Non Hodgkin Lymphoma Clinical Trial
Study of TRM-1 (TRAIL-R1 Monoclonal Antibody) in Subjects With Relapsed or Refractory Non-Hodgkin’s Lymphoma (NHL)
Summary
The purpose of this study is to evaluate the safety, efficacy and exposure to TRM-1 in subjects with relapsed or refractory Non-Hodgkin's Lymphoma (NHL).
Eligibility Criteria
Primary Inclusion Criteria:
Relapsed or refractory histologically confirmed Non-Hodgkin's Lymphoma
Previously treated with at least 1 therapeutic regimen and relapsed or progressed or failed to achieve a response after the last regimen
18 years of age or older
Primary Exclusion Criteria:
Received a non-FDA approved investigational agent within the last 4 weeks
Received cancer therapies (chemotherapy, biological therapy [including hormonotherapy], radiation therapy or immunosuppressants within the last 3 weeks, 8 weeks for monoclonal antibodies, radioimmunotherapy or nitrosourea
Eligible for a hematopoietic stem cell transplant (HSCT) or have had an autologous HSCT within the last 16 weeks
Prior history of an allogeneic HSCT
HIV, AIDS-related lymphoma, central nervous system (CNS) lymphoma, Hepatitis-B or Hepatitis-C
Infection requiring antibiotics within the last 4 weeks
Major surgery within the last 4 weeks
Pregnant or breast-feeding women
History of other cancers within the past 5 years
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There are 7 Locations for this study
Rochester Minnesota, 55905, United States
Omaha Nebraska, 68198, United States
Buffalo New York, 14263, United States
New York New York, 10021, United States
Philadelphia Pennsylvania, 19111, United States
Nashville Tennessee, 37203, United States
Houston Texas, 77230, United States
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