Last update 01 Nov 2024
IXALTIS SAS
Last update 01 Nov 2024
Overview
Tags
Urogenital Diseases
Small molecule drug
Disease domain score
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A Double-Blind Randomised Placebo-Controlled Phase I/IIa Dose Titration Trial to Evaluate the Safety, Tolerability and Efficacy of Oral Litoxetine up to 30 mg vs Placebo BID in Subjects With Urinary Incontinence
A Double-Blind, Randomised, Placebo-Controlled, Parallel Group, Phase II, Dose Ranging Trial to Evaluate the Efficacy, Safety and Tolerability of oral Litoxetine 10mg, 20mg and 40mg Twice Daily (BID) versus placebo in women with Mixed Urinary Incontinence
A Double-Blind, Randomised, Placebo-Controlled, Parallel-Group, Phase 2, Dose Ranging Trial to Evaluate the Efficacy, Safety, and Tolerability of Oral Litoxetine 10mg,20mg and 40mg Twice Daily (BID) versus Placebo in Women with Mixed Urinary Incontinence - IXA-CSP-001 Litoxetine v Placebo in Urinary Incontinence 2016-12-09 V1
100 Clinical Results associated with IXALTIS SAS
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100 Deals associated with IXALTIS SAS
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100 Translational Medicine associated with IXALTIS SAS
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Pipeline
Pipeline Snapshot as of 24 Dec 2024
The statistics for drugs in the Pipeline is the current organization and its subsidiaries are counted as organizations,Early Phase 1 is incorporated into Phase 1, Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3
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