Abbott Reports Second-Quarter 2026 Results and Raises Full-Year EPS Guidance

On July 16, 2026 Abbott (NYSE: ABT) reported financial results for the second quarter ended June 30, 2026.

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Second-quarter sales increased 13.0 percent on a reported basis and 4.8 percent on a comparable basis.
Second-quarter GAAP diluted EPS of $0.53 and adjusted diluted EPS of $1.31, which excludes specified items.
Abbott reaffirms full-year 2026 comparable sales growth guidance of 6.5% to 7.5%1.
Abbott raises full-year 2026 adjusted diluted EPS guidance range to $5.45 to $5.60, compared to previous range of $5.38 to $5.58.
In April, Abbott completed enrollment in its TECTONIC U.S. pivotal trial. This trial is designed to evaluate Abbott’s investigational Coronary Intravascular Lithotripsy (IVL) System for treating severe calcification in coronary arteries prior to stent implantation.
In April, at the Heart Rhythm Society (HRS) conference, Abbott presented new late-breaking data from four clinical trials that demonstrated strong clinical outcomes across the company’s pulsed field ablation (PFA) and conduction system pacing (CSP) portfolios.
In May, Abbott announced it secured CE Mark for Libre Duo, the world’s first dual glucose-ketone biowearable sensor. By providing real-time visibility into glucose and ketone levels, this new technology helps optimize the management of diabetes by detecting rising ketone levels, which can lead to diabetic ketoacidosis, a serious health condition for people with diabetes.
In May, Abbott completed its submission to the U.S. Food and Drug Administration (FDA) seeking approval for the company’s Amulet 360 left atrial appendage (LAA) device.
In May, the American Cancer Society (ACS) issued updated colorectal cancer (CRC) screening guidelines that reaffirmed Cologuard and Cologuard Plus as preferred screening options for adults age 45 and older who are at average risk for CRC.
"Our second-quarter results reflect the momentum we are building," said Robert B. Ford, chairman and chief executive officer, Abbott. "We expect this momentum to continue and drive accelerating sales and earnings growth in the second half of the year."

SECOND-QUARTER BUSINESS OVERVIEW

Comparable sales growth:
Management believes that measuring sales growth on a comparable basis is an appropriate way for investors to best understand the underlying performance of the business. Comparable sales growth includes the prior and current year sales of Exact Sciences, a cancer diagnostics company that Abbott acquired on March 23, 2026. Comparable sales growth excludes the impact of foreign exchange and revenue in both the prior and current year related to compensation payments that Abbott’s Structural Heart business received as part of a multi-year agreement with a competitor. The final payment under this agreement was recognized in the first quarter of 2026.

Note: In order to compute results excluding the impact of exchange rates, current year U.S. dollar sales are multiplied or divided, as appropriate, by the current year average foreign exchange rates and then those amounts are multiplied or divided, as appropriate, by the prior year average foreign exchange rates.

Second Quarter 2026 Results (2Q26)

Sales 2Q26 ($ in millions)

Total Company


Nutrition


Diagnostics


Established
Pharmaceuticals


Medical Devices

U.S.

5,216


871


1,660



2,680

International

7,377


1,273


1,432


1,499


3,173

Total reported

12,593


2,144


3,092


1,499


5,853


% Change vs. 2Q25


U.S.

22.0


(9.0)


104.8


n/a


7.0

International

7.5


1.4


5.1


8.4


10.7

Total reported

13.0


(3.1)


42.3


8.4


9.0

Total reported excl. foreign exchange impact

12.2


(3.6)


41.3


8.7


7.9

Comparable sales growth

4.8


(3.6)


2.9


8.7


8.4


U.S.

3.5


(9.0)


4.0


n/a


8.0

International

5.8


0.6


1.6


8.7


8.7

First Half 2026 Results (1H26)


Sales 1H26 ($ in millions)

Total Company


Nutrition


Diagnostics


Established
Pharmaceuticals


Medical Devices

U.S.

9,490


1,715


2,565



5,203

International

14,267


2,446


2,707


2,925


6,189

Total reported

23,757


4,161


5,272


2,925


11,392


% Change vs. 1H25


U.S.

