CompletedPhase 3NCT01191060
Study Comparing Conventional Dose Combination RVD to High-Dose Treatment With ASCT in the Initial Myeloma up to 65 Years
Studying Multiple myeloma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University Hospital, Toulouse
- Principal Investigator
- MICHEL ATTAL, MD PhDUniversity Hospital of Toulouse
- Intervention
- Lenalidomide, Bortezomib(drug)
- Enrollment
- 700 enrolled
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2010 – 2018
Study locations (30)
- CH du Pays D'Aix, Aix-en-Provence, France
- CHRU - Hôpital Sud Amiens, Amiens, France
- CHU d'Angers, Angers, France
- Centre Hospitalier Argenteuil Victor Dupouy, Argenteuil, France
- Centre Hospitalier H.Duffaut, Avignon, France
- Centre Hospitalier de la côte basque, Bayonne, France
- Hôpital Jean Minjoz, Besançon, France
- Centre Hospitalier de Blois, Blois, France
- Hôpital Avicenne, Bobigny, France
- Polyclinique Bordeaux Nord Aquitaine, Bordeaux, France
- Hôpital A.Morvan, Brest, France
- CHU Caen Côte de Nacre, Caen, France
- Centre François Baclesse, Caen, France
- CH René Dubos, Cergy-Pontoise, France
- Centre Hospitalier William Morey, Chalon-sur-Saône, France
- +15 more locations on ClinicalTrials.gov
Collaborators
Dana-Farber Cancer Institute · Celgene Corporation · Janssen-Cilag Ltd.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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