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Venus Remedies Limited (IN:VENUSREM)
:VENUSREM
Enoxaparin Sodium (Venus Remedies Limited), Enoxaparin Sodium (Sanofi)
Healthy
Phase I
Completed
Bioequivalence Study of a Generic Enoxaparin Sodium to Clexane® After Single Subcutaneous Dose in Healthy Human Subjects
Feb 22, 2022
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Meropenem, Cse-1034 (Ceftriaxone + Sulbactam + Edta)
Urinary Tract Infection Complicated, Acute Pyelonephritis
Phase III
Completed
CSE-1034 (Ceftriaxone+ Sulbactam+ EDTA) Compared to Meropenem in Complicated Urinary Tract Infections (cUTIs) Caused by ESBL Producing Gram Negative Bacteria
Mar 09, 2018
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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
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 Venus Remedies Limited (VENUSREM) have in its pipeline
VENUSREM is currently developing the following drugs: Enoxaparin Sodium (Venus Remedies Limited), Enoxaparin Sodium (Sanofi), Meropenem, Cse-1034 (Ceftriaxone + Sulbactam + Edta). These drug candidates are in various stages of clinical development as the company works toward FDA approval.