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Dalantercept

Alternative Names: dalantercept, ace-041, ace041, ace 041
Latest Update: 2022-10-06
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: TGFR Inhibitor

Novel Mechanism: No

Modality: Fusion Protein

Route of Administration: Oral,Subcutaneous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Dalantercept

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Squamous Cell Carcinoma|Mucinous Cystadenocarcinoma|Serous Cystadenocarcinoma|Mucinous Adenocarcinoma|Transitional Cell Carcinoma|Clear Cell Adenocarcinoma|Endometrial Cancer|Renal Cell Carcinoma|Ovarian Cancer|Head and Neck Cancer|Hepatocellular Carcinoma

Phase 1: Multiple Myeloma

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

A041-05

P2

Completed

Hepatocellular Carcinoma

2017-07-05

A041-04

P2

Terminated

Renal Cell Carcinoma

2017-06-01

GOG-0229N

P2

Completed

Serous Cystadenocarcinoma|Endometrial Cancer|Clear Cell Adenocarcinoma|Mucinous Cystadenocarcinoma|Transitional Cell Carcinoma|Squamous Cell Carcinoma|Mucinous Adenocarcinoma

2016-01-01

GOG-0170R

P2

Completed

Ovarian Cancer

2015-10-31

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