Fusidic acid

Ceapro Inc. Reports Record Financial Results for First Quarter 2022 and Provides Corporate Update

Retrieved on: 
Wednesday, May 18, 2022

Our strong financial results this quarter reflect our employees dedication to respond to increased demand in a timely manner.

Key Points: 
  • Our strong financial results this quarter reflect our employees dedication to respond to increased demand in a timely manner.
  • This quarter, we announced a strengthened distribution and supply agreement with long time distributor and partner, Symrise, which will take us throughthe end of 2024.
  • This agreement will provide Ceapro with an additional three years of visibility, stable revenue and cashflows, commented Gilles Gagnon, M.Sc., MBA, President and CEO .
  • Subsequent to quarter, results from development of sodium alginate using PGX Technology were published in the peer review Journal of CO2 Utilization.

Sodium Fusidate Oral: A Bacterial Protein Synthesis Inhibitor by Preventing the Turnover Ofelongation Factor G (EF-G) from the Ribosome - Global Emerging Insight and Market Forecast 2021-2030 - ResearchAndMarkets.com

Retrieved on: 
Wednesday, April 7, 2021

"SODIUM FUSIDATE ORAL - Emerging Insight and Market Forecast - 2030" the report provides comprehensive insights about an investigational product for Prosthetic Joint Infection in 7 Major Markets.

Key Points: 
  • "SODIUM FUSIDATE ORAL - Emerging Insight and Market Forecast - 2030" the report provides comprehensive insights about an investigational product for Prosthetic Joint Infection in 7 Major Markets.
  • Further, it also consists of future market assessments inclusive of the market forecast, SWOT analysis, market competitors, and other emerging therapies.
  • Sodium Fusidate oral, (also known as Fusidic acid, FA or sodium fusidate) acts as a bacterial protein synthesis inhibitor by preventing the turnover ofelongation factor G (EF-G) from the ribosome.
  • What are the other emerging products available and how these are giving competition to SODIUM FUSIDATE ORAL?

Enteris BioPharma to Host Webinar on Strategies for Initiating Phase 1 Clinical Development with Limited API

Retrieved on: 
Tuesday, January 12, 2021

During the webinar, Mr. Daggs and Mr. Consalvo will discuss their expertise in developing CMC approaches for advancing pharmaceutical companies into Phase 1 clinical development, while managing limited access to active pharmaceutical ingredients, also known as API.

Key Points: 
  • During the webinar, Mr. Daggs and Mr. Consalvo will discuss their expertise in developing CMC approaches for advancing pharmaceutical companies into Phase 1 clinical development, while managing limited access to active pharmaceutical ingredients, also known as API.
  • This webinar, which is the second in a series of virtual events that Enteris is hosting, is designed to share our knowledge and expertise with those who desire novel strategies for initiating clinical programs with limited API quantities."
  • The technologies have been the subject of numerous feasibility studies and active development programs, several of which are in late-stage clinical development.
  • TobrateTM (oral tobramycin tablet) is also being developed by Enteris BioPharma for the treatment of uncomplicated urinary tract infection (uUTI).

Recce Pharmaceuticals Announces More Positive Data on RECCE® 327 Against MRSA Superbug in Burn Wound Animal Model

Retrieved on: 
Thursday, April 23, 2020

The study was conducted by an independent Contract Research Organization to assess the dose-dependency of RECCE 327 and in-vivo antibacterial activity against MRSA in rats with topical burns.

Key Points: 
  • The study was conducted by an independent Contract Research Organization to assess the dose-dependency of RECCE 327 and in-vivo antibacterial activity against MRSA in rats with topical burns.
  • RECCE 327 was effective in reducing bacterial load within a wound and showed enhanced wound contraction in comparison to the best in class - Soframycin.
  • RECCE 327 showed repeated efficacy at different dosing levels on topical skin conditions even at low doses.
  • RECCE 327 continued to show efficacy at different dose levels with significant reduction in bacterial count in the infected wound when compared to the vehicle control (p