Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00430365
Other study ID # 0400401
Secondary ID French PHRC
Status Completed
Phase Phase 3
First received
Last updated
Start date June 2006
Est. completion date September 2018

Study information

Verified date April 2019
Source University Hospital, Toulouse
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Maintenance treatment of myeloma.


Recruitment information / eligibility

Status Completed
Enrollment 614
Est. completion date September 2018
Est. primary completion date September 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- No signs of progression after transplant

- Effective contraception if necessary (oral contraception for females and barrier methods of contraception for sexually active males)

- No active severe infection

- Satisfactory restoration of the haematological parameters defined by: PN >1,000/mm3 and Platelets > 75,000/mm3

- Bilirubin < 35 umol/l and GOT/GPT/PAL<3N

- Creatinine < 160 umol/l.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
lenalidomide
oral drug
placebo
oral placebo

Locations

Country Name City State
Belgium Algemeen Centrumziekenhuis Antwerpen Antwerpen
Belgium UZA Antwerpen Antwerpen
Belgium ZNA Middelheim Antwerpen
Belgium Hôpital Saint Joseph Arlon
Belgium Institut Jules Bordet Bruxelles
Belgium UCL St Luc Bruxelles
Belgium Hôpital Saint Joseph Gilly
Belgium Hôpital Jolimont Haine Saint Paul
Belgium Heilig Hart Ziekenhuis Roeselare
Belgium UCL Mont-Godinne Yvoir
France CH Aix-en-Provence
France CHRU Amiens
France CHRU Hôpital du Bocage Angers
France Centre hospitalier Argenteuil Victor Dupouy Argenteuil
France Centre hospitalier Duffaut Avignon
France Centre hospitalier de la côte basque Bayonne
France Hôpital Jean Minjoz Besançon
France CH Blois
France Hôpital Avicenne Bobigny
France CHRU Hôpital haut Lévêque Bordeaux
France Polyclinique Bordeaux Nord Aquitaine Bordeaux
France Hôpial Morvan Brest
France Centre Baclesse Caen
France Polyclinique du Parc Caen
France CH William Morey Châlon-sur-Saône
France CH Chartres
France Hôpital Antoine Béclère Clamart
France Hôpital d'instruction des Armées Percy Clamart
France CHRU Hôtel Dieu Clermont Ferrand
France CH Louis Pasteur Colmar
France CHU Henri Mondor Créteil
France CHRU Dijon Dijon
France Centre hospitalier général Dunkerque
France CHRU Hôpital Michallon Grenoble
France Centre hospitalier départemental La Roche sur Yon
France CH Le Mans
France CHRU Hôpital Claude Huriez Lille
France Centre hospitalier Bodelio Lorient
France Centre Léon Bérard Lyon
France CHU Hôpital Edouard Herriot Lyon
France Hôpital Nord Marseille
France Institut Paoli Calmette Marseille
France Hôpital Notre Dame de Bon Secours Metz
France CHRU Hôpitaux de Brabois Nancy
France CHRU Hôtel Dieu Nantes
France Centre Antoine Lacassagne Nice
France Hôpital Archet Nice
France Hôpital de l'Archet Nice
France CHU Hôpital St Antoine Paris
France Hôpital Cochin Paris
France Hôtel Dieu Paris
France Centre hospitalier Lyon Sud Pierre Bénite
France CHRU Hôpital Jean Bernard Poitiers
France Centre hospitalier de la région d'Annecy Pringy
France Hôpital Debré Reims
France CHRU Hôpital de Pontchaillou Rennes
France CHRU Hôpital Sud Rennes
France Centre hospitalier de Roanne Roanne
France Centre Henri Becquerel Rouen
France Centre hospitalier de la Réunion Saint-Denis
France Centre hospitalier Yves Le Foll St Brieuc
France Institut de Cancérologie de la Loire St-Priest-en-Jarez
France CHRU Hôpital de Hautepierre Strasbourg
France CHU Toulouse Purpan Toulouse
France CHU Toulouse Rangueil Toulouse
France CHRU Hôpital Bretonneau Tours
France Centre hospitalier Troyes
France CH Chubert Vannes
Switzerland Center of Oncology/Hematology and transfusion Medicine, Kantonsspital Aarau
Switzerland Universitäts Spital Basel
Switzerland Istituto Oncologico Sviss. Italiana IOSI Ospedale Regionale Bellinzona e Valli Bellinzona
Switzerland Inselspital Bern
Switzerland Hôpital cantonal Genêve
Switzerland CHUV Lausanne
Switzerland Onkologie/Hämatologie Kantonsspital st Gallen St Gallen
Switzerland Spital Thun-Simmental Onkologiezentrum Thun
Switzerland Institute of Oncology and Hematology Stadtspital Triemli Zürich

