Interleukin-7 (CYT107) Treatment of Idiopathic CD4 Lymphocytopenia: Expansion of CD4 T Cells (ICICLE)
Status:
Terminated
Trial end date:
2014-09-01
Target enrollment:
Participant gender:
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.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
National Institute of Allergy and Infectious Diseases (NIAID)