Ozmosi | CDX-527 Drug Profile
Drug Search Results
Using advanced filters...
Advanced Search [+]

CDX-527

Alternative Names: cdx-527, cdx527, cdx 527
Clinical Status: Inactive
Latest Update: 2023-06-19
Latest Update Note: Clinical Trial Update

Product Description

CDX-527 is the first candidate from Celldexs bispecific antibody platform. It uses Celldexs proprietary highly active anti-PD-L1 and CD27 human antibodies to couple CD27 costimulation with blockade of the PD-L1/PD-1 pathway to help prime and activate anti-tumor T cell responses through CD27 costimulation, while preventing PD-1 inhibitory signals that subvert the immune response.

Mechanisms of Action: PD-1 Inhibitor, CD27 Inhibitor

Novel Mechanism: Yes

Modality: Bispecific Antibody

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Celldex
Company Location: HAMPTON NJ 08827
Company CEO: Anthony S. Marucci
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for CDX-527

Countries in Clinic: United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Bladder Cancer|Breast Cancer|Cholangiocarcinoma|Colorectal Cancer|Esophageal Cancer|Fallopian Tube Cancer|Gastrointestinal Cancer|Head and Neck Cancer|Liver Cancer|Non-Small-Cell Lung Cancer|Ovarian Cancer|Peritoneal Cancer|Renal Cell Carcinoma|Transitional Cell Carcinoma

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT04440943

CDX527-01

P1

Completed

Ovarian Cancer|Esophageal Cancer|Fallopian Tube Cancer|Breast Cancer|Liver Cancer|Colorectal Cancer|Transitional Cell Carcinoma|Non-Small-Cell Lung Cancer|Cholangiocarcinoma|Bladder Cancer|Head and Neck Cancer|Peritoneal Cancer|Renal Cell Carcinoma|Gastrointestinal Cancer

2023-04-06

23%

2023-06-19

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status