Press Releases & Media Statements

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Collaboration with Mary Tyler Moore Vision Initiative

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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

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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

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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

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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

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U.S. FDA Grants Breakthrough Therapy designation

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J-Code Issued for SPEVIGO

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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

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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

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