A Study of PCI-32765 (Ibrutinib) in Patients With Refractory Follicular Lymphoma - Full Text View

Purpose

The purpose of this study is to evaluate the efficacy and safety of PCI-32765 (ibrutinib) administered to patients with chemoimmunotherapy-resistant follicular lymphoma (FL).

Condition	Intervention	Phase
Lymphoma	Drug: PCI-32765 (Ibrutinib)	Phase 2

Study Type:	Interventional
Study Design:	Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment
Official Title:	An Open-label, Multicenter, Single-arm, Phase 2 Study of PCI-32765 (Ibrutinib) in Subjects With Refractory Follicular Lymphoma

Resource links provided by NLM:

MedlinePlus related topics: Lymphoma

U.S. FDA Resources

Further study details as provided by Janssen Research & Development, LLC:

Primary Outcome Measures:

Overall response rate [ Time Frame: Up to 2 years after the last patient is enrolled ] [ Designated as safety issue: No ]

Secondary Outcome Measures:

Duration of response [ Time Frame: Every 12 weeks during the first 24 months, followed by every 24 weeks thereafter until disease progression (up to 2 years after the last patient is enrolled) ] [ Designated as safety issue: No ]
Progression-free survival [ Time Frame: Up to progressive disease, death, lost to follow-up, withdrawal of consent, or study end (up to 2 years after the last patient is enrolled) ] [ Designated as safety issue: No ]
Overall survival [ Time Frame: Up to death, lost to follow-up, withdrawal of consent, or study end (up to 2 years after the last patient is enrolled) ] [ Designated as safety issue: No ]
Time to response [ Time Frame: Every 12 weeks during the first 24 months, followed by every 24 weeks thereafter until disease progression (up to 2 years after the last patient is enrolled) ] [ Designated as safety issue: No ]
Number of patients experiencing resolution of lymphoma-related B symptoms [ Time Frame: Day 1 of every cycle during the first 12 months, thereafter every other cycle (up to 2 years after the last patient is enrolled) ] [ Designated as safety issue: No ]
Number of patients identified with blood biomarkers that alter B-cell receptor signaling or activate alternative signaling pathways [ Time Frame: Day 1 of Cycles 1-3, and time of disease progression, or at end-of treatment visit for patients who discontinue treatment without disease progression ] [ Designated as safety issue: No ]
Minimum plasma concentration of PCI-32765 [ Time Frame: Pre-dose Day 1 of Cycles 1-3, post-dose Day 1 of Cycles 1, 2 at 1, 2, and 4 hours ] [ Designated as safety issue: No ]
Oral plasma clearance of PCI-32765 [ Time Frame: Pre-dose Day 1 of Cycles 1-3, post-dose Day 1 of Cycles 1, 2 at 1, 2, and 4 hours ] [ Designated as safety issue: No ]
Oral volume of distribution at steady state of PCI-32765 [ Time Frame: Pre-dose Day 1 of Cycles 1-3, post-dose Day 1 of Cycles 1, 2 at 1, 2, and 4 hours ] [ Designated as safety issue: No ]
Area under the plasma-concentration time curve of PCI-32765 [ Time Frame: Pre-dose Day 1 of Cycles 1-3, post-dose Day 1 of Cycles 1, 2 at 1, 2, and 4 hours ] [ Designated as safety issue: No ]
Number of participants affected by an adverse event [ Time Frame: Up to 30 days after the last dose of study medication ] [ Designated as safety issue: Yes ]

Estimated Enrollment:	110
Study Start Date:	April 2013
Estimated Study Completion Date:	September 2016
Estimated Primary Completion Date:	September 2016 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
Experimental: PCI-32765 (Ibrutinib)	Drug: PCI-32765 (Ibrutinib) 560 mg capsules administered orally once daily, continuously on a 21-day cycle

Detailed Description:

