A Single-arm, Dose-escalation Trial of Long-acting Recombinant Human IL-7 (NT-I7, Efineptakin Alfa) for Idiopathic CD4 Lymphopenia

Last updated: March 6, 2026
Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)
Overall Status: Active - Recruiting

Phase

1/2

Condition

Aids And Aids Related Infections

White Cell Disorders

Treatment

Recombinant human interleukin (IL) 7-hyFc

Clinical Study ID

NCT05600920
10000821
000821-I
  • Ages 18-75
  • All Genders

Study Summary

Background:

Idiopathic CD4 lymphopenia (ICL) is a syndrome characterized by low levels of certain immune cells called CD4 T cells. The low CD4 T cells renders people with ICL prone to many types of severe infections, autoimmune diseases, and cancers. Although these infections and diseases can be treated whenever occur, there is currently no treatment that targeting the underlying deficiency of CD4 T cells can provide a definitive treatment for people with ICL.

Objective:

To test a new drug (NT-17) in people with ICL which can increase the number of CD4 T cells

Eligibility:

People aged 18 to 75 years with ICL who are also enrolled in NIH protocol 09-I-0102.

Design:

Participants will be screened. They will have a physical exam and blood tests. Some participants with high suspicion of central nervous system infection or history of such infections may also undergo a lumbar puncture. A thin needle will be inserted into their lower back to draw out a sample of the fluid around their spinal cord.

Participants will receive 3 doses of NT-17, each about 12 weeks apart. NT-17 is injected into the muscle of the upper arm, thigh, or buttock. They will visit the clinic 5 days before each dose and again 2 and 4 weeks after each dose. Blood will be drawn at all visits.

Participants will undergo leukapheresis 3 times. Blood will be drawn from a needle in one arm. The blood will pass through a machine that separates out the white blood cells. The remaining blood will be given back through a second needle in the other arm.

Some visits will include a rectal swab.

Some participants may have additional tests, including a skin exam, skin biopsies, and medical imaging.

Participants will have 3 follow-up visits every 3 months after they finish treatment.

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:

Individuals must meet all of the following criteria to be eligible for study participation:

  1. Aged 18 to 75 years.

  2. Able to provide informed consent.

  3. Co-enrolled in NIH protocol 09-I-0102, Etiology, Pathogenesis, and Natural Historyof Idiopathic CD4+ Lymphocytopenia (EPIC) study (NCT0086726).

  4. Documented ICL, defined as CD4 T-cell count <300 cells/microliter in at least 2different measurements at least 6 weeks apart, at any point in the past.

  5. Participants who can become pregnant or who can impregnate their partner must agreeto remain abstinent or to use 2 highly effective methods of contraception, at least 1 of which must be a barrier method, when engaging in sexual activities that canresult in pregnancy, beginning at the first pre-injection visit until the 30 daysafter the last injection. Acceptable methods of contraception include the following:

  6. Male or female condom.

  7. Diaphragm or cervical cap with a spermicide.

  8. Hormonal contraception.

  9. Intrauterine device.

Note: Contraception requirements do not apply to participants who are post-menopause (age >=45 years plus no menses for 12 consecutive months without an alternative medical cause).

Exclusion

EXCLUSION CRITERIA:

Individuals meeting any of the following criteria will be excluded from study participation:

  1. Current moderate or severe acute illness (eg, febrile illness, seizure, myocardialinfarction, cerebrovascular accident, pulmonary embolism) that in the opinion of thestudy team would make the individual unsuitable for the study.

  2. Clinical or microbiologic evidence of active progressive cryptococcal centralnervous system (CNS) disease or nontuberculous mycobacterial (NTM) infections withinthe last year. History of stable cryptococcal CNS disease or NTM diseases since morethan 1 year can be enrolled but will need to have undetectable CSF cryptococcalantigen and initiate/maintain antifungal or antimycobacterial treatment,respectively.

  3. Pregnant or breastfeeding.

  4. HIV infection, chronic hepatitis B or C infection, and any other recognizedcongenital or acquired immunodeficiency (eg, SCID IL-2/JAK3/ADA, MAGT1, MHC1deficiency, CVID, DOCK8).

  5. Serum creatinine >1.5 X ULN, platelets <50,000/microliter, hemoglobin <9 g/dL,AST/ALT>2.5 X ULN, total bilirubin >1.5 X ULN (except if due to Gilbert's syndrome),or immunoglobulin (Ig) G level <450 mg/L.

  6. Current (within 3 months of screening) use of systemic glucocorticosteroids orimmunomodulants other than corticosteroid nasal spray or inhaler and topicalsteroids.

