WHO ICTRP trial
A study to explore heart function during first dose administration of fingolimod…
EUCTR2012-000653-32-DE · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2012-000653-32-DE |
|---|---|
| Public title | A study to explore heart function during first dose administration of fingolimod in patients with relapsing-remitting multiple sclerosis |
| Scientific title | A 1-week, open-label, multi-center study to explore conduction abnormalities during first dose administration of fingolimod in patients with relapsing-remitting multiple sclerosis (START) - START |
| Primary sponsor | Novartis Pharma GmbH |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): yes |
| Countries | Germany |
| Conditions | Conduction abnormalities in patients with relapsing-remitting multiple sclerosis MedDRA version: 18.1 Level: PT Classification code 10063399 Term: Relapsing-remitting multiple sclerosis System Organ Class: 10029205 - Nervous system… |
| Interventions | Trade Name: Gilenya Product Name: Fingolimod Product Code: FTY720 Pharmaceutical Form: Capsule, hard CAS Number: 162359-56-0 Current Sponsor code: FTY720 Other descriptive name: Fingolimod Hydrochloride Concentration unit: mg milligram(s)… |
| Registration date | Dec 4, 2012 |
| Secondary IDs | CFTY720DDE17 |
| Registry page | clinicaltrialsregister.eu |
At a glance
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: