Boehringer Ingelheim USA Corporation

🇺🇸United States
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medpagetoday.com
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Novel Drug Maintained Clinical Improvements in IBD

Tulisokibart maintained clinical and endoscopic improvements in IBD patients through week 50 in phase II trial extensions, with 48% of ulcerative colitis patients and 56% of Crohn's disease patients achieving clinical remission. The drug was well-tolerated with no identified safety signals.

New MASH drug development could reshape the treatment paradigm

Several Phase III trials for MASH, including FGF21 analogues like efruxifermin and pegozafermin, FASN inhibitor denifanstat, and GLP-1 receptor agonists like semaglutide, are underway, aiming to revolutionize MASH treatment. Noninvasive tests (NITs) are gaining traction as alternatives to liver biopsies, potentially accelerating trial processes. These developments highlight diverse therapeutic approaches to address MASH's multifactorial nature, with combination therapies offering comprehensive management strategies.
pharmavoice.com
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Want to launch a blockbuster? An AstraZeneca exec breaks it down.

AstraZeneca's Farxiga, initially approved for type 2 diabetes, has exceeded $6 billion in sales and is projected to reach $7.4 billion next year. Success factors include addressing unmet needs, clear value propositions, and strategic market access. Farxiga expanded its indications to chronic kidney disease and heart failure, driving sales. Keytruda exemplifies a blockbuster drug with multiple indications. Market access strategies and pricing considerations are crucial for drug commercialization. The definition of a blockbuster is evolving, focusing on high-value drugs that justify R&D investments.
euronews.com
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European countries and non-profits pledge nearly €630 million in new funding for WHO

Germany, Norway, Luxembourg, Denmark, and Ireland lead new $700 million WHO funding commitments, aiming to prevent 40 million deaths over four years. Germany pledges nearly $400 million, including $262.6 million in new funds. The WHO seeks more discretion in spending to address health emergencies and improve staff retention.
psychiatrictimes.com
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Revolutionizing Pharma: The Power of AI and Chatbots in Clinical Trials and Beyond

AI revolutionizes pharmaceutical industry with advancements in clinical trials, drug discovery, and communication, addressing challenges like data privacy and bias while offering significant cost and time savings.
openpr.com
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Congestive Heart Failure Treatment Market 2034: Clinical

DelveInsight's report on Congestive Heart Failure Market (2020-2034) covers epidemiology, market trends, key companies, and therapies. Market size was ~USD 6,900 million in 2023, expected to grow significantly. Key companies include Novartis, Bayer, and Eli Lilly. Therapies like ENTRESTO and JARDIANCE are highlighted. Market drivers include aging population and disease prevalence, while barriers include generic therapies and diagnostic challenges.
liverdiseasenews.com
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Survodutide wins FDA's breakthrough therapy for treatment of fatty...

The FDA granted breakthrough therapy status to Boehringer Ingelheim's survodutide for MASH, based on Phase 2 trial results showing significant MASH reduction without fibrosis worsening. Two global Phase 3 trials, LIVERAGE and LIVERAGE-Cirrhosis, are underway to further assess survodutide's safety and efficacy in MASH patients with moderate to advanced liver fibrosis and compensated cirrhosis, respectively.

Comprehensive biomarker and modeling approach to support dose finding for BI 836880

Studies 1336.1 and 1336.6, non-randomized, open-label, dose escalation studies, enrolled adult patients with advanced solid tumors refractory to standard therapy or lacking effective standard therapy. Patients received BI 836880, a VEGF/Ang-2 inhibitor, via intravenous infusion. Data from study 1336.1 demonstrated target engagement for different q3w dose levels using a multiple biomarker approach. Combined data from both studies were used for PopPK/PD modeling. PK and PD sampling, including quantification of free/total VEGF-A and Ang-2, was conducted at predefined timepoints. DCE-MRI scans assessed microvascular structure and function properties within tumor lesions. PopPK/PD modeling of BI 836880 was performed based on combined measurements of total BI 836880 and free/total Ang-2 in plasma, with simulations predicting the probability of achieving minimal inhibition levels of free Ang-2.
pharmexec.com
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How to Rally a Team Around Building a New Business

Oncology evolution requires partnerships, clear communication, agility, and strategic hiring to address unmet needs and rare cancers, fostering a culture of excellence and empowerment.
mmm-online.com
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Rx Rundown: AstraZeneca, Danco Laboratories, GSK and more

AstraZeneca to pay $2B to CSPC for a cardiovascular drug, Astellas Pharma licenses gene therapy from AviadoBio, Merck partners with Mestag Therapeutics for fibrosis treatments, Insitro signs three agreements with Eli Lilly for metabolic diseases, MiNK Therapeutics and Autonomous Therapeutics collaborate on metastatic tumors, Bayer and MOMA Therapeutics partner in oncology, Wonderskin names 5W Public Relations as AOR, Eversana signs with Oracle Argus Cloud, Qinotto and Eli Lilly collaborate, Onspire Health acquires Aesthetic Brand Marketing, Reunion Neuroscience partners with Seleni Institute, Danco Laboratories to seek FDA approval for Mifeprex use in miscarriages, Exact Sciences' Cologuard Plus wins FDA approval, Boehringer Ingelheim's survodutide gets Breakthrough Therapy designation, Lunds & Byerlys recalls Lone Star Dip, Kezar Life Sciences' zetomipzomib development halted by FDA, Bayer's elinzanetant NDA accepted by FDA, Biogen's felzartamab gets Breakthrough Therapy Designation, Black Diamond Therapeutics to cut jobs, Upstream Bio targets $182M for IPO, City Therapeutics launches with $135M, Purespring Therapeutics raises $105M, Judo Bio launches with $100M, Orasis Pharmaceuticals raises $78M, CAMP4 Therapeutics targets $67M for IPO, Basecamp Research closes $60M Series B, Arda Therapeutics raises $43M Series A, Crinetics Pharmaceuticals announces public offering, GSK to pay $2.2B to settle Zantac lawsuits, Scholar Rock's SMA drug shows muscle function improvement, CDC to screen travelers due to Marburg virus outbreak in Rwanda, Ad Council, AMA, and CDC launch flu vaccination campaign, Sage Therapeutics' Sage-718 fails in Alzheimer's study, WeightWatchers adds GLP-1 obesity treatments, Gritstone Bio files for Chapter 11, BioPharmCatalyst launches AI-powered chatbot Aiden, Otsuka Precision Health and Amalgam Rx launch Alzheimer's app Elevmi, PatientPoint unveils interactive communication solution, Curia rebrands, Switzerland's COMCO terminates Novartis investigation, Bluebird Bio's Skysona linked to blood cancer in seven children, Solera Health rebrands, HearingLife launches pickleball sweepstakes, Alfasigma launches Morpho brand, Healthy Minds Innovations launches Our World Of Emotions campaign.
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