| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 15.90B | 15.40B | 14.98B | 14.41B | 13.87B | 11.36B |
| Gross Profit | 5.37B | 5.38B | 5.24B | 5.03B | 4.64B | 3.86B |
| EBITDA | 3.44B | 3.45B | 3.26B | 2.91B | 2.77B | 2.08B |
| Net Income | 1.28B | 1.37B | 1.36B | 1.09B | 966.00M | 279.00M |
Balance Sheet | ||||||
| Total Assets | 28.73B | 26.90B | 26.68B | 25.34B | 24.69B | 24.56B |
| Cash, Cash Equivalents and Short-Term Investments | 1.97B | 1.84B | 1.50B | 1.31B | 1.48B | 1.90B |
| Total Debt | 15.19B | 14.16B | 13.90B | 13.01B | 12.44B | 12.90B |
| Total Liabilities | 22.44B | 20.83B | 20.57B | 19.57B | 18.65B | 18.28B |
| Stockholders Equity | 6.16B | 6.07B | 6.11B | 5.76B | 6.04B | 6.00B |
Cash Flow | ||||||
| Free Cash Flow | 2.64B | 2.11B | 1.50B | 1.59B | 2.30B | 1.34B |
| Operating Cash Flow | 2.80B | 2.72B | 2.15B | 2.26B | 2.94B | 1.96B |
| Investing Cash Flow | -1.51B | -1.44B | -1.60B | -2.01B | -2.10B | -796.00M |
| Financing Cash Flow | -1.06B | -878.00M | -382.00M | -329.00M | -1.24B | -217.00M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
| ― | $16.35B | 40.59 | 73.70% | ― | 13.88% | 23.92% | |
| ― | $36.86B | 29.72 | 19.55% | ― | 3.85% | -4.74% | |
| ― | $151.90B | 44.04 | 6.84% | 0.57% | 2.22% | -7.60% | |
| ― | $210.04B | 32.27 | 13.16% | 0.30% | 3.22% | 8.26% | |
| ― | $19.57B | 20.65 | 13.69% | 1.79% | 13.74% | 14.87% | |
| ― | $13.36B | 23.23 | 6.27% | ― | -2.46% | -17.89% | |
| ― | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
IQVIA Holdings Inc. is a global leader in providing clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries, leveraging advanced analytics and AI technologies. In its third-quarter 2025 earnings report, IQVIA announced a revenue increase of 5.2% year-over-year, reaching $4.1 billion, with a GAAP net income of $331 million and an adjusted EBITDA of $949 million. The company also reported a significant free cash flow increase of 35% year-over-year, amounting to $772 million. Key financial highlights include a robust performance in its Research & Development Solutions segment, with quarterly bookings of $2.6 billion and a contracted backlog of $32.4 billion, indicating strong future revenue potential. Additionally, the Technology & Analytics Solutions and Contract Sales & Medical Solutions segments also showed solid growth. Looking forward, IQVIA remains confident in sustaining its growth trajectory, supported by strong demand indicators and a strategic focus on leveraging its comprehensive portfolio of solutions.
IQVIA Holdings’ recent earnings call conveyed a positive sentiment, highlighting strong financial performance and record-high free cash flow. The company demonstrated significant growth in net bookings and backlog, despite facing challenges in the R&D Solutions segment and delays in mega trials. IQVIA’s focus on AI and technology advancements underscores its optimism for future efficiencies and growth.
Study Overview: The study titled Observational Cohort Study on Adult Patients With Not-adequately Controlled Focal-onset Seizures Treated With Cenobamate as Early Adjunctive Therapy in a Real-world Setting – FOCUS aims to evaluate the clinical response to cenobamate in adult patients with focal epilepsy in France, Germany, and Spain. The study is significant as it seeks to provide real-world data on the effectiveness of cenobamate for patients whose seizures are not adequately controlled by two or three anti-seizure medications (ASMs).
Study Overview: The study titled ‘A Prospective, Open-Label, Multi-Country, Multicentre, Observational PoSt Market SurvEillance of VIVO ISAR’ aims to assess the safety and performance of the Polymer-Free Sirolimus Eluting Coronary Stent System in patients with coronary artery disease. The key objective is to evaluate clinical outcomes in patients undergoing percutaneous coronary intervention (PCI) with a short dual antiplatelet therapy (DAPT) regimen, highlighting its significance in real-world applications.
Study Overview: The Carry Life@ UF System Clinical Study, officially titled ‘A Clinical Study With the Carry Life® UF System in Continuous Ambulatory Peritoneal Dialysis (CAPD) Patients,’ aims to evaluate the effectiveness of the Carry Life UF system in enhancing ultrafiltration in CAPD patients. This study is significant as it could improve treatment outcomes for patients with End Stage Renal Disease by optimizing peritoneal dialysis processes.
Study Overview: The study titled A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of Taplucainium Inhalation Powder (NOC-110) in Adults With Refractory or Unexplained Chronic Cough aims to evaluate the effectiveness, safety, and tolerability of NOC-110. This research is significant as it targets adults suffering from chronic coughs that are either unexplained or resistant to existing treatments.
IQVIA Holdings (IQV) has recently provided an update on a clinical study titled ‘Prospective, Multi-center, Single-arm Investigational Study of SWM-831 to Treat Moderate and Severely Calcified Femoropopliteal Arteries.’ The study aims to evaluate the safety and effectiveness of the SWM-831 device in treating peripheral arterial disease, specifically targeting calcified femoropopliteal arteries. This research is significant as it could offer new treatment options for patients with this condition.
IQVIA Holdings and Swedish Orphan Biovitrum are collaborating on a clinical study titled ‘A Single Arm, Long-term, Multicentre Observational Study to Evaluate Effectiveness of Pegcetacoplan Under Real World Conditions in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH).’ The study aims to assess the real-world effectiveness of pegcetacoplan, a treatment for PNH, over a period of up to 72 months. This research is significant as it seeks to provide comprehensive data on the long-term impact of pegcetacoplan in a real-world setting.
Study Overview: The QUVIVIQ® Pregnancy Registry, officially titled ‘Registry to Collect Information on Pregnancy, Neonatal, and Infant Outcomes in Pregnant Women Exposed to QUVIVIQ®,’ aims to explore the effects of QUVIVIQ exposure on pregnancy, neonatal, and infant outcomes. This study is significant as it seeks to provide insights into the safety and implications of using QUVIVIQ, a treatment for insomnia, during pregnancy.
On September 2, 2025, IQVIA Holdings announced the appointment of Michael J. Fedock as Executive Vice President and Chief Financial Officer, effective February 28, 2026. This transition is part of the company’s CFO succession plan, with Fedock succeeding Ronald E. Bruehlman, who will retire and transition to a Senior Advisor role to the CEO. Fedock, with over 25 years of experience in the healthcare industry, has held several senior financial roles within IQVIA since joining in 2016. The transition aims to ensure continuity and support IQVIA’s long-term growth strategy, with Bruehlman having played a crucial role in the company’s transformation and growth since 2011.
The most recent analyst rating on (IQV) stock is a Buy with a $221.00 price target. To see the full list of analyst forecasts on IQVIA Holdings stock, see the IQV Stock Forecast page.