Viewing Study NCT02518568


Ignite Creation Date: 2025-12-24 @ 6:27 PM
Ignite Modification Date: 2026-01-04 @ 4:41 AM
Study NCT ID: NCT02518568
Status: TERMINATED
Last Update Posted: 2016-09-28
First Post: 2015-08-04
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Ferrous Sulphate Supplement (V0355) in Women With Iron Deficiency Anaemia
Sponsor: Pierre Fabre Medicament
Organization:

Study Overview

Official Title: Study of the Pharmacokinetics of Serum Iron After a Single Oral Administration of Ferrous Sulphate Supplement Synthetic Formula in Women With Iron Deficiency Anaemia.
Status: TERMINATED
Status Verified Date: 2016-09
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 purpose of this study is to investigate the pharmacokinetics of serum iron after a single oral administration of 160 mg (2 tablets of 80 mg) V0355 in women with iron deficiency anaemia.
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
2015-000544-42 EUDRACT_NUMBER None View