A Study to Evaluate Safety and Efficacy of Subcutaneous Administration of Anakinra in Patients With CF (ANAKIN)

A Phase IIa, Randomized, Placebo-controlled, Double-blind, Cross-over Study to Evaluate Safety and Efficacy of Subcutaneous Administration of Anakinra in Patients With Cystic Fibrosis

OBJECTIVES

Primary:

To evaluate efficacy of treatment with anakinra in subjects with CF who are ≥ 12 years of age by means of lung clearance index (LCI).

Secondary To evaluate safety and tolerability of treatment with anakinra as well as to investigate further effects of anakinra on lung function and quality of life (QOL) in subjects with CF.

Study Overview

• Status: Recruiting
• Conditions: Cystic Fibrosis, 10011762
• Intervention / Treatment: Drug: Anakinra

• Study Type: Interventional
• Enrollment (Estimated): 52
• Phase: Phase 2

Contacts and Locations

Study Locations

• Germany
  • Berlin, Germany, 13353
    • Recruiting
    • Charité - Universitätsmedizin Berlin
    • Contact: Mirjam Stahl, Prof. Dr.; Phone Number: +4930450566552; Email: mirjam.stahl@charite.de
    • Contact: Phone Number: +4930450666564; Email: cf-studienzentrum@charite.de
  • Baden-Württemberg
    • Heidelberg, Baden-Württemberg, Germany, 69120
      • Recruiting
      • University Children's Hospital Heidelberg, Cystic Fibrosis Centre
      • Contact: Olaf Sommerburg, MD; Phone Number: +49 6221 56 5696; Email: Olaf.Sommerburg@med.uni-heidelberg.de
      • Contact: Mirjam Stahl, MD; Phone Number: +49 6221 56 37049; Email: Mirjam.Stahl@med.uni-heidelberg.de
      • Principal Investigator: Olaf Sommerburg, MD
  • Nordrhein-Westfalen
    • Essen, Nordrhein-Westfalen, Germany, 45239
      • Recruiting
      • Universitätsmedizin Essen, Ruhrlandklinik
      • Contact: Thea Schwarzer; Phone Number: +492014334621; Email: Thea-Lisa.Schwarzer@rlk.uk-essen.de
      • Contact: Nadine Zmudzinski; Phone Number: +492014334659; Email: Nadine.Zmudzinski@uk-essen.de

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 12 years and older (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

1. Age ≥ 18 years (1st cohort). If justified by interim analysis, 18 > age ≥ 12 years (2nd cohort),
2. Informed consent of the patient (if applicable) and/or all legal guardians,
3. Sufficient fluency of patient and/or his/her representative in German language to comply with study-specific procedures (e.g. to complete required quality of life questionnaires),

4. Confirmed diagnosis of cystic fibrosis, fulfilling at least one of the following three criteria:

   1. sweat chloride ≥ 60mEq/L,
   2. two CF causing mutations in the CFTR gene,
   3. alterations of transepithelial potential difference of nasal or rectal epithelia typical for CF,
5. FEV1 ≥ 50 % pred. at screening,
6. LCI2.5 ≥ 7.05 at screening,
7. Ability to perform reproducible multiple breath washout and spirometry,
8. Oxyhaemoglobin saturation of ≥ 90% on room air at screening,
9. No changes in the medication for cystic fibrosis lung disease for at least 4 weeks prior to the first administration of the IMP of each treatment period (in case of medication changes in Period 1 and/or the washout phase the wash-out may be extended for up to 12 weeks in order to fulfill this criterion),
10. Adequate bone marrow function assessed on the basis of: neutrophils >1.5 x 109/L, platelets >100 x 109/L, hemoglobin >9.0 g/dL,
11. Adequate liver function assessed on the basis of: GGT, ASAT, and ALAT <3 x upper limit of normal (ULN),
12. Adequate blood clotting assessed on the basis of: aPTT <39 sec., INR <1.2,
13. Negative serology for HIV (anti-HIV 1/2 IgG/IgM and p24-Ag), HBV (anti-HBs quantitative and anti-HBc IgG/IgM) and HCV (anti-HCV IgG), negative Interferon-gamma release assay,
14. Negative Beta-HCG blood/urine test in women of childbearing potential (of childbearing potential are females who have experienced menarche and are not permanently sterile or postmenopausal (postmenopausal: 12 consecutive months with no menses without an alternative medical cause)),
15. Use of adequate contraception in sexually active female subjects (sexual abstinence, hormonal contraceptives or intrauterine device).

