- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03280160
Protocol GELLC-7: Ibrutinib Followed by Ibrutinib Consolidation in Combination With Ofatumumab
A Multicenter, Non-randomized, Open Label Study to Evaluate the Efficacy and Security of Ibrutinib Followed by Ibrutinib Consolidation in Combination With Ofatumumab in Previously Untreated Patients With Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Multicenter, non- randomized, open-label, double agent, phase II study of the Spanish Group of CLL (GELLC).
Patients with untreated CLL/SLL. Ibrutinib will be administered orally 420 mg (3 x 140 mg capsules) once daily on a continuous schedule on an outpatient basis until disease progression or unacceptable toxicity.
After 12 cycles of ibrutinib, patients that do not achieve a complete response (CR) will be treated with the combination of ibrutinib and ofatumumab. Patients in CR after 12 cycles of ibrutinib will continue with ibrutinib alone.
Ofatumumab will be administered by IV infusion, 300mg on Day 1 and 1,000 mg on Day 8 of cycle 13, followed by 5 monthly infusions of 1,000 mg (Day 1 of subsequent 28-day cycles for cycles C14, C15, C16, C17, and C18).
A treatment cycle will be defined as lasting 28 days. Patients will be treated with ibrutinib, within the study frame, until progression, unacceptable toxicity or cycle C42 of treatment).
All patients still on study treatment at the time of cycle C42, or if the study is stopped early, will be transitioned to prescribed ibrutinib.
Study Type
Enrollment (Actual)
Phase
- Phase 2
Contacts and Locations
Study Locations
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Badalona, Spain
- Hospital de Badalona Germans Trias i Pujol
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Barcelona, Spain
- Hospital Clínic de Barcelona
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Barcelona, Spain
- Hospital de la Santa Creu i Sant Pau
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Barcelona, Spain
- Hospital Universitario Vall d'Hebrón
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Barcelona, Spain
- ICO Hospitalet - Hospital Duran i Reynals
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Córdoba, Spain
- Hospital Reina Sofía de Córdoba
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Madrid, Spain
- Fundacion Jimenez Diaz
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Madrid, Spain
- Hospital Universitario 12 de octubre
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Madrid, Spain
- Hospital Universitario La Paz
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Madrid, Spain
- Hospital Universitario de La Princesa
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Madrid, Spain
- Hospital Infanta Leonor
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Madrid, Spain
- Hospital Universitario Puerta de Hierro
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Oviedo, Spain
- Hospital Universitario Central de Asturias
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Salamanca, Spain
- Hospital Universitario de Salamanca
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Santander, Spain
- Hospital Universitario Marqués de Valdecilla
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Sevilla, Spain
- Hospital Nuestra Señora de Valme
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Toledo, Spain
- Hospital Virgen de la Salud de Toledo
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Valencia, Spain
- Hospital Clinico de Valencia
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Valencia, Spain
- Hospital La Fe de Valencia
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Illes Balears
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Palma De Mallorca, Illes Balears, Spain, 07010
- Hospital Son Espases (Son Dureta)
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adult patients with previously untreated CLL or SLL defined following IWCLL criteria (Hallek, 2008).
- Must understand and voluntarily sign an informed consent form.
- Age ≥ 18 years at the time of signing the informed consent form and must be able to adhere to the study visit schedule and other protocol requirements.
- Must have a documented diagnosis of CLL or SLL [IWCLL guidelines for diagnosis and treatment of CLL (Hallek, 2008)] meeting at least one of the following criteria:
Evidence of progressive marrow failure as manifested by the development of, or worsening of, anemia and/or thrombocytopenia.
Massive (i.e. > 6 cm below the left costal margin) or progressive or symptomatic splenomegaly.
Massive nodes (i.e. > 10 cm in longest diameter) or progressive or symptomatic lymphadenopathy.
Progressive lymphocytosis with an increase of > 50% over a 2-month period, or lymphocyte doubling time (LDT) of less than 6 months.
A minimum of any one of the following disease-related symptoms: unintentional weight loss ≥ 10% within the previous 6 months, significant fatigue (i.e., ECOG PS 2; cannot work or unable to perform usual activities), fevers of greater than 38.0° C or 100.5F for 2 or more weeks without other evidence of infection, or night sweats for more than 1 month without evidence of infection
- Physically fit patients defined as CIRS < 6 (CIRS Scale, Appendix E).
