Ozmosi | BGB-DXP604 Drug Profile
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BGB-DXP604

Alternative Names: bgb-dxp604, bgb dxp604, bgbdxp604
Clinical Status: Inactive
Latest Update: 2024-03-15
Latest Update Note: Clinical Trial Update

Product Description

monoclonal antibodies for SARS-CoV-2 infection (Sourced from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479899/)

Mechanisms of Action: Mpro Inhibitor

Novel Mechanism: Yes

Modality: Antibody

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: BeiGene
Company Location: GRAND CAYMAN E9 KY1-1108
Company CEO: John V. Oyler
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Healthy Volunteers

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT04669262

BGB-DXP604-101

P1

Completed

Healthy Volunteers

2021-05-21

12%

2024-03-16

Primary Endpoints

Recent News Events

Date

Type

Title