BridgeBio Pharma Q3 revenue more than doubles on Attruby sales and Bayer milestone
Overview
U.S. biopharma firm's Q3 revenue more than doubled yr/yr, driven by Attruby sales and Bayer milestone
Company posted Q3 operating loss as costs rose with commercialization and R&D investments
Attruby growth led by more newly diagnosed patients starting treatment, boosting first-line share
Outlook
BridgeBio expects U.S. launch of BBP-418 for LGMD2I/R9 upon FDA approval in November 2026
Company anticipates U.S. launch of oral infigratinib for achondroplasia after February 2027 FDA decision
Encaleret for ADH1 has a May 2027 PDUFA date; U.S. launch expected upon approval
Result Drivers
ATTRUBY SALES GROWTH - Co said revenue increase was primarily driven by higher U.S. Attruby net product sales, with growth led by treatment-naïve segment and increased share of new patient starts
BAYER MILESTONE - Co recognized a one-time $75 mln sales milestone from Bayer under license agreement, contributing to higher license and services revenue
OPERATING COSTS - Higher selling, general and administrative expenses and increased R&D spending contributed to Q3 operating loss, reflecting investment in commercialization and late-stage product development
Company press release:
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q3 Loss Per Share | $0.42 | ||
Q3 Net Loss | $60.50 mln | ||
Q3 Operating Income | -$11.64 mln |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 21 "strong buy" or "buy", 2 "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 $108.50, about 53.2% above its October 28 closing price of $70.82
Reuters Recommended Reads
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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.)