Worst Performing Large-Cap Stocks Last Week
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Feb 22 2026
0mins
Should l Buy BBIO?
Source: Benzinga
- GPC Earnings Miss: Genuine Parts Company (NYSE:GPC) saw a 19.51% drop this week after reporting disappointing fourth-quarter results and issuing FY26 EPS guidance below estimates, prompting multiple analysts to lower their price targets, indicating market concerns over its future profitability.
- FLUT Earnings Awaited: Flutter Entertainment plc (NYSE:FLUT) decreased by 11.86% this week as the company announced it will release its fourth quarter and full year 2025 financial results after market close on February 26, leading investors to adopt a cautious stance ahead of the earnings report, which may impact stock performance.
- OKTA Price Target Cuts: Okta, Inc. (NASDAQ:OKTA) fell 12.86% this week after several firms lowered their price targets, reflecting diminished market confidence in its growth potential and possibly prompting investors to reassess its investment value.
- TEAM Executive Change: Atlassian Corporation (NASDAQ:TEAM) decreased by 5.33% this week following the announcement of James Chuong as the new Chief Financial Officer effective March 30, 2026; while executive changes may bring new strategic directions, they failed to boost the stock price in the short term.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy BBIO?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
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: 76.750
Low
85.00
Averages
98.50
High
157.00
Current: 76.750
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.
BridgeBio Pharma (BBIO.US) Director Plans to Sell $8.9 Million in Common Stock via Form 144
Share Sale Announcement: Bridge Bio Pharma intends to sell 120,000 shares of its common stock on April 9, with a total market value of approximately $8.9 million.
Reduction in Holdings: Kumar Haldea has reduced his shareholding in Bridge Bio Pharma by 188,050 shares since February 10, 2026, with a total value of approximately $13.25 million.
See More
Healthcare Stocks Mixed as NYSE Health Care Index Edges Up 0.1%
- Mixed Market Performance: Late Thursday afternoon, healthcare stocks showed mixed results, with the NYSE Health Care Index rising by 0.1%, indicating a cautious market sentiment towards the healthcare sector amid economic uncertainties.
- Investor Sentiment Fluctuations: While the overall index saw a slight increase, individual healthcare stocks exhibited varied performances, influenced by company earnings reports and market dynamics, highlighting the volatility and uncertainty in investor sentiment.
- Uncertain Industry Outlook: The future of the healthcare industry faces challenges, particularly in light of changing policies and economic conditions, prompting investors to closely monitor potential impacts from regulatory changes on the sector.
- Long-Term Trends to Watch: Despite the mixed short-term performance of healthcare stocks, the sector is still viewed as having growth potential in the long run, driven by an aging population and increasing health demands.
See More
Acoramidis Shows Significant Long-Term Benefits in Heart Failure Treatment
- Significant Risk Reduction: In the ATTRibute-CM open-label extension trial, acoramidis achieved a 44.7% reduction in all-cause mortality (ACM) (p<0.0001) and a 49.3% reduction in cardiovascular mortality (CVM) (p<0.0001) at Month 54, marking the earliest timepoint for such significant risk reduction in this field, indicating its potential in heart disease treatment.
- Quality of Life Improvement: Early and continuous treatment with acoramidis effectively stabilized and maintained heart failure-related quality of life scores (KCCQ-OS), demonstrating a sustained improvement in the quality of life for ATTR-CM patients, thereby enhancing their overall health status.
- Good Safety Profile: Throughout the 54-month observation period, acoramidis exhibited a favorable long-term safety profile with no severe adverse reactions, providing confidence for its acceptability and tolerability in heart disease treatment for future clinical applications.
- Clinically Significant Findings: These study results underscore the importance of early diagnosis and timely treatment, as the sustained clinical benefits of acoramidis offer new hope for heart disease patients, potentially altering the treatment trajectory of this condition.
