AI
AbbVie Inc. (ABBV)·Q4 2024 Earnings Summary
Executive Summary
- Q4 2024 revenue grew to $15.10B (+5.6% reported, +6.1% operational) with adjusted EPS of $2.16; GAAP EPS was a loss of $0.02 due to a $3.5B after-tax emraclidine impairment and elevated acquired IPR&D expense (10.4% of sales) .
- Immunology drove the quarter: Skyrizi $3.78B (+57.7% YoY) and Rinvoq $1.83B (+46.2% YoY) more than offset Humira decline ($1.68B, -49.1% YoY), while Neuroscience (+19.8% YoY) and Oncology (+12.0% YoY) added breadth .
- 2025 guidance: adjusted EPS $12.12–$12.32; revenue ~ $59B (5.7% operational growth), including Skyrizi $15.9B, Rinvoq $7.9B, Humira $5.6B; adjusted tax rate ~15.6% and operating margin ~47% (all excl. IPR&D) .
- Long-term: raised 2027 Skyrizi+Rinvoq outlook to >$31B (from >$27B), reaffirmed high-single-digit revenue CAGR through 2029; Aesthetics long-term updated to high-single-digit CAGR (2025–2029) .
- Stock-relevant catalysts: accelerating IBD share capture for Skyrizi/Rinvoq; 2025 Part D redesign a ~4% net sales headwind (mix-driven uptick vs prior commentary); near-term Aesthetics headwinds but program changes (reinstated Alle) and pipeline (BoNT/E) aim to stabilize/rehaccelerate .
What Went Well and What Went Wrong
-
What Went Well
- Immunology outperformance: “ex-Humira platform” revenue up 22% in Q4; Skyrizi and Rinvoq combined expected to be nearly $24B in 2025, with raised 2027 target >$31B; strong IBD traction highlighted .
- Neuroscience strength: Vraylar $924M (+17.1% YoY), Botox Therapeutic $873M (+12.5% YoY), oral CGRPs Ubrelvy $303M (+29.6%) and Qulipta $201M (+76.4%), with Parkinson’s portfolio expansion (Vyalev launch; tavapadon Phase 3 positive) .
- Operational discipline: Q4 adjusted gross margin 83.8% and adjusted operating margin 34.7% despite IPR&D drag; 2025 guided ~84% adjusted GM and ~47% adjusted OM as mix shifts to higher-margin growth assets .
-
What Went Wrong
- Aesthetics softness: Q4 Aesthetics $1.30B (-5.2% YoY) on U.S./China macro and initial provider pushback to new loyalty program; share loss “a few points”; company reverted to original Alle in January .
- Cerevel emraclidine Phase 2 miss triggered a $3.5B after-tax impairment and GAAP loss; company pursuing adjunct indications and dose optimization, but monotherapy path is now more risk-adjusted and delayed .
- Medicare Part D redesign: net ~4% 2025 headwind (vs earlier ~3%); especially affecting oncology and immunology; only modest volume offset expected .
Financial Results
Headline results vs prior periods
Margins and operating ratios
Segment and key products – Q4 2024 (YoY reported growth)
KPIs and non-GAAP adjustments – Q4 2024
- Acquired IPR&D expense = 10.4% of sales; adjusted EPS impact -$0.88; GAAP loss driven by partial emraclidine impairment ($3.5B after-tax) .
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “We are entering 2025 with significant momentum and expect net revenues to exceed their previous peak in just the second full year following the U.S. Humira loss of exclusivity.” – CEO Rob Michael .
- “We now expect Skyrizi and Rinvoq to exceed more than $31 billion of combined sales in 2027… driven by strong performance across all approved indications, especially in IBD.” – CEO Rob Michael .
- “Fourth quarter… adjusted EPS of $2.16, which is $0.08 above our guidance midpoint… ex-Humira platform delivered reported growth of 22%.” – CFO Scott Reents .
- “We reinstated our original Alle consumer loyalty program… with encouraging early indicators for sales and market share recovery.” – Carrie Strom (Allergan Aesthetics) .
- “A thorough analysis… shows a path forward for emraclidine as an adjunct… and potentially monotherapy at higher doses” – Roopal Thakkar (R&D/CSO) .
Q&A Highlights
- Skyrizi/Rinvoq trajectory: Upside drivers are primarily share capture across indications; 2027 breakdown: Skyrizi ~$20B (psoriatic ~$12.5B; IBD ~$7.5B), Rinvoq ~$11B (Rheum $4.8B; Derm $2.5B; IBD $3.7B) .
- Part D redesign: Net ~4% growth headwind; modest volume offsets concentrated in standard-eligible segment; no spillover to commercial contracting observed .
- Aesthetics trough and BoNT/E: 2025 modeled as trough with HSD CAGR to 2029; BoNT/E expected to activate “considerer” patients and funnel to Botox over time .
- Inventory/gross-to-net: No unusual Q4 stocking or GTN dynamics for Skyrizi/Rinvoq ahead of Part D changes .
- AD uptake/AtoDerm: Rinvoq in-play share >20% with differentiation on stringent endpoints; pipeline (lutikizumab) targeted to augment franchise .
Estimates Context
- S&P Global (Capital IQ) consensus for Q4 2024 EPS and revenue was unavailable at the time of retrieval due to vendor rate limits; therefore, we cannot quantify beat/miss vs Street consensus. Values from S&P Global could not be retrieved at this time.
- Company vs guidance: Adjusted EPS of $2.16 was $0.08 above AbbVie’s internal guidance midpoint for Q4; revenue of $15.10B was described as “robust,” with ex-Humira +22% and total +6.1% operational growth .
Key Takeaways for Investors
- Immunology engine accelerating: Skyrizi/Rinvoq momentum (esp. IBD) supports 2025 growth and raised 2027 target >$31B; this is the primary multi-year stock driver .
- 2025 setup resilient despite headwinds: ~5.7% operational revenue growth and mid-teens tax rate guided, absorbing ~4% Part D and ~$3B U.S. Humira erosion .
- Aesthetics near-term weak but stabilizing: Reversion to prior loyalty program and product cadence aim to recapture share; long-term HSD CAGR reset provides a more conservative, achievable base .
- Mixed neuroscience update: Emraclidine impairment is a headline negative; tavapadon and Vyalev expand Parkinson’s platform and maintain optionality into late decade .
- ADC franchise scaling: Elahere EU approval, Teliso-V potential 1H25 approval, and ABBV-400 progression underpin oncology optionality .
- Watch Part D dynamics intra-year: Expect pressure in oncology/immunology with modest volume offsets; company pricing commentary implies ongoing low single-digit rebate pressure but volume-led growth .
- Catalyst path: Regulatory milestones (Teliso-V), IBD share data points for Skyrizi/Rinvoq, aesthetics KPIs post-Alle reversion, and neuroscience readouts should shape estimate revisions and sentiment .
Appendix: Other Relevant Press Releases (Q4 2024 window)
- EC approval of Elahere for FRα-positive platinum‑resistant ovarian cancer (first novel therapy in EU for this population) .
- Emraclidine Phase 2 EMPOWER trials did not meet primary endpoints (schizophrenia); safety acceptable; post-hoc analysis/plans described on call .
- Aliada Therapeutics acquisition (BBB-crossing tech; ALIA‑1758 in AD) and EvolveImmune collaboration (multispecific T-cell engagers) .