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Ardelyx (CH:41X)
:41X
Switzerland Market

Ardelyx (41X) Drug Pipeline

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Drug Name
Condition
Stage
Status
Study Name
Trial Start Date
Article
Tenapanor 25 Mg Bid, Tenapanor 5 Mg Bid, Tenapanor 50 Mg Bid
Chronic Idiopathic Constipation (Cic)
Phase III
Recruiting
A 26-Wk Study to Assess Safety & Efficacy of Tenapanor for T/t of Chronic Idiopathic Constipation in Adults
Jan 26, 2026
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Tenapanor
Irritable Bowel Syndrome With Constipation (Ibs-C)
Phase II
Active Not Recruiting
4-Week, Multi-center Dose-Ranging Study for the IBS-C in Pts. 6 to <12 Yrs
Aug 12, 2024
Tenapanor
Irritable Bowel Syndrome With Constipation (Ibs-C)
Phase III
Enrolling By Invitation
Safety Study of Tenapanor for the Treatment of Pediatric Patients (6 to Less Than 18 Years Old) With IBS-C
Mar 07, 2023
Tenapanor 50 Mg, Tenapanor 25 Mg Bid
Irritable Bowel Syndrome With Constipation (Ibs-C)
Phase III
Active Not Recruiting
Study to Assess Safety and Efficacy of Tenapanor for Treatment of IBS-C in Pediatric Patients 12 to Less Than 18 Years
Nov 30, 2022

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 Ardelyx (41X) have in its pipeline
      41X is currently developing the following drugs: Tenapanor 25 Mg Bid, Tenapanor 5 Mg Bid, Tenapanor 50 Mg Bid, Tenapanor, Tenapanor. These drug candidates are in various stages of clinical development as the company works toward FDA approval.