12.4


(10.3)


52.5


n/a


7.4

International

9.3



6.4


10.7


14.2

Total reported

10.5


(4.5)


24.7


10.7


11.0

Total reported excl. foreign exchange impact

8.2


(5.6)


22.4


8.9


8.0

Comparable sales growth

4.3


(5.6)


2.4


8.9


8.4


U.S.

3.0


(10.3)


3.0


n/a


8.3

International

5.3


(1.9)


1.6


8.9


8.5

Refer to table titled "Non-GAAP Revenue Reconciliation" for a reconciliation of comparable sales growth.

Nutrition

Second Quarter 2026 Results (2Q26)

Sales 2Q26 ($ in millions)

Total


Pediatric


Adult

U.S.

871


525


346

International

1,273


500


773

Total reported

2,144


1,025


1,119


% Change vs. 2Q25


U.S.

(9.0)


(10.7)


(6.4)

International

1.4


7.3


(2.0)

Total reported

(3.1)


(2.7)


(3.4)

Total reported excl. foreign exchange impact

(3.6)


(3.1)


(4.0)

Comparable sales growth

(3.6)


(3.1)


(4.0)


U.S.

(9.0)


(10.7)


(6.4)

International

0.6


6.4


(2.8)

Worldwide Nutrition sales decreased 3.1 percent on a reported basis and 3.6 percent on a comparable basis in the second quarter.

Results in the quarter reflect the impact of lower sales volumes compared to the prior year and the effect of strategic pricing actions implemented in the fourth quarter of 2025. These pricing actions, together with the launch of new products, are contributing to improving performance. Nutrition sales increased $127 million on a sequential basis compared to the first quarter of 2026.

First Half 2026 Results (1H26)

Sales 1H26 ($ in millions)

Total


Pediatric


Adult

U.S.

1,715


1,036


679

International

2,446


942


1,504

Total reported

4,161


1,978


2,183


% Change vs. 1H25


U.S.

(10.3)


(11.9)


(7.8)

International


2.4


(1.5)

Total reported

(4.5)


(5.6)


(3.5)

Total reported excl. foreign exchange impact

(5.6)


(6.4)


(4.9)

Comparable sales growth

(5.6)


(6.4)


(4.9)


U.S.

(10.3)


(11.9)


(7.8)

International

(1.9)


0.7


(3.5)

Diagnostics*

Second Quarter 2026 Results (2Q26)

Sales 2Q26 ($ in millions)

Total


Core Laboratory


Cancer Diagnostics


Rapid/Molecular
Diagnostics

U.S.

1,660


377


890


393

International

1,432


1,041


29


362

Total reported

3,092


1,418


919


755


% Change vs. 2Q25


U.S.

104.8


7.5


n/a


(14.5)

International

5.1


3.4


n/a


2.0

Total reported

42.3


4.4


n/a


(7.3)

Total reported excl. foreign exchange impact

41.3


3.2


n/a


(8.0)

Comparable sales growth

2.9


3.2


13.3


(8.0)


U.S.

4.0


7.5


13.3


(14.5)

International

1.6


1.7


13.8


0.5

Worldwide Diagnostics sales increased 42.3 percent on a reported basis and 2.9 percent on a comparable basis in the second quarter.

Worldwide Core Laboratory Diagnostics results were driven by strong growth in the U.S. and Latin America.

Rapid and Molecular Diagnostics results reflect lower sales of respiratory virus tests compared to the prior year.

Cancer Diagnostics results were driven by mid-teens growth of Cologuard, which is benefiting from a growing base of both new and repeat users. Results in the quarter also reflect contributions to growth from the precision oncology and international businesses.

First Half 2026 Results (1H26)

Sales 1H26 ($ in millions)

Total


Core Laboratory


Cancer Diagnostics


Rapid/Molecular
Diagnostics

U.S.

2,565


724


983


858

International

2,707


1,966


32


709

Total reported

5,272


2,690


1,015


1,567


% Change vs. 1H25


U.S.

