Cormedix Inc. ((CRMD)) announced an update on their ongoing clinical study.
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CorMedix Inc. is conducting a Phase 3 clinical study titled ‘A Phase 3, Prospective, Multicenter, Double-Blind, Randomized, Controlled, Adaptive Study To Demonstrate The Safety And Efficacy Of DEFENCATH® In Reducing Central Line-Associated Bloodstream Infections (CLABSIs) In Adult Participants Receiving Total Parenteral Nutrition (TPN) Via Central Venous Catheter (CVC)’. The study aims to evaluate the safety and effectiveness of DEFENCATH® in reducing CLABSIs in adults receiving TPN through a central venous catheter, highlighting its potential significance in improving patient outcomes.
The study tests an experimental intervention, DEFENCATH®, a catheter lock solution composed of taurolidine and heparin, against a control group using heparin alone. This intervention is intended to prevent infections associated with central venous catheters.
The study follows an interventional design with randomized allocation and a parallel intervention model. It employs triple masking, meaning the participant, care provider, and investigator are unaware of the group assignments. The primary purpose of the study is prevention.
Key dates for the study include its start on May 14, 2025, with the latest update submitted on July 8, 2025. These dates mark the study’s progression and provide a timeline for stakeholders to anticipate results and potential market impacts.
The study’s progress could significantly impact CorMedix’s stock performance and investor sentiment, especially if DEFENCATH® proves effective. This could position CorMedix favorably against competitors in the infection prevention market, potentially influencing industry dynamics.
The study is currently recruiting, with further details available on the ClinicalTrials portal.