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Resatorvid

Alternative Names: resatorvid, tak-242, tak 242, tak242
Latest Update: 2024-06-17
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: TLR4 Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Injection

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Takeda
Company Location: TOKYO M0 103-8668
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Resatorvid

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Respiratory Insufficiency|Sepsis|Shock, Septic

Phase 2: Hepatitis C, Chronic|Liver Cirrhosis, Alcoholic|Liver Failure, Acute|Hepatitis, Alcoholic|Acute-On-Chronic Liver Failure|Respiratory Insufficiency|Kidney Diseases|Acute Kidney Injury|Liver Cirrhosis|Hepatic Insufficiency|End Stage Liver Disease|Hepatitis, Chronic

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

G-TAK-ES-01

P2

Withdrawn

Liver Cirrhosis|Liver Failure, Acute|Acute Kidney Injury|Respiratory Insufficiency|Kidney Diseases

2025-01-31

TAK-242-2001

P2

Unknown status

Hepatic Insufficiency|End Stage Liver Disease|Acute-On-Chronic Liver Failure|Hepatitis, Chronic|Liver Failure, Acute|Hepatitis, Alcoholic

2022-12-01

24%

Phase 2a Study of TAK-242 to Treat Acute-on-Chronic Liver Failure

P2

Unknown status

Liver Cirrhosis, Alcoholic|Liver Failure, Acute|Hepatitis, Alcoholic|Acute-On-Chronic Liver Failure|Hepatitis C, Chronic

2022-04-28

JapicCTI-080588

P3

Terminated

Respiratory Insufficiency|Sepsis

2012-11-01

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