52.5


6.0


n/a


(14.1)

International

6.4


6.1


n/a


2.4

Total reported

24.7


6.1


n/a


(7.4)

Total reported excl. foreign exchange impact

22.4


3.2


n/a


(8.8)

Comparable sales growth

2.4


3.2


13.3


(8.8)


U.S.

3.0


6.0


13.2


(14.1)

International

1.6


2.2


16.5


(1.1)

*Beginning in 2026, Abbott aggregated its previously reported Rapid Diagnostics, Molecular Diagnostics, and Point of Care businesses into the Rapid and Molecular Diagnostics business. On March 23, 2026, Abbott completed the acquisition of Exact Sciences. Following the acquisition, the sales of Exact Sciences are presented as Abbott’s Cancer Diagnostics business.

Refer to table titled "Non-GAAP Revenue Reconciliation" for a reconciliation of comparable sales growth.

Established Pharmaceuticals

Second Quarter 2026 Results (2Q26)

Sales 2Q26 ($ in millions)

Total


Key Emerging
Markets


Other

U.S.



International

1,499


1,164


335

Total reported

1,499


1,164


335


% Change vs. 2Q25


U.S.

n/a


n/a


n/a

International

8.4


9.8


3.7

Total reported

8.4


9.8


3.7

Total reported excl. foreign exchange impact

8.7


10.7


2.1

Comparable sales growth

8.7


10.7


2.1


U.S.

n/a


n/a


n/a

International

8.7


10.7


2.1

Established Pharmaceuticals sales increased 8.4 percent on a reported basis and 8.7 percent on a comparable basis in the second quarter.

Key Emerging Markets include several emerging countries that represent the most attractive long-term growth opportunities for Abbott’s branded generics product portfolio. Sales in these geographies increased 9.8 percent on a reported basis and 10.7 percent on a comparable basis, led by double-digit growth in several countries across the Latin America and Asia Pacific regions.

First Half 2026 Results (1H26)

Sales 1H26 ($ in millions)

Total


Key Emerging
Markets


Other

U.S.



International

2,925


2,253


672

Total reported

2,925


2,253


672


% Change vs. 1H25


U.S.

n/a


n/a


n/a

International

10.7


11.3


8.6

Total reported

10.7


11.3


8.6

Total reported excl. foreign exchange impact

8.9


10.1


4.9

Comparable sales growth

8.9


10.1


4.9


U.S.

n/a


n/a


n/a

International

8.9


10.1


4.9

Medical Devices

Second Quarter 2026 Results (2Q26)

Sales 2Q26 ($ in millions)

Total


Rhythm
Management


Electro-
physiology*


Heart
Failure


Vascular


Structural
Heart*


Neuro-
modulation


Diabetes
Care

U.S.

2,680


377


420


313


294


225


189


862

International

3,173


366


441


88


509


372


71


1,326

Total reported

5,853


743


861


401


803


597


260


2,188


% Change vs. 2Q25


U.S.

7.0


10.7


15.9


10.9


3.9


(9.8)


(2.1)


8.6

International

10.7


10.0


12.3


3.0


7.5


12.1


14.7


11.7

Total reported

9.0


10.4


14.0


9.0


6.1


2.7


2.0


10.5

Total reported excl. foreign exchange impact

7.9


9.5


13.4


8.7


5.1


1.7


1.2


9.0

Comparable sales growth

8.4


9.5


13.4


8.7


5.1


5.7


1.2


9.0


U.S.

8.0


10.7


15.9


10.9


3.9


(0.9)


(2.1)


8.6

International

8.7


8.3


11.1


1.3


5.8


10.2


11.3


9.2

Worldwide Medical Devices sales increased 9.0 percent on a reported basis and 8.4 percent on a comparable basis in the second quarter.

Sales growth in the quarter was led by low-teens growth in Electrophysiology and high-single-digit growth in Rhythm Management, Diabetes Care, and Heart Failure.

In Diabetes Care, sales of continuous glucose monitors grew 11.0 percent on a reported basis and 9.5 percent on a comparable basis.

