Viewing Study NCT01106508


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Study NCT ID: NCT01106508
Status: COMPLETED
Last Update Posted: 2020-12-17
First Post: 2010-04-16
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: A Dose Finding and Safety Study of Oral LEQ506 in Patients With Advanced Solid Tumors
Sponsor: Novartis Pharmaceuticals
Organization:

Study Overview

Official Title: A Phase I, Multi-center, Open Label, Dose Escalation Study of LEQ506, an Oral Smoothened Inhibitor, in Patients With Advanced Solid Tumors
Status: COMPLETED
Status Verified Date: 2016-01
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: This first-in-human dose-escalation study is to characterize the safety, tolerability, pharmacokinetics and pharmacodynamics of LEQ506 given orally on a daily dosing schedule in patients with advanced solid tumors.
Detailed Description: None

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 ID Infos

Secondary ID Type Domain Link View
2009-017969-30 EUDRACT_NUMBER None View