BridgeBio to Release Q4 and Full Year 2025 Financial Results
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 5 days ago
0mins
Should l Buy BBIO?
Source: Newsfilter
- Earnings Release Schedule: BridgeBio Pharma will announce its fourth quarter and full year 2025 financial results after market close on February 24, 2026, highlighting the company's latest advancements and financial status in the genetic treatment sector.
- Conference Call Details: The company will host a conference call at 4:30 PM ET on the same day to discuss the financial results and program updates, aiming to bolster investor confidence in the company's future growth.
- Webcast Access: Investors can access the live webcast of the earnings release through the 'Events & Presentations' page on BridgeBio's website, ensuring transparency and fostering interaction with stakeholders.
- Company Mission and Model: BridgeBio focuses on developing transformative medicines for genetic conditions, utilizing a decentralized hub-and-spoke model to enhance the speed and precision of drug development, addressing the needs of small patient populations.
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Analyst Views on BBIO
Wall Street analysts forecast BBIO stock price to rise
13 Analyst Rating
13 Buy
0 Hold
0 Sell
Strong Buy
Current: 70.720
Low
85.00
Averages
98.50
High
157.00
Current: 70.720
Low
85.00
Averages
98.50
High
157.00
About BBIO
BridgeBio Pharma, Inc. is a biopharmaceutical company. It discovers, creates, tests, and delivers transformative medicines to treat patients who suffer from genetic diseases. Its pipeline of development programs ranges from early science to advanced clinical trials, which includes Attruby, an oral small molecule near-complete transthyretin (TTR) stabilizer, for the treatment of cardiomyopathy of wild-type or variant transthyretin-mediated amyloidosis (ATTR-CM); Beyonttra for the treatment of TTR Amyloidosis; Low-dose Infigratinib, an oral FGFR1-3 selective tyrosine kinase inhibitor (TKI) for the treatment of children with achondroplasia and hypochondroplasia; Encaleret, an oral small molecule antagonist of the calcium sensing receptor (CaSR) that it is developing for the treatment of Autosomal Dominant Hypocalcemia Type 1 (ADH1), and BBP-418, for the treatment of Limb Girdle Muscular Dystrophy Type 2I. It also conducting a Phase 1/2 study (CANaspire) for BBP-812 for Canavan disease.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Equity Grant Program: On February 12, 2026, BridgeBio Pharma approved equity grants totaling 76,701 restricted stock units to 34 new employees, aimed at attracting and retaining talent, thereby enhancing the company's competitive edge in genetic drug development.
- Vesting Schedule: One-fourth of the restricted stock units will vest on February 16, 2027, with the remaining shares vesting quarterly, ensuring employees remain with the company to receive their incentives, which boosts employee loyalty and motivation.
- Compliance and Plan Background: The equity grants comply with Nasdaq Listing Rule 5635(c)(4) and are granted under an incentive plan adopted in November 2019, demonstrating the company's strategic planning and compliance in talent acquisition.
- Company Mission and Vision: BridgeBio focuses on developing transformative medicines for genetic conditions, aiming to bridge the gap between advancements in genetic science and patient needs, utilizing a decentralized operational model to enhance R&D efficiency and market responsiveness.
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- Earnings Release Schedule: BridgeBio Pharma will announce its fourth quarter and full year 2025 financial results after market close on February 24, 2026, highlighting the company's latest advancements and financial status in the genetic treatment sector.
- Conference Call Details: The company will host a conference call at 4:30 PM ET on the same day to discuss the financial results and program updates, aiming to bolster investor confidence in the company's future growth.
- Webcast Access: Investors can access the live webcast of the earnings release through the 'Events & Presentations' page on BridgeBio's website, ensuring transparency and fostering interaction with stakeholders.
- Company Mission and Model: BridgeBio focuses on developing transformative medicines for genetic conditions, utilizing a decentralized hub-and-spoke model to enhance the speed and precision of drug development, addressing the needs of small patient populations.
See More
- Clinical Trial Results: BridgeBio Pharma's PROPEL 3 Phase 3 trial for oral infigratinib in children demonstrated a significant annualized height velocity increase, with an LS mean treatment difference of +1.74 cm/year compared to placebo, highlighting the drug's potential in treating achondroplasia.
- Statistical Significance: In a pre-specified exploratory analysis of children under 8, infigratinib showed statistical significance against placebo with an LS mean decrease of -0.05, marking a significant breakthrough in randomized trials for achondroplasia treatment.
- Regulatory Plans: BridgeBio intends to meet with regulatory authorities in the second half of 2026 to discuss plans for submitting a New Drug Application (NDA) and Marketing Authorization Application (MAA) for infigratinib, reflecting the company's confidence in future market opportunities.
- Competitive Landscape: While BioMarin's Voxzogo is the first FDA-approved drug for achondroplasia, the positive results from BridgeBio's infigratinib clinical trials may shift the competitive dynamics and enhance the company's position in the rare disease market.
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Positive Trial Results: BridgeBio's drug for treating an oral genetic disorder has shown a 10.44% improvement in late-stage trial results.
Impact on Patients: The positive outcomes from the trial suggest potential benefits for patients suffering from this specific genetic condition.
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