Study of a new drug combination for the treatment of Non Hodgkin’s Lymphoma

Phase 1

• Conditions: Indolent B-cell Non-Hodgkin’s Lymphoma; MedDRA version: 20.0 Level: HLGT Classification code 10025320 Term: Lymphomas non-Hodgkin's B-cell System Organ Class: 10005329 - Blood and lymphatic system disorders; Therapeutic area: Diseases [C] - Cancer [C04]

• Registration Number: EUCTR2008-004177-17-AT
• Lead Sponsor: ovartis Pharma Services AG

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2010-11-25
• Last Update Posted: 28 February 2019

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: Not specified
• Target Recruitment: 346

Inclusion Criteria

Subjects eligible for enrollment in the study must meet all of the following criteria:

1. Small lymphocytic lymphoma (SLL), lymphoplasmacytic lymphoma, marginal
zone lymphoma, and follicular lymphoma; grades 1, 2 and 3A, defined
according to World Health Organization guidelines. Subjects with a diagnosis
of SLL who have a peripheral blood monoclonal B lymphocyte count of
=5,000/µL are considered to have CLL and are not eligible for this study.
• Tumor verified to be CD20+ positive from a previous or current tissue
biopsy.
•CT imaging in screening phase (based on local evaluation) showing 2 or
more clearly demarcated lesions/nodes with a long axis >1.5 cm and short
axis = 1.0 cm or 1 clearly demarcated lesion/node with a long axis >2.0 cm
and short axis =1.0 cm (Section 6.2.5 of Study Protocol). CT imaging performed at screening as baseline image.
2. Indolent B-cell NHL with failure to achieve at least a partial response lasting 6
months beyond the end of treatment with rituximab or a rituximab-containing
regimen (See Section 6.2.5.4– Section 6.2.5.5 of study protocol for details on response criteria),
i.e.:
•Stable disease (SD) after rituximab or a rituximab-containing regimen
(imaging will support this finding. NOTE: in cases of SD after rituximab
monotherapy as induction treatment, the minimum time to confirm SD
by imaging is 60 days from start of first rituximab infusion) or,
• Disease progression during or within 6 months of treatment with
rituximab or a rituximab-containing regimen. Imaging must support this
finding and will be done = 6 months after the last infusion of rituximab.
Note: Subjects must have received a minimum of 4 rituximab infusions as monotherapy or 3 infusions as part of rituximab-containing combination regimens
3. ECOG Performance Status of 0, 1, or 2
4. Age = 18 years
5. Life expectancy of at least 6 months
6. Signed written informed consent prior to performing any study-specific
procedures

French subjects: In France, a subject will be eligible for inclusion in this study only if
either affiliated to or a beneficiary of a social security category
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 137
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 130

Exclusion Criteria

Subjects meeting any of the following criteria will not be enrolled in the study:

1. Grade 3b FL or evidence that the indolent lymphoma has transformed to
aggressive lymphoma as verified by biopsy confirmation
2. Previous autologous stem cell transplant in the last 6 months or previous
allogeneic stem cell transplant at any time.
3. High dose steroids = 25 mg prednisolone/day (or equivalent) for 7 consecutive
days, given as concomitant medication, within 3 months prior to randomization.
No more than 10 mg prednisone daily at the time of randomization
4. Prior bendamustine treatment within 1 year of randomization not resulting in a
CR or PR for at least 6 months
5. Prior use of any monoclonal antibody (other than anti-CD20) within 3 months
prior to randomization
6. Known central nervous system (CNS) involvement by indolent lymphoma
7. Other past or current malignancy. Subjects who have been free of malignancy
for at least 5 years, or have a history of definitively treated non-melanoma skin
cancer, or successfully treated in situ carcinoma, are eligible*
8. Chronic or current active infectious disease requiring systemic antibiotics,
antifungal, or antiviral treatment such as, but not limited to, chronic renal
infection, chronic chest infection with bronchiectasis, tuberculosis, and active
Hepatitis C
9. Clinically significant cardiac disease as judged by the investigator including
unstable angina, acute myocardial infarction within 6 months of randomization,
congestive heart failure, and arrhythmia requiring therapy
10. History of significant cerebrovascular disease or event with significant
symptoms or sequelae
11. Significant concurrent, uncontrolled medical condition that in the opinion of the investigator or GSK medical monitor contraindicates participation this study
12. Positive serology for Hepatitis B (HB) defined as a positive test for Hepatitis B
surface antigen (HbsAg). In addition, if negative for HBsAg but Hepatits B core
antibody (HBcAb) positive (regardless of HBsAb status), a HBV DNA test will
be performed and if positive the subject will be excluded
? Consult with a physician experienced in care and management of subjects
with Hepatitis B to manage/treat subjects who are anti-HBc positive
? If HBV DNA is negative, subject may be included but must undergo HBV
DNA monitoring (see Section 6.5.7.1 of study protocol). Prophylactic antiviral therapy may be initiated at the discretion of the investigator
13. Current active liver or biliary disease (subjects with Gilbert’s syndrome or
asymptomatic gallstones, liver metastases related to indolent NHL or otherwise
stable chronic liver disease per investigator assessment, are eligible)
14. Known human immunodeficiency virus (HIV) positive
15. Screening laboratory values:
? platelets < 100 x 109/L (

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified