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BMS-986263

Alternative Names: bms-986263, bms986263, bms 986263, nd-l02-s0201, ndl02s0201, nd l02 s0201
Latest Update: 2024-02-14
Latest Update Note: Clinical Trial Update

Product Description

BMS-986263 is a lipid nanoparticle delivering small interfering RNA designed to degrade HSP47 mRNA, for the treatment of advanced fibrosis. (Sourced from: https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/hep.32181)

Mechanisms of Action: HSP47 Antagonist

Novel Mechanism: Yes

Modality: Nucleic Acid

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Bristol-Myers Squibb
Company Location: NEW YORK NY 10016
Company CEO: Giovanni Caforio
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for BMS-986263

Countries in Clinic: Argentina, Belgium, Brazil, Canada, France, Germany, Israel, Italy, Japan, Korea, Spain, Switzerland, Taiwan, United Kingdom, United States, Unknown Location

Active Clinical Trial Count: 5

Highest Development Phases

Phase 2: Hepatitis, Alcoholic|Idiopathic Pulmonary Fibrosis|Liver Cirrhosis|Non-alcoholic Steatohepatitis

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2019-003932-22

P2

Active, not recruiting

Liver Cirrhosis|Non-alcoholic Steatohepatitis|Hepatitis, Alcoholic

2026-09-04

jRCT2011200024

P2

Recruiting

Liver Cirrhosis|Non-alcoholic Steatohepatitis

2024-02-29

jRCT2080225045

P2

Completed

Idiopathic Pulmonary Fibrosis

2023-12-31

JUNIPER

P2

Completed

Idiopathic Pulmonary Fibrosis

2022-08-24

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