NAVX-010-Phase I Tolerability and Pharmacokinetic Study in Healthy Male Subjects

Algenis SpA30 enrolled

Overview

This was a double-blind, placebo-controlled, randomized, single ascending dose, sequential group study. Each subject participated in only 1 treatment period. The primary objective was to determine the safety of single intramuscular (IM) injections of NAVX-010 in healthy subjects. The secondary objective was to determine the single dose pharmacokinetics (PK) of Gonyautoxin 2 (GTX 2) and Gonyautoxin 3 (GTX 3) following IM administration of NAVX-010 in healthy subjects. Thirty subjects were studied in 5 groups (Groups A to E); each group consisted of 6 subjects, of which 4 subjects received the Investigational Medicinal Product (IMP; NAVX-010) and 2 subjects received placebo. All subjects completed the study and data for all subjects were included in the safety analyses. A total of 20 subjects received NAVX-010 and were included in the PK population and subsequent PK analysis. This study comprised healthy male subjects of any ethnic origin, aged between 18 and 45 years, inclusive, and with a body mass index (BMI) between 18.0 and 32.0 kg/m2, inclusive. Dose levels of NAVX-010 were 2, 8, 25, 50, and 75 mcg. Doses were administered as IM injections into the deltoid muscle in the fasted state. The IMP was supplied in glass vials containing 1.2 mL solution at a total GTX 2 and GTX 3 concentration of 42 mcg/mL (at a relative epimer ratio of 62% GTX 2:38% GTX 3). Placebo was of identical appearance to the IMP, and was administered into the deltoid muscle in the fasted state. Single IM injections were administered in each group. Blood and urine samples were collected for the analysis of plasma and urinary concentrations of GTX 2 and GTX 3, and the following PK parameters for GTX 2 and GTX 3 were calculated: area under the concentration-time curve (AUC) from time 0 up to the time of last quantifiable plasma concentration (AUC0 t), AUC from time 0 to 24 hours postdose (AUC0-24), AUC from time 0 extrapolated to infinity (AUC0 ∞), percentage of AUC that is due to extrapolation from the time of last quantifiable concentration to infinity (%AUCextrap), maximum observed plasma concentration (Cmax), time of the maximum observed plasma concentration (tmax), time of last quantifiable plasma concentration (tlast), time before the start of absorption (tlag), apparent plasma terminal elimination half life (t½), apparent total plasma clearance (CL/F), apparent volume of distribution during the terminal elimination phase (Vz/F), amount of drug excreted in urine (Ae), percentage of dose excreted in urine (Fe), and renal clearance (CLR). Safety evaluations included adverse events (AEs), vital signs, 12 lead electrocardiogram (ECG), telemetry, clinical laboratory evaluations, physical examination, and clinical study questionnaires.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

DOUBLE

Enrollment

Interventions

NAVX-010DRUG

Dose levels of NAVX-010 were 2, 8, 25, 50, and 75 mcg. Four patients per active group. Each subject participated in only 1 treatment period.

PlaceboDRUG

There were two Placebos per group.

