Viewing Study NCT00002226



Ignite Creation Date: 2024-05-05 @ 10:00 AM
Last Modification Date: 2024-10-26 @ 9:02 AM
Study NCT ID: NCT00002226
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 1999-11-02

Brief Title: Safety and Effectiveness of Giving SU5416 to HIV-Infected Patients With AIDS-Related Kaposis Sarcoma
Sponsor: SUGEN
Organization: NIH AIDS Clinical Trials Information Service

Study Overview

Official Title: A Multicenter Dose Escalating Study in Patients With Cutaneous AIDS-Related Kaposis Sarcoma
Status: COMPLETED
Status Verified Date: 2000-06
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 see if it is safe and effective to give SU5416 to HIV-infected patients with AIDS-related Kaposis sarcoma KS SU5416 may prevent the growth of KS tumors
Detailed Description: Groups of 3-6 patients are sequentially assigned to receive escalating doses of SU5416 in 33 increments Study drug is administered as a twice-weekly intravenous injection for 4 weeks In the absence of unacceptable toxicity responding patients may continue on SU5416 in 4-week treatment cycles for a maximum of 1 year or until the presence of unacceptable toxicity or tumor progression

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
Secondary ID Type Domain Link
5416003 None None None