Press Releases & Media Statements

Developing treatments for people with mental health conditions

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Boehringer Ingelheim collaborates with Circle Pharma

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Boehringer receives U.S. FDA Breakthrough Therapy designation for MASH

Lab Research

Topline results from Boehringer's Phase III IPF Study

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Positive results reported in HER2 mutated lung cancer

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Boehringer Ingelheim to unveil oncology research at WCLC

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First half of 2024: Boehringer Ingelheim progresses pipeline at pace and reaches major milestones

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New affordability initiative with GoodRx for our biosimilar

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New effort to help improve C-R-M health outcomes

Results from Phase II MASH trial presented at EASL 2024

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Boehringer inhalers now available at $35 a month for eligible patients

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New agreement with Quallent expands biosimilar access

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Improving Access to Clinical Trials

Scientists

FDA Approves Additional Formulation of Our Biosimilar

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Boehringer Ingelheim reports strong growth in 2023 and accelerates late-stage pipeline.

Boehringer Ingelheim reports strong growth in 2023 and accelerates late-stage pipeline.

Results announced from EMPACT-MI phase III trial

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New FDA approval for the treatment of GPP

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Update on sNDA for fibrosing ILD in children and adolescents

Boehringer Ingelheim caps patient out-of-pocket costs for its inhaler portfolio at $35 per month

Boehringer Ingelheim caps patient out-of-pocket costs for its inhaler portfolio at $35 per month

Top-line Phase II Data for treatment of MASH

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National Psoriasis Foundation Releases Consensus Statement on Management of Generalized Pustular Psoriasis (GPP)

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Investigational Compound Granted FDA Orphan Drug Designation

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Promising Phase II Results in Chronic Kidney Disease

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AI-Driven Model Validated to Predict Risk of CKD Progression

Kidney Illustration

Hip-Hop Classic “It Takes Two” Takes on New Meaning in Remix to Elevate Importance of Testing for Kidney Disease

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Life forward - Boehringer Ingelheim unveils its evolved company brand

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Boehringer Ingelheim wins 2023 Prix Galien USA

Recipients of the 2023 Prix Galien USA

Low-WAC interchangeable biosimilar is now available

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FDA Approved Treatment Option for Adults with CKD

Patient talking to doctor

Statement by Boehringer Ingelheim on selection of Jardiance® (empagliflozin) by the Centers for Medicare and Medicaid Services (CMS) Drug Price Negotiation Program

First half of 2023: Boehringer Ingelheim sees strong growth and expansion in key therapy areas

For download: © 2020, Peter Ginter

FDA accepts OFEV sNDA for 6–17-year-olds with fibrosing ILD

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Interchangeable Biosimilar Now on Express Scripts® Formulary

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Boehringer Ingelheim presents Effisayil™ 2 trial results

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Interchangeable biosimilar now available in the U.S.

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Boehringer Ingelheim and FIT Unveil Fifth Piece for The Unwearable Collection

Trapped by Uncertainty

Optum Rx Places Interchangeable Biosimilar on its Commercial Formulary

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FDA approves treatment option for T2D in children 10 and older

DINAMO

FDA approves autoinjector pen for Interchangeable biosimilar

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IL-11 inhibitor antibody clinical development launched

Fibroblasts

U.S. FDA Grants Breakthrough Therapy designation

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J-Code Issued for SPEVIGO

Spevigo-J-code

Boehringer Ingelheim reaches more patients than ever in 2022 as innovative medicines drive growth

Press Release

FDA accepts Jardiance sNDA for T2D in children 10 and older

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Intensive education about multidisciplinary care improved likelihood that adults with type 2 diabetes and cardiovascular disease were receiving guideline-directed medicines

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Boehringer Ingelheim announces new partnership to support awareness of GPP

The Unwearable Collection Designs

US FDA accepts supplemental New Drug Application for Jardiance® for adults with chronic kidney disease.

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New cancer therapeutics collaboration with 3T Bio

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Boehringer Ingelheim and Click Therapeutics Expand their Existing Collaboration to Develop Prescription Digital Therapeutics for Schizophrenia

New Digital Tx collab with Click

Full data announced in DINAMO trial in young people with T2D

Boehringer Ingelheim Welcomes New 2023 GOLD Report Positioning LAMA/LABA as the Preferred Treatment for the Majority of Patients with COPD

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Full data announced in phase III EMPA-KIDNEY trial

