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Bucillamine

Alternative Names: bucillamine, rev-002, rev002, rev 002
Latest Update: 2024-11-12
Latest Update Note: News Article

Product Description

For the treatment of patients with mild to moderate COVID-19 (Sourced from: https://pubmed.ncbi.nlm.nih.gov/35044238/)

Mechanisms of Action: VEGF Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: Orphan Drug - Reperfusion Injury|Liver Transplant *

Approval Status: Not Approved

Approved Countries: Korea

Approved Indications: None

Known Adverse Events: None

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

Clinical Description

Map of Global Clinical Trials for Bucillamine

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 4: Arthritis, Rheumatoid

Phase 3: COVID-19

Phase 2: Cystinuria|Gout

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

RT-003

P3

Terminated

COVID-19

2023-06-12

39%

REV401

P2

Unknown status

Cystinuria

2018-03-01

REV-201

P2

Completed

Gout

2015-11-01

SMC-94

P4

Unknown status

Arthritis, Rheumatoid

2011-12-01

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