First Half 2026 Results (1H26)

Sales 1H26 ($ in millions)

Total


Rhythm
Management


Electro-
physiology*


Heart
Failure


Vascular


Structural
Heart*


Neuro-
modulation


Diabetes
Care

U.S.

5,203


716


798


605


585


449


366


1,684

International

6,189


711


851


185


995


726


137


2,584

Total reported

11,392


1,427


1,649


790


1,580


1,175


503


4,268


% Change vs. 1H25


U.S.

7.4


11.1


14.8


11.1


6.2


(9.6)


(0.7)


9.2

International

14.2


15.9


15.7


13.5


8.7


18.1


20.4


14.0

Total reported

11.0


13.4


15.3


11.7


7.7


5.7


4.3


12.1

Total reported excl. foreign exchange impact

8.0


10.9


13.0


10.4


5.0


2.6


2.6


8.2

Comparable sales growth

8.4


10.9


13.0


10.4


5.0


6.2


2.6


8.2


U.S.

8.3


11.1


14.8


11.1


6.2


(2.2)


(0.7)


9.2

International

8.5


10.7


11.2


7.8


4.3


12.4


13.2


7.5

*Abbott’s Amplatzer Amulet Left Atrial Appendage Occluder device and related accessories were transferred from Structural Heart to Electrophysiology on January 1, 2026. As a result, $55 million of sales in the second quarter of 2025 and $101 million of sales in the first half of 2025 were moved from Structural Heart to Electrophysiology.

(Press release, Abbott, JUL 16, 2026, View Source [SID1234669268])

Second Quarter 2026

On July 15, 2026 Johnson & Johnson reported second quarter 2026 results.

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(Press release, Johnson & Johnson, JUL 15, 2026, View Source [SID1234669384])

Rakovina Therapeutics Announces $1.5 Million Private Placement

On July 15, 2026 Rakovina Therapeutics Inc. (TSX-V: RKV)( FSE: 7JO0), a biopharmaceutical company advancing innovative cancer therapies through artificial intelligence (AI)-powered drug discovery, reported a non-brokered private placement offering (the "Offering") of up to $1.5 million.

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Pursuant to the Offering, Rakovina will issue up to 15 million equity units ("Units") at an offering price of $0.10 per Unit, with each Unit consisting of one common share and one-half of one common share purchase warrant (a "Warrant"). Each whole Warrant will entitle the holder to acquire one additional common share at an exercise price of $0.20 exercisable for a period of 24 months from issuance.

Proceeds from the Offering will be used to advance Rakovina’s pipeline, with a primary focus on in vivo ADME and efficacy testing for the kt-5000AI dual ATR/mTOR inhibitor program and continued AI-driven lead optimization through the Company’s collaboration with Variational AI. Funds will also support advancement of the kt-3000 LNP formulation program through in vitro and in vivo characterization, ongoing kt-2000AI compound development, and the continued expansion of the Company’s AI-enabled drug discovery collaborations. Remaining proceeds will be used for general working capital purposes.

The Units will be sold on a non-brokered "private placement" basis in accordance with applicable Canadian securities laws and under applicable exemptions from prospectus and registration requirements and the securities will be subject to resale restrictions for a period of four months plus one day from the date of issue.

(Press release, Rakovina Therapeutics, JUL 15, 2026, View Source;utm_medium=rss&utm_campaign=rakovina-therapeutics-announces-1-5-million-private-placement [SID1234669272])

First Patients Dosed in OPTIMAL-e Trial for Earlier Stage Prostate Cancer

On July 15, 2026 Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, "Telix") and St Vincent’s Hospital reported that the first patients have been dosed with TLX597-Tx (177Lu-DOTA-HYNIC-panPSMA) in the OPTIMAL-e trial, led by Professor Louise Emmett for patients with metastatic hormone-sensitive prostate cancer (mHSPC) at St Vincent’s Hospital in Sydney, Australia.

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OPTIMAL-e is a single-arm, open-label trial, evaluating adaptive-dosed TLX597-Tx in combination with androgen deprivation therapy (ADT) and an androgen receptor pathway inhibitor (ARPI) in men with mHSPC. The study will evaluate the impact of TLX597-Tx on PSA4 response rate in an earlier treatment setting, assessing its potential to improve both the depth and durability of PSA response, while further evaluating the safety of dose intensification.

