Ozmosi | Resminostat Drug Profile
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Resminostat

Alternative Names: resminostat, 4sc-201, ras-2410, ras 2410, ras2410
Clinical Status: Active
Latest Update: 2025-03-14
Latest Update Note: Clinical Trial Update

Product Description

Resminostat is an orally administered histone deacetylase (HDAC) inhibitor that potentially represents a novel therapy for a broad spectrum of oncology indications, both in monotherapy and particularly in combination with other anti-cancer drugs. (Sourced from: https://www.4sc.com/product-pipeline/resminostat/)

Mechanisms of Action: HDAC Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: 4SC
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Resminostat

Countries in Clinic: Austria, Belgium, France, Germany, Greece, Italy, Japan, Netherlands, Poland, Spain, Switzerland, United Kingdom

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Mycosis Fungoides|Sezary Syndrome|T-Cell Cutaneous Lymphoma

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT02953301

RESMAIN

P2

Completed

T-Cell Cutaneous Lymphoma|Mycosis Fungoides|Sezary Syndrome

2023-03-01

65%

2024-09-04

Primary Endpoints|Study Completion Date|Treatments|Trial Status