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Trial record 3 of 21 for:    BGB-3111

Study of Zanubrutinib (BGB-3111) in Patients With Marginal Zone Lymphoma

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ClinicalTrials.gov Identifier: NCT03846427
Recruitment Status : Recruiting
First Posted : February 19, 2019
Last Update Posted : June 11, 2019
Sponsor:
Information provided by (Responsible Party):
BeiGene

Brief Summary:
This is a single arm study to evaluate the efficacy, safety and tolerability of zanubrutinib (BGB-3111) in patients with relapsed/refractory marginal zone lymphoma (R/R MZL).

Condition or disease Intervention/treatment Phase
Marginal Zone Lymphoma Drug: Zanubrutinib Phase 2

Detailed Description:
This is a Phase 2, open-label study of zanubrutinib in approximately 65 patients with R/R MZL. The study will evaluate efficacy, as measured by overall response rate, safety and tolerability.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 65 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 2, Open-label Study of Zanubrutinib (BGB-3111) in Patients With Relapsed or Refractory Marginal Zone Lymphoma
Actual Study Start Date : February 19, 2019
Estimated Primary Completion Date : April 1, 2021
Estimated Study Completion Date : August 1, 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Lymphoma

Arm Intervention/treatment
Experimental: Zanubrutinib Drug: Zanubrutinib
Zanubrutinib at a dose of 160 mg PO BID
Other Name: BGB-3111




Primary Outcome Measures :
  1. Overall response rate (ORR) determined by independent central review [ Time Frame: Up to 3 years ]

Secondary Outcome Measures :
  1. ORR by investigator assessment [ Time Frame: Up to 3 years ]
  2. Progression-free survival (PFS) [ Time Frame: Up to 3 years ]
  3. Overall survival (OS) [ Time Frame: Up to 3 years ]
  4. Duration of response (DOR) [ Time Frame: Up to 3 years ]
  5. Time to response (TTR) [ Time Frame: Up to 3 years ]
  6. Patient-reported outcomes (PROs) as measured by the EQ-5D-5L questionnaire [ Time Frame: Up to 3 years ]
  7. PROs as measured by the EORTC QLQ-C30 questionnaire [ Time Frame: Up to 3 years ]
  8. Occurrence and severity of treatment-emergent adverse events (safety and tolerability) [ Time Frame: Up to 3 years ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Age 18 years or older
  2. Histologically confirmed diagnosis of MZL including splenic, nodal, and extranodal subtypes
  3. Previously received one or more lines of therapy including at least one CD20-directed regimen (either as monotherapy or as chemoimmunotherapy) with documented failure to achieve at least PR or documented PD after, the most recent systemic treatment
  4. Current need for systemic therapy for MZL
  5. Measurable disease by CT or MRI
  6. ECOG of 0-2
  7. Life expectancy ≥ 6 months
  8. Adequate bone marrow function
  9. Adequate organ function
  10. Male and female patients must use highly effective methods of contraception

Exclusion Criteria:

  1. Known transformation to aggressive lymphoma, eg, large cell lymphoma.
  2. Clinically significant cardiovascular disease
  3. Prior malignancy within the past 2 years, except for curatively treated basal or squamous cell skin cancer, superficial bladder cancer, carcinoma in situ of the cervix or breast, or localized Gleason score 6 prostate cancer
  4. History of severe bleeding disorder such as hemophilia A, hemophilia B, von Willebrand disease, or history of spontaneous bleeding requiring blood transfusion or other medical intervention
  5. History of stroke or intracranial hemorrhage
  6. Severe or debilitating pulmonary disease
  7. Active fungal, bacterial and/or viral infection requiring systemic therapy
  8. Known central nervous system involvement by lymphoma
  9. Known infection with HIV, or serologic status reflecting active viral hepatitis B (HBV) or viral hepatitis C (HCV) infection
  10. Major surgery within 4 weeks of the first dose of study drug
  11. Prior treatment with a BTK inhibitor
  12. Pregnant or lactating women
  13. Requires ongoing treatment with a strong CYP3A inhibitor or inducer
  14. Concurrent participation in another therapeutic clinical trial

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03846427


Contacts
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Contact: William Reed, MD 1-877-828-5568 clinicaltrials@beigene.com
Contact: Melannie Co, MD 1-877-828-5568 clinicaltrials@beigene.com

Locations
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United States, New York
Clinical Research Alliance Recruiting
Lake Success, New York, United States, 11042
Principal Investigator: Morton Coleman         
United States, North Carolina
Levine Cancer Institute - Carolinas Medical Center Recruiting
Charlotte, North Carolina, United States, 28204
Principal Investigator: Bei Hu, MD         
Australia, New South Wales
Concord Repatriation General Hospital Recruiting
Concord, New South Wales, Australia
Principal Investigator: Judith Trotman         
St George Hospital Recruiting
Kogarah, New South Wales, Australia
Principal Investigator: Shir-Jing Ho         
Australia, Queensland
Princess Alexandra Hospital (AUS) Recruiting
Woolloongabba, Queensland, Australia
Principal Investigator: Sally Mapp, MD         
Australia, South Australia
Flinders Medical Centre Recruiting
Bedford Park, South Australia, Australia, 5042
Principal Investigator: Magdalena Sobieraj-Teague         
Australia, Victoria
Box Hill Hospital (AUS) Recruiting
Box Hill, Victoria, Australia
Principal Investigator: Eliza Hawkes, MD         
Peninsula Private Hospital Recruiting
Frankston, Victoria, Australia
Principal Investigator: Patricia Walker         
Australia
Peter MacCallum Cancer Centre Not yet recruiting
Melbourne, Australia
Principal Investigator: Constantine Tam, MD         
Royal Perth Hospital Not yet recruiting
Perth, Australia
Principal Investigator: Michael Leahy, MD         
China, Henan
Henan Cancer Hospital Recruiting
Zhengzhou, Henan, China
Principal Investigator: Keshu Zhou, MD         
China, Zhejiang
The First Affiliated Hospital, College of Medicine, Zhejiang University Recruiting
Hangzhou, Zhejiang, China
Principal Investigator: Jie Jin, MD         
China
Peking University Third Hospital Recruiting
Beijing, China
Principal Investigator: Xiaoyan Ke, MD         
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences Recruiting
Tianjin, China
Principal Investigator: Junyuan Qi, MD         
Institute of Hematology and Hospital of Blood Disease Recruiting
Tianjin, China
Principal Investigator: Junyuan Qi         
New Zealand
Auckland City Hospital Recruiting
Auckland, New Zealand
Principal Investigator: Peter Browett, MD         
North Shore Hospital (NZ) Recruiting
Auckland, New Zealand
Principal Investigator: David Simpson, MD         
Sponsors and Collaborators
BeiGene

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Responsible Party: BeiGene
ClinicalTrials.gov Identifier: NCT03846427     History of Changes
Other Study ID Numbers: BGB-3111-214 (MAGNOLIA)
First Posted: February 19, 2019    Key Record Dates
Last Update Posted: June 11, 2019
Last Verified: June 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by BeiGene:
BGB-3111
Zanubrutinib

Additional relevant MeSH terms:
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Lymphoma
Lymphoma, B-Cell, Marginal Zone
Neoplasms by Histologic Type
Neoplasms
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Lymphoma, B-Cell
Lymphoma, Non-Hodgkin
Zanubrutinib
Antineoplastic Agents
Protein Kinase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action