Idiopathic CD4+ T-Lymphocytopenia
Conditions
Keywords
Idiopathic CD4+ T-Lymphocytopenia, Interleukin-7, Clinical Trial, T-Lymphocytes, Idiopathic CD4 Lymphocytopenia (ICL), ICL
Brief summary
Background: * Idiopathic CD4 lymphocytopenia (ICL) is a condition in which patients have low levels of T cells, a type of white blood cell that helps fight infection. Animal studies have shown that an experimental drug Interleukin 7 (IL-7), which is named CYT107, can increase the number and function of T cells. CYT107, however, has not been used in people with ICL. Objectives: * To determine the safety of CYT107 in people with ICL. * To determine whether CYT107 will increase the number and function of T cells in people with ICL. Eligibility: * Patients 18 years of age and older diagnosed with ICL and who are at risk of becoming sick because of this condition are eligible for this study. In addition, patients must not be pregnant, or have other illnesses that would cause low CD4 T cell counts, such as human immunodeficiency virus (HIV) or human T-lymphotrophic virus (HTLV) infection. Design: * The initial screening visit will include the following examinations and tests: * A complete physical exam and medical history * Blood analysis, including CD4 T cell count; complete blood count and additional blood tests to determine clotting ability and blood composition; thyroid, liver, kidney, and pancreatic function tests; HIV and HTLV tests; and tests for anti-IL-7 antibodies that block normal IL-7 activity * Routine urine test * Urine or blood pregnancy test for women * Chest X-ray * Electrocardiogram * Spleen ultrasound. * The baseline visit will include blood tests to determine levels of each of the major types of antibodies, a test of genetic background, and more detailed CD4 and protein analysis. In addition, leukapheresis (a procedure to collect large numbers of immune cells without red blood cells) will be done. Participants will also have the option of having colon and lymph node biopsies. * The schedule will be as follows: * Weeks 1, 2, and 3 (Cycle 1): Three weekly IL-7 dosing visits. * Weeks 5, 8, and 12: Follow-up visits. * Weeks 24, 25, and 26 (Cycle 2): Three more weekly IL-7 dosing visits. * Weeks 28, 31, and 35: Follow-up visits. * Week 48: End of study visit. * Tests conducted before getting IL-7 will be repeated during the IL-7 cycles and follow-up visits to compare with earlier values. Optional colon and lymph node biopsies done at baseline will be repeated 1 6 weeks prior to Cycle 2 and 1 6 weeks prior to Week 48.
Detailed description
Interleukin-7 (CYT107) Treatment of Idiopathic CD4 Lymphocytopenia: Expansion of CD4 T Cells (ICICLE) is a Phase I/IIa open-label, single arm clinical trial evaluating the safety profile of glycosylated recombinant human interleukin-7 (rhIL-7) as an immunostimulatory therapy in patients with idiopathic CD4 T cell lymphocytopenia (ICL) at risk of disease progression. Secondary analyses will assess the immunostimulatory effects of rhIL-7 on T cell number and function. ICL was first characterized in the early 1990 s and is a primary immune disorder of CD4 T cell lymphocytopenia (less than 300 cells/microL or less than 20% of lymphocytes), which is not due to any known infectious process, exogenous medication, autoimmune cytopenia, or other underlying disorder associated with lymphocytopenia. ICL patients are at risk for a wide spectrum of opportunistic and other serious infections, autoimmune disorders, and other types of lymphocytopenia. At present, no validated treatment exists for ICL, and treatment is directed primarily toward infectious complications once they arise. A first-generation form of rhIL-7 was shown in pre-clinical and Phase I studies in oncology and human immunodeficiency virus (HIV)-infected patients to be well tolerated in repeated dose trials, with long-lasting increases in both CD4 and CD8 T cells. CYT107 is a second-generation rhIL-7 product made by Cytheris via a recombinant mammalian cell culture system. DESIGN - Open-label, single-arm, Phase I/IIa interventional clinical trial. Participants will be evaluated at baseline (prior to study treatment) and according to the protocol follow-up schedule, receiving a total of 2 cycles of rhIL-7 (CYT107) during the induction phase and up to 8 cycles during the maintenance phase. Safety assessments of rhIL-7 will be the primary focus at each study visit, with secondary analyses of immune parameters, including changes from baseline in T cell number and function at Weeks 24 and 48. DURATION - Enrollment is expected to take 3 to 4 years. Each volunteer will be followed for at least 48 weeks. Thus, total duration of the study will be approximately 5 years. SAMPLE SIZE - Approximately 35-40 patients will be screened over a 3-year period to achieve the desired sample of 18 ICL patients, allowing for a primary safety assessment of CYT107 in this Phase I/IIa clinical trial, as well as exploring the immunomodulatory effects of rhIL-7. POPULATION - Men and women, aged greater than or equal to 18 years, with a confirmed diagnosis of ICL (CD4 less than 300 cells/micromL or less than 20% of lymphocytes) deemed at risk for complications due to concurrent CD8 T cell lymphocytopenia and/or history of opportunistic or otherwise serious infection, without autoimmunity or hematologic or lymphoid malignancy. REGIMEN - During the induction phase, subjects will receive 2 cycles of subcutaneous rhIL-7 dosed once weekly for 3 weeks in a dose escalation fashion: 3 microg/kg (first 3 subjects-completed), 10 microg/kg (next 5 subjects-completed) and 20 microg/kg (last 5 subjects), with an additional 5 subjects at the highest achieved dose level. Cycles of rhIL-7 will be administered starting at Week 1 and Week 24. For subjects who tolerate the induction phase and elect to participate in the maintenance phase, additional cycles of rhIL-7 may be offered at 3-6 month intervals. These participants will receive rhIL-7 at the highest dose for which at least 8 weeks of safety data for 5 subjects has been reviewed provided no more than 1 DLT is reported.
