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Completed

NCT Number: NCT04865393

Phase 1 Study of PK and Safety of SPR206 in Subjects With Various Degrees Of Renal Function

Evaluation of the pharmacokinetics (PK) of SPR206 in subjects with normal renal function, subjects with various degrees of renal insufficiency, and subjects with end-stage renal disease (ESRD) receiving hemodialysis (HD) therapy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Medical Facility, Auckland, New Zealand

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • BMI ≥ 18.5 and ≤ 39.9 (kg/m2) and weight between 50.0 and 130.0 kg (inclusive)
  • Medically healthy without clinically significant abnormalities (Healthy Volunteers) or medically stable without clinically significant acute or chronic illness (Subjects with varying degrees of Renal Disease)
  • Normal renal function with eGFR ≥90 mL/min/1.73m2 (Cohort 1), or renal insufficiency with eGFR 60 to <90 mL/min/1.73m2 (Cohort 2), 30 to <60 mL/min/1.73m2 (Cohort 3), or <30 mL/min/1.73m2 (Cohort 4), calculated using Modification of Diet in Renal Disease (MDRD). Subjects with ESRD must be receiving hemodialysis at least 3 times per week for at least 3 months at Screening (Cohort 5 only)
  • Non-smoker for at least 1 month prior to screening for the study
  • Ability and willingness to abstain from alcohol, caffeine, xanthine-containing beverages or food
  • Other inclusion criteria per protocol

Key Exclusion Criteria:

  • Any clinically significant medical history or abnormal findings upon physical examination, or clinical laboratory tests, not specifically excluded in other criteria below that, in the opinion of the Investigator, might confound the results of the study or pose an additional risk in administering study drug to the subject
  • Electrocardiogram (ECG) with QTcF interval duration equal or greater than 500 msec
  • Hemoglobin (HB), hematocrit (HCT), white blood cell count (WBC), or platelet count less than the lower limit of normal range of the reference laboratory (Cohort 1). HB <8.5 gm/dL, WBC ≤3,000 cells/μL or platelet count ≤100,000 cells/μL (Cohorts 2-5)
  • Results of biochemistry tests for alanine aminotransferase (ALT), aspartate aminotransferase (AST) and bilirubin greater than 1.5 X the upper limit of normal (ULN) for the reference laboratory
  • Recent history (within 6 months) of known or suspected Clostridium difficile infection
  • History of chronic liver disease, cirrhosis, or biliary disease
  • History of seizure disorder except childhood history of febrile seizures
  • Positive urine drug/alcohol testing
  • Positive testing for human immunodeficiency virus1/2 (HIV 1/2), hepatitis B surface antigen (HBsAg) or hepatitis C (HCV) antibodies
  • History of substance abuse or alcohol abuse
  • Known history of clinically significant hypersensitivity reaction or anaphylaxis to any medication
  • Other exclusion criteria per protocol

