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Cormedix (CRMD)
NASDAQ:CRMD
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Cormedix (CRMD) Drug Pipeline

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1,505 Followers
Drug Name
Condition
Stage
Status
Study Name
Trial Start Date
Article
Heparin, (Taurolidine And Heparin) Catheter Lock Solution
Central Line Associated Blood Stream Infections (Clabsi)
Phase III
Recruiting
Comparing The Safety And Efficacy Of DEFENCATH® In Reducing Central-Line Bloodstream Infections (CLABSIs) In Adults Receiving Total Parenteral Nutrition Through A Central Venous Catheter (CVC)
Jan 15, 2025
Standard of Care, (Taurolidine And Heparin) Catheter Lock Solution
Catheter-Related Infections
Phase IV
Recruiting
Open-Label Study to Assess Safety and Time to Catheter-related Bloodstream Infections (CRBSI) in Subjects From Birth to < 18 Years of Age
Dec 02, 2024
Heparin, Neutrolin
Kidney Failure, Chronic, Catheter-Related Infections
Phase III
Completed
Study Assessing Safety & Effectiveness of a Catheter Lock Solution in Dialysis Patients to Prevent Bloodstream Infection
Jan 07, 2016

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases:
a. Preclinical testing
b. Phase 1 – Safety and dosage
c. Phase 2 – Effectiveness and side effects
d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments
e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
    What is a clinical trial?
    A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
      What drugs does Cormedix (CRMD) have in its pipeline
      CRMD is currently developing the following drugs: Heparin, (Taurolidine And Heparin) Catheter Lock Solution, Standard of Care, (Taurolidine And Heparin) Catheter Lock Solution, Heparin, Neutrolin. These drug candidates are in various stages of clinical development as the company works toward FDA approval.
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