  7. Any established diagnosis of autoimmune disease requiring systemic treatment exceptfor vitiligo or endocrine disease (including diabetes, thyroid disease, and adrenaldisease) controlled by replacement therapy.

  8. Malignancy requiring systemic chemotherapy or immunotherapy within 2 months ofscreening.

  9. Receipt of any other investigational agents within 3 months of screening.

  10. Any condition that, in the opinion of the study team contraindicates participationin this study.

Participants will be selected in an equitable manner from the available pool of potentially eligible individuals, without regard to factors such as sex, gender, race, ethnicity, or socioeconomic status, except for age.

Study Design

Total Participants: 60
Treatment Group(s): 1
Primary Treatment: Recombinant human interleukin (IL) 7-hyFc
Phase: 1/2
Study Start date:
November 06, 2024
Estimated Completion Date:
November 01, 2026

Study Description

Study Description:

Open-label trial of efineptakin alfa (NT-I7) to manage idiopathic CD4 lymphopenia (ICL). After baseline assessments, NT-I7 will be administered intramuscularly (IM) at the NIH Clinical Center (CC) once every 12 weeks for 3 total doses, with the final dose at week 24, in 3 cohorts of 10 participants each. The doses for each cohort are 240, 480, or 720 microgram/kg. Blood will be drawn at each dose visit, as well as 5 days before and 14 and 30 days after each dose visit. Blood laboratory evaluations will be performed at the NIH CC or by remote laboratory providers, with results shared with the NIH study team. Primary and secondary evaluations include assessment of adverse events (AEs) and T-cell counts. Questionnaires will be administered to assess patient health perceptions and quality of life. The final study visit will be at week 60.

Primary Objective:

Evaluate the safety (all AEs) of NT-I7 in patients with ICL.

Secondary Objective:

  1. Evaluate the immunologic effects of NT-I7 on peripheral CD4 T-cell counts in ICL patients.

  2. Evaluate the safety (study drug-related AEs) of NT-I7 in patients with ICL.

Exploratory Objectives:

  • Evaluate the ability of NT-I7 to increase CD4 T-cell counts.

  • Evaluate the clinical effects of NT-I7 administration in participants with treatment-refractory human papillomavirus (HPV)-related diseases.

  • Evaluate the effect of NT-I7 on clinical sequelae, radiologic or laboratory findings associated with previous opportunistic infections.

  • Evaluate effects of NT-I7 administration on presence/titer of clinical autoantibodies.

  • Evaluate the immunogenicity of NT-I7.

  • Evaluate the pharmacokinetics (PK) of NT-I7 and explore exposure-safety and exposure-efficacy relationships.

Primary Endpoint:

Number and severity of AEs observed after NT-I7 administration evaluated at week 60 (end-of-study visit).

Secondary Endpoints:

  • Evaluation of the trajectory of absolute lymphocyte count (ALC), and CD4, CD8, B, and NK counts measured at all study visits up to week 60 (end-of-study visit).

  • Evaluation of the trajectory of ALC and CD4, CD8, B, and NK counts measured at all study visits up to week 36 (interim analysis).

  • Evaluation of the trajectory of ALC and CD4, CD8, B, and NK counts measured between week 36 (12 weeks after last dose of NT-I7) and week 60.

  • Number and severity of AEs possibly, probably, or definitely related to NT-I7 administration evaluated at week 60 (end-of-study visit).

Exploratory Endpoints:

  • Proportion of participants with CD4 T-cell counts >=300 cells/microliter with NT-I7 treatment evaluated at week 60 (end-of-study visit).

  • Time (cumulative number of days or weeks) that participants with baseline CD4 T-cell counts <200 cells/microliter maintain CD4 T-cell counts >= 200 cells/microliter after initiating treatment with NT-I7.

  • Changes in skin or mucosal manifestations of HPV diseases as evaluated by clinical photography, and dermatologic and histologic evaluation.

  • Changes in the clinical, radiologic, or laboratory findings associated with previous history of opportunistic infections.

  • Changes in presence and titer of clinical autoantibodies.

  • Incidence of antidrug antibodies (ADA) to NT-I7 in the study population.

  • Serum concentration of NT-I7 administered at specified timepoints for the maximum observed concentration (Cmax).

Connect with a study center

  • National Institutes of Health Clinical Center

    Bethesda, Maryland 20892
    United States

    Active - Recruiting

  • National Institutes of Health Clinical Center

    Bethesda 4348599, Maryland 4361885 20892
    United States

    Site Not Available

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