Treatment and study plan

SPR206

Drug

SPR206 100 mg single-dose IV infused over 1 hour

Primary outcomes

  1. Time to the maximum plasma concentration (Tmax)

    Time frame: 36 hours after start of study drug IV infusion

  2. Maximum plasma concentration (Cmax)

    Time frame: 36 hours after start of study drug IV infusion

  3. Area under the concentration-time curve from time 0 to last measurable timepoint (AUC0-t)

    Time frame: 36 hours after start of study drug IV infusion

  4. Area under the concentration-time curve from time 0 to infinity (AUC0-∞)

    Time frame: 36 hours after start of study drug IV infusion

Secondary outcomes

  1. Area under the concentration-time curve from time 0 to 8 hours (AUC0-8)

    Time frame: 8 hours after start of study drug IV infusion

  2. Terminal Elimination Rate Constant (kel)

    Time frame: 36 hours after start of study drug IV infusion

  3. Terminal half-life (t1/2)

    Time frame: 36 hours after start of study drug IV infusion

  4. Total body clearance (CL)

    Time frame: 36 hours after start of study drug IV infusion

  5. Renal clearance (CLR)

    Time frame: 36 hours after start of study drug IV infusion

  6. Steady-state volume of distribution (Vss)

    Time frame: 36 hours after start of study drug IV infusion

  7. Amount of drug excreted in urine by interval (Aet) for Cohorts 1-4

    Time frame: 36 hours after start of study drug IV infusion

  8. Cumulative amount of drug excreted in urine at the end of each interval (Aeu) for Cohorts 1-4

    Time frame: 36 hours after start of study drug IV infusion

  9. Fraction of drug excreted in the urine expressed as a percentage (Ae%) for Cohorts 1-4

    Time frame: 36 hours after start of study drug IV infusion

  10. Fraction of dose excreted in the urine over a collection interval (Fe) for Cohorts 1-4

    Time frame: 36 hours after start of study drug IV infusion

  11. Cumulative fraction of dose excreted in the urine over (Feu) for Cohorts 1-4

    Time frame: 36 hours after start of study drug IV infusion

  12. Extraction ratio (ER) for subjects on dialysis (Cohort 5)

    Time frame: Up to 1 day post dose - between start and end of hemodialysis

  13. Estimated hemodialysis clearance (CLHD) for subjects on dialysis (Cohort 5)

    Time frame: Up to 1 day post dose - between start and end of hemodialysis

  14. Amount of the dose removed by hemodialysis (XHD) for subjects on dialysis (Cohort 5)

    Time frame: Up to 1 day post dose - between start and end of hemodialysis

  15. Incidence of Treatment-Emergent Adverse Events

    Time frame: 14 days post start of last study drug IV infusion

    To assess the incidents of treatment-emergent adverse events following SPR206 intravenous dose administration. AEs will be classified by System Organ Class (SOC) and Preferred Term (PT). Incidence, frequency, severity and duration will be presented.

  16. Incidence of abnormal vital sign assessments - blood pressure

    Time frame: 14 days post study drug IV infusion

    To assess the incidents of abnormal systolic and diastolic blood pressure assessments following SPR206 intravenous dose administration. Values and changes from baseline at each scheduled time-point will be summarized using descriptive statistics (n, mean, SD, median, minimum, and maximum). Significant changes from baseline will be presented.

  17. Incidence of abnormal vital sign assessments - body temperature

    Time frame: 14 days post study drug IV infusion

    To assess the incidents of abnormal body temperature assessments following SPR206 intravenous dose administration. Values and changes from baseline at each scheduled time-point will be summarized using descriptive statistics (n, mean, SD, median, minimum, and maximum). Significant changes from baseline will be presented.

  18. Incidence of abnormal physical exam assessments

    Time frame: 14 days post study drug IV infusion

    To assess the incidents of abnormal body system assessments following SPR206 intravenous dose administration. Changes from baseline in physical examination findings will be classified as Normal, Abnormal NCS, and Abnormal CS. Frequency counts will be presented.

  19. Incidence of abnormal ECG assessments - heart rate

    Time frame: 14 days post study drug IV infusion

    To assess the incidents of abnormal heart rate assessment following SPR206 intravenous dose administration. Cardiac (12-Lead ECG) for heart rate will be classified as normal, abnormality that is NCS, and CS abnormality. Frequency counts by dose group and timepoint of collection will be presented.

  20. Incidence of abnormal ECG assessments - PR, RR, QRS, QT and QTcF interval

    Time frame: 14 days post study drug IV infusion

    To assess the incidents of abnormal PR interval, RR interval, QRS interval, QT interval and QTcF interval assessments following SPR206 intravenous dose administration. Cardiac (12-Lead ECG) results will be classified as normal, abnormality that is NCS, and CS abnormality. Frequency counts by dose group and timepoint of collection will be presented.

  21. Incidence of abnormal safety laboratory assessments

    Time frame: 14 days post study drug IV infusion

    To assess the incidents of abnormal hematology, serum chemistry, coagulation and urinalysis assessments following SPR206 intravenous dose administration. Values and changes from baseline at each scheduled time-point will be summarized using descriptive statistics (n, mean, SD, median, minimum, and maximum). Frequency counts of significant changes from baseline will be presented.

Sponsors and collaborators

Lead sponsor

Spero Therapeutics

Industry

Collaborators

  • United States Department of Defense

Registry information

Official study title

A Phase 1, Open-label Study to Assess the Safety and Pharmacokinetics of SPR206 Following a Single IV Dose of SPR206 in Subjects With Varying Degrees of Renal Function

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Apr 29, 2021
Registry last updated
Apr 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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