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Toulouse Celgene, Intergroupe Francophone du Myelome

Countries where clinical trial is conducted

Belgium,  France,  Switzerland, 

References & Publications (1)

Combination chemotherapy versus melphalan plus prednisone as treatment for multiple myeloma: an overview of 6,633 patients from 27 randomized trials. Myeloma Trialists' Collaborative Group. J Clin Oncol. 1998 Dec;16(12):3832-42. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Determine the efficacy of Revlimid® at prolonging the duration of the post-transplant response. 2 years
Secondary Assess the impact of Revlimid® on the post-transplant complete response rate 2 years
Secondary Compare survival without events and overall survival of patients in the lenalidomide arm with the control 2 years
Secondary Evaluate the long-term tolerance of Revlimid® in post-transplant maintenance therapy. 3 years
See also
  Status Clinical Trial Phase
Recruiting NCT03832127 - Evaluation of PET 18F-Fludarabine for the Initial Assessment and End-treatment of Symptomatic Multiple Myeloma Patients Phase 1
Completed NCT01413178 - A Randomized Trial to Compare Busulfan + Melphalan 140 mg/m2 With Melphalan 200 mg/m2 as Preparative Regimen for Autologous Hematopoietic Stem Cell Transplantation for Multiple Myeloma Phase 3
Recruiting NCT03641456 - VRD as Induction Followed by VR Maintenance in Patients With Newly Diagnosed High Risk Multiple Myeloma Phase 2
Terminated NCT02907073 - Positron Emission Tomography (PET) Imaging Studies With NIS Reporter Phase 1/Phase 2
Completed NCT03135925 - Feasibility of Pre Transplant Exercise (Pre-habilitation) for Multiple Myeloma Patients Awaiting Autologous Stem Cell Transplantation N/A
Withdrawn NCT02114502 - Carfilzomib/SAHA Combined With High-Dose Gemcitabine/Busulfan/Melphalan With Autologous Stem Cell Transplant in Myeloma Phase 2
Completed NCT00794261 - Stem Cell Mobilization With Pegfilgrastim in Lymphoma and Myeloma Phase 2
Completed NCT01700608 - Prospective Observational Study on Plerixafor After Chemotherapy N/A
Completed NCT00800839 - Busulfan and Fludarabine Followed by Post-transplant Cyclophosphamide Phase 2
Completed NCT00606437 - Total Body Irradiation With Fludarabine Followed by Combined Umbilical Cord Blood (UCB) Transplants Phase 1
Recruiting NCT05528887 - Study of CAR-T Cell Therapy in the Treatment of Relapsed/Refractory Hematological Malignancies Phase 1
Recruiting NCT05625971 - Non-invasive MRD Assessment in Multiple Myeloma
Active, not recruiting NCT02931942 - Changing Over Time of Ascorbic Acid After Chemotherapy
Active, not recruiting NCT05889221 - Multicenter Phase 2 Study of Subcutaneous Isatuximab Plus Bortezomib, Lenalidomide and Dexamethasone in the Treatment of Newly Diagnosed Transplant Ineligible Multiple Myeloma N/A
Recruiting NCT03836690 - Transfer of Effector Memory T Cells (Tem) Following Allogeneic Stem Cell Transplantation Phase 1
Active, not recruiting NCT02542657 - Ixazomib With Pomalidomide, Clarithromycin and Dexamethasone in Treating Patients With Multiple Myeloma Phase 1/Phase 2
Completed NCT01279694 - Trial of Carfilzomib Plus Melphalan and Prednisone in Elderly Untreated Patients With Multiple Myeloma (CARMYSAP) Phase 1/Phase 2
Completed NCT01191060 - Study Comparing Conventional Dose Combination RVD to High-Dose Treatment With ASCT in the Initial Myeloma up to 65 Years Phase 3
Terminated NCT00983346 - Effect of Low Dose Bortezomib on Bone Formation in Smoldering Myeloma Patients Phase 2
Completed NCT00476294 - Long-Term Follow Up Study for AMD3100 Patients N/A