See More
BridgeBio Submits NDA for BBP-418 to Treat LGMD2I/R9
- Clinical Trial Success: BridgeBio's BBP-418 met all pre-specified primary and secondary endpoints in the Phase 3 FORTIFY trial, demonstrating rapid and consistent treatment effects with a favorable safety profile, laying a solid foundation for future FDA approval.
- NDA Submission: The company has submitted a New Drug Application for BBP-418 to the FDA, with approval anticipated in late 2026 to early 2027, which, if successful, would be the first treatment for LGMD2I/R9, addressing a significant unmet need in this area.
- Significant Market Potential: Approval of BBP-418 would provide the first effective treatment option for thousands of LGMD2I/R9 patients, potentially improving their quality of life and representing the first approved therapy for any form of LGMD, highlighting its substantial market significance.
- Expedited Approval Pathway: BridgeBio is actively engaging with regulatory agencies to identify an expedited approval pathway for BBP-418 in Europe, while the drug has already received Orphan Drug, Fast Track, and Rare Pediatric Disease designations from the FDA, enhancing its market prospects.
See More
BridgeBio Pharma (BBIO.US) Director Plans to Sell $9.52 Million in Common Stock via Form 144
Share Sale Announcement: Bridge Bio Pharma intends to sell 140,000 shares of its common stock, valued at approximately $9.52 million, on March 13.
Reduction in Holdings: The Kumar Haldea Family Irrevocable Trust has reduced its shareholding in Bridge Bio Pharma by 25,806 shares since December 15, 2025, with a total value of around $18.78 million.
See More
BridgeBio Presents Positive Interim Data for BBP-418 in LGMD2I/R9
- Clinical Trial Results: BridgeBio presented positive interim analysis results for BBP-418 at the MDA conference, highlighting early separation from placebo in the 100-meter timed test, with improvements evident as early as three months, indicating the drug's rapid onset of action.
- FDA Submission Plans: Following the positive interim results, BridgeBio intends to submit a New Drug Application (NDA) to the FDA in the first half of 2026, with a U.S. launch anticipated in late 2026 to early 2027, potentially making it the first approved therapy for LGMD2I/R9, which holds significant market potential.
- Safety Analysis: BBP-418 demonstrated a safety profile comparable to placebo, with 93.2% of patients reporting treatment-emergent adverse events, and similar rates of serious adverse events, indicating good tolerability and laying a foundation for future clinical use.
- Efficacy Sustainability: Among patients treated with BBP-418 for 12 months, 59.6% achieved significant reductions in serum creatine kinase (CK) levels, and 38.3% normalized CK levels, demonstrating the drug's sustained efficacy in improving muscle function, which could transform the treatment landscape for LGMD2I/R9.
See More
BridgeBio Pharma (BBIO.US) Director Plans to Sell $8.9 Million in Common Stock via Form 144
Share Sale Announcement: Bridge Bio Pharma intends to sell 120,000 shares of its common stock on April 9, with a total market value of approximately $8.9 million.
Reduction in Holdings: Kumar Haldea has reduced his shareholding in Bridge Bio Pharma by 188,050 shares since February 10, 2026, with a total value of approximately $13.25 million.
See More
Healthcare Stocks Mixed as NYSE Health Care Index Edges Up 0.1%
- Mixed Market Performance: Late Thursday afternoon, healthcare stocks showed mixed results, with the NYSE Health Care Index rising by 0.1%, indicating a cautious market sentiment towards the healthcare sector amid economic uncertainties.
- Investor Sentiment Fluctuations: While the overall index saw a slight increase, individual healthcare stocks exhibited varied performances, influenced by company earnings reports and market dynamics, highlighting the volatility and uncertainty in investor sentiment.
- Uncertain Industry Outlook: The future of the healthcare industry faces challenges, particularly in light of changing policies and economic conditions, prompting investors to closely monitor potential impacts from regulatory changes on the sector.
- Long-Term Trends to Watch: Despite the mixed short-term performance of healthcare stocks, the sector is still viewed as having growth potential in the long run, driven by an aging population and increasing health demands.
