infigratinib in oncology.
Completed acquisition of Eidos Therapeutics, Inc.
BridgeBio anticipates major milestones in 2021 or early 2022 for its four core value drivers, including Acoramidis, Encaleret, Low-dose infigratinib and BBP-631.