Ozmosi | Bezetabart debotansine Drug Profile
Drug Profile
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Bezetabart debotansine

Pronounced as: bez-eh-tuh-bart dee-boh-tan-seen

Alternative Names: Bezetabart debotansine, BN-301, BN301, stro-001, stro001, stro 001
Clinical Status: Active
Latest Update: 2024-06-11
Latest Update Note: Clinical Trial Update

Product Description

STRO-001 is a CD74-targeting ADC currently being investigated in a Phase 1 clinical trial of patients with advanced B-cell malignancies, including multiple myeloma and non-Hodgkin lymphoma. (Sourced from: https://www.sutrobio.com/sutro-biopharma-presents-data-from-ongoing-phase-1-dose-escalation-study-for-stro-001-for-the-treatment-of-b-cell-non-hodgkin-lymphoma-at-the-62nd-american-society-of-hematology-annual-meeting/)

Mechanisms of Action: CD74 Inhibitor

Novel Mechanism: Yes

Modality: Antibody Drug Conjugate

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Sutro Biopharma, Inc.
Company Location: Western America
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Bezetabart debotansine

Countries in Clinic: United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Diffuse Large B-Cell Lymphoma|Follicular Lymphoma|Mantle-Cell Lymphoma|Multiple Myeloma

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT03424603

STRO-001-BCM1

P1

Completed

Multiple Myeloma|Diffuse Large B-Cell Lymphoma|Mantle-Cell Lymphoma|Follicular Lymphoma

2024-02-15

2024-06-12

Primary Endpoints