Viewing Study NCT00432068



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Last Modification Date: 2024-10-26 @ 9:30 AM
Study NCT ID: NCT00432068
Status: COMPLETED
Last Update Posted: 2015-12-03
First Post: 2007-02-05

Brief Title: Open Label Study of a Single Dose of a New Extended Long Acting Formulation of Octreotide Pamoate in Healthy Volunteers
Sponsor: Novartis Pharmaceuticals
Organization: Novartis

Study Overview

Official Title: A Phase I Open Label Single Center Dose Escalation Study to Assess the Pharmacokinetics Safety and Tolerability of a Single Dose of a New Extended Long-acting Formulation of Octreotide Pamoate Administered im in Healthy Cholecystectomized Volunteers
Status: COMPLETED
Status Verified Date: 2015-12
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 study will assess the pharmacokinetic profile safety and tolerability of an octreotide extended long-acting formulation after a single dose in humans It will investigate the profile of a single dose of drug in a healthy volunteer subject in order to understand the timing and extent of fluctuations in octreotide concentrations in the blood with this formulation the relationship of drug concentration with dose and how long the drug remains in the body system
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