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Minesapride

Alternative Names: Minesapride, dsp-6952, dsp6592, dsp 6952
Latest Update: 2020-12-01
Latest Update Note: PubMed Publication

Product Description

The pharmacological profile of DSP-6952, a novel 5-HT4 receptor partial agonist, was investigated to evaluate the potential use for GI disorders, and to compare its effects in some GI dysfunction models with those of clinically efficacious prokinetic agents. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/29428470/)

Mechanisms of Action: 5-HT4 Agonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Sumitomo Dainippon Pharma Co
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Minesapride

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Constipation|Irritable Bowel Syndrome

Phase 1: Healthy Volunteers

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

JapicCTI-163459

P2

Completed

Constipation|Irritable Bowel Syndrome

2018-04-20

JapicCTI-173785

P1

Completed

Healthy Volunteers

2018-03-31

JapicCTI-205093

P1

Completed

Healthy Volunteers

2017-12-17

JapicCTI-122041

P2

Completed

Constipation|Irritable Bowel Syndrome

2013-12-31

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