Ignite Creation Date:
2024-05-05 @ 6:34 PM
Last Modification Date:
2024-10-26 @ 9:34 AM
Study NCT ID:
NCT00500461
Status:
COMPLETED
Last Update Posted:
2017-08-07
First Post:
2007-07-10
Brief Title:
Study To Examine Safety Tolerability And Pharmacokinetics Of Intravenous Doses And Oral Dose Of GSK233705
Sponsor:
GlaxoSmithKline
Organization:
GlaxoSmithKline
Study Overview
Official Title:
A Single-centre Open-label Sequential Ascending Cross Over Study to Examine Safety Tolerability Pharmacodynamics and Pharmacokinetics of Ascending Single Doses Nominally 10 30 70 and 110µg Intravenous Doses and a Single 250µg Oral Dose of GSK233705 in Healthy Volunteers
Status:
COMPLETED
Status Verified Date:
2017-08
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:
GSK233705 is being developed for the treatment of chronic obstructive pulmonary disease This will be an open-label dose-ascending study in 7 healthy male subjects to establish well tolerated intravenous doses and an oral dose of GSK233705 The main objective of the study is to confirm an IV and oral dose for a definitive human radiolabel metabolic study
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