Overview
US rare disease drugmaker's Q1 revenue rose yr/yr on strong Attruby sales and royalty growth
Company posted a Q1 net loss per share of $0.84, narrowing from $0.88 a year earlier
Board authorized a $500 mln share repurchase program
Outlook
Company anticipates U.S. launch of BBP-418 for LGMD2I/R9 in late 2026 or early 2027
BridgeBio expects to submit NDA for encaleret in ADH1 in 1H 2026, with U.S. launch in early 2027
Company plans NDA submission for infigratinib in achondroplasia in Q3 2026, U.S. launch expected early to mid 2027
Result Drivers
ATTRUBY SALES GROWTH - Q1 revenue increase was primarily driven by a $143.9 mln rise in net product revenue from Attruby, reflecting strong prescribing growth and patient persistence
BROAD ATTRUBY UPTAKE - Company cited continued broad uptake among all patient types and healthcare provider segments, with particularly strong and growing demand in treatment-naïve patients
HIGHER OPERATING COSTS - Operating expenses rose due to increased SG&A for commercialization of Attruby and pre-commercial activities for late-stage pipeline products, as well as higher R&D spending
Company press release: ID:nGNXcd3h6W
Key Details
Metric
Beat/Miss
Actual
Consensus Estimate
Q1 EPS
-$0.84
Q1 Net Income
-$166.56 mln
Q1 Operating Income
-$105.96 mln
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 24 "strong buy" or "buy", no "hold" and no "sell" or "strong sell"
The average consensus recommendation for the pharmaceuticals peer group is "buy"
Wall Street's median 12-month price target for BridgeBio Pharma Inc is $99.00, about 45.4% above its May 6 closing price of $68.09
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(This story was created using Reuters automation and AI based on LSEG and company data. It was checked and edited by a Reuters journalist prior to publication.)