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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01198717
Other study ID # SPD422-404
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 28, 2010
Est. completion date March 1, 2016

Study information

Verified date March 2021
Source Takeda
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate the progression of ET in children (aged 6-17years inclusive) over a period of 5 years maximum. The study will also assess how children are diagnosed, treatment options for those children with symptoms and events related to their ET and the outcomes of those treatments.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date March 1, 2016
Est. primary completion date March 1, 2016
Accepts healthy volunteers No
Gender All
Age group 6 Years to 17 Years
Eligibility Inclusion Criteria: - 6 years or over and less than 18 years patient has ET according to the WHO criteria as guidance Exclusion Criteria: - Interventional clinical study participation

Study Design


Locations

Country Name City State
Czechia Paediatric Clinic University Hospital Olomouc Olomouc
Czechia Clinic of Paediatric haematology and oncology University Hospital Motol Prague
France Paediatric Oncology Unit, Hopital Cote De Nacre Caen
France Practicen Hospitalier , Institute d'Hematologie et Oncologie Pediatrique Lyon
France Centre Hospitalier Lyon Sud - service Hématologie Pierre Benite
France Hopitaux de Brabois Vandoeuvre Les Nancy
Germany Klinikum Chemnitz GmbH, Klinik für Kinder-und Jugendmedizin Chemnitz
Germany Zentrum für Kinder- und Jugendmedizin Klinik II / III Frankfurt
Greece "Agia Sophia" Children's Hospital Athens
Italy Dipartimento di Biomedicina dell'Eta Evolutiva. University of Bari Bari
Italy Servico de Oncoematologia Peditrica Cagliari
Italy UO Oncoematologia AOU Meyer Florence
Italy Pediatric Hamatology Unit. Department of Hematology and Oncology. G Gaslini Children's hospital. Largo Genova
Italy Chairmen of Pediatric Hamatooncology Outpatient Clinic. Hospital San Gerardo Monza
Italy Department of Oncology, Pausilipon Hospital, AORN Santobono Napoli
Italy Azienda Ospedaliera di Padova Padova
Italy Department of Cellular Biotechnologies and Hematology. Sapienza University Rome
Italy Ospedale Casa Sollievo della Sofferenza San Giovanni
Italy Hamatology Unit. Paediatric Department. University of Torino Torino
Spain Hospital Universitario Mutua de Terrassa Barcelona
Spain Jefe de Servicio Oncología Y Hematología Pediátricas Barcelona
Spain Sección de Hematología Pediátrica. Hospital de la Santa Creu i Sant Pau Barcelona
Spain Servicio de Hematología Clínica, Hospital Sant Joan de Déu Barcelona Barcelona
Spain Department Haematology, Hospital Ramon y Caja Madrid
Spain Servicio de Transfusión, Hospital Universitario Niño Jesús Madrid
Spain Hospital Universitario Virgen de la Arrixac Murcia
Spain Complexo Hospitalario Universitario, Santiago Santiago de Compostela
Switzerland Leitender Arzt, Pädiatrische Hämatologie/Onkologie Kinderspital Luzern
United Kingdom St James University Hospital Leeds
United Kingdom Royal Manchester Childrens Hospital, Manchester
United Kingdom Children's Clinic, Royal Berkshire Hospital Reading
United Kingdom Sheffield Childrens Hospital Sheffield

Sponsors (1)

Lead Sponsor Collaborator
Shire

Countries where clinical trial is conducted

Czechia,  France,  Germany,  Greece,  Italy,  Spain,  Switzerland,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Treatment effects on platelet count in children ages 6-17 years inclusive. 60 months
Secondary Drug utilization of cytoreductive therapy in children ages 6-17 years inclusive 60 months
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