TLX597-Tx is a highly-targeted next generation small molecule RLT5 designed to improve efficacy and quality of life in earlier-stage metastatic prostate cancer. It has demonstrated a favorable biodistribution and dosimetry profile in prior studies including OPTIMAL-PSMA6, suggesting low exposure to salivary glands and the kidneys, the healthy organs of concern with PSMA RLT, and high uptake in PSMA-expressing tumors.

Louise Emmett, MD, Director of Theranostics and Nuclear Medicine, St. Vincent’s Hospital, and Lead Investigator of the OPTIMAL-e study, said, "I am excited to lead the OPTIMAL-e trial, which is evaluating an adaptive treatment approach designed to tailor therapy to each patient’s response. By using PSMA-PET7 imaging and PSA measurements to monitor disease burden, treatment can be continued when the PSMA target persists, and paused when there is a significant reduction in tumor burden. This individualized strategy aims to maintain disease control while minimizing unnecessary treatment exposure, with the potential to keep patients in a low-volume disease state for longer and support quality of life. The findings from OPTIMAL-e may help shape future treatment strategies and advance precision medicine for men living with prostate cancer."

David N. Cade, MD, Group Chief Medical Officer, Telix, said, "The initiation of OPTIMAL-e marks an important evolution of PSMA-targeted radioligand therapy for earlier metastatic prostate cancer, where maintaining quality of life is paramount. While the currently approved radioligand therapy has demonstrated a modest improvement in overall survival in advanced-stage disease, we believe earlier intervention may offer the potential to further improve outcomes and prolong quality of life for patients."

TLX597-Tx has not received marketing authorization in any jurisdiction.

About OPTIMAL-e

OPTIMAL-e is a Phase 2, non-randomized pilot study evaluating adaptive-dosed TLX597-Tx (177Lu-DOTA-HYNIC-panPSMA) in combination with ADT and an ARPI in patients with metastatic hormone-sensitive prostate cancer (mHSPC). Adaptive dosing of 177-Lu-PSMA is the concept of only treating if the PSMA target is persistent, while pausing treatment if there is a marked reduction in the tumor target, with re-treatment at first confirmed PSA rise (once the target has returned). The study is investigating whether intensified, response-adapted PSMA-targeted radioligand therapy can deepen responses, improve disease control and enable treatment pauses for selected patients based on PSMA-PET imaging and PSA outcomes.

TLX597-Tx is being developed alongside TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan), Telix’s lead antibody-based prostate cancer therapy candidate, currently the subject of the Phase 3 ProstACT Global8 trial in mCRPC9, which is actively dosing patients in jurisdictions with regulatory approval. TLX591-Tx and TLX597-Tx exhibit complementary modes-of-action, suggesting the potential for distinct applications in mCRPC and mHSPC settings as part of Telix’s portfolio approach to treating prostate cancer.

(Press release, Telix Pharmaceuticals, JUL 15, 2026, View Source [SID1234669249])

Boehringer Ingelheim reports first-half 2026 sales growth, driven by JARDIANCE® and new product launches in the U.S.

On July 15, 2026 Boehringer Ingelheim reported continued sales growth in the first half of 2026, driven by strong growth in the U.S. due to increased demand for JARDIANCE (empagliflozin) and successful new launches. Group net sales increased by 16.2%* to EUR 15.8 billion, with Human Pharma contributing EUR 13.1 billion and Animal Health EUR 2.6 billion.

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Shashank Deshpande, Chairman of the Board of Managing Directors and Head of Human Pharma, Boehringer Ingelheim said: "The strong uptake of our new products JASCAYD and HERNEXEOS show the value of the scientific innovation behind these medicines for patients, bringing real progress in areas with significant unmet medical need. In an era of accelerated medical discovery, where the boundaries of what is possible are continuously expanding, innovation-friendly environments such as the United States play a critical role in ensuring new therapies reach patients more rapidly."

