AbbVie Inc.

Abbvie Inc.

Drug Manufacturers - General Healthcare North Chicago, IL, United States ABBV (NYQ)
Quarter: Q2 2025 Reported: April 3, 2025 Sentiment: Neutral

AbbVie Inc., a research-based biopharmaceutical company, engages in the research and development, manufacture, commercialization, and sale of medicines and therapies worldwide. The company offers Humira, an injection for autoimmune and intestinal Behçet's diseases, generalized pustular psoriasis, and pyoderma gangrenosum; Skyrizi to treat autoimmune diseases, erythrodermic psoriasis, generalized pustular psoriasis, and palmoplantar pustulosis; Rinvoq to treat inflammatory diseases; Imbruvica for the treatment of adult patients with blood cancers; Venclexta/Venclyxto to treat blood cancers; Elahere to treat various cancer; and Epkinly to treat lymphoma. It also provides facial injectables, plastics and regenerative medicine, body contouring, and skincare products; botox therapeutic to treat neurologic diseases; Vraylar to treat schizophrenia, bipolar disorder, and depressive disorder; Duopa and Duodopa to treat Parkinson's disease; Ubrelvy to treat migraine; and Qulipta for episodic and chronic migraine, as well as other neuroscience products. In addition, the company offers Ozurdex for eye diseases; Lumigan/Ganfort and Alphagan/Combigan for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension; Restasis to increase tear production; and other eye care products. Further, it provides Mavyret/Maviret to treat chronic hepatitis C virus genotype 1-6 infection; Creon, a pancreatic enzyme therapy; and Linzess/Constella to treat irritable bowel syndrome with constipation and chronic idiopathic constipation. The company was incorporated in 2012 and is headquartered in North Chicago, Illinois.

Analysis Summary

AbbVie Inc. has released preliminary financial updates for the first quarter and full-year 2025, primarily focusing on the impact of acquired IPR&D (In-Process Research & Development) and milestones expense. The company reported a pre-tax expense of $248 million for acquired IPR&D and milestones in Q1 2025, which translates to an unfavorable impact of $0.13 on both GAAP and adjusted non-GAAP diluted earnings per share. Consequently, AbbVie's full-year 2025 adjusted diluted EPS guidance has been revised to $11.99 - $12.19, now including this Q1 IPR&D impact, a change from previous guidance that excluded such expenses due to their uncertain nature. The first quarter 2025 adjusted diluted EPS guidance is set at $2.34 - $2.38. It's important to note that these figures are preliminary and subject to the company's financial statement closing procedures, with no assurance that final results will not differ. Additionally, the guidance does not yet reflect the impact of the recently closed licensing agreement with Gubra for the development of GUB014295, as this transaction occurred after the first quarter. Management's commentary highlights the inherent uncertainty in forecasting IPR&D expenses, which are incurred upon execution of strategic collaborations and asset acquisitions. The company maintains its commitment to providing updated, comprehensive guidance as these transactions materialize. Competitive positioning and market trends are not explicitly detailed in this snippet, but ongoing strategic agreements like the Gubra deal suggest continued investment in pipeline expansion. Risk factors include the preliminary nature of these estimates, the unpredictable timing and occurrence of future IPR&D expenses, and general risks associated with forward-looking statements such as intellectual property challenges, competition, R&D difficulties, adverse litigation, and regulatory changes. Analyst Q&A highlights are not available in this specific transcript excerpt.

Key Highlights

  • Preliminary Q1 2025 adjusted diluted EPS guidance set at $2.34 - $2.38.
  • Full-year 2025 adjusted diluted EPS guidance updated to $11.99 - $12.19, now including Q1 IPR&D impact.
  • Acquired IPR&D and milestones expense of $248 million pre-tax incurred in Q1 2025.
  • This expense resulted in an unfavorable $0.13 impact on both GAAP and adjusted diluted EPS.
  • Guidance does not yet reflect the impact of the Gubra licensing agreement, which closed post-Q1.
  • All reported results are preliminary and subject to finalization procedures.

Financial Metrics

eps
revenue
Not provided N/A
YoY: Not provided
guidance
net income
Not provided N/A
YoY: Not provided

Stock Performance (90 Days)

Data through Dec 26, 2025
Layoff Events
Earnings Calls

Positive Signals

  • Transparency in updating guidance to include IPR&D expenses.
  • Proactive communication of preliminary results and their potential impact.
  • Ongoing strategic business development indicated by the Gubra licensing agreement.
  • Management's clear explanation of IPR&D expense uncertainty.

Risks & Concerns

  • Preliminary nature of financial results, subject to finalization.
  • Uncertainty regarding the future occurrence and timing of acquired IPR&D and milestones expenses.
  • Challenges to intellectual property rights.
  • Competition from other products.
  • Difficulties inherent in the research and development process.

Full Transcript

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