schachlehrling's News: Ibezapolstat. Nov 2, 2023 · Ibezapolstat is a novel, orally administered antibioti

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Nov 2, 2023 · Ibezapolstat was well-tolerated, with three patients each experiencing one mild adverse event assessed by the blinded investigator to be drug-related. All three events were gastrointestinal in ... Poster Presentation and Abstract from ID Week (October 2021) titled “An Open-label Phase 2a study of Ibezapolstat, a Unique Gram-positive Selective Spectrum (GPSS®) Antibiotic, for Patients with Clostridioides difficile Infection.” presented by Dr. Kevin Garey, Professor and Chair, University of Houston College of Pharmacy”.WebAcurx Announces Publication of Positive Phase 2a Clinical Trial Results of Ibezapolstat for CDI in Clinical Infectious Diseases. Clinical results of 10 of 10 patients (100%) enrolled met the study ...In the event non-inferiority of ibezapolstat to vancomycin is demonstrated, further analysis will be conducted to test for superiority. Additionally, due to slower than expected enrollment during ...Kevin Garey, PharmD, MS, Professor and Chair, University of Houston College of Pharmacy, the Principal Investigator for microbiome aspects of the ibezapolstat clinical trial program and Acurx Scientific Advisory Board member stated: " These results confirm and extend data from the open-label component of the Phase 2 study and …Three scientific posters highlighting novel anti-virulence pharmacologic properties of oral ibezapolstat for C. difficile Infection; effects on toxin production, biofilm and the gut microbiome; A ...Aug 10, 2020 · Further derisking of ibezapolstat is likely to represent a far more significant value inflection point for investors than successful outcomes in phase 3 would be for Summit. Acurx is selling shares direct to the public in a late crossover round, one that closes 30 September 2020, for $3.25 per share (no warrants). ABSTRACT BACKGROUND OBJECTIVES RESULTS CONCLUSIONS METHODS •Ibezapolstat maintains its efficacy against clinical isolates with reduced susceptibility to metronidazole, vancomycin, and fidaxomicin. Unexpected, Novel Findings •Ibezapolstat reduces C. difficile’smotility as visualized with CD 630 reference strain in a motility assay. …Feb 7, 2022 · Ibezapolstat has potent activity as demonstrated by the eradication of C. difficile by day three of treatment. Our data also show it unexpectedly spares other Firmicutes along with the important ... - Ibezapolstat, is the first of a new class of antibiotics with a novel mechanism of action, a DNA polymerase IIIC inhibitor, to enter clinical efficacy trials - 10 of 10 patients (100%) enrolled in a Ph2A trial met the study's primary and secondary efficacy endpoints of Clinical Cure at end of treatment and Sustained Clinical Cure of no ...While extensive in vitro studies demonstrating the effects of ibezapolstat on the broader gut microbiome are lacking, it has an MIC 90 to C. difficile of 4 μg/mL . In an in vivo hamster model, ibezapolstat had identical survival rates (33%) to vancomycin at 34 days following only 3 days of therapy . However, when the treatment was extended to ...FDA has accepted an Interim Analysis Plan for an IDMC to assess clinical outcome when 36 patients are enrolled in the Company's Ph2b clinical trial of ibezapolstat in patients with CDIA scientific...In the currently enrolling Phase 2b, trial segment, patients with CDI will be enrolled and randomized in a 1:1 ratio to either ibezapolstat 450 mg every 12 hours or vancomycin 125 mg orally every ...About the Ibezapolstat Phase 2 Clinical Trial The completed multicenter, open-label single-arm segment (Phase 2a) study was followed by a double-blind, randomized, active-controlled, ...Oct 2, 2023 · About the Ibezapolstat Phase 2 Clinical Trial The completed multicenter, open-label single-arm segment (Phase 2a) study was followed by a double-blind, randomized, active-controlled, ... Acurx Announces Positive Top-Line Ibezapolstat Phase 2 Efficacy Results with 96% Clinical Cure Rate in Patients with C. difficile Infection . Nov 2, 2023. Acurx Pharmaceuticals to Discuss Third Quarter 2023 Financial Results and Provide Business Update . Oct 25, 2023. Acurx Announces Ibezapolstat Scientific Posters and Presentations at ...4 Oct 2022 ... ... (Ibezapolstat) is in progress for treatment of Clostridium difficile (11). These compounds compete with deoxynucleotide triphosphate (dNTP) ...Nov 2, 2023 · Ibezapolstat was well-tolerated, with three patients each experiencing one mild adverse event assessed by the blinded investigator to be drug-related. All three events were gastrointestinal in ... Ibezapolstat was as effective as the currently-used anti-C. difficile agents fidaxomicin, vancomycin and metronidazole to reduce biofilm-embedded C. difficile quantity and biofilm biomass; Metagenomic Evaluation of Ibezapolstat Compared to Other Anti-Clostridioides difficile Agents. Presented by Jinhee Jo, University of Houston College of Pharmacy

