Clostridioides difficile

Acurx Pharmaceuticals Announces Presentation of Ibezapolstat Phase 2 Clinical Trial Results at ESCMID Global 2024 Scientific Conference

Retrieved on: 
Thursday, May 2, 2024

The presentation included additional analyses of clinical and microbiological data from the Phase 2b Segment of the trial.

Key Points: 
  • The presentation included additional analyses of clinical and microbiological data from the Phase 2b Segment of the trial.
  • Commenting on his presentation, Dr. Garey stated: "This randomized, active-controlled study showed ibezapolstat was comparable to vancomycin in achieving clinical cure in patients with mild-to-moderate CDI.
  • The presentation and poster are available on the Acurx Pharmaceuticals website following their respective presentations at the conference.
  • www.acurxpharma.com
    The complete Phase 2 results are being prepared for submission to a prominent scientific journal.

Phathom Pharmaceuticals Launches Direct-to-Consumer Campaign, “VOQUEZNA Can Kick Some Acid”

Retrieved on: 
Tuesday, March 26, 2024

FLORHAM PARK, N.J., March 26, 2024 (GLOBE NEWSWIRE) -- Phathom Pharmaceuticals, Inc. (Nasdaq: PHAT), a biopharmaceutical company focused on developing and commercializing novel treatments for gastrointestinal (GI) diseases, today announces the launch of its new broadcast ad and full-scale, Direct-to-Consumer (DTC) campaign, “VOQUEZNA Can Kick Some Acid,” to raise awareness of its powerful first-in-class treatment and encourage people to speak to their doctor about this new treatment option. VOQUEZNA (vonoprazan) is indicated for the healing and maintenance of healing of all severities of Erosive Esophagitis (EE), also referred to as Erosive GERD, and for the relief of related heartburn. VOQUEZNA represents the first major innovation to the U.S. Erosive GERD market in over 30 years.1

Key Points: 
  • The campaign will also be featured on consumer-facing platforms across Facebook, Instagram, waiting room TVs in doctor offices, and digital banner ads.
  • “Phathom is excited to launch our first campaign directly to, and for, the people whose lives we strive to improve every day.
  • To view a video of the “VOQUEZNA Can Kick Some Acid” commercial, click here.
  • Talk with your healthcare provider about the possibility of fundic gland polyps if you have been on VOQUEZNA for a long time.

NRx Pharmaceuticals, Inc. (Nasdaq: NRXP) Announces FDA Qualified Infectious Disease Product (QIDP) and Fast Track Designation of NRX-101 in Complicated Urinary Tract Infection and Pyelonephritis

Retrieved on: 
Tuesday, January 16, 2024

Receipt of QIDP designation confers Priority Review, and critically, five additional years of data-exclusivity to NRX-101's already strong Intellectual Property position.

Key Points: 
  • Receipt of QIDP designation confers Priority Review, and critically, five additional years of data-exclusivity to NRX-101's already strong Intellectual Property position.
  • The FDA also granted NRX-101 Fast Track designation for cUTI, which additionally allows for rolling submission of the Company's New Drug Application.
  • On the basis of this advance, NRx is seeking partners with active involvement in urology, infectious disease and/or women's health for commercialization of NRX-101.
  • NRx thanks the US FDA for its rapid award of QIDP designation for cUTI and pyelonephritis.

Immuron Clinical Trials Update

Retrieved on: 
Friday, December 22, 2023

MELBOURNE, Australia, Dec. 22, 2023 (GLOBE NEWSWIRE) -- Immuron Limited (ASX: IMC; NASDAQ: IMRN), an Australian based and globally integrated biopharmaceutical company is pleased to provide shareholders and the market with an update on the company’s clinical development portfolio.

Key Points: 
  • The NMRC has recently completed the in-patient stage of the campylobacter challenge clinical study.
  • Headline results from the clinical trial are anticipated to be reported in H2 2024.
  • The Phase 2 clinical trial is designed to evaluate the safety and protective efficacy of the new product manufactured by Immuron compared to a placebo in a controlled human infection model (CHIM).
  • The inpatient challenge phase of the Travelan clinical study led by Principal Investigator Dr Mohamed Al-Ibrahim at the Pharmaron CPC FDA inspected Clinical Research Facility Inpatient Unit located in Baltimore, Maryland US, has been completed.

Phathom Pharmaceuticals Announces Commercial Availability of VOQUEZNA® (vonoprazan) Tablets, a Powerful First-In-Class PCAB for the Treatment of Erosive GERD and Relief of Associated Heartburn

Retrieved on: 
Tuesday, November 28, 2023

“We are thrilled to announce the commercial availability of our first-in-class medication, VOQUEZNA, now available for the millions of people in the U.S. suffering from Erosive GERD,” said Martin Gilligan, Chief Commercial Officer at Phathom Pharmaceuticals.

Key Points: 
  • “We are thrilled to announce the commercial availability of our first-in-class medication, VOQUEZNA, now available for the millions of people in the U.S. suffering from Erosive GERD,” said Martin Gilligan, Chief Commercial Officer at Phathom Pharmaceuticals.
  • “Erosive GERD is a highly prevalent condition affecting over 20 million people in the U.S.,3,4 many of whom experience troubling symptoms, including painful heartburn.
  • Phathom is offering programs for eligible patients who face coverage or affordability issues, including co-pay assistance for patients with commercial insurance.
  • for up to 6 months to maintain healing of Erosive Acid Reflux and for relief of heartburn related to Erosive Acid Reflux.

Do you think you have a penicillin allergy? You might be wrong

Retrieved on: 
Wednesday, November 8, 2023

Originally derived from a fungus, penicillin antibiotics such as amoxicillin are used to treat common infections, including chest, sinus, ear, urinary tract and skin infections.

