SPR206
DrugSPR206 100 mg single-dose IV infused over 1 hour
NCT Number: NCT04865393
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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Notify Me18 year and older
All sexes
Interventional
Phase 1
Medical Facility, Auckland, New Zealand
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
SPR206 100 mg single-dose IV infused over 1 hour
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 8 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: 36 hours after start of study drug IV infusion
Time frame: Up to 1 day post dose - between start and end of hemodialysis
Time frame: Up to 1 day post dose - between start and end of hemodialysis
Time frame: Up to 1 day post dose - between start and end of hemodialysis
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.
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.
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.
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.
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.
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.
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.
Spero Therapeutics
Industry
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
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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