ABBV: SKYRIZI Approval vs Rich Valuation | ABBV Research
π On October 23, 2026, the FDA approved a subcutaneous induction regimen for SKYRIZI in Crohn's disease, expanding patient access via an on-body injector.
π° AbbVie reported Q2 2026 EPS of $3.65, beating estimates of $3.61, driven by resilient revenue from specialty biologics.
π The stock trades at a trailing P/E of 80.47 with limited implied upside to the consensus price target of $294.
β οΈ Liquidity metrics warrant monitoring as the current ratio stands at 0.81, indicating current liabilities exceed short-term assets.
π Goldman Sachs maintained a Strong Buy rating and raised its price target from $258 to $294 following the FDA action.
π Upcoming earnings on October 30, 2026, will focus on SKYRIZI uptake, margin expansion, and capital allocation revisions.
π The stock has largely stopped making Humira central to its investor narrative as it pivots toward newer assets like SKYRIZI.
- AbbVie secured FDA approval for a subcutaneous induction regimen of SKYRIZI in Crohn's disease, expanding the label and improving patient convenience.
- The company delivered an EPS beat of $3.65 versus estimates of $3.61 for the quarter ended July 31, 2026.
- Goldman Sachs raised its price target to $294 following the regulatory win, signaling confidence in SKYRIZI's commercial potential.
- AbbVie maintains a durable dividend profile and a large market capitalization while transitioning revenue streams toward newer biologics.
- Liquidity metrics are concerning with a current ratio of 0.81, indicating that current liabilities exceed short-term assets.
- Return on equity is negative and price-to-book is negative, reflecting large share buybacks and accumulated intangible assets rather than operational weakness.
- Implied upside to the consensus price target is only about 2.9%, suggesting the stock is fairly valued to slightly rich on a near-term basis.