Frank Hübler, Member of the Board of Managing Directors responsible for Finance, added: "Our business results show that, in Human Pharma and Animal Health, we successfully navigated a challenging macroeconomic environment and political uncertainties. We remain focused on delivering innovative medicines to patients and animals worldwide. Looking ahead, we need to direct our long-term investments to where they are closest to our growth markets and where they can create the best possible impact for patients. This also includes engaging with governments around the globe to create an environment that appropriately recognizes the value of innovative medicines and ensures patient access."

Human Pharma: Growth supported by key launches

Human Pharma sales grew 20.1%* to EUR 13.1 billion, supported by the new product launches. Established products such as JARDIANCE for the treatment of chronic kidney disease, type 2 diabetes and heart failure remained major growth drivers, contributing EUR 5.7 billion in net sales in the first half of the year. The positive development of JARDIANCE was supported by a large and growing patient base, as well as changes in the U.S. pricing and reimbursement environment, which drove significant volume growth. This trend is in line with Boehringer’s commitment to ensuring continued patient access and affordability. Without the JARDIANCE volume effect, the growth of the Human Pharma Business Unit in the first six months would have been in line with the overall pharma market.

The company also saw a successful uptake of its most recent product launches, JASCAYD (nerandomilast) and HERNEXEOS (zongertinib), particularly in the U.S., as both medicines were able to gain significant traction thanks to the innovation-friendly climate in the U.S. but also in China and Japan. Streamlined processes as well as stronger incentives for innovation in these geographies paved the way for swiftly making these breakthrough medicines available to patients.

JASCAYD, for the treatment of idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF), saw a strong uptake reflecting the urgent need for new treatment options in a disease area that has seen limited therapeutic progress for many years. Following approvals in the United States, China and Japan, as well as Thailand, the United Arab Emirates, the UK and Brazil, JASCAYD is awaiting EU approval from the European Medicines Agency (EMA).

HERNEXEOS, an oral treatment for HER2-mutant advanced non-small cell lung cancer, marked the company’s successful re-entry into oncology after ten years with launches in the U.S., China and Japan. The company expects that HERNEXEOS will be available for European patients only from 2028 after Phase III data becomes available.

Boehringer continued to advance its late-stage pipeline programs during the first half of 2026, realizing significant progress in oncology and cardio-renal-metabolic diseases. Positive Phase III data for survodutide demonstrated the medicine’s potential to address metabolic and liver health in addition to overweight and obesity. Progress with a next-generation triple agonist underlines Boehringer’s ambition to build a broad obesity and metabolic health portfolio.

At the same time, Boehringer Ingelheim initiated three Phase III oncology trials, reinforcing its goal to expand precision cancer care. The company also advanced key assets such as obrixtamig, an experimental cancer immunotherapy, and apecotrep, an investigational drug targeting kidney disease. Research momentum also continued to be strong, with five new compounds entering clinical trials. The Boehringer Human Pharma R&D pipeline spans around 80 projects.

Animal Health: Focus on new launches and emerging disease outbreaks response

The Animal Health business reported net sales of EUR 2.6 billion in the first six months of 2026, a 0.4%* increase compared to the previous year. The performance reflected a modestly growing animal health market, with increased consumer price sensitivity and fewer veterinary visits in several countries.

The company continues to execute its 2026 launch plan, including LENZELTA, a new vaccine that advances mastitis prevention in dairy cows and has launched in several EU countries, and Eko Vet+ | CANINEBEAT AI, an AI-based solution that helps detect heart murmurs in dogs and has already launched in the U.S., the UK and Germany. Boehringer Ingelheim also continues to support responses to emerging animal disease outbreaks, including New World screwworm in the U.S., after receiving Emergency Use Authorizations (EUAs) earlier this year from the U.S. Food and Drug Administration.

The company continues to progress its R&D pipeline in Animal Health, with strong candidates across infectious and non-infectious diseases as well as parasiticides, building a solid innovation foundation for the future in pets, equine, and livestock animals.

(Press release, Boehringer Ingelheim, JUL 15, 2026, View Source [SID1234669248])