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Carotuximab

Alternative Names: carotuximab, trc105
Latest Update: 2024-02-02
Latest Update Note: Clinical Trial Update

Product Description

A human/murine chimeric monoclonal antibody directed against endoglin (CD105) with potential antiangiogenic and antineoplastic activities. Carotuximab binds to endoglin, which may result in inhibition of tumor angiogenesis and decreased tumor cell proliferation. The glycoprotein endoglin is a transforming growth factor beta-1 (TGF beta-1) accessory receptor that is highly expressed on tumor vessel endothelial cells and appears to be essential for angiogenesis. (Sourced from: https://www.cancer.gov/publications/dictionaries/cancer-drug/def/carotuximab?redirect=true)

Mechanisms of Action: Endoglin Inhibitor

Novel Mechanism: Yes

Modality: Antibody

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Tracon
Company Location: San Diego CA 92122
Company CEO: Charles P. Theuer
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Carotuximab

Countries in Clinic: United States

Active Clinical Trial Count: 1

Highest Development Phases

Phase 2: Breast Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

F150701004 (UAB 1514)

P2

Completed

Breast Cancer

2022-12-01

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