BridgeBio (BBIO) Q1 2025 earnings summary
Event summary combining transcript, slides, and related documents.
Q1 2025 earnings summary
9 Jul, 2026Executive summary
Q1 2025 marked the first full quarter of net product revenue from the US launch of Attruby, generating $36.7 million in product sales and $116.6 million in total revenue, including a $75 million EU regulatory milestone; BEYONTTRA approved in EU, Japan, and UK.
Early uptake of Attruby was strong, with 2,072 unique patients and 756 healthcare providers prescribing by April 25, 2025.
The pipeline remains robust, with three phase three readouts expected in the next year for limb-girdle muscular dystrophy type 2i, achondroplasia, and ADH1, and additional programs advancing.
Attruby's clinical profile includes a 42% relative risk reduction in cardiovascular hospitalization and mortality at 30 months, and a 50% reduction in cardiovascular hospitalization.
Ended Q1 2025 with $540.6 million in cash and equivalents, not including $105 million in anticipated Q2 regulatory milestone payments.
Financial highlights
Total Q1 2025 revenue was $116.6 million, with $36.7 million from Attruby sales and $79.9 million from license and services revenue; revenue declined year-over-year due to lower license revenue.
Operating expenses were $218.4 million to $221.0 million, up year-over-year, reflecting continued investment in Attruby and late-stage pipeline.
R&D expense decreased to $111.4 million from $141 million year-over-year due to divestitures and focus on late-stage programs.
SG&A expense rose to $106.4 million from $65.8 million, driven by the commercial rollout of Attruby.
Net loss widened to $169.6 million in Q1 2025 from $36.2 million in Q1 2024, reflecting higher SG&A and interest expenses.
Outlook and guidance
Expect modest growth in quarterly operating expenses for the remainder of 2025, with Attruby sales offsetting cash burn.
Anticipate $105 million in regulatory milestone payments in Q2 2025 for ex-U.S. BEYONTTRA approvals and $30 million milestone from Japan approval.
Three phase three program readouts expected: ADH1 and LGMD2i in H2 2025, achondroplasia in early 2026; plans to advance encaleret to registration and initiate new studies.
Long-term goal for Attruby is 30-40% market share, aiming for $4.3 billion in peak year sales.
Cash and equivalents expected to fund operations for at least 12 months under current plans.
Latest events from BridgeBio
- Q2 2026 revenue surged on strong product sales and $1B in new preferred equity financing.BBIO
Q2 2026 - Multiple first-in-class rare disease therapies advance toward US launches, backed by $1.7B cash.BBIO
Corporate presentation - ATTR-CM launch outperformed, with three late-stage pipeline catalysts expected within 18 months.BBIO
Bank of America 2025 Healthcare Conference - Accelerating sales and robust clinical data drive growth and pipeline momentum in rare diseases.BBIO
UBS Global Healthcare Conference 2025 - Oral infigratinib significantly improved growth and body proportions in children with achondroplasia.BBIO
Conference presentation - All proposals, including director elections and stock plan amendments, were approved by majority vote.BBIO
AGM 2026 - Oral infigratinib delivers record growth and proportionality benefits with strong safety in achondroplasia.BBIO
Study result - Q3 revenue surged on new launches; pipeline and cash position support 2026 NDA filings.BBIO
Q3 2025 - Infigratinib delivers sustained growth and proportionality gains in achondroplasia with strong safety.BBIO
Study Result