Acurx Pharmaceuticals, Inc. (NASDAQ: ACXP) ("Acurx" or the "Company"), a clinical stage biopharmaceutical company developing a new class of antibiotics for difficult-to-treat bacterial infections ...Ibezapolstat will now move forward to Phase 3 clinical trials. Further data will be provided when available on all of the secondary and exploratory endpoints in the Phase 2b trial, including sustained clinical cure data, extended clinical cure data up to 94 days and impact on the microbiome compared to vancomycin.We anticipate that these ...Dec 1, 2020 · Ibezapolstat was well tolerated with a safety signal similar to placebo. Ibezapolstat had minimal systemic absorption with the majority of plasma concentrations less than 1 µg/mL. In the multiday, ascending dose study, ibezapolstat concentrations of 2000 µg/g of stool were observed by Day 2 and for the remainder of the dosing time period. In the event non-inferiority of ibezapolstat to vancomycin is demonstrated, further analysis will be conducted to test for superiority. Phase 2a data demonstrated complete eradication of colonic C. difficile by day three of treatment with ibezapolstat as well as the observed overgrowth of healthy gut microbiota, Actinobacteria and Firmicute …WebStool samples were evaluated for microbiome changes and bile acid concentrations. Ibezapolstat 450 mg and vancomycin, but not ibezapolstat 300 mg, showed statistically significant changes in alpha diversity over time compared to that of a placebo. Beta diversity changes confirmed that microbiota were significantly different between study groups. About the Ibezapolstat Phase 2 Clinical Trial The multicenter, open-label single-arm segment of this study (Phase 2a) is to be followed by a double- blind, randomized, active-controlled segment (Phase 2b) which, together, comprise the Phase 2 clinical trial. The Phase 2 clinical trial is designed to evaluate ibezapolstat in the treatment of CDI.Acurx Pharmaceuticals, Inc. gab die Wirksamkeitsergebnisse der klinischen Phase-2-Studie für Ibezapolstat zur Behandlung von C. difficile-Infektionen ...Ibezapolstat is FDA QIDP and Fast Track Designated for priority review. Robert J. DeLuccia, Executive Chairman of Acurx, stated, "With the excellent clinical results and very good safety and tolerability demonstrated in the Phase 2a segment of this ongoing trial, we validated the bacterial pol IIIC enzyme as a therapeutic target for ...Ibezapolstat has been granted QIDP (Qualified Infectious Disease Product) status; FDA Fast Track designation granted. ACX375C is QIDP and FDA Fast-Track eligible and is planned to be applied for pre-IND and post-IND, respectively.19 Nov 2023 ... ... ibezapolstat, for the treatment of C difficile Infection (CDI). Specifically, in 26 ibezapolstat-treated patients in phases 2a and 2b, the ...Ibezapolstat and Vancomycin Head-to-Head: Phase 2b. The new trial is a double-blind, randomized 1:1 ratio to either ibezapolstat 450 mg every 12 hours or vancomycin 125 mg orally every 6 hours, in each case, for 10 days and followed for 28 ± 2 days following the end of treatment for a recurrence of CDI.Acurx Pharmaceuticals’ ibezapolstat completed primary and secondary treatment objectives in trial patients with a 100% success rate, successfully curing C. difficile infection in all ...Due to observed clinical success, Acurx Pharmaceuticals, Inc. has discontinued the Phase IIb clinical trial of its lead antibiotic candidate, ibezapolstat, for Clostridioides difficile infection (CDI). In the trial, ibezapolstat and the control antibiotic vancomycin, a standard treatment for C. difficile infection, delivered high rates of clinical …In the currently enrolling Phase 2b, trial segment, patients with CDI will be enrolled and randomized in a 1:1 ratio to either ibezapolstat 450 mg every 12 hours or vancomycin 125 mg orally every ...Ibezapolstat is a novel, orally administered antibiotic being developed as a Gram-Positive Selective Spectrum (GPSS™) antibacterial. It is the first of a new class of DNA polymerase IIIC ...

