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Polaprezinc

Alternative Names: polaprezinc
Latest Update: 2024-11-07
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: HO1 Inducer

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: Australia | China | Korea

Approved Indications: None

Known Adverse Events: None

Company: ZERIA
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Polaprezinc

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Taste Disorders

Phase 2: Lymphoma|Intestinal Diseases|Leukemia|Digestive System Cancer|Mucositis|Prostate Cancer|Mouth Cancer|Gastrointestinal Cancer|Liver Cancer|Colorectal Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
GER

N/A

Not yet recruiting

Gastroesophageal Reflux|Esophagitis, Peptic

2025-04-01

ChiCTR2300070469

N/A

Not yet recruiting

Helicobacter Infections

2024-02-29

PEACe

P2

Completed

Prostate Cancer

2023-01-20

ChiCTR1900028329

N/A

Recruiting

Unknown

2022-12-31

Recent News Events

Date

Type

Title

04/04/2024

PubMed

 Expression analysis of zinc-metabolizing enzymes in the saliva as a new method of evaluating zinc content in the body: two case reports and a review of the literature.

04/02/2024

PubMed

 Efficacy of Normalising Serum Zinc Level for Patients with Olfactory Dysfunction and Zinc Deficiency.

03/01/2024

PubMed

 Zinc supplementation with polaprezinc was associated with improvements in albumin, prothrombin time activity, and hemoglobin in chronic liver disease.

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