Stock Markets March 11, 2026

JPMorgan Adds BridgeBio to Focus List and Lifts December 2026 Target to $94

Brokerage cites steady uptake of Attruby, modest post-generic share loss and undervalued late-stage programs

By Ajmal Hussain BBIO
JPMorgan Adds BridgeBio to Focus List and Lifts December 2026 Target to $94
BBIO

JPMorgan elevated BridgeBio Pharma to its U.S. Equity Analyst Focus List and raised its December 2026 price target to $94 from $89 while reaffirming an Overweight rating. The bank's conclusions rest on physician survey results showing steady adoption of Attruby for transthyretin amyloid cardiomyopathy and an assessment that BridgeBio's late-stage pipeline remains underappreciated.

Key Points

  • JPMorgan added BridgeBio to its U.S. Equity Analyst Focus List and raised the December 2026 price target to $94 from $89 - Sectors impacted: Biotechnology, Healthcare, Pharmaceuticals.
  • Physician survey of 28 ATTR-CM specialists shows steady adoption of Attruby among newly diagnosed patients and those progressed after tafamidis - Sectors impacted: Clinical therapeutics, Specialty pharma.
  • JPMorgan views BridgeBio’s late-stage programs (infigratinib, encaleret, BBP-418) as undervalued; further commercial and regulatory progress could support the stock - Sectors impacted: Drug development, Biotech R&D.

JPMorgan has moved BridgeBio Pharma onto its U.S. Equity Analyst Focus List and nudged up the firm's December 2026 price target to $94, from $89, while keeping an Overweight recommendation in place. The brokerage’s view is grounded in physician feedback on clinical adoption patterns and a reassessment of the value in BridgeBio’s late-stage drug programs.

In a survey of 28 physicians who treat transthyretin amyloid cardiomyopathy (ATTR-CM), JPMorgan found that uptake of BridgeBio’s stabilizer drug, Attruby, is progressing among newly diagnosed patients and among those whose disease has advanced despite prior treatment with tafamidis. The bank highlighted that clinicians continue to prefer stabilizer therapies such as Attruby and tafamidis over so-called knockdown agents that reduce production of the transthyretin protein.

About one-third of the surveyed doctors indicated that Attruby offers a slight or meaningful advantage in overall clinical profile compared with tafamidis products, including Vyndaqel and Vyndamax. JPMorgan said efficacy was the principal reason cited for that perceived edge.

JPMorgan acknowledged investor concerns about potential competition from generic tafamidis. The bank views the base-case scenario as loss of exclusivity for Pfizer’s tafamidis franchise occurring in December 2028. Even with generic entry, JPMorgan projects Attruby would surrender only incremental market share among newly diagnosed patients, a dynamic the firm expects to be partly offset by rising diagnosis rates over time.

Beyond the commercial outlook for Attruby, JPMorgan described BridgeBio’s late-stage pipeline as undervalued. The bank called out several programs specifically, naming:

  • infigratinib for achondroplasia
  • encaleret for autosomal dominant hypocalcemia
  • BBP-418 for limb-girdle muscular dystrophy

JPMorgan said that continued commercial traction for Attruby together with regulatory progress across these programs could underpin further upside in BridgeBio’s shares. The firm’s recalibration combines observed prescribing behavior, an expectation of modest competitive impact from future generics, and potential value tied to multiple late-stage assets.

Investors assessing BridgeBio will likely weigh ongoing commercial performance for Attruby against the timing of tafamidis generic competition and the upcoming regulatory milestones for the company’s pipeline candidates.

Risks

  • Potential loss of exclusivity for the tafamidis franchise developed by Pfizer expected in December 2028 could increase competition from generic tafamidis - Impact on the Pharmaceuticals and Specialty Pharma sectors.
  • Attruby may incur incremental market-share erosion in newly diagnosed patients after generic tafamidis entry, even if partially offset by higher diagnosis rates - Impact on Biotechnology and Commercial therapeutics.
  • Realization of upside depends on regulatory milestones for BridgeBio’s late-stage programs; delays or adverse outcomes could limit share gains - Impact on Biotech R&D and Capital markets.

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