Viewing Study NCT02171637



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Last Modification Date: 2024-10-26 @ 11:26 AM
Study NCT ID: NCT02171637
Status: COMPLETED
Last Update Posted: 2014-06-24
First Post: 2014-06-20

Brief Title: Dose Escalation Study of Oral Treatment With BIBW 2992 in Patients With Advanced Solid Tumors
Sponsor: Boehringer Ingelheim
Organization: Boehringer Ingelheim

Study Overview

Official Title: A Phase I Open Label Dose Escalation Study of Once-daily Oral Treatment With BIBW 2992 for 14 Days in Patients With Advanced Solid Tumors
Status: COMPLETED
Status Verified Date: 2014-06
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: Evaluation of maximum Tolerated Dose MTD safety pharmacokinetics efficacy of BIBW 2992 pharmacodynamic modulation of biomarkers correlation of Epidermal Growth Factor Receptor EGFR and Human EGF-like Receptor number 2 HER2 immunohistochemical status with objective tumour responses
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