- Must have an Eastern Cooperative Oncology Group (ECOG) performance status score of ≤2.
- All sexually active subjects with the capacity to reproduce (male and female) must use high-efficacy contraceptive methods during the course of the study. These restrictions apply for 12 months after the last dose of ofatumumab or 3 months after the last dose of ibrutinib, whichever happens later. High-efficacy contraceptive methods include:
Total abstinence when consistent with the subject's typical and preferred lifestyle (periodic abstinence [e.g. calendar methods, ovulation, symptothermal and post-ovulation methods] and the withdrawal method are not acceptable contraceptive methods).
Female sterilisation defined as surgical hysterectomy, bilateral oophorectomy, or tubal ligation at least six weeks prior to the study treatment (a simple oophorectomy does not meet the definition of female sterilisation).
Male sterilisation (at least six months before screening). A man who has undergone a vasectomy must be the only partner who is a study subject.
Combination of two of the following methods (a+b or a+c or b+c):
- Use of oral, injected or implanted hormonal contraceptives, or other hormonal contraceptive methods that have a comparable efficacy (failure rate < 1%), for example, hormonal vaginal ring or transdermal hormonal contraceptive. If an oral contraceptive is used, women must use the same pill for a minimum of three months before taking the study treatment.
- Placement of an intrauterine device (IUD) or an intrauterine system (IUS).
Barrier contraceptive methods: condom or cervical cap (cervical/vault diaphragm or cap) with foam/gel/film/spermicidal cream/vaginal suppository.
- Female subjects of childbearing potential must have a negative pregnancy test at screening. Females of child bearing potential are defined as sexually mature women without prior hysterectomy or who have had any evidence of menses in the past 12 months. However, women who have been amenorrheic for 12 or more months are still considered to be of childbearing potential if the amenorrhea is possibly due to other causes, including prior chemotherapy, anti-estrogens, or ovarian suppression
Exclusion Criteria:
- Prior treatment for CLL or SLL.
- Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the patient from signing the informed consent form.
- Systemic infection that has not resolved prior to initiating study treatment in spite of adequate anti-infective therapy.
- Pregnant or lactating females.
- Participation in any clinical study or having taken any investigational therapy within 28 days prior to initiating study therapy.
- Central nervous system (CNS) involvement as documented by spinal fluid cytology or imaging.
- Prior history of malignancies, other than CLL, unless the patient has been free of the disease for ≥ 3 years.
Exceptions include the following:
Basal cell carcinoma of the skin Squamous cell carcinoma of the skin Carcinoma in situ of the cervix Carcinoma in situ of the breast Incidental histologic finding of prostate cancer (TNM stage of T1a or T1b)
- Known Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV) and/or Hepatitis C Virus (HCV) infection.
- Any of the following laboratory abnormalities:
Serum creatinine ≥ 2 x ULN or estimated Glomerular Filtration Rate (Cockroft-GaultAppendix C) ≤ 40 mL/min/1.73m2 Absolute neutrophil count (ANC) < 1.0 X 109/L, unless secondary to bone marrow involvement by CLL.
Platelet count <100,000/mm3 or <50,000/mm3 if bone marrow involvement independent of transfusion support in either situation Serum aspartate aminotransferase (AST)/serum glutamic-oxaloacetictransaminase (SGOT) or alanine transaminase (ALT)/serum glutamate pyruvate transaminase (SGPT) >3 x upper limit of normal (ULN).
Serum total bilirubin > 1.5 x ULN, except in cases of Gilbert's syndrome.
- Presence of autoimmune haemolytic anemia or autoimmune thrombocytopenia.
- Disease transformation [i.e. Richter's Syndrome (lymphomas) or prolymphocytic leukemia.
- Major surgery within the last 28 days prior to registration.
- History of stroke or intracranial hemorrhage within 6 months prior to enrolment.
- Currently active, clinically significant cardiovascular disease or a history of myocardial infarction within 3 months prior to enrolment.
- Requires or receiving anticoagulation with warfarin or equivalent vitamin K antagonists within 28 days of first dose of study drug.
- Any life-threatening illness, medical condition, or organ system dysfunction which, in the investigator's opinion, could compromise the subject's safety, interfere with the absorption or metabolism of ibrutinib capsules, or put the study outcomes at undue risk.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Efficacy in terms of response rate
Time Frame: 18 months
|
To determine the complete response rate obtained with the combination of Ibrutinib and ofatumumab
|
18 months
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GELLC-7
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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