Study of the Safety and Pharmacokinetics of KSP-1007 Alone and Coadministered With Meropenem in Healthy Subjects

Sumitovant Biopharma

Status and phase: Completed; Phase 1

Conditions: Bacterial Infections

Treatments: Drug: Meropenem; Other: Placebo:0.9% sodium chloride; Drug: KSP-1007

Study type: Interventional

Funder types: Industry

Identifiers

NCT05226923

KSP-1007-101

Details and patient eligibility

About

This study is a first-in-human, Phase 1, randomized, double- blind, four-part, dose-escalation study to assess the safety, tolerability, and pharmacokinetics of single (Part 1) and repeat (Part 2) escalating intravenous doses of KSP-1007. Repeated escalating doses of KSP-1007 will be co-administered with meropenem (Part 3) and single, ascending doses of KSP-1007 will be administered alone in healthy Japanese subjects (Part 4)

Full description

Carbapenem-resistant Gram-negative bacteria are responsible for serious, life-threatening infections and are regarded as an urgent threat by the Centers for Disease Control and Prevention and the World Health Organizations. One principal mechanism of carbapenem resistance is bacterial production of carbapenemases, which reduce the effectiveness of meropenem and other carbapenem class antibiotics. Sumitovant Biopharma is developing a fixed combination of meropenem and KSP-1007 for the treatment of serious bacterial infections.

Enrollment: 123 patients

Sex: All

Ages: 18 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy male or female subjects 18 to 55 years of age, inclusive
• Females that engage in heterosexual activity must agree to use a highly selective birth control (BC) method (< 1% failure rate per year) throughout the study, or have a documented reproductive status of non-childbearing based on medical history, or is postmenopausal
• Males that engage in heterosexual activity that has the risk of pregnancy must agree to use effective BC and agree to not donate sperm during the study and for at least 90 days after the last dose of the study medication
• Body mass index (BMI) 2: 18 kg/m2 and :s 32 kg/m2

Exclusion criteria

• History of Gilbert's Syndrome
• History of severe allergic reactions to β-lactams or β-lactamase inhibitors or a history allergic reactions to multiple medications.
• Pregnant female, determined by positive serum or urine human chorionic gonadotropin pregnancy test at Screening, or prior to dosing
• Lactating female
• Donation of plasma within 7 days prior to dosing. Donation or loss of blood (excluding volume drawn at Screening) of > 499 mL within 56 days prior to Day 1
• Participation in a study with an investigational drug or device study with last dose of investigational drug within 30 days (90 days if the study involved a biologic, cellular, or vaccine product) or 5 half-lives, whichever is longer, before study treatment administration
• Subjects with abnormal hepatic and/or renal function, that could interfere with the metabolism, and/or excretion of the study treatments
• Abnormal blood pressure, either low (defined as < 90 mmHg systolic and/ or < 45 mmHg diastolic) or high (defined as > 140 mmHg systolic and/ or > 90 mmHg diastolic) at Screening
• Positive serology for hepatitis B virus (HBV), hepatitis C virus (HCV), or HIV at Screening. Subjects who test positive for hepatitis B core antibody (HBcAb) or hepatitis B surface antigen (HBsAg) also will be ineligible. Evidence of prior HBV vaccination (positive hepatitis B surface antibody [HBsAb)) is not exclusionary.
• Subjects unable to abstain from alcohol for 48 hours prior to admission through to completion of the Follow-up visit

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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123 participants in 6 patient groups, including a placebo group

KSP-1007 single ascending dose

Experimental group

Description:

Single, ascending intravenous dose of KSP-1007

Treatment:

Drug: KSP-1007

Placebo single dose

Placebo Comparator group

Description:

Single dose of placebo (0.9% normal saline)

Treatment:

Other: Placebo:0.9% sodium chloride

KSP-1007 multiple ascending dose

Experimental group

Description:

Multiple, ascending, intravenous doses of KSP-1007

Treatment:

Drug: KSP-1007

Placebo multiple dose

Placebo Comparator group

Description:

Multiple doses of placebo (0.9% saline)

Treatment:

Other: Placebo:0.9% sodium chloride

KSP-1007 multiple ascending dose + Meropenem multiple dose

Experimental group

Description:

Multiple, ascending intravenous doses of KSP-1007 and multiple doses of meropenem (fixed dose)

Treatment:

Drug: Meropenem

Drug: KSP-1007

Placebo + Meropenem multiple dose

Placebo Comparator group

Description:

Multiple doses of placebo (0.9% normal saline) plus multiple doses of meropenem (fixed dose)

Treatment:

Drug: Meropenem

Other: Placebo:0.9% sodium chloride