First patient enrolled in FIBRONEER™-IPF Phase III trial

First patient enrolled in FIBRONEER™-IPF Phase III trial

Boehringer Ingelheim announces expanded access program

New Expanded Access Program for children and adolescents with fibrosing ILD

Boehringer Ingelheim announces InPedILD PhaseIII trial results

New Phase III data in children presented at ERS 2022

Boehringer Ingelheim introduces Tune In To Lung Health

Photo of Tune In To Lung Health spokesperson Bernie Williams seated at piano, playing guitar and smiling at three women who are affected by interstitial lung disease

FDA approves the first treatment option for generalized pustular psoriasis flares in adults

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First Half of 2022: Boehringer Ingelheim continues growth pace and strengthens research pipeline

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Real-world data announced for adults with type 2 diabetes

Boehringer Ingelheim Enters Global Licensing Agreement to Develop and Commercialize Innovative Antibodies from A*star for Targeted Cancer Therapies

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Investigational treatment slowed lung function decline in IPF

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Boehringer Ingelheim Statement on Idiopathic Pulmonary Fibrosis and Progressive Pulmonary Fibrosis

New global guidelines for progressive pulmonary fibrosis now available

Tackling Health Disparities and Inequities for Women with Heart Failure: New Program Encourages Black and Latina Women to Demand More From Their Care

Boehringer Ingelheim strengthens investment in R&D

Research and development laboratory

Phase III EMPA-KIDNEY trial will stop early

FDA Grants Breakthrough Therapy Designation for IPF

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U.S. FDA grants priority review for spesolimab for the treatment of flares in patients with generalized pustular psoriasis (GPP), a rare, life-threatening skin disease

Yankees Legend Bernie Williams Teams Up With Multi-Platinum Recording Artist and Actress Jordin Sparks to Unveil New Song Featuring Lyrics From The Breathless® Ballad Challenge Winner

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Boehringer Ingelheim’s Carine Boustany Appointed to BIO Board

US FDA accepts supplemental New Drug Application and grants Priority Review for Jardiance® for adults with heart failure independent of left ventricular ejection fraction

Weill Cornell Medicine and NewYork-Presbyterian Hospital join Boehringer Ingelheim to study the incidence of progressive Interstitial Lung Disease in COVID-19 patients

Jardiance® shows consistent cardio-renal benefits in adults with heart failure with left ventricular ejection fraction over 40% regardless of chronic kidney disease status

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Boehringer Ingelheim and King’s College London join forces to progress new therapeutic concepts in major depressive disorder and schizophrenia

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Boehringer Ingelheim Partners with Thoeris to Investigate a Novel Approach to Treat Urea Cycle Disorders

Boehringer Ingelheim increases commitments to sustainable development, investing in health innovation and collaborations to expand access and improve healthcare for 50 million people in vulnerable communities by 2030

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Boehringer Ingelheim and Partners to Accelerate Development of First-In-Class Gene Therapy for Patients with Cystic Fibrosis

U.S. FDA Approves Cyltezo® (adalimumab-adbm) as First Interchangeable Biosimilar with Humira®

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Ready for the Challenge? Boehringer Ingelheim and Eli Lilly and Company Launch First Ever Online Game on Cardio-Renal-Metabolic Conditions for Healthcare Professionals

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Boehringer Ingelheim Acquires Abexxa Biologics to Further Expand its Research Efforts in Cancer Immunology and Novel Immunotherapeutic Approaches

Boehringer Ingelheim Enters Clinical Collaboration with Amgen to Study BI 1701963, a SOS1::pan-KRAS Inhibitor, in Combination with LUMAKRAS™ (sotorasib), a KRASG12C Inhibitor

FDA grants Jardiance® Breakthrough Therapy designation for heart failure with preserved ejection fraction

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Boehringer Ingelheim and Twist Bioscience Enter Therapeutic Antibody Discovery Collaboration

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Landmark trial demonstrates Jardiance® (empagliflozin) is the first therapy to show statistically significant improvement in heart failure outcomes in adults with preserved ejection fraction

US FDA approves Jardiance® (empagliflozin) to treat adults living with heart failure with reduced ejection fraction

Media Contacts

Head, U.S. Communications Human Pharma

900 Ridgebury Rd.
P.O. Box 368
Ridgefield, CT 06877

michele.baer@boehringer-ingelheim.com

Head, U.S. Communications
Animal Health

Phone +1 (913) 620-0026

rene.ward@boehringer-ingelheim.com

U.S. Communications

Phone +1 (203) 791-6487

belinda.martin@boehringer-ingelheim.com

Boehringer Ingelheim Animal Health USA Inc.
U.S. Communications

Phone +1 (516) 527-5456

christine.jones@boehringer-ingelheim.com