Eligibility

Sex: MALEMin age: 18 YearsMax age: 45 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * males * between 18 and 45 years of age * body mass index (BMI) between 18.0 and 32.0 kg/m2 inclusive * body weight between 50 kg and 100 kg inclusive * Subjects must be in good health, as determined by: * medical history * physical examination (at check-in) * vital sign assessment * 12-lead ECG * clinical laboratory evaluations * Subjects must be able to understand and respond to the clinical study questionnaire * Subjects will have given their written informed consent to participate in the study and to abide by the study restrictions Exclusion Criteria: * Male subjects who are not willing, or whose partners are not willing, to use appropriate contraception (such as a condom with spermicidal oam/gel/film/cream/suppository), or to refrain from donating sperm from the time of dosing until 3 months after study drug administration. * Male subjects whose partners are of child-bearing potential must also agree to use an additional highly effective method of contraception. * Subjects who have donated; * blood or platelets in the 3 months prior to screening * plasma in the 7 days prior to screening * Subjects who have a significant history of alcoholism or drug/chemical abuse as determined by the Investigator or consume alcohol within 48 hours prior to the screening visit and prior to check-in. * Subjects who have smoked more than 10 cigarettes per day or the equivalent in tobacco use (e.g. chewing tobacco, eCigarettes and smoking cessation products \[nicotine patch or gum\]) during the 3 months prior to screening. * Subjects who have used the following within 7 days prior to study drug administration, unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety: * any over-the-counter systemic or topical medication * herbal remedies * vitamin supplements * mineral supplements * Subjects who have received any medications, including St John's Wort, known to chronically alter drug absorption or elimination processes within 30 days prior to study drug administration unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety. * Subjects who have received: * any prescribed systemic or topical medication within 15 days prior to study drug administration unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety. * slow release medicinal formulations considered to still be active within 15 days prior to study drug administration, unless in the opinion of the Investigator, the medication will not interfere with the study procedures or compromise safety. * coumarins (e.g. warfarin) at any time in the subject's lifetime. * Subjects who have an abnormality in heart rate, blood pressure, temperature, oxygen saturation or respiration rate that, in the opinion of the Investigator, increases the risk of participating in the study, at screening and prior to study drug administration. * Specific exclusion criteria at screening and/or prior to dosing are heart rate \<40 bpm or \>110 bpm, systolic blood pressure \<90 mmHg or \>150 mmHg, diastolic blood pressure \<40 mmHg or \>90 mmHg, oxygen saturation \<94%, confirmed by a repeat assessment. * Subjects with a positive urine drug or alcohol screen at screening or first admission. * Subjects who have an abnormality in the 12-lead ECG that, in the opinion of the Investigator, increases the risk of participating in the study, at screening and prior to study drug administration. * Specific exclusion criterion at screening and/or prior to dosing is QTcF value \>450 ms, confirmed by a repeat assessment. * Subjects who are still participating in a clinical study (e.g. attending follow-up visits) or who have been administered an investigational drug (new chemical entity) in the 30 days prior to study drug administration. * Subjects with a significant history of drug allergy as determined by the Investigator, including known or suspected allergy to any of the study drug components. * Subjects with a known or suspected shellfish allergy or a positive skin prick test for shellfish allergy at screening or first admission. * Subjects who have any clinically significant abnormal physical examination finding at check-in (Day -1 or Day -2). Specific exclusion criterion is any skin condition or finding that would limit a local injection site examination. * Subjects who have any clinically significant allergic condition (excluding non-active hayfever) as determined by the Investigator. * Subjects with, or with a history of, any clinically significant neurological, gastrointestinal, renal, hepatic, cardiovascular, psychiatric, respiratory, metabolic, endocrine, haematological or other major disorders as determined by the Investigator. * Subjects who have had a clinically significant illness within 4 weeks of the start of dose administration as determined by the Investigator. * Subjects who have any clinically significant abnormal laboratory safety findings, in the opinion of the Investigator (one repeat assessment is acceptable), at screening and prior to study drug administration. * Specific exclusion criteria at screening and/or prior to dosing are fasting serum glucose \<60 mg/dL or \>115 mg/dL, serum phosphorous \>1.5 х upper limit of normal (ULN), serum blood urea nitrogen \>1.5 х ULN, serum alanine aminotransferase (ALT) \>1.5 х ULN, serum aspartate aminotransferase (AST) \>1.5 х ULN, serum total bilirubin \>1.5 х ULN, serum creatinine \>1.5 х ULN, hemoglobin \<12 g/100 mL. * Subjects who: * are known to have serum hepatitis * are carriers of the hepatitis B surface antigen (HBsAg) * are carriers of the hepatitis C antibody * have a positive result to the test for human immunodeficiency virus (HIV) antibodies. * Subjects who have previously received a dose in this study. * Subjects who, in the opinion of the Investigator, should not participate in the study. * Subjects with a history of complications with anesthesia, such as malignant hyperthermia.

Outcomes

Primary Outcomes

Adverse events related to NAVX-010

Any signs or symptoms will be observed and elicited at least once a day by open questioning. Subjects will also be encouraged to spontaneously report AEs occurring at any other time during the study. Any AEs and remedial action required will be recorded in the subject's source data. Subjects experiencing AEs will be followed clinically until their health has returned to baseline status or until all parameters have returned to normal or have otherwise been explained.

Time frame: Monitored from dosing day until 5 days after dosed

Oral body temperature changes

Oral body temperature in °C (BT) will be measured. All measurements will be taken as single readings. Measurements will be repeated once if outside the relevant clinical reference ranges. If repeated, the repeat value will be used in the data analysis. Clinical research unit reference ranges will be applied.

Time frame: BT measured at screening day, check in day, -1 hour relative to dose, 24 hrs postdose and at day 5 after dosed.

12-lead ECG measurements changes

At check-in, 12-lead ECG will be recorded in triplicate in the supine position for baseline measurements. The average value for each ECG parameter will be calculated as the baseline value. At all other times, a single 12-lead resting ECG with a 10-second rhythm strip will be recorded after the subject has been supine for at least 5 minutes.The 12-lead ECG will be repeated once if either of the following criteria apply:The QTcF is \>450 ms; The QTcF change from baseline (check-in) is \>60 ms. Additional 12-lead ECGs will be performed at other times if judged to be clinically appropriate or if the ongoing review of the data suggests a more detailed assessment of ECGs is required. The ECG machine will compute the PR, QT and QTc intervals, QRS duration and heart rate. The QT interval will be corrected for heart rate using Fridericia's formula.

