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Vorinostat

Alternative Names: vorinostat, suberoylanilide hydroxamic acid, zolinza, mk-0683, mk0683, suberoylanilide hydroxamic acid (saha), saha
Latest Update: 2024-12-16
Latest Update Note: Clinical Trial Update

Product Description

Vorinostat is a new drug used in the management of cutaneous T cell lymphoma when the disease persists, gets worse or comes back during or after treatment with other medicines. It is an efficacious and well tolerated drug and has been considered a novel drug in the treatment of this condition.  (Sourced from: https://pubmed.ncbi.nlm.nih.gov/26288427/)

Mechanisms of Action: HDAC Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Approved

Approved Countries: Argentina | Australia | Canada | Chile | Colombia | Dominican Republic | Ecuador | Ireland | Japan | Korea | Mexico | Peru | Russia | Taiwan | United Kingdom | United States

Approved Indications: Lymphoma | T-Cell Cutaneous Lymphoma | T-Cell Lymphoma

Known Adverse Events: Dysgeusia | Thrombocytopenia | Anorexia | Diarrhea

Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Vorinostat

Countries in Clinic: France, United States

Active Clinical Trial Count: 7

Highest Development Phases

Phase 2: Adenocarcinoma|Anus Cancer|Cervical Cancer|Head and Neck Cancer|Lung Cancer|Melanoma|Neuroblastoma|Penile Cancer|Primitive Neuroectodermal Tumors|Prostate Cancer|Squamous Cell Carcinoma|Uterine Cancer|Vulvar Cancer

Phase 1: Breast Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

RG1123920

P2

Recruiting

Prostate Cancer|Adenocarcinoma

2025-12-30

Pro00020138

P1

Recruiting

Breast Cancer

2025-09-01

PEVOsq

P2

Active, not recruiting

Squamous Cell Carcinoma|Head and Neck Cancer

2024-11-18

NANT2017-01

P1

Active, not recruiting

Neuroblastoma

2024-02-23

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