Key Points: 
  • Originally derived from a fungus, penicillin antibiotics such as amoxicillin are used to treat common infections, including chest, sinus, ear, urinary tract and skin infections.
  • Up to 20% of Australians admitted in hospital say they have a penicillin allergy.
  • Read more:
    Weekly Dose: penicillin, the mould that saves millions of lives

Why does it matter?

  • People who mistakenly think they’re allergic to penicillin may not get the most effective or safest antibiotics to treat their infection.
  • They are also at greater risk of developing multidrug-resistant infections or “superbugs”.
  • People who receive second-line antibiotics are more likely to have complications, such as antibiotic-induced gut infections.

Why do people think they’re allergic?

  • They may have experienced side effects from penicillin, such as nausea or diarrhoea.
  • An Epstein-Barr viral infection treated with amoxicillin, for example, causes a fine, red rash.
  • But there is no evidence penicillin allergy is inherited.
  • Then there are people who have had a genuine and serious reaction to penicillin.

Testing for penicillin


When someone says they have a penicillin allergy, we first get them to explain what happened with the reaction, including to what antibiotic, in what context and how severe it was. Then we perform skin tests to further assess the person’s risk of reaction. If skin tests are negative, we can then give the patient the penicillin in question under supervision (a “challenge”) to see if they react.

  • Our study followed 195 patients who reported a penicillin allergy across six Sydney hospitals.
  • In the first phase, we assessed 85 people and found 82% weren’t allergic to penicillin.
  • In our study, eight weeks after their test, just 54% of participants in phase one correctly knew their penicillin allergy status.

Reducing long waits for allergy tests

  • The wait time from someone first being referred to an allergy clinic to having testing can be up to two years.
  • We need to improve access to testing and also look at when people can access allergy services.
  • We also need to ensure the results of allergy tests translate to the real world so people know their true allergy status.
  • Winnie Tong has received funding from Maridulu Budyari Gumal, the Sydney Partnership for Health, Education, Research and Enterprise (SPHERE), Triple I Clinical Academic Group seed grant 2017, and the Balnaves Foundation.
  • The authors would like to acknowledge Professor Andrew Carr, their collaborators and participants on this project.

PCT and HypoClean Team Up to Help Grow Veteran Commercial Cleaning, LLC

Retrieved on: 
Monday, October 30, 2023

Eagle Guard is a ready-to-use fluid product produced with proprietary technology, salt, and water.

Key Points: 
  • Eagle Guard is a ready-to-use fluid product produced with proprietary technology, salt, and water.
  • It replaces bleach and other harsh chemicals referred to as Quaternary Ammonium Compounds (aka QACs) and has no VOC (Volatile Organic Compounds).
  • It has been proven that Eagle Guard kills contagious pathogens and infectious diseases when used as directed on the EPA approved label.
  • Eagle Guard Disinfectant is a broad-spectrum disinfectant which kills 99.9% of bacteria in 2 minutes.

ACG 2023 Presentations for REBYOTA® (fecal microbiota, live – jslm) Explore Association Between Gut Microbiome Composition and Health-Related Quality of Life and Evaluate Efficacy and Safety in Older Patients With Comorbidities

Retrieved on: 
Monday, October 23, 2023

Patients were categorized as improved if Cdiff32 scores improved 10 points or more from baseline to week 8.

Key Points: 
  • Patients were categorized as improved if Cdiff32 scores improved 10 points or more from baseline to week 8.
  • The average microbiome profiles were then compared between baseline and week 8 within the improved and unchanged groups, respectively.
  • The analysis found that the quartile with the highest Cdiff32 score showed a significantly different microbiome composition from most other groups with lower scores.
  • “Seeing efficacy and safety consistent with previous clinical trials of REBYOTA among these higher-risk patients is encouraging.”

UMF Corporation Calls for Nominations for 15th Annual National Hygiene Specialist® Excellence Award

Retrieved on: 
Wednesday, October 18, 2023

NORTHBROOK, Ill., Oct. 18, 2023 /PRNewswire/ -- Nominations are open for UMF|PerfectCLEAN's 15th annual National Hygiene Specialist® Excellence Award. The award acknowledges exemplary environmental services (EVS) workers who help reduce the spread of preventable healthcare-associated infections (pHAIs) caused by numerous superbugs including C. auris, C. diff, COVID-19, MRSA, and Norovirus. Nominations are open through Dec. 15, 2023.

Key Points: 
  • NORTHBROOK, Ill., Oct. 18, 2023 /PRNewswire/ -- Nominations are open for UMF|PerfectCLEAN's 15th annual National Hygiene Specialist® Excellence Award .
  • We established our National Hygiene Specialist Excellence Award 15 years ago to acknowledge and celebrate the EVS staff who work tirelessly to prevent the spread of pHAIs."
  • The National Hygiene Specialist Excellence Award is a testament to that commitment.
  • The National Hygiene Specialist Excellence Award is an opportunity to recognize their critical contributions.

More Real-World Data and New Analyses of Data for REBYOTA® (fecal microbiota, live – jslm) Presented at IDWeek 2023

Retrieved on: 
Wednesday, October 11, 2023

Electronic health records, administration records and internal databases were reviewed for patient demographics, setting of care, time from order to treatment, logistics from order to administration and payor details.

Key Points: 
  • Electronic health records, administration records and internal databases were reviewed for patient demographics, setting of care, time from order to treatment, logistics from order to administration and payor details.
  • Early experience with REBYOTA showed an administration time of six minutes followed by 15 minutes of observation.
  • No one was denied insurance coverage for REBYOTA or the instillation procedure.
  • Within a modified intent-to-treat (mITT) population (n=402), 98 had renal comorbidity, including chronic kidney disease (CKD) (n=29) and end-stage renal failure (n=5).