Time frame: 12-lead ECG will be measured at: screening day; check in day; 0.5, 1, 6, 12 and 24 hous postdose and day 5 after dosed.

Changes in cardiac rhythm monitored by telemetry

Cardiac rhythm will be monitored by telemetry. Telemetry strips will be printed out at the times indicated in the Study Plan. In addition, staff members will be instructed to print out ECGs if either of the following criteria apply: The QTcF is \>450 ms; The QTcF change from baseline (check-in) is \>60 ms. In such an event, ECGs will continue to be printed out every 20 minutes until the QTcF value has returned to normal.

Time frame: Continuous telemetry monitoring from -1 hour to 24 hour relative to dose. Telemetry strips will be printed out at 2, 3, 4 and 5 hours postdose.

Changes in clinical laboratory evaluations

Blood and urine samples will be collected for clinical laboratory evaluations at the times indicated in the Study Plan. Additional clinical laboratory evaluations will be performed at other times if judged to be clinically appropriate or if the ongoing review of the data suggests a more detailed assessment of clinical laboratory safety is required. The following evaluations will be performed: Serum biochemistry, hematology, coagulation, urinalysis and serology.

Time frame: Clinical laboratories evaluations will be measured at: screening day; check in day; -1 hour and 24 hour relative to dose and day 5 after dosed.

Changes in blood glucose and phosphorous evaluations

Blood samples will be collected for serum glucose (mg/dL) and phosphorous (mg/dL) evaluations.

Time frame: The evaluations will be measured 30 minutes and 1 hour post adminitration of the drug.

Physical examination changes

A full physical examination will be performed at the times indicated in the Study Plan and an abbreviated physical examination may be performed at other times.

Time frame: Physical examination will be performed at: check in day, 1 and 24 hours after dose administration and at day 5 after dosed.

Changes in the general wellbeing of the subject

Subjects will be asked to complete a clinical study questionnaire to assess tolerance to the study drug, with the assistance of a suitably trained CRU staff member. Subjects will be asked questions about their general wellbeing and the injection site over the period either since dosing or since the last questionnaire, as applicable. In addition, the injection site will be assessed by the CRU staff member conducting the questionnaire.

Time frame: The questionnaire will be conducted every hour for 12 hours postdose and at approximately 24 hours postdose.

Blood pressure changes

Systolic and Diastolic blood pressure in mmHg (BP), will be measured. At check-in, blood pressure, will be measured in triplicate within a 10-minute window. The median value for systolic and diastolic blood pressure, will be used as the baseline value in the data analysis. All other measurements will be taken as single readings. Measurements will be repeated once if outside the relevant clinical reference ranges. If repeated, the repeat value will be used in the data analysis. Clinical research unit reference ranges will be applied.

Time frame: BP: measured at screening day, check in day, continuous monitoring during dose day (until 24 hrs) and day 5 after dosed.

Heart rate changes

Heart rate in bpm (HR) will be measured. At check-in, heart rate will be measured in triplicate within a 10-minute window. The median value for heart rate will be used as the baseline value in the data analysis. All other measurements will be taken as single readings. Measurements will be repeated once if outside the relevant clinical reference ranges. If repeated, the repeat value will be used in the data analysis. Clinical research unit reference ranges will be applied.

Time frame: HR: measured at screening day, check in day, continuous monitoring during dose day (until 24 hrs) and day 5 after dosed.

Respiratory rate changes

Respiratory rate in breaths/min (RR) will be measured. At check-in, respiratory rate will be measured in triplicate within a 10-minute window. The median value for respiratory rate will be used as the baseline value in the data analysis. All other measurements will be taken as single readings. Measurements will be repeated once if outside the relevant clinical reference ranges. If repeated, the repeat value will be used in the data analysis. Clinical research unit reference ranges will be applied.

Time frame: RR: measured at screening day, check in day, continuous monitoring during dose day (until 24 hrs) and day 5 after dosed.

Oxygen saturation changes

Oxygen saturation in % (OS) will be measured. All measurements will be taken as single readings. Measurements will be repeated once if outside the relevant clinical reference ranges. If repeated, the repeat value will be used in the data analysis. Clinical research unit reference ranges will be applied.

Time frame: OS: measured at screening day, check in day, continuous monitoring during dose day (until 24 hrs) and day 5 after dosed.

Secondary Outcomes

Pharmacokinetic of NAVX-010: Area under the curve from time 0 up to the time of last quantifiable (AUC0-t) plasma concentration.

Blood samples (approximately 1 x 10 mL) will be taken by venipuncture or cannulation at the times indicated in the Study Plan to calculate the AUC0-t of GTX 2 and GTX 3. The Area under the concentration-time curve from time 0 up to the time of last quantifiable plasma concentration (tlast), calculated using the linear trapezoidal rule for increasing concentrations and the logarithmic rule for decreasing concentrations.