BridgeBio Pharma, Inc. (BBIO) Stock Analysis
Range Bound setup
Healthcare · Biotechnology
Sell if holding. Multiple concerning factors at $67.03: Consecutive earnings misses (3); Concentration risk — Product: Attruby and Beyonttra.
BridgeBio Pharma commercializes Attruby (acoramidis) for ATTR-CM in the U.S. and develops therapies for genetic diseases. Attruby generated $362.4 million in U.S. net product revenues in 2025; Beyonttra contributed $105.0 million in license revenue via Bayer (Europe) and Alexion... Read more
Sell if holding. Multiple concerning factors at $67.03: Consecutive earnings misses (3); Concentration risk — Product: Attruby and Beyonttra. Chart setup: RSI 47 mid-range, Bollinger mid-band. Score 5.4/10, moderate confidence.
Passes 8/8 gates (positive momentum, favorable risk/reward ratio, clean insider activity, no SEC red flags, news events none recent, earnings proximity 50d clear, semi cycle peak clear, materials cycle peak clear). Suitability: moderate.
Recent developments
updated 2026-06-15Recent Developments — BridgeBio Pharma, Inc.
Latest news
- NEWS BBIO Reiterated by HC Wainwright & Co. -- Price Target Maintained at $100 - GuruFocus — GuruFocus positive
- NEWS BridgeBio: Attruby's Early Dominance Makes The Bull Case Hard To Ignore (NASDAQ:BBIO) - Seeking Alpha — Seeking Alpha positive
- NEWS Why BridgeBio Pharma (BBIO) Is Down 6.4% After Attruby’s Faster-Than-Expected Commercial Ramp - And What's Next - simply — simplywall.st negative
- NEWS Analysts Are Bullish on Top Healthcare Stocks: BridgeBio Pharma (BBIO), Wave Life Sciences (WVE) - The Globe and Mail — The Globe and Mail positive
- NEWS BBIO Maintained by Truist Securities -- Price Target Raised to $102 - GuruFocus — GuruFocus positive
Generated 2026-06-15T18:11:46Z.
Upcoming dated catalysts
Thesis
Key Metrics
Quality Signals
Options Flow
Concentration Risks(10-K Item 1A)
- HIGHProductAttruby and Beyonttra10-K Item 1A: 'Our business is substantially dependent on the commercial success of Attruby and Beyonttra'
Material Events(8-K, last 90d)
- 2026-05-08Item 1.01LOWBridgeBio entered an Equity Distribution Agreement with Goldman Sachs and Leerink Partners on May 7, 2026 for an at-the-market offering of up to $500 million in common stock, filed alongside a Form S-3ASR registration statement.SEC filing →
Model-generated analysis — not investment advice. Not a registered investment advisor. Past performance does not guarantee future results.
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Rating Breakdown
3 floor-breakers·1 ceiling hit
No near-term catalyst priced in. Thesis progression will come from fundamentals grinding, not event reaction.static
Priced at a premium — multiples above sector norms. Needs delivery on growth + margins to justify.static
Ranks in the bottom of its industry peers on the composite signal. Better names in the same sector exist.static
Price Targets
Position Sizing
Analyst Consensus
Earnings
Verdict History
Frequently Asked Questions
Sell if holding. Multiple concerning factors at $67.03: Consecutive earnings misses (3); Concentration risk — Product: Attruby and Beyonttra. Chart setup: RSI 47 mid-range, Bollinger mid-band. Prior stop was $62.36. Score 5.4/10, moderate confidence.
Take-profit target: $92.44 (+37.9% upside). Prior stop was $62.36. Stop-loss: $62.36.
Concentration risk — Product: Attruby and Beyonttra; Consecutive earnings misses (3); Expensive valuation.
BridgeBio Pharma, Inc. trades at a P/E of N/A (forward 134.9). TrendMatrix value score: 3.2/10. Verdict: Sell.
29 analysts cover BBIO with a consensus score of 4.2/5. Average price target: $103.
What does BridgeBio Pharma, Inc. do?BridgeBio Pharma commercializes Attruby (acoramidis) for ATTR-CM in the U.S. and develops therapies for genetic...
BridgeBio Pharma commercializes Attruby (acoramidis) for ATTR-CM in the U.S. and develops therapies for genetic diseases. Attruby generated $362.4 million in U.S. net product revenues in 2025; Beyonttra contributed $105.0 million in license revenue via Bayer (Europe) and Alexion (Japan). Three Phase 3 programs—infigratinib, BBP-418, and encaleret—each reported positive data in 2025-2026 with NDA submissions planned for 2026.