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Search / Trial NCT02348216

Study Evaluating the Safety and Efficacy of KTE-C19 in Adult Participants With Refractory Aggressive Non-Hodgkin Lymphoma

Launched by KITE, A GILEAD COMPANY · Jan 27, 2015

Trial Information

Current as of May 07, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Key Inclusion Criteria
  • 1. Histologically confirmed:
  • Diffuse Large B Cell Lymphoma (DLBCL)
  • Primary Mediastinal Large B Cell Lymphoma (PMBCL)
  • Transformation Follicular Lymphoma (TFL)
  • High grade B-cell lymphoma (HGBCL)
  • 2. Chemotherapy-refractory disease, defined as one of more of the following:
  • No response to last line of therapy i. Progressive disease (PD) as best response to most recent therapy regimen ii. Stable disease (SD) as best response to most recent therapy with duration no longer than 6 month from last dose of therapy OR
  • Refractory post-autologous stem cell transplant (ASCT) i. Disease progression or relapsed less than or equal to 12 months of ASCT (must have biopsy proven recurrence in relapsed individuals) ii. If salvage therapy is given post-ASCT, the individual must have had no response to or relapsed after the last line of therapy
  • 3. Individuals must have received adequate prior therapy including at a minimum:
  • Anti-cluster of differentiate 20 (CD20) monoclonal antibody unless investigator determines that tumor is CD20-negative and
  • an anthracycline containing chemotherapy regimen
  • for individual with transformed FL must have chemorefractory disease after transformation to DLBCL.
  • 4. At least one measurable lesion per revised international working group (IWG Response Criteria
  • 5. Eastern cooperative oncology group (ECOG) performance status of 0 or 1
  • 6. Absolute neutrophil count (ANC) ≥ 1000/microliters (uL)
  • 7. Absolute lymphocyte count ≥ 100/uL
  • 8. Platelet count ≥ 75,000/uL
  • 9. Adequate renal, hepatic, pulmonary and cardiac function defined as:
  • Creatinine clearance (as estimated by Cockcroft Gault) \> 60 mL/min
  • Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) \< 2.5 upper limit of normal (ULN)
  • Total bilirubin \< 1.5 mg/dL, except in individuals with Gilbert's syndrome
  • Cardiac ejection fraction \>50%, no evidence of pericardial effusion as determined by an echocardiogram (ECHO), and no clinically significant pleural effusion
  • Baseline oxygen saturation \>92% on room air
  • 10. All individuals or legally appointed representatives/caregivers, must personally sign and date the Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved consent form before initiating any study specific procedures or activities.
  • 11. Relapsed or refractory large B-cell lymphoma including DLBCL, PMBCL, TFL, and HGBCL after two systemic lines of therapy
  • Key Exclusion Criteria
  • 1. History of malignancy other than nonmelanoma skin cancer or carcinoma in situ (e.g. cervix, bladder, breast) or follicular lymphoma unless disease free for at least 3 years
  • 2. History of allogeneic stem cell transplantation
  • 3. Prior chimeric antigen receptor (CAR) therapy or other genetically modified T cell therapy
  • 4. Presence of fungal, bacterial, viral, or other infection that is uncontrolled or requiring intravenous (IV) antimicrobials for management. Simple urinary tract infection (UTI) and uncomplicated bacterial pharyngitis are permitted if responding to active treatment
  • 5. History of human immunodeficiency virus (HIV) infection or acute or chronic active hepatitis B or C infection. Individuals with history of hepatitis infection must have cleared their infection as determined by standard serological and genetic testing per current Infectious Diseases Society of America (IDSA) guidelines
  • 6. Individuals with detectable cerebrospinal fluid malignant cells, or brain metastases, or with a history of central nervous system (CNS) lymphoma or primary CNS lymphoma, cerebrospinal fluid malignant cells or brain metastases
  • 7. History or presence of CNS disorder such as seizure disorder, cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease, or any autoimmune disease with CNS involvement
  • Note: Other protocol defined Inclusion/Exclusion criteria may apply.

About Kite, A Gilead Company

Kite, a Gilead Company, is a leading biopharmaceutical organization focused on innovative cell therapy solutions for cancer treatment. With a commitment to advancing the field of oncology, Kite specializes in developing groundbreaking therapies, particularly in the area of chimeric antigen receptor T-cell (CAR T) therapy. Leveraging Gilead's extensive expertise and resources, Kite aims to transform the lives of patients with hematologic malignancies and solid tumors through rigorous research, clinical trials, and a patient-centric approach. The company's dedication to scientific excellence and collaboration positions it at the forefront of the fight against cancer.

Locations

Rochester, Minnesota, United States

Palo Alto, California, United States

Nashville, Tennessee, United States

Bronx, New York, United States

Iowa City, Iowa, United States

Saint Louis, Missouri, United States

Maywood, Illinois, United States

Hackensack, New Jersey, United States

Groningen, , Netherlands

Utrecht, , Netherlands

Boston, Massachusetts, United States

Vancouver, British Columbia, Canada

Tampa, Florida, United States

Rochester, New York, United States

Miami, Florida, United States

Omaha, Nebraska, United States

Amsterdam, , Netherlands

Detroit, Michigan, United States

Tel Aviv, , Israel

Rotterdam, , Netherlands

Paris, , France

Rennes, , France

Cleveland, Ohio, United States

Dresden, , Germany

Gilbert, Arizona, United States

Duarte, California, United States

Santa Monica, California, United States

La Jolla, California, United States

Denver, Colorado, United States

Nashville, Tennessee, United States

Houston, Texas, United States

San Antonio, Texas, United States

Toronto, Ontario, Canada

Pessac, , France

Essen, , Germany

Würzburg, , Germany

Patients applied

0 patients applied

Trial Officials

Kite Study Director

Study Director

Kite, A Gilead Company

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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