Ibezapolstat (ACX-362E) is under development for the treatment of Clostridium difficile Infections. The drug candidate is administered through oral route in the ...3 Aug 2020 ... Ibezapolstat has patent protection through 2039. ACX-375C, chemically related to ibezapolstat, is nearing IND (investigational new drug). (3) ...2 Oct 2023 ... 在与艰难梭菌定植后,该细菌会产生并释放出主要的毒力因子,即两种大型的Clostridial毒素A(TcdA)和B(TcdB)。TcdA和TcdB是外毒素,它们与人类肠上皮 ...Mar 16, 2023 · About the Ibezapolstat Phase 2 Clinical Trial The completed multicenter, open-label single-arm segment (Phase 2a) study is now followed by a double-blind, randomized, active-controlled, non ... Mar 16, 2023 · About the Ibezapolstat Phase 2 Clinical Trial The completed multicenter, open-label single-arm segment (Phase 2a) study is now followed by a double-blind, randomized, active-controlled, non-inferiority, segment (Phase 2b ) at 28 US clinical trial sites which together comprise the Phase 2 clinical trial (see https://clinicaltrials.gov/ct2/show ... Ibezapolstat is currently enrolling in a Phase 2b trial for C. difficile infection in U.S. centers across the country and nearing its goal to reach a targeted 36 patients at which point an Interim ...WebAbout the Ibezapolstat Phase 2 Clinical Trial. On November 2, 2023, we reported top-line data from the Phase 2 clinical trial including the ibezapolstat clinical cure rate at end of treatment, or ...Ibezapolstat demonstrated an increased proportion of Actinobacteria, including the Bifidobacteriaceae family. Using a linear regression analysis, vancomycin …Oct 2, 2023 · About the Ibezapolstat Phase 2 Clinical Trial The completed multicenter, open-label single-arm segment (Phase 2a) study was followed by a double-blind, randomized, active-controlled, non-inferiority, segment (Phase 2b) at 28 US clinical trial sites which together comprise the Phase 2 clinical trial (see https://clinicaltrials.gov/ct2/show ... 14 Nov 2023 ... The company can now expedite advancement of ibezapolstat into phase III clinical trials. H.C. Wainwright & Co. analysts noted that even though ...3 Aug 2020 ... Ibezapolstat has patent protection through 2039. ACX-375C, chemically related to ibezapolstat, is nearing IND (investigational new drug). (3) ...Nếu bạn tìm thấy bất kỳ địa chỉ nào trong đó thì có khả năng chúng được sử dụng trong một mạng riêng và nên được loại bỏ theo hướng có lợi cho những địa chỉ khác để tìm kiếm …Ibezapolstat was minimally absorbed in a hamster model, leading to high colonic and low systemic concentrations and was shown to be effective for CDI . A phase …

