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Pegozafermin Enters Phase 3 Clinical Trial Program for MASH, Fibrosis

The phase 3 ENLIGHTEN program will consist of 2 phase 3 trials evaluating the safety and efficacy of pegozafermin in patients with MASH. ....

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Bristol Myers Squibb's Investigational LPA1 Antagonist Reduces Rate of Lung Function Decline in Progressive Pulmonary Fibrosis Cohort of Phase 2 Study

Results show 26 weeks of treatment with twice-daily 60 mg dose of BMS-986278 resulted in a 69% relative reduction in the rate of decline in percent predicted forced vital capacity versus placeboTreatment effect was consistent with or without background therapy and BMS-986278 was well tolerated, with rates of adverse. ....

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Bristol-Myers Squibb's (BMY) LPA1 Antagonist Reduces Rate of Lung Function Decline in Progressive Pulmonary Fibrosis Cohort of Phase 2 Study

Bristol-Myers Squibb's (BMY) LPA1 Antagonist Reduces Rate of Lung Function Decline in Progressive Pulmonary Fibrosis Cohort of Phase 2 Study
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Bristol Myers Squibb's Investigational LPA1 Antagonist Reduces Rate of Lung Function Decline in Progressive Pulmonary Fibrosis Cohort of Phase 2 Study

Results show 26 weeks of treatment with twice-daily 60 mg dose of BMS-986278 resulted in a 69% relative reduction in the rate of decline in percent predicted forced vital capacity versus. ....

United States , Tameraj Corte , Bristol Myers Squibb , Jonathan Sadeh , Department Of Respiratory Medicine , European Respiratory Society , American Thoracic Society , Exchange Commission , Immunology Development , International Congress , Abstracts Leading , Respiratory Medicine Trials , Professor Tamera , Consultant Respiratory Physician , Interstitial Lung Disease , Respiratory Medicine , Royal Prince Alfred Hospital , Bristol Myers , International Conference , Fibrosis Trial , Myers Squibb , Pioneering Paths Forward , Transform Patient , Private Securities Litigation Reform Act , Annual Report , Quarterly Reports ,

Bristol Myers Squibb's Investigational LPA1 Antagonist Reduces Rate of Lung Function Decline in Progressive Pulmonary Fibrosis Cohort of Phase 2 Study - Bristol-Myers Squibb (NYSE:BMY)

Results show 26 weeks of treatment with twice-daily 60 mg dose of BMS-986278 resulted in a 69% relative reduction in the rate of decline in percent predicted forced vital capacity versus placebo Treatment effect was ....

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