Status:
TERMINATED
A Phase 2 Study of Velcade™ in Subjects With Relapsed or Refractory Follicular B-Cell Lymphoma
Lead Sponsor:
Lymphoma Study Association
Collaborating Sponsors:
Janssen-Cilag International NV
Conditions:
Follicular Lymphoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This is a prospective, randomized, sequential, international, multicentric, 2-arm, non-comparative, open-label, 2-stage clinical study to determine disease response rates to Velcade™ therapy in subjec...
Detailed Description
This is a prospective, randomized, sequential, international, multicentric, 2-arm, non-comparative, open-label, 2-stage clinical study to determine disease response rates therapy of Velcade™ in subjec...
Eligibility Criteria
Inclusion
- Male or female subject 18 years or older.
- Initial diagnosis of follicular B-cell lymphoma (CD20+) (grades 1, 2, and 3 based on the World Health Organization 1997 classification), in first or subsequent relapse or progression after prior anti-neoplastic treatment including previous rituximab treatment. Relapse or progression since previous anti-neoplastic therapy must be documented by new lesions or objective evidence of progression of existing lesions.
- At least 1 measurable lymph node mass that is \>1.5 cm in 2 perpendicular dimensions, and has not been previously irradiated or has grown since previous irradiation.
- No active central nervous system (CNS) lymphoma
- Karnofsky Performance Status (KPS) \>50% (Eastern Cooperative Oncology Group \[ECOG\] 0-2)
- The following laboratory values at screening, unless abnormalities are related to the lymphoma:
- Absolute neutrophil count (ANC) \>1000 cells/dL;
- Platelets \>50,000 cells/dL;
- Aspartate transaminase (AST) \<3 x upper limit of normal (ULN);
- Alanine transaminase (ALT) \<3 x ULN;
- Total bilirubin \<2 x ULN;
- Creatinine level \<150 µmol/L
- Toxic effects of previous therapy or surgery resolved to Grade 2 or better.
- Female subject is either post-menopausal or surgically sterilized or willing to use an acceptable method of birth control (i.e., a hormonal contraceptive, intra-uterine device, diaphragm with spermicide, condom with spermicide, or abstinence) for the duration of the study. Women are neither breast feeding nor pregnant for the duration of the study. Confirmation that the subject is not pregnant must be established by a negative serum beta-human chorionic gonadotropin pregnancy test result obtained during screening. Pregnancy testing is not required for post-menopausal or surgically sterilized women. Male subject agrees to use an acceptable method of contraception for the duration of the study.
- Voluntary signed informed consent before performance of any study-related procedure not part of normal medical care.
- Patient with minimum life expectancy of 3 months.
Exclusion
- Any other type of lymphoma.
- Previous treatment with Velcade™.
- Anti-neoplastic or experimental or radiation therapy within 3 weeks before Day 1 of Cycle 1.
- Major surgery within 2 weeks before Day 1 of Cycle 1.
- Rituximab, alemtuzumab (Mabcampath®), or other unconjugated therapeutic antibody within 10 weeks before Day 1 of Cycle 1.
- Nitrosoureas within 6 weeks before Day 1 of Cycle 1.
- Radioimmunoconjugates or toxin immunoconjugates such as ibritumomab tiuxetan (Zevalin™), or tositumomab (Bexxar®) within 10 weeks before Day 1 of Cycle 1.
- Peripheral neuropathy or neuropathic pain of Grade 3 or worse.
- History of allergic reaction attributable to compounds containing boron or mannitol.
- Diagnosed or treated for a malignancy other than non-Hodgkin's lymphoma (NHL) within 5 years before Day 1 of Cycle 1, with the exception of complete resection of basal cell carcinoma, squamous cell carcinoma of the skin, or in situ malignancy.
- Active systemic infection requiring treatment.
- Previously known HIV positive serology.
- Serious medical or psychiatric illness likely to interfere with participation in this clinical study.
- Concurrent treatment with another investigational agent.
- Adult patient under guardian.
Key Trial Info
Start Date :
September 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2010
Estimated Enrollment :
87 Patients enrolled
Trial Details
Trial ID
NCT00136591
Start Date
September 1 2005
End Date
January 1 2010
Last Update
October 26 2010
Active Locations (4)
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1
Groupe d'Etude des Lymphomes de l'adulte
Mont-Godinne, Belgium
2
Service d'Hématologie - Centre Hospitalier Lyon-Sud
Pierre-Bénite, France, 69495
3
Centre Henri Becquerel
Rouen, France, 76038
4
Institut Gustave Roussy
Villejuif, France