Exclusion Criteria:

1. Expected non-compliance, i.e. inability or unwillingness to comply with study-specific procedures,
2. Known allergy to anakinra or any ingredient of the pharmaceutical formulation of Kineret®,
3. Planned immunization with attenuated (live) vaccine(s) during the treatment with the IMP or completed immunization with attenuated (live) vaccine(s) within 4 weeks prior to the first administration of the IMP,
4. Renal failure (creatinine in serum above ULN),
5. History of tuberculosis or repeated detection of non-tuberculous mycobacteria from airway samples in the last 12 months before start of each treatment period,
6. History of detection of Burkholderia cenocepacia species in the last 12 months before start of each treatment period,
7. Colonization with multi-resistant Staphylococcus aureus (MRSA) and/or 4-multi-resistant gram negative (MRGN) Pseudomonas aeruginosa is only an exclusion criterion if the treating physician judges that this is an increased risk for the patient,
8. Acute bronchopulmonary exacerbation (defined by modified Fuchs criteria (1) (see Appendix 1), modification includes all ways of application of an antibiotic (e.g., oral, i.v., inhaled)) within 14 days prior to the screening and before start of each treatment period,
9. Signs of other active infection within 14 days prior to the screening and before start of each treatment period (clinical symptoms (e.g. burning sensation while urinating, skin, wound or dental infection) and/or fever and/or deterioration of infection-specific laboratory parameters beyond changes driven by the underlying disease),
10. Immunosuppressive treatment due to organ transplantation, rheumatic or autoimmune diseases as well as treatment with Anakinra in the last 3 months before Day 1 of Period 1,
11. Participation in another interventional trial within the last 30 days prior to screening,
12. Current oral corticosteroid use,
13. Current oxygen supplementation,
14. Current treatment with etanercept,
15. Medical history of lung transplantation,
16. Pregnant or nursing females (females of childbearing potential must have a negative pregnancy test at Screening),
17. Known hypersensitivity to hypertonic saline (used for induction of sputum).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Placebo Comparator: Placebo	Drug: Anakinra; Application of Anakinra once daily for 28 days
Experimental: Anakinra	Drug: Anakinra; Application of Anakinra once daily for 28 days

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Absolute pre-post change of the lung clearance index (LCI)	28 days

Collaborators and Investigators

• Sponsor: Heidelberg University

Study record dates

Study Major Dates

• Study Start (Actual): December 1, 2022
• Primary Completion (Estimated): December 1, 2024
• Study Completion (Estimated): June 1, 2025

Study Registration Dates

• First Submitted: April 19, 2019
• First Submitted That Met QC Criteria: April 19, 2019
• First Posted (Actual): April 24, 2019

Study Record Updates

• Last Update Posted (Actual): December 13, 2023
• Last Update Submitted That Met QC Criteria: December 12, 2023
• Last Verified: December 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Digestive System Diseases; Pathologic Processes; Respiratory Tract Diseases; Lung Diseases; Infant, Newborn, Diseases; Genetic Diseases, Inborn; Pancreatic Diseases; Fibrosis; Cystic Fibrosis; Antirheumatic Agents; Interleukin 1 Receptor Antagonist Protein
• Other Study ID Numbers: EudraCT No.: 2016-004786-80-A

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No