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Anetumab ravtansine

Alternative Names: anetumab ravtansine, bay-94-9343, bay949343, bay 949343, bay94-9343, bay94 9343
Latest Update: 2024-12-18
Latest Update Note: Clinical Trial Update

Product Description

A fully human IgG1 monoclonal antibody directed against the cell surface glycoprotein mesothelin and conjugated to the maytansinoid DM4 with potential antineoplastic activity. The monoclonal antibody moiety of anetumab ravtansine targets and binds to the tumor associated antigen mesothelin; upon internalization, the DM4 moiety binds to tubulin and disrupts microtubule assembly/disassembly dynamics, resulting in inhibition of cell division and cell growth of mesothelin-expressing tumor cells. Mesothelin is overexpressed on all mesotheliomas as well as many ovarian and pancreatic cancers while minimally expressed on normal tissue. (Sourced from: https://www.cancer.gov/publications/dictionaries/cancer-drug/def/anetumab-ravtansine)

Mechanisms of Action: Mesothelin Inhibitor

Novel Mechanism: Yes

Modality: Antibody Drug Conjugate

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Elanco Animal Health
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Anetumab ravtansine

Countries in Clinic:

Active Clinical Trial Count: 1

Highest Development Phases

Phase 2: Oncology Solid Tumor Unspecified

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2019-000061-20

P2

Active, not recruiting

Oncology Solid Tumor Unspecified

2024-05-23

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