Interventions
DRUGCYT107
Sponsors
National Institute of Allergy and Infectious Diseases (NIAID)
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
-INCLUSION CRITERIA: 1. Age greater than or equal to 18 years 2. CD4 T cell count less than 300 cells/microL or less than 20% of total T lymphocytes on 2 occasions at least 6 weeks apart (and at the time of screening) in the absence of any illness accounting for CD4 lymphocytopenia 3. ICL diagnosis that indicates a risk for disease progression, defined as one or both of the following: * CD8 T cell lymphocytopenia (less than 180 cells/microL) * History of opportunistic or otherwise significant infection (e.g., AIDS-defining or highly morbid illnesses, such as Cryptococcus or Mycobacteria infection, severe herpes zoster, JC virus causing progressive multifocal leukoencephalopathy, Kaposi s sarcoma, or severe human papilloma virus condylomata) 4. HIV-1 and HIV-2 seronegativity and below detection of HIV-1 viral load 5. HTLV-1 and HTLV-2 seronegativity 6. Adequate venous access, as determined by the study team, although participants unable to undergo leukapheresis will not be excluded 7. Normal thyroid-stimulating hormone (TSH) 8. Negative serum or urine pregnancy test at time of study enrollment for women of childbearing potential 9. Ability to understand and give informed consent 10. Capacity and willingness to adhere to study procedures, including scheduled follow-up visits 11. Willingness to allow blood and tissue sample storage 12. Established primary care provider
Exclusion criteria
1. History of prior cytotoxic, chemotherapeutic, immunosuppressant (e.g., systemic corticosteroids), immunomodulatory (e.g., IL-2, IL-7, interferon-gama), or growth factor therapy within the last 6 months; chemotherapy or immunomodulatory therapy given to treat an underlying disease or condition may be permitted at the protocol team's discretion, provided diagnosis of ICL was established prior to starting this treatment. The treatment has been stable for over 6 months and is being administered at stable doses as maintenance therapy. 2. History of prior participation in another investigational intervention study within the last 6 months. Co-enrollment in other NIAID stem cell mobilization protocols will be permitted at the protocol team s discretion, but CYT107 may be dosed no sooner than 6 months after last dose of that protocol s medications have been given. 3. Active uncontrolled opportunistic infection at the time of enrollment 4. Current or recent history (less than 28 days prior to screening) of a viral, bacterial, parasitic or fungal infection requiring hospitalization and/or systemic treatment, other than long-term maintenance pharmacotherapy 5. Serious illness requiring systemic treatment and/or hospitalization within 56 days (8 weeks) of screening, unless the subject is clinically stable, in the opinion of the Principal Investigator, and has completed therapy or has been on appropriate therapy for greater than 28 days (4 weeks) prior to screening 6. Current or history of hematologic or lymphoid (lymphoma) malignancy 7. Established or planned pregnancies or refusal to use effective birth control (e.g., barrier methods, oral contraceptives, intrauterine devices) for the duration of study involvement, regardless of gender 8. Concurrent breastfeeding 9. Renal insufficiency (e.g., estimated glomerular filtration rate less than 60 mL/min/1.73 m(2)) 10. Any of the following screening laboratory abnormalities: platelets less than 100,000 cells/microL; lipase greater than 1.5 times the ULN; AST, ALT, or alkaline phosphatase greater than 2.5 times the ULN; total bilirubin greater than 1.5 times the ULN 11. History of splenectomy or hematologic disease associated with hypersplenism, such as alpha- or beta-thalassemia, hereditary spherocytosis, Gaucher s disease, or autoimmune hemolytic anemia 12. Cirrhosis of any origin, including alcoholic or non-alcoholic steatohepatitis, either suspected by history or histologically proven 13. History of hepatitis B or C infection, i.e., positive hepatitis B surface antigen, positive anti-hepatitis B core antibody with a detectable hepatitis B DNA viral load, positive anti-hepatitis C antibody and/or detectable hepatitis C RNA viral load (subjects who became negative for hepatitis B DNA or hepatitis C RNA following anti-viral treatment will not qualify for study treatment) 14. Need for anticoagulant medication (e.g., warfarin, heparin), other than aspirin, clopidogrel, or other antiplatelet agent as CYT107 may co-precipitate with heparin if taken together. 