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Pregnancy Registry Trial

This study is currently recruiting participants.
See Contacts and Locations
Verified July 2017 by Novartis ( Novartis Pharmaceuticals )
Sponsor:
Information provided by (Responsible Party):
Novartis ( Novartis Pharmaceuticals )
ClinicalTrials.gov Identifier:
NCT01285479
First received: January 26, 2011
Last updated: July 30, 2017
Last verified: July 2017
January 26, 2011
July 30, 2017
October 15, 2011
September 25, 2023   (Final data collection date for primary outcome measure)
Major malformations, minor congenital anomalies & overall pregnancy outcomes will be collected; Complications during pregnancy, potential AEs on the physical & immune system development of the offspring, & any other adverse pregnancy/maternal outcomes. [ Time Frame: Throughout the entirety of a patient's participation in the study which would include 9 months of pregnancy and 1 year of follow up post pregnancy ]
Same as current
Complete list of historical versions of study NCT01285479 on ClinicalTrials.gov Archive Site
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Pregnancy Registry Trial
The Multi-National Pregnancy Fingolimod Exposure Registry in Multiple Sclerosis (Epidemiological Study Protocol FTY720D2404)
The purpose of the Multi-National Gilenya Pregnancy Exposure Registry in Multiple Sclerosis (MS) is to continuously monitor, evaluate, and assess for major and minor teratogenic effects in the offspring of women exposed to Gilenya before (up to 8 weeks before last menstrual period) and during pregnancy in routine clinical practice. The overall aim is to collect and evaluate data on maternal, fetal, and infant outcomes and compare it with reference populations.
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Observational
Observational Model: Cohort
Time Perspective: Prospective
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Non-Probability Sample
Women with MS who become pregnant and were exposed to at least one dose of Gilenya during pregnancy (or up to 8 weeks before last menstrual period).
Multiple Sclerosis
Drug: Fingolimod
prescribed fingolimod 0.5 mg/day
Intervention: Drug: Fingolimod
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
500
September 25, 2023
September 25, 2023   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Pregnancy and reported confirmed or suspected maternal exposure to Gilenya any time during pregnancy or shortly before pregnancy (up to 8 weeks before LMP).
  • Informed consent

Exclusion Criteria:

  • There are no specific exclusion criteria for this registry.

Other protocol-defined inclusion/exclusion criteria may apply

Sexes Eligible for Study: Female
Child, Adult, Senior
No
Contact: Novartis Pharmaceuticals 1-888-669-6682
Contact: Novartis Pharmaceuticals +41613241111
Argentina,   Australia,   Belgium,   Canada,   Cyprus,   Czechia,   Denmark,   Finland,   France,   Germany,   Greece,   Ireland,   Italy,   Lebanon,   Mexico,   Netherlands,   Poland,   Portugal,   Russian Federation,   Saudi Arabia,   Spain,   Sweden,   Switzerland,   United Arab Emirates,   United Kingdom,   United States
Austria,   Czech Republic,   Norway
 
NCT01285479
CFTY720D2404
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Novartis ( Novartis Pharmaceuticals )
Novartis Pharmaceuticals
Not Provided
Study Director: Novartis Pharmaceuticals Novartis Pharmaceuticals
Novartis
July 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP