This Study Will Investigate the Safety, Tolerability and Pharmacokinetic Profile of Repeat Oral Doses of GSK2140944 in Healthy Adult Subjects

NCT01706315 | Completed Phase 1

• 1 other identifier: 116778
• Study Type: interventional
• Target: 72
• Locations: 1 country
• Sites: 1

Brief Summary

This will be a randomized, placebo-controlled, single blind study to investigate the safety, tolerability and pharmacokinetic (PK) profile of GSK2140944 following repeat oral doses in healthy adult subjects. The study will include a Screening period (40 days), Treatment period (16 days) and a Follow-up period (26 to 30 days). A single dose will be administered on Day 1 for characterization of single dose PK, followed by twice-daily (BID) or thrice-daily (TID) dosing on Days 3 to 16. Subjects may only be randomized to one cohort per the randomization schedule. Up to 6 cohorts will be enrolled using a sequential panel. Subjects in Cohort 1 will receive GSK2140944 (6) and placebo (2). Subsequent cohorts will enroll 16 subjects such that 12 subjects will receive GSK2140944 and 4 subjects will receive placebo, per dose level according to the randomization schedule. Dose escalations are planned to run in successive weeks. Cohort 2 may begin dosing once subjects in Cohort 1 have completed 7 days of BID dosing, PK data is reviewed and safety data from at least 6 subjects is available. Each subsequent dose escalation will commence only when GSK2140944 safety data and available PK data of at least 12 subjects dosed at the previous dose level have been reviewed. The number of cohorts may be reduced or expanded if needed. The first planned dose is 400 milligram (mg) BID but may be modified based upon emergent PK, safety and tolerability data from ongoing clinical study BTZ115198 evaluating single and repeat intravenous (IV) doses of GSK2140944. The projected dose for Cohort 2 is 800 mg BID, Cohort 3 is 1500 mg BID, Cohort 4 is 2300 mg BID or 1500 mg TID and Cohort 5 and cohort 6 will be decided later. The planned maximum dose is 2500 mg TID but may be modified based upon emergent safety, tolerability and PK data. Doses of GSK2140944 or placebo will be administered following a moderate fat meal.

Conditions

Infections, Respiratory Tract

Outcome Measures

Primary Outcomes (19)

• GSK2140944 clinical safety data assessed as change from baseline in 12-lead ECG

  12-lead ECGs will be obtained at each timepoint using an ECG machine, after the subject has rested in a semi-supine position for at least 10 minutes

  Day 1, Day 4, Day 7, Day 10, Day 13, Day 16, Day 18 and at the Follow-up visit

• GSK2140944 clinical safety data from dual-lead cardiac monitoring

  Continuous dual-lead cardiac monitoring will be obtained at each timepoints using an ECG machine

  Day 1

• GSK2140944 clinical safety data assessed as change from baseline in clinical laboratory tests

  Clinical laboratory assessments will include hematology, clinical chemistry, routine urinalysis and additional parameters

  Day -2 and pre-morning dose on Day 2, Day 5, Day 8, Day 11, and Day 14; on the morning of Day 17 and at the Follow-up visit

• GSK2140944 clinical safety data assessed as by number of adverse events (AE)

  Safety and tolerability parameters will include recording of AEs, throughout the study

  Up to the Follow-up visit

• GSK2140944 clinical safety data assessed as change from baseline in blood pressure

  Vital sign measurements will be done in semi-supine position and will include systolic and diastolic blood pressure

  Day -1, Day 1, Day 4, Day 7, Day 10, Day 13, Day 16, Day 18 and the Follow-up visit

• GSK2140944 clinical safety data assessed as change from baseline in heart rate

  Vital sign measurements will be done in semi-supine position and will include pulse rate

  Day -1, Day 1, Day 4, Day 7, Day 10, Day 13, Day 16, Day 18 and the Follow-up visit

• Pharmacokinetic parameter: AUC(0-12) following single dose of GSK2140944

  Pharmacokinetic data will include area under the curve from time zero (pre-dose) to 12 hour post-dose (AUC(0-12)) following single dose of GSK2140944

  Day 1

• Pharmacokinetic parameter: AUC(0-24) following single dose of GSK2140944

  Pharmacokinetic data will include area under the curve from time zero (pre-dose) to 24 hour post-dose (AUC(0-24)) following single dose of GSK2140944

  Up to Day 2

• Pharmacokinetic parameter: AUC(0-t) following single dose of GSK2140944

  Pharmacokinetic data will include area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC(0-t)) following single dose of GSK2140944

  Up to Day 3

• Pharmacokinetic parameter: AUC(0-infinity) following single dose of GSK2140944

  Pharmacokinetic data will include area under the concentration-time curve from time zero (pre-dose) extrapolated to infinite time (AUC(0-infinity)) following single dose of GSK2140944

  Up to Day 3

• Pharmacokinetic parameter: Cmax following single dose of GSK2140944

  Pharmacokinetic data will include maximum observed concentration (Cmax) following single dose of GSK2140944

  Up to Day 3

• Pharmacokinetic parameter: tmax following single dose of GSK2140944

  Pharmacokinetic data will include time of occurrence of Cmax (tmax) following single dose of GSK2140944

  Up to Day 3

• Pharmacokinetic parameter: t1/2 following single dose of GSK2140944

  Pharmacokinetic data will include terminal phase half-life (t1/2) following single dose of GSK2140944

  Up to Day 3

• Pharmacokinetic parameter: AUC(0-tau) following repeat dose of GSK2140944

  Pharmacokinetic data will include area under the concentration-time curve over the dosing interval (AUC(0-tau)) following repeat dose of GSK2140944

  Day 14, Day 15 and Day 16

• Pharmacokinetic parameter: Cmax following repeat dose of GSK2140944

  Pharmacokinetic data will include Cmax following repeat dose of GSK2140944

  Day 14, Day 15 and Day 16

• Pharmacokinetic parameter: tmax following repeat dose of GSK2140944

  Pharmacokinetic data will include tmax following repeat dose of GSK2140944

  Day 14, Day 15 and Day 16

• Pharmacokinetic parameter: Ctau following repeat dose of GSK2140944

  Pharmacokinetic data will include pre-dose (trough) concentration at the end of the dