Viewing Study NCT00630760


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Study NCT ID: NCT00630760
Status: TERMINATED
Last Update Posted: 2014-05-21
First Post: 2008-02-28
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Oral NRX 194204 in Patients With Refractory Malignancies
Sponsor: University of Southern California
Organization:

Study Overview

Official Title: A Multiple-Center, Open-Label, Dose Escalation Study of the Safety and Pharmacokinetics of Oral NRX 194204 Capsule Administered Daily for a Minimum of 4 Weeks in Patients With Refractory Malignancies
Status: TERMINATED
Status Verified Date: 2014-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Sponsor withdrew study. Accrual not completed
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This phase I study will determine the safety profile of NRX 194204 on this schedule; it will evaluate the pharmacokinetic profile of NRX 194204 in cancer patients; and will investigate anti-tumor activity as manifested by standard response criteria, or by tumor markers.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: