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Spots Global Cancer Trial Database for Ofatumumab and Bendamustine Followed by Maintenance Ofatumumab for Rituximab Relapsed Indolent B-cell Non-Hodgkin's Lymphoma (B-NHL)

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Trial Identification

Brief Title: Ofatumumab and Bendamustine Followed by Maintenance Ofatumumab for Rituximab Relapsed Indolent B-cell Non-Hodgkin's Lymphoma (B-NHL)

Official Title: A Phase II Open-Label Study of Ofatumumab and Bendamustine Followed by Maintenance Ofatumumab for Indolent B-cell Non-Hodgkin's Lymphoma (B-NHL) Which Has Relapsed After Rituximab or a Rituximab Containing Therapy

Study ID: NCT01294579

Study Description

Brief Summary: The purpose of this phase II open label study was is to evaluate the safety and efficacy of ofatumumab and bendamustine followed by maintenance ofatumumab in subjects with indolent B-NHL who had relapsed after Rituximab treatment. A maximum of 53 subjects at least 18 years old with Small lymphocytic, lymphoplasmacytic, marginal zone lymphoma, or follicular lymphoma; Grades 1, 2 and 3a, would have been enrolled (34 in Stage 1 and 19 in Stage 2). Subjects should have had Rituximab-sensitive disease, defined as a Partial Remission (PR) or Complete Remission (CR) to the last rituximab-containing therapy lasting at least 6 months following completion of therapy or subjects should have relapsed or have had disease progression following response to prior rituximab-based therapy a Eastern Cooperative Oncology Group (ECOG) Performance status of 0 1 or 2. During the induction phase, ofatumumab 1000 mg IV on day 1 of each cycle (cycles 1-6) were followed by Bendamustine 90 mg/m2 IV on days 1, 2 of each cycle (cycles 1-6).During the maintenance phase, subjects with a PR or CR after the induction phase received ofatumumab 1000 mg IV every 2 months for 2 years.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Novartis Investigative Site, Chandler, Arizona, United States

Novartis Investigative Site, Burbank, California, United States

Novartis Investigative Site, Fresno, California, United States

Novartis Investigative Site, Oxnard, California, United States

Novartis Investigative Site, Aurora, Colorado, United States

Novartis Investigative Site, Orange Park, Florida, United States

Novartis Investigative Site, Burlington, Massachusetts, United States

Novartis Investigative Site, Omaha, Nebraska, United States

Novartis Investigative Site, Las Vegas, Nevada, United States

Novartis Investigative Site, Cary, North Carolina, United States

Novartis Investigative Site, Charlotte, North Carolina, United States

Novartis Investigative Site, Raleigh, North Carolina, United States

Novartis Investigative Site, Kettering, Ohio, United States

Novartis Investigative Site, Eugene, Oregon, United States

Novartis Investigative Site, Charleston, South Carolina, United States

Novartis Investigative Site, Greenville, South Carolina, United States

Novartis Investigative Site, San Antonio, Texas, United States

Novartis Investigative Site, Sherman, Texas, United States

Novartis Investigative Site, Tyler, Texas, United States

Novartis Investigative Site, Waco, Texas, United States

Novartis Investigative Site, Vancouver, Washington, United States

Novartis Investigative Site, Yakima, Washington, United States

Contact Details

Name: Novartis Pharmaceuticals

Affiliation: Novartis Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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