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AR-42

Alternative Names: ar-42, ar42, ar 42
Clinical Status: Inactive
Latest Update: 2024-03-01
Latest Update Note: PubMed Publication

Product Description

AR-42 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT01129193)

Mechanisms of Action: HDAC6 Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Alison Walker
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Prolymphocytic T-Cell Leukemia|Prolymphocytic B-Cell Leukemia|Follicular Lymphoma|Waldenstrom Macroglobulinemia|Lymphomatoid Granulomatosis|Sezary Syndrome|Lymphoma, Non-Hodgkin|Burkitt Lymphoma|Prolymphocytic Leukemia|Mycosis Fungoides|Lymphoproliferative Disorders|Plasmablastic Lymphoma|Chronic Lymphoid Leukemia|Precursor B-Cell Lymphoblastic Leukemia-Lymphoma|Lymphocytic Chronic B-Cell Leukemia|Extranodal NK-T-Cell Lymphoma|Large-Cell Immunoblastic Lymphoma|Precursor T-Cell Lymphoblastic Leukemia-Lymphoma|Mantle-Cell Lymphoma|Intraocular Lymphoma|Precursor Cell Lymphoblastic Leukemia-Lymphoma|Immunoblastic Lymphadenopathy|Diffuse Large B-Cell Lymphoma|Adult T-Cell Leukemia-Lymphoma|T-Cell Cutaneous Lymphoma|Multiple Myeloma|Large-Cell Anaplastic Lymphoma|Leukemia, Plasma Cell|T-Cell Peripheral Lymphoma|Testicular Cancer|B-Cell Marginal Zone Lymphoma|Acute Myeloid Leukemia|Neurofibromatosis 2|Neurofibromatoses|Neurilemmoma|Neuroma, Acoustic|Meningioma|Renal Cell Carcinoma|Kidney Diseases|Sarcoma

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

OSU-15004

P1

Completed

Multiple Myeloma

2020-11-14

2021-06-16

Patient Enrollment|Primary Completion Date|Primary Endpoints|Start Date|Study Completion Date|Treatments|Trial Status

14-078H

P1

Terminated

Meningioma|Neurofibromatosis 2|Neurilemmoma|Neuroma, Acoustic|Neurofibromatoses

2017-05-30

2022-05-12

Primary Endpoints

OSU-09102

P1

Completed

Mantle-Cell Lymphoma|Testicular Cancer|Intraocular Lymphoma|Burkitt Lymphoma|T-Cell Cutaneous Lymphoma|Precursor Cell Lymphoblastic Leukemia-Lymphoma|T-Cell Peripheral Lymphoma|Prolymphocytic Leukemia|Sezary Syndrome|Prolymphocytic T-Cell Leukemia|Mycosis Fungoides|Adult T-Cell Leukemia-Lymphoma|Precursor B-Cell Lymphoblastic Leukemia-Lymphoma|Diffuse Large B-Cell Lymphoma|Follicular Lymphoma|B-Cell Marginal Zone Lymphoma|Plasmablastic Lymphoma|Leukemia, Plasma Cell|Lymphoproliferative Disorders|Precursor T-Cell Lymphoblastic Leukemia-Lymphoma|Immunoblastic Lymphadenopathy|Large-Cell Immunoblastic Lymphoma|Large-Cell Anaplastic Lymphoma|Lymphomatoid Granulomatosis|Multiple Myeloma|Lymphocytic Chronic B-Cell Leukemia|Extranodal NK-T-Cell Lymphoma|Chronic Lymphoid Leukemia|Lymphoma, Non-Hodgkin|Waldenstrom Macroglobulinemia|Prolymphocytic B-Cell Leukemia

2017-01-07

2019-03-19

Treatments

MCC-14-10774

P1

Terminated

Renal Cell Carcinoma|Sarcoma|Kidney Diseases

2016-11-24

2019-04-04

Patient Enrollment|Primary Completion Date|Study Completion Date|Treatments|Trial Status

OSU-11130

P1

Completed

Acute Myeloid Leukemia

2015-02-19

2019-03-19

Treatments