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Aviptadil / Zyesami? (Twitter) - Mar 31, 2022
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A Safety Monitoring Framework for Critical Care Trials of Agents with Potential to Lower Blood Pressure (Room 3009/3011 (West Building, Level 3), Moscone Center) - Feb 19, 2022 - Abstract #ATS2022ATS_2353; P3 The monitoring framework will be validated in the ongoing TESICO trial and could be adapted for other trials of vasoactive investigational agents targeting critically ill patients. Comprehensive AE grading criteria designed specifically for critically ill patients could improve trials’ ability to meaningfully monitor and report safety outcomes in this population.FUNDING: National Institutes of Health (1OT2HL156821-01).
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He needs Aviptadil . (Twitter) - Feb 18, 2022
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Zyesami (aviptadil)? (Twitter) - Feb 10, 2022
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RECOVERY AND SURVIVAL IN COVID-19 RESPIRATORY FAILURE‚ WHEN TREATED WITH AVIPTADIL ([VIRTUAL]) - Feb 7, 2022 - Abstract #CROI2022CROI_1105; Multiple organ dysfunction syndrome (6.9% vs 13.8%) and respiratory failure (12.2% vs 13.8%) occurred more commonly in placebo-treated patients. Treatment with aviptadil demonstrates efficacy in improving the likelihood of recovering from respiratory failure, surviving to 60 days, and reducing hospital stay in critically ill patients with respiratory failure caused by COVID-19.
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Review, Journal: Anticipated pharmacological role of Aviptadil on COVID-19. (Pubmed Central) - Jan 27, 2022 However, such drugs like Aviptadil in COVID-19 patients have peculiar safety profiles. Thus, adequate clinical trials are necessary for these compounds.
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Trial primary completion date: Inhaled Aviptadil for the Treatment of COVID-19 in Patients at High Risk for ARDS (clinicaltrials.gov) - Jan 11, 2022 P2, N=82, Recruiting, In addition, the role of vasoactive intestinal peptide in the human maternal-fetal interface suggests that vasoactive intestinal peptide is a safe treatment of severe coronavirus disease 2019 respiratory failure during pregnancy. Trial primary completion date: Dec 2021 --> Mar 2022
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Phase classification, Enrollment change: AVICOVID-2: Inhaled ZYESAMI (Aviptadil Acetate) for Treatment of Severe COVID-19 (clinicaltrials.gov) - Dec 25, 2021 P3, N=498, Not yet recruiting, Trial primary completion date: Dec 2021 --> Mar 2022 Phase classification: P2/3 --> P3 | N=270 --> 498
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ZYESAMI/AVIPTADIL. THERE YOU GO (Twitter) - Nov 20, 2021
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Clinical, Adverse events, Cytokine storm: Why not #Aviptadil, #RLF100 from Relief Therapeutics? Works as an antiviral, stops the cytokine storm & prevents & perhaps heals (!) Type 2 pneumocytes & has no side effects. It is in 4 Clinical Trials, 2x against severe Covid-19. Waiting for > 150 days => answer from FDA, EUA! (Twitter) - Nov 5, 2021
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#Aviptadil, #RLF100, #Zysami - whatever you call it, it's the solution to a growing need to help battle Covid and you're sitting on the EUA. What's the hold up? @CNBC, @FoxNews, @CBSNews, @ABC (Twitter) - Oct 22, 2021
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Aviptadil ???? (Twitter) - Oct 12, 2021
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Trial completion date, Trial primary completion date: AVINALI: Inhaled ZYESAMI (clinicaltrials.gov) - Sep 8, 2021 P2/3, N=144, Recruiting, Phase classification: P2/3 --> P3 | N=270 --> 498 Trial completion date: Sep 2021 --> Dec 2021 | Trial primary completion date: Aug 2021 --> Dec 2021
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