$72.01+1.77 (+2.52%)
BridgeBio Pharma, Inc., a biopharmaceutical company, discovers, develops, and delivers medicines for patients with genetic diseases.
BridgeBio Pharma, Inc. in the Healthcare sector is trading at $72.01 with a market capitalization of $12.8B. Wall Street consensus targets $102.28 (23 analysts), implying a +42.0% move over the next 12 months. The stock is currently 15% below its 52-week high of $84.94, remaining 5.8% above its 200-day moving average. On fundamentals, Piotroski 2/9 flags weak fundamentals, Altman Z in the distress zone. The Whystock Score of 70/100 reflects bullish alignment across trend, valuation and analyst targets.
| Metric (USD) | Q1 2026 | Q4 2025 | Q3 2025 | Q2 2025 | Q1 2025 |
|---|---|---|---|---|---|
| Total Revenue | $194.51M↑ | $154.18M↑ | $120.70M↑ | $110.56M↓ | $116.63M |
| Gross Profit | $184.58M↑ | $146.07M↑ | $114.14M↑ | $106.91M↓ | $113.99M |
| Operating Income | -$105.96M↑ | -$128.43M↑ | -$136.36M↓ | -$133.47M↓ | -$103.80M |
| Net Income | -$164.04M↑ | -$192.86M↓ | -$182.74M↓ | -$181.90M↓ | -$167.42M |
BridgeBio Pharma, Inc., a biopharmaceutical company, discovers, develops, and delivers medicines for patients with genetic diseases. The company offers Attruby, a next-generation oral small molecule near-complete TTR stabilizer for the treatment of c...
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BridgeBio Pharma recently announced that the FDA has accepted and granted Priority Review to its New Drug Application for oral BBP-418 to treat limb-girdle muscular dystrophy type 2I/R9, with a PDUFA target action date set for November 27, 2026. If approved, BBP-418 would be the first and only therapy for LGMD2I/R9 and the first approved treatment for any form of limb-girdle muscular dystrophy, highlighting its potential importance for a rare disease community with limited options. We will...
David Chang will leave his post after an eight-year run at the cell therapy maker. Elsewhere, a next-generation blood disease drug stumbled and an acquisition yielded an FDA approval for AbbVie.
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