Viewing Study NCT00150462



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Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00150462
Status: COMPLETED
Last Update Posted: 2017-05-02
First Post: 2005-09-06

Brief Title: Safety Study of the Proteasome Inhibitor PR-171 Carfilzomib for Injection in Patients With Hematological Malignancies
Sponsor: Amgen
Organization: Amgen

Study Overview

Official Title: A Phase I Study of the Safety and Pharmacokinetics of Escalating Intravenous Doses of the Proteasome Inhibitor PR-171 in Patients With Hematological Malignancies
Status: COMPLETED
Status Verified Date: 2017-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to test the safety and tolerability of carfilzomib at different dose levels on hematological cancers such as multiple myeloma non-Hodgkins lymphoma Hodgkins disease or Waldenstroms macroglobulinemia Carfilzomib is a proteasome inhibitor an enzyme responsible for degrading a wide variety of cellular proteins
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None