This is an open-label (identity of assigned study drug will be known) study of PCI-32765 (ibrutinib) in approximately 110 patients with chemoimmunotherapy-resistant FL whose disease has relapsed from at least 2 prior lines of therapy, including at least 1 rituximab combination chemotherapy regimen. Each patient must have resistant disease to the last therapy (defined as progression of disease during or within 12 months of the last dose of a CD20 antibody combination chemotherapy regimen). The study will include the following phases: screening (up to 30 days prior to the first dose of study drug), treatment (until disease progression or unacceptable toxicity), and posttreatment follow-up (until death, lost to follow up, withdrawal of consent, or study end [defined as 2 years after the last patient is enrolled]). Patients will receive 560 mg of PCI-32765 by mouth once daily on a 21-day cycle. Treatment will be continuous (without interruption) and self-administered at home. The treatment phase will extend from administration of the first dose of study medication until disease progression or unacceptable toxicity. Posttreatment follow-up will extend from the end of treatment until death, lost to follow up, withdrawal of consent, or study end. Every patient, except for those who explicitly withdraw consent from further site contact, will be followed for survival status until the study ends. In addition, data on subsequent antineoplastic therapy will also be collected. Serial pharmacokinetic samples will be collected and efficacy and safety will be monitored throughout the study.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Histologic proof of Grade 1, 2, or 3a follicular lymphoma (FL) without clinical or pathological evidence of transformation
Previously treated with at least 2 prior lines of therapy, including at least 1 rituximab combination chemotherapy regimen; last prior line of therapy includes an anti CD20 monoclonal antibody-containing chemotherapy regimen (separate lines of therapy are defined as different regimens that are either separated by disease progression, refractory disease, or relapsed disease)
Resistant disease to the last therapy, defined as progression of disease during or within 12 months of the last dose of a CD20 antibody combination chemotherapy regimen
At least 1 measurable site of disease according to International Working Group Revised Response Criteria for Malignant Lymphoma
Eastern Cooperative Oncology Group performance status grade 0 or 1
Hematology and biochemical laboratory values must be within protocol-defined parameters within 7 days prior to enrollment
Agrees to protocol-defined use of effective contraception
Women of childbearing potential must have a negative serum or urine pregnancy test at screening

Exclusion Criteria:

Prior nitrosoureas within 6 weeks, chemotherapy within 3 weeks, therapeutic anticancer antibodies within 4 weeks, radio- or toxin-immunoconjugates within 10 weeks, radiation therapy or other investigational agents within 3 weeks, or major surgery within 4 weeks of first dose of study drug
Prior treatment with PCI-32765, other Bruton's tyrosine kinase inhibitors, or phosphoinositide 3-kinase delta inhibitors
Concurrent enrollment in another therapeutic investigational clinical treatment study
Received a prior allogeneic hematopoietic stem cell transplant (prior autologous hematopoietic stem cell transplant is allowed)
Known central nervous system lymphoma
History of prior malignancy (except malignancy treated with curative intent and with no known active disease present for >=3 years before enrollment, adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease, or adequately treated cervical carcinoma in situ without evidence of disease)
History of stroke or intracranial hemorrhage within 6 months prior to enrollment
Requires anticoagulation with warfarin or equivalent vitamin K antagonists
Requires treatment with strong cytochrome P450 (CYP)3A4/5 inhibitors
Clinically significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, congestive heart failure, or myocardial infarction within 6 months of screening, or any Class 3 (moderate) or Class 4 (severe) cardiac disease as defined by the New York Heart Association Functional Classification
Known history of Human Immunodeficiency Virus (HIV) or Hepatitis C or active infection with Hepatitis B or any uncontrolled active systemic infection requiring intravenous antibiotics
Women who are pregnant or breastfeeding
Any life-threatening illness, medical condition, or organ system dysfunction which, in the investigator's opinion, could compromise the patient's safety, interfere with the absorption or metabolism of PCI-32765 capsules, or put the study outcomes at undue risk

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT01779791

Contacts

Contact: Use link at the bottom of the page to see if you qualify for an enrolling site (see list). If you still have questions:

JNJ.CT@sylogent.com

Show 51 Study Locations

Sponsors and Collaborators

Janssen Research & Development, LLC

Pharmacyclics

Investigators

Study Director:

Janssen Research & Development, LLC Clinical Trial

Janssen Research & Development, LLC

More Information

Additional Information:

To learn how to participate in this trial please click here. This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party:	Janssen Research & Development, LLC
ClinicalTrials.gov Identifier:	NCT01779791 History of Changes
Other Study ID Numbers:	CR100956, 2012-004097-26, PCI-32765FLR2002
Study First Received:	January 25, 2013
Last Updated:	May 13, 2013
Health Authority:	Australia: Department of Health and Ageing Therapeutic Goods Administration United States: Food and Drug Administration Germany: Ethics Commission

Keywords provided by Janssen Research & Development, LLC:

Lymphoma
Refractory follicular lymphoma
Chemoimmunotherapy-resistant follicular lymphoma
PCI-32765
Ibrutinib

Additional relevant MeSH terms:

Lymphoma
Lymphoma, Follicular
Neoplasms by Histologic Type
Neoplasms
Lymphoproliferative Disorders

Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Lymphoma, Non-Hodgkin

ClinicalTrials.gov processed this record on May 21, 2013