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Vorsetuzumab mafodotin

Alternative Names: vorsetuzumab mafodotin, denintuzumab mafodotin, sgn-cd19a, sgn-75, abt-414
Latest Update: 2024-02-20
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: Tubulin Inhibitor,Mitosis Inhibitor

Novel Mechanism: No

Modality: Bispecific Antibody

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: AbbVie
Company Location: NORTH CHICAGO IL 60064
Company CEO: Richard A. Gonzalez
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Vorsetuzumab mafodotin

Countries in Clinic: Argentina, Australia, Austria, Belgium, Brazil, Canada, China, Colombia, Czech Republic, France, Germany, Hong Kong, Ireland, Israel, Italy, Korea, Mexico, Netherlands, New Zealand, Portugal, Russia, Singapore, South Africa, Spain, Switzerland, Taiwan, United Kingdom, United States

Active Clinical Trial Count: 2

Highest Development Phases

Phase 3: Glioblastoma|Gliosarcoma

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2015-001166-26

P3

Completed

Glioblastoma|Gliosarcoma

2022-04-04

Intellance1

P3

Completed

Glioblastoma|Gliosarcoma

2022-04-04

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