Ozmosi | Alizapride Drug Profile
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Alizapride

Alternative Names: alizapride
Clinical Status: Inactive
Latest Update: 2025-04-24
Latest Update Note: Clinical Trial Update

Product Description

Dopamine D2 receptor antagonist with prokinetic and antiemetic effects which can also be used in the treatment of nausea and vomiting, including postoperative nausea and vomiting. (Sourced from: https://www.guidetopharmacology.org/GRAC/LigandDisplayForward?ligandId=11141)

Mechanisms of Action: DR Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: Belgium | Brazil | Colombia | Dominican Republic | Egypt | France | Italy | Luxembourg | Peru | Portugal | Taiwan

Approved Indications: None

Known Adverse Events: None

Company: Institut Jules Bordet
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 4: Breast Cancer

Phase 2: Oncology Unspecified

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

2023-505360-11-00

IJB-IRAES-2020

P2

Recruiting

Oncology Unspecified

2027-06-30

2025-05-02

Treatments

NCT01298193

GEICAM/2009-02

P4

Completed

Breast Cancer

2013-03-01

2024-10-16

Primary Endpoints|Treatments