15. Active drug or alcohol use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements (subjects must agree to refrain from substance abuse use during the entire course of the study) 16. Past or current psychiatric illness that, in the opinion of the investigator, would interfere with protocol adherence or the ability and willingness to give written informed consent 17. Current autoimmune conditions requiring systemic (oral, injection, or other parenteral) therapy, as well as psoriasis and optic neuritis regardless of treatment and/or a diagnosis of systemic lupus erythematous based on the screening rheumatologic work up. 18. Cardiac, pulmonary, thyroid, renal, hepatic, neurological (central or peripheral) disease or disorder of hemostasis requiring therapy and considered to be significant by the protocol team 19. History of cardiovascular disease, arrhythmias, or clinically significant ECG abnormalities, including a corrected QT interval (QTc) greater than or equal to 470 milliseconds 20. Family history consistent with an inherited cardiomyopathy or arrhythmia such as the following: * Arrhythmogenic Right Ventricular Dysplasia (ARVD) * Brugada syndrome (BrS) * Congenital Long QT (LQT) * Congenital Short QT intervals (SQT) * Early Repolarization Syndrome * Idiopathic Ventricular Fibrillation (IVF) 21. Uncontrolled hypertension (i.e., resting systolic blood pressure greater than160 mmHg or resting diastolic blood pressure greater than 90 mmHg), despite pharmacologic antihypertensive treatment, confirmed with a second blood pressure measurement done later in the same day. 22. Evidence of circulating neutralizing anti-IL-7 antibodies (prior to initial rhIL-7 administration) To be eligible for rhIL-7 administration, all
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse Events and Toxicities Associated With CYT107. | 48 weeks per patient with a 3-4 year enrollment period |
Other
| Measure | Time frame |
|---|---|
| Change: CD4/CD8 T Cell Cts After CYT107; in Immunophenotype (Naive, Memory, Regulatory T Cell Subsets) & Amp; Antigen-specific T Cell Function After CYT107; in T Cell Activation/Proliferation Status & Amp; TCR Repertoire After CYT107; ... | 48 weeks per patient with a 3-4 year enrollment period |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| 3 mcg/kg Cohort | 3 |
| 10 mcg/kg Cohort | 5 |
| 20 mcg/kg Cohort | 1 |
| Total | 9 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 |
|---|---|---|---|---|
| Overall Study | Developed exclusionary condition | 1 | 0 | 0 |
| Overall Study | Study drug no longer available | 0 | 0 | 1 |
| Overall Study | Withdrawal by Subject | 0 | 1 | 0 |
Baseline characteristics
| Characteristic | 3 mcg/kg Cohort | 10 mcg/kg Cohort | 20 mcg/kg Cohort | Total |
|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 1 Participants | 0 Participants | 1 Participants |
| Age, Categorical Between 18 and 65 years | 3 Participants | 4 Participants | 1 Participants | 8 Participants |
| Age, Continuous | 49 years | 56 years | 33 years | 51 years |
| CD4 T cell count | 13 cells/microliter | 52 cells/microliter | 15 cells/microliter | 18 cells/microliter |
| Region of Enrollment United States | 3 participants | 5 participants | 1 participants | 9 participants |
| Sex: Female, Male Female | 3 Participants | 3 Participants | 1 Participants | 7 Participants |
| Sex: Female, Male Male | 0 Participants | 2 Participants | 0 Participants | 2 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — | — / — |
| other Total, other adverse events | 3 / 3 | 5 / 5 | 1 / 1 |
| serious Total, serious adverse events | 2 / 3 | 2 / 5 | 0 / 1 |
Outcome results
Primary
Adverse Events and Toxicities Associated With CYT107.
Time frame: 48 weeks per patient with a 3-4 year enrollment period
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| 3 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 3 Adverse Events | 3 Events |
| 3 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 4 Adverse Events | 0 Events |
| 3 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 1 Adverse Events | 103 Events |
| 3 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 5 Adverse Events | 0 Events |
| 3 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 2 Adverse Events | 21 Events |
| 10 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 4 Adverse Events | 0 Events |
| 10 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 1 Adverse Events | 112 Events |
| 10 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 5 Adverse Events | 0 Events |
| 10 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 3 Adverse Events | 0 Events |
| 10 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 2 Adverse Events | 45 Events |
| 20 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 2 Adverse Events | 0 Events |
| 20 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 3 Adverse Events | 0 Events |
| 20 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 1 Adverse Events | 8 Events |
| 20 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 4 Adverse Events | 0 Events |
| 20 mcg/kg Cohort | Adverse Events and Toxicities Associated With CYT107. | Grade 5 Adverse Events | 0 Events |
Other Pre-specified
Change: CD4/CD8 T Cell Cts After CYT107; in Immunophenotype (Naive, Memory, Regulatory T Cell Subsets) & Amp; Antigen-specific T Cell Function After CYT107; in T Cell Activation/Proliferation Status & Amp; TCR Repertoire After CYT107; ...
Time frame: 48 weeks per patient with a 3-4 year enrollment period