avenciguat (BI 685509) / Boehringer Ingelheim 
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  • ||||||||||  avenciguat (BI 685509) / Boehringer Ingelheim
    VITALISSCE (Poster Area) -  Feb 13, 2024 - Abstract #SSWC2024SSWC_349;    
    P2
    Recruiting --> Active, not recruiting The VITALISScE
  • ||||||||||  BI 685509 / Boehringer Ingelheim
    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.
  • ||||||||||  avenciguat (BI 685509) / Boehringer Ingelheim
    Enrollment open:  A Study in Healthy Men to Test How BI 685509 is Processed in the Body (clinicaltrials.gov) -  Sep 16, 2022   
    P1,  N=12, Recruiting, 
    Currently, BI-685509 is in Phase II clinical trial to be tested for CKD and DKD. Not yet recruiting --> Recruiting
  • ||||||||||  avenciguat (BI 685509) / Boehringer Ingelheim
    Trial completion, Trial completion date, Trial primary completion date:  A Study in Healthy Men to Find the Best Formulation of BI 685509 and to Test How it is Taken up in the Body (clinicaltrials.gov) -  Mar 8, 2022   
    P1,  N=39, Completed, 
    Trial completion date: Feb 2023 --> Aug 2023 | Trial primary completion date: Jan 2023 --> Jul 2023 Active, not recruiting --> Completed | Trial completion date: May 2022 --> Feb 2022 | Trial primary completion date: May 2022 --> Feb 2022
  • ||||||||||  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.