Clinical trial

Anti-Cytokine Therapy for Hemodialysis InflammatION (ACTION): A Phase II Multi-center Study to Evaluate the Safety and Tolerability of Anakinra, an IL-1 Receptor Antagonist, for Patients Treated With Maintenance Hemodialysis

Name
826900
Description
Anti-Cytokine Therapy for Hemodialysis InflammatION (ACTION) is a phase II multi-center study to evaluate the safety and tolerability of anakinra, an IL-1 receptor antagonist, for patients treated with maintenance hemodialysis.
Trial arms
Trial start
2017-12-15
Estimated PCD
2021-09-02
Trial end
2021-09-02
Status
Completed
Phase
Early phase I
Treatment
Anakinra
Anakinra (Kineret®) is a therapeutic agent that blocks the effects of IL-1α and IL-1β by competitively binding to the interleukin-1 type I receptor (IL-1RI). It is a recombinant, non-glycosylated form of the naturally occurring human interleukin-1 receptor antagonist (IL-1Ra) but differs from human IL-1Ra in that it has the addition of a single methionine residue at the amino terminus. It is supplied commercially in single use 1 ml prefilled glass syringes as a sterile, clear, colorless-to-white, preservative free solution. Each syringe contains: 0.67 ml (100 mg) of anakinra in a solution (pH 6.5) containing sodium citrate (1.29 mg), sodium chloride (5.48 mg), disodium EDTA (0.12 mg) and polysorbate 80 (0.70 mg) in Water for Injection, USP.
Arms:
Anakinra
Other names:
Kineret®
Placebo
Saline (0.9%) will be used as the placebo, in single use 1 ml prefilled glass syringes as a sterile, clear, colorless-to-white, preservative free solution.
Arms:
Placebo
Size
80
Primary endpoint
Safety and Tolerability of Anakinra, for Patients Receiving Maintenance Hemodialysis
48 Weeks (after the 24-week treatment period and the 24-week post-treatment period)
Change in Log-transformed Circulating CRP Concentration After 24 Weeks of Treatment for Patients Receiving Maintenance Hemodialysis
Change from Baseline to 24 Weeks (end of treatment phase)
Eligibility criteria
Inclusion Criteria: 1. Maintenance hemodialysis therapy 3 times per week for end-stage renal disease 2. ≥6 months since hemodialysis initiation 3. C-reactive protein measured by high sensitivity assay (hsCRP) ≥2.0 mg/L at screening and within 10 days prior to randomization 4. Most recent single pool Kt/V \> or = 1.2 within 30 days prior to first screening visit 5. Negative tuberculosis interferon gamma release assay (e.g. Quantiferon-TB Gold) for tuberculosis unless documented treatment for a) positive PPD, b) positive interferon gamma release assay, or c) tuberculosis. 6. Negative human immunodeficiency virus (HIV) antibody test, negative hepatitis C Ab test unless viral clearance following direct antiviral therapy is documented, and negative hepatitis B surface antigen positivity. 7. For women of childbearing potential, willingness to use a highly effective method of birth control for up to 4 weeks after the last dose of anakinra. 8. Ability to provide informed consent Exclusion Criteria: 1. Current or anticipated use of a hemodialysis central venous catheter 2. Acute bacterial infection, including vascular access infection, within 60 days prior to screening unless treated with antibiotics and resolved. Any chronic bacterial infection (e.g., osteomyelitis or bronchiectasis) 3. Hospitalization within 30 days unless for vascular access procedure 4. Cirrhosis 5. Malignancy within the past 5 years with exception of basal or squamous cell carcinoma 6. Use of an immunosuppressive drug within the past 3 months except low doses of oral corticosteroids (total daily dose ≤10 mg/day of prednisone or equivalent) 7. Receipt of live vaccine within the past 3 months. Live vaccines include Varicella zoster, measles, oral polio, rotavirus, yellow fever, and the nasal spray influenza vaccine 8. Absolute neutrophil count (ANC) \<2,500 cells/mm3 (2.5 x 109 cells/L) 9. Platelet count \<100,000/mm3 (100 x 109/L) 10. Known allergy to anakinra 11. Anticipated kidney transplantation, change to peritoneal dialysis, or transfer to another dialysis unit within 9 months 12. Expected survival less than 9 months 13. Pregnancy, anticipated pregnancy, or breastfeeding 14. Incarceration 15. Receipt of an investigational drug within the past 30 days 16. Current or anticipated participation in another intervention study
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 80, 'type': 'ACTUAL'}}
Updated at
2023-03-14

1 organization

1 product

1 drug

1 indication

Product
Anakinra