Ruxolitinib Phosphate in Reducing Fatigue in Patients With Chronic Lymphocytic Leukemia

Running, not enrolling · Phase 2

Conditions studied: Chronic Lymphocytic Leukemia

In brief

This phase II trial studies how well ruxolitinib phosphate works in reducing fatigue in patients with chronic lymphocytic leukemia. Ruxolitinib phosphate may stop the growth of cancer cells by blocking a protein called Janus kinase (JAK) that is needed for cell growth and may also help control fatigue, decrease the size of lymph nodes and/or lower the number of chronic lymphocytic leukemia cells in the blood.

Key facts

Study ID

NCT02131584

Run by

M.D. Anderson Cancer Center

People needed

10

Starts

2014-09-02

Expected to finish

2026-09-30

Last updated by the study team

2026-04-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects who are able to understand and sign an informed consent document
• Subjects must be diagnosed with CLL and do not meet the IWCLL criteria for treatment
• Patients may have been previously treated or previously untreated
• Symptomatic patients with a BFI symptom scale of 2 points or greater
• Subjects with hemoglobin values at the screening visit equal to or greater than 12.0 g/dL
• Subjects with a platelet count of at least 75 x 10\^9/L at the screening visit
• Subjects with an absolute neutrophil count (ANC) of equal to or higher than 0.5 x 10\^9/L at the screening visit
• Subjects must have discontinued all drugs used to treat CLL no later than day -30
• Subjects with an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2

You may not qualify if…

• Females who are pregnant or are currently breastfeeding
• Subjects of childbearing potential who are unwilling to take appropriate precautions (throughout the study from screening, including 30 days after discontinuation of the study drug) to avoid becoming pregnant or fathering a child
• Females of non-childbearing potential are defined as women who (a) are equal to or greater than 55 years of age with history of amenorrhea for 1 year, or (b) are surgically sterile for at least 3 months
• For females of childbearing potential, or for males, appropriate precautions are those that are at least 99% effective in preventing the occurrence of pregnancy; these methods should be communicated to the subjects and their understanding confirmed:
• Complete abstinence from sexual intercourse
• Double barrier methods
• Condom with spermicide in conjunction with use of an intrauterine device (IUD)
• Condom with spermicide in conjunction with use of a diaphragm
• Oral, injectable, or implanted contraceptives
• Tubal ligation or vasectomy (surgical sterilization)
• Subjects with recent history of inadequate bone marrow reserve as demonstrated by previous transfusions except for acute blood loss (e.g. surgery) in the month prior to screening
• Alanine aminotransferase (ALT) > 2.5 x upper limit of normal (ULN)
• Modification of diet in renal disease (MDRD) calculated glomerular filtration rate (GFR) < 30 mL/min
• Subjects with active uncontrolled infection or who are human immunodeficiency virus (HIV) positive (subjects with acute infections requiring treatment should delay screening/enrollment until the course of therapy has been completed and the event is considered controlled)
• Subjects with an invasive malignancy over the previous 2 years except treated basal or squamous carcinomas of the skin completely resected intraepithelial carcinoma of the cervix and completely resected papillary thyroid and follicular thyroid cancers; other completely resected cancers greater than 2 years may be considered after review by the principal investigator (PI)
• Subjects with clinically significant uncontrolled cardiac disease
• Subjects being treated concurrently with any prohibited medications, including investigational medication, rifampin, St. John's wort, and potent cytochrome P450, family 3, subfamily A, polypeptide 4 (CYP3A4) inhibitors (excluding ketoconazole) unless continuation of such medications are determined by the investigator to be in the best interest of the patient
• Subjects who have previously received JAK inhibitor therapy
• Subjects with active alcohol or drug addiction that would interfere with their ability to comply with the study requirements
• Subjects with any concurrent condition that, in the investigator's opinion, would jeopardize the safety of the subject or compliance with the protocol
• Subjects who have unknown transfusion history for at least the 12 weeks prior to screening
• Subjects who are unable to complete the symptom diary
• Subjects who will need conventional therapy during the course of the study

Where it is running

• M D Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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