Viewing Study NCT00504842



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Last Modification Date: 2024-10-26 @ 9:34 AM
Study NCT ID: NCT00504842
Status: TERMINATED
Last Update Posted: 2008-04-15
First Post: 2007-07-18

Brief Title: Transcranial Ultrasound in Clinical SONothrombolysis
Sponsor: ImaRx Therapeutics
Organization: ImaRx Therapeutics

Study Overview

Official Title: A Phase 1-2 Randomized Placebo-Controlled Single-Blind Dose Escalation Study to Evaluate the Safety Tolerability and Activity of Ascending Single Doses of MRX-801 With Continuous Ultrasound Administration in Subjects With Acute Ischemic Stroke Receiving Treatment With Intravenous Tissue Plasminogen Activator
Status: TERMINATED
Status Verified Date: 2008-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Sponsor decision
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: TUCSON
Brief Summary: This is a randomized placebo controlled parallel group dose escalation trial to evaluate the safety tolerability and activity of four sequential dose tiers of MRX-801 and ultrasound as an adjunctive therapy to tissue plasminogen activator tPA treatment in subjects with acute ischemic stroke
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