See More
Acoramidis Shows Significant Long-Term Benefits in Heart Failure Treatment
- Significant Risk Reduction: In the ATTRibute-CM open-label extension trial, acoramidis achieved a 44.7% reduction in all-cause mortality (ACM) (p<0.0001) and a 49.3% reduction in cardiovascular mortality (CVM) (p<0.0001) at Month 54, marking the earliest timepoint for such significant risk reduction in this field, indicating its potential in heart disease treatment.
- Quality of Life Improvement: Early and continuous treatment with acoramidis effectively stabilized and maintained heart failure-related quality of life scores (KCCQ-OS), demonstrating a sustained improvement in the quality of life for ATTR-CM patients, thereby enhancing their overall health status.
- Good Safety Profile: Throughout the 54-month observation period, acoramidis exhibited a favorable long-term safety profile with no severe adverse reactions, providing confidence for its acceptability and tolerability in heart disease treatment for future clinical applications.
- Clinically Significant Findings: These study results underscore the importance of early diagnosis and timely treatment, as the sustained clinical benefits of acoramidis offer new hope for heart disease patients, potentially altering the treatment trajectory of this condition.
See More
BridgeBio Submits NDA for BBP-418 to Treat LGMD2I/R9
- Clinical Trial Success: BridgeBio's BBP-418 met all pre-specified primary and secondary endpoints in the Phase 3 FORTIFY trial, demonstrating rapid and consistent treatment effects with a favorable safety profile, laying a solid foundation for future FDA approval.
- NDA Submission: The company has submitted a New Drug Application for BBP-418 to the FDA, with approval anticipated in late 2026 to early 2027, which, if successful, would be the first treatment for LGMD2I/R9, addressing a significant unmet need in this area.
- Significant Market Potential: Approval of BBP-418 would provide the first effective treatment option for thousands of LGMD2I/R9 patients, potentially improving their quality of life and representing the first approved therapy for any form of LGMD, highlighting its substantial market significance.
- Expedited Approval Pathway: BridgeBio is actively engaging with regulatory agencies to identify an expedited approval pathway for BBP-418 in Europe, while the drug has already received Orphan Drug, Fast Track, and Rare Pediatric Disease designations from the FDA, enhancing its market prospects.
See More
BridgeBio Pharma (BBIO.US) Director Plans to Sell $9.52 Million in Common Stock via Form 144
Share Sale Announcement: Bridge Bio Pharma intends to sell 140,000 shares of its common stock, valued at approximately $9.52 million, on March 13.
Reduction in Holdings: The Kumar Haldea Family Irrevocable Trust has reduced its shareholding in Bridge Bio Pharma by 25,806 shares since December 15, 2025, with a total value of around $18.78 million.
See More
BridgeBio Presents Positive Interim Data for BBP-418 in LGMD2I/R9
- Clinical Trial Results: BridgeBio presented positive interim analysis results for BBP-418 at the MDA conference, highlighting early separation from placebo in the 100-meter timed test, with improvements evident as early as three months, indicating the drug's rapid onset of action.
- FDA Submission Plans: Following the positive interim results, BridgeBio intends to submit a New Drug Application (NDA) to the FDA in the first half of 2026, with a U.S. launch anticipated in late 2026 to early 2027, potentially making it the first approved therapy for LGMD2I/R9, which holds significant market potential.
- Safety Analysis: BBP-418 demonstrated a safety profile comparable to placebo, with 93.2% of patients reporting treatment-emergent adverse events, and similar rates of serious adverse events, indicating good tolerability and laying a foundation for future clinical use.
- Efficacy Sustainability: Among patients treated with BBP-418 for 12 months, 59.6% achieved significant reductions in serum creatine kinase (CK) levels, and 38.3% normalized CK levels, demonstrating the drug's sustained efficacy in improving muscle function, which could transform the treatment landscape for LGMD2I/R9.
See More
