BridgeBio Oncology Therapeutics

BBOT · NASDAQ

$2.72−$0.13 (−4.56%)TodayMarket closed ·
Prev close $2.85

BBOT analyst rating

BuyConsensus of 10 analysts over the last 12 months. 100% rate it a buy.
  • Strong buy0
  • Buy10
  • Hold0
  • Underperform0
  • Sell0

12-month price target · 12 analysts

Average $22.33 (+720.8% upside)

Low
$15.15
Now
$2.72
High
$30.45

Upgrades and downgrades

The latest rating actions, newest first

BBOT analyst upgrades, downgrades and rating actions
FirmDateActionRating
OppenheimerOct 20, 2026MaintainsOutperform
JP MorganSep 11, 2026MaintainsOverweight
Leerink PartnersSep 10, 2026MaintainsOutperform
Canaccord GenuitySep 9, 2026MaintainsBuy
Raymond JamesSep 9, 2026MaintainsOutperform
StifelSep 9, 2026MaintainsBuy
WedbushSep 9, 2026MaintainsOutperform
JP MorganAug 14, 2026MaintainsOverweight
JP MorganJul 8, 2026InitiatesOverweight
OppenheimerJun 22, 2026InitiatesOutperform

The case for and against

Updated Oct 16, 2026

Bull case

BridgeBio Oncology is attractive because BBO-8520 is showing strong clinical differentiation, with 63% ORR and 100% DCR in G12C-naive patients, 75% of eligible patients still on treatment beyond 6 months, and no grade 3 liver enzyme elevations. Its pivot toward BBO-8520 plus pembrolizumab in 2L+ KRAS G12C inhibitor-experienced NSCLC is strategically sound, targeting a less crowded setting with favorable efficacy versus current standards and peers while preserving the upside of a faster path to market. Beyond that, the company’s broader RAS pipeline adds meaningful optionality: BBO-11818 and BBO-10203 combinations are advancing in CRC and PDAC, supported by a highly synergistic platform with modeled total worldwide peak sales of about $7.5 billion.

Bear case

BridgeBio Oncology is facing a negative fundamental setup because its pipeline remains early-stage, with BBO-8520, BBO-10203, and BBO-11818 all still in Phase 1 and dependent on unproven therapeutic windows, tolerability, and clinical activity. The company’s recent narrowing away from breast cancer and other legacy indications signals internal prioritization and has likely reduced investor confidence, while the crowded KRAS market raises the risk of weaker eventual market share versus better-positioned competitors. Although early safety data are encouraging, any need for large randomized Phase 3 trials would require significant capital and likely equity issuance, creating dilution risk in a business that still has no approved products or meaningful revenue.

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