- |||||||||| Jardiance (empagliflozin) / Eli Lilly, Boehringer Ingelheim, avenciguat (BI 685509) / Boehringer Ingelheim
Enrollment closed, Combination therapy: A Study to Test Whether BI 685509 Alone or in Combination With Empagliflozin Helps People With Liver Cirrhosis Caused by Viral Hepatitis or Non-alcoholic Steatohepatitis (NASH) Who Have High Blood Pressure in the Portal Vein (Main Vessel Going to the Liver) (clinicaltrials.gov) - Mar 6, 2024 P2, N=80, Active, not recruiting, Active, not recruiting --> Completed Recruiting --> Active, not recruiting
- |||||||||| avenciguat (BI 685509) / Boehringer Ingelheim
VITALISSCE (Poster Area) - Feb 13, 2024 - Abstract #SSWC2024SSWC_349; P2 Recruiting --> Active, not recruiting The VITALISScE
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Bi 685509: a Potent Activator of Soluble Guanylate Cyclase as a Novel Treatment of Vasculopathy and Fibrosis in Systemic Sclerosis () - Feb 8, 2024 - Abstract #CRAAHPA2024CRA_AHPA_116; In the mouse model of bleomycin-induced skin and lung fibrosis, sGC activation via BI 685509 resulted in significant improvement in skin thickness and lung fibrosis, comparable to mice treated with Nintedanib (60mg/kg) or Riociguat (1 mg/kg). Collectively, these results point to the use of the sGC activator BI 685509 as a novel treatment for SSc and suggests potential superior effects vs. sGC stimulators like Riociguat in this autoimmune disease.
- |||||||||| BI 690517 / Boehringer Ingelheim
[VIRTUAL] Phase 1c Study of the Aldosterone Synthase Inhibitor BI 690517 in Diabetic Patients with Kidney Disease () - Oct 17, 2021 - Abstract #KIDNEYWEEK2021KIDNEY_WEEK_2107; P1 Methods Patients with type 1 or type 2 diabetes, estimated glomerular filtration rate (eGFR) 20–75 mL/min/1.73m 2 and urine albumin creatinine ratio (UACR) 200–3500 mg/g, receiving stable angiotensin receptor blocker/angiotensin-converting enzyme inhibitor treatment were randomised to receive daily oral BI 690517 (3/10/40 mg), eplerenone (25–50 mg) or PBO for 28 days...Changes seen in SBP did not differ between PBO and BI 685509 dose groups...Conclusion BI 690517 was generally well tolerated and appears to have an early effect on UACR, with over 50% of treated patients being classed as responders. These data need to be confirmed in larger studies.
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