17 Nov 2023 ... ... Ibezapolstat drug, a treatment for patients with Clostridioides difficile Infections (CDI). Based on positive data from Phase 2a and Phase ...Sep 6, 2020 · Ibezapolstat was well tolerated with a safety signal similar to placebo. Ibezapolstat had minimal systemic absorption with the majority of plasma concentrations less than 1 µg/mL. In the multiday, ascending dose study, ibezapolstat concentrations of 2000 µg/g of stool were observed by Day 2 and for the remainder of the dosing time period. He further stated: "The totality of the data, including the pioneering vancomycin-controlled healthy volunteer study, suggests that ibezapolstat's effects on the gut microbiome could be predictive of an anti-recurrence effect in CDI patients." More simply stated, ibezapolstat is showing potential to be a curative treatment.Ibezapolstat is a novel DNA polymerase IIIC inhibitor with in vitro activity against C. difficile. Objectives and methods: Randomized, double-blind, placebo-controlled study to assess the safety ...About the Ibezapolstat Phase 2 Clinical Trial The completed multicenter, open-label single-arm segment (Phase 2a) study was followed by a double-blind, randomized, active-controlled, non-inferiority, segment (Phase 2b) at 28 US clinical trial sites which together comprise the Phase 2 clinical trial (see https://clinicaltrials.gov/ct2/show ...Ibezapolstat is a novel, first-in-class, orally administered antibacterial. It is the first of a new class of DNA polymerase IIIC inhibitors in clinical development by Acurx to treat bacterial ...Acurx has completed its Phase 2b clinical trial of ibezapolstat compared to vancomycin, a standard of care to treat C. difficile infection or CDI. The Phase 2b ...Ibezapolstat Vs. Vancomycin- A Phase 2b Trial Showdown. The new trial arm is a double-blind, randomized 1:1 ratio to either ibezapolstat 450 mg every 12 hours or vancomycin 125 mg orally every 6 hours, in each case, for 10 days and followed for 28 ± 2 days following the end of treatment for a recurrence of CDI.Efficacy, Safety, Pharmacokinetics, and Microbiome Changes of Ibezapolstat in Adults with Clostridioides difficile Infection: A Phase 2a Multicenter Clinical ...In a total of 26 ibezapolstat-treated patients in Phases 2a and 2b, the Clinical Cure rate is 96%. Meets protocol primary objective of assessing the primary efficacy …Feb 7, 2022 · Ibezapolstat has potent activity as demonstrated by the eradication of C. difficile by day three of treatment. Our data also show it unexpectedly spares other Firmicutes along with the important ... Ibezapolstat colonic concentrations averaged 400 ug/g stool at day 3 and greater than 1,000 ug/g by day 10 of dosing. Six of the seven available baseline stool samplesOct 19, 2023 · Three scientific posters highlighting novel anti-virulence pharmacologic properties of oral ibezapolstat for C. difficile Infection; effects on toxin production, biofilm and the gut microbiome; A ... Ibezapolstat was minimally absorbed in a hamster model, leading to high colonic and low systemic concentrations and was shown to be effective for CDI . A phase …In the now completed Phase 2b trial segment, 32 patients with CDI were enrolled and randomized in a 1:1 ratio to either ibezapolstat 450 mg every 12 hours or vancomycin 125 mg orally every 6 hours ...Sep 6, 2020 · Ibezapolstat was well tolerated with a safety signal similar to placebo. Ibezapolstat had minimal systemic absorption with the majority of plasma concentrations less than 1 µg/mL. In the multiday, ascending dose study, ibezapolstat concentrations of 2000 µg/g of stool were observed by Day 2 and for the remainder of the dosing time period. ibezapolstat Acurx Pharmaceuticals Clostridium difficile infections Phase II (DNA polymerase III inhibitor) White Plains, NY (Fast Track) www.acurxpharma.com IDP-120 gel Bausch Health Americas acne vulgaris Phase III (benzoyl peroxide/tretinoin) Bridgewater, NJ www.bauschhealth.com JNJ-63871860 (ExPEC4V) Janssen Escherichia coli …

14 Aug 2023 ... Since ibezapolstat treatment leads to minimal dis!

David P. Luci, the Company's President and Chief Executive Officer, stated: "We also look forward to reporting the full ibezapolstat data which will include the most extensive data for any antibiotic on sustained clinical cure to date in patients with CDI, as well as a comparison of the effect on the microbiome between oral ibezapolstat and oral …WebThis drug entry is a stub and has not been fully annotated. It is scheduled to be annotated soon. Generic Name. Ibezapolstat. DrugBank Accession Number. DB16189. Background. Ibezapolstat is under investigation in clinical trial NCT04247542 (ACX-362E Ibezapolstat for Oral Treatment of Clostridioides Difficile Infection).Mar 16, 2023 · About the Ibezapolstat Phase 2 Clinical Trial The completed multicenter, open-label single-arm segment (Phase 2a) study is now followed by a double-blind, randomized, active-controlled, non ...

Jul 1, 2021 · Methods: As part of the completed Phase 1 clinical study of ibezapolstat, stool samples were collected daily from healthy volunteers given ten days of ibezapolstat (300 or 450 mg given twice daily ... Remember, data supports the potential for ibezapolstat to become the front-line therapy to treat over 500,000 patients who get CDI each year. Of those 500,000, more than 20,000 patients per year die.Ibezapolstat has previously received FDA QIDP and Fast-Track Designation. STATEN ISLAND, N.Y., Oct. 19, 2023 /PRNewswire/ -- Acurx Pharmaceuticals, Inc. (NASDAQ: ACXP) ("Acurx" or the "Company"), a clinical stage biopharmaceutical company developing a new class of antibiotics for difficult-to-treat bacterial infections, today announced three ...

Ibezapolstat 450 mg was given twice daily for 10 days to patients with . mild-moderate CDI de ned as diarrhea plus a positive C. di cile toxin test. T est of . cure was evaluated at day 12 and ...WebCompany Overview. Acurx Pharmaceuticals is a publicly held clinical stage biopharmaceutical company focused on developing new antibiotics for difficult to treat infections. Acurx's approach is to develop antibiotic candidates that target the DNA polymerase IIIC enzyme and its R&D pipeline includes early stage antibiotic candidates …Ibezapolstat (IBZ) is currently in a phase 2 trial against Clostridioides difficile infection, and inhibits bacterial DNA polymerase IIIC (pol IIIC) by interfering with addition of guanine (G) to ...

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