A 6 month safety, tolerability, efficacy and pharmacokinetic study with ANF-Rho to treat patients with chronic neutropenia.
Chronic neutropenia patients who are eligible for participation will be screened and enrolled to received open-label ANF-Rho for a period of 6 months. Study participation will be separated into 2 periods, Induction (8 weeks) and Maintenance (16 weeks). Blood samples to measure neutrophil levels and biochemistry labs will be drawn throughout the study to monitor efficacy response and patient safety. Pharmacokinetic samples will be collected during both periods and questionnaires will be completed by the patient and investigator for bone pain, quality of life (QOL) and injection site reaction.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Pegylated version of recombinant human granulocyte-colony stimulating factor (G-CSF)
Neutrophil response rate to ANF Rho following a 6 month treatment period (induction, stabilization and maintenance periods) in patients with Chronic Neutropenia.
Median Absolute Neutrophil Count (ANC) of ≥1.0 x 109/L over the 6 months total treatment period
Time frame: 6 months
Serum concentration of ANF-Rho over time
Pharmacokinetic parameter measuring ANF-Rho levels over time
Time frame: 6 months
The peak plasma concentration of ANF-Rho after administration (Cmax) over time
Pharmacokinetic Parameter measuring ANF-Rho levels over time
Time frame: 6 months
Total ANF-Rho exposure (AUC)
Pharmacokinetic parameter measuring ANF-Rho levels from time 0 through last dose.
Time frame: 6 months
Time to peak plasma concentration of ANF-Rho (Tmax)
Pharmacokinetic parameter measuring the time to Cmax.
Time frame: 6 months
Half-Life of ANF-Rho (T1/2)
Pharmacokinetic parameter to measure the time required for the concentration of the drug to reach half of its original value
Time frame: 6 months
Rate of subject reported infection related morbidities (infections, hospitalisations and antibiotic use) in Chronic Neutropenia patients treated with ANF Rho
Time frame: 6 months
Evaluate the effect of ANF Rho on the Quality of Life and Bone Pain in Chronic Neutropenia patients.
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Change in Quality of life over 6 months measured by the Short Form 36, change in bone pain over 6 months measured by the Bone Pain Questionnaire, Wong and Baker Scale and FLACC Behavioral Pain Assessment Scale
Time frame: 6 months
Evaluate safety and tolerability of subcutaneous injections of ANF Rho in chronic neutropenia patients.
Composite endpoint with multiple vital signs, bone scans, biopsies, splenic ultrasounds, electrocardiographic assessments, clinical signs, and bio-analytical measures (e.g., biochemistry), and reported adverse events following repeated dosing.
Time frame: 6 months