Viewing Study NCT00483093



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Last Modification Date: 2024-10-26 @ 9:33 AM
Study NCT ID: NCT00483093
Status: COMPLETED
Last Update Posted: 2014-05-30
First Post: 2007-06-05

Brief Title: Study of NGR-hTNF in Combination With Cisplatin in Solid Tumor
Sponsor: AGC Biologics SpA
Organization: AGC Biologics SpA

Study Overview

Official Title: NGR004A Phase IB Study of NGR-hTNF in Combination With Cisplatin in Patient Affected by Advanced or Metastatic Solid Tumor
Status: COMPLETED
Status Verified Date: 2014-05
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 main objective of the trial is to document the safety of the combination escalation doses of NGR-hTNF from 02 mcgsqm to 16 mcgsqm with a fixed dose of cisplatin 80 mgsqm Safety will be established by clinical and laboratory assessment according to National Cancer Institute Common Toxicity Criteria NCI-CTC
Detailed Description: This is a phase IB open-label non-randomized dose-escalation study that will be conducted in sequential cohorts of patients Three patients per each cohort are planned

Patients with advanced or metastatic solid tumor not amenable of standard therapy will be enrolled

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
Secondary IDs
Secondary ID Type Domain Link
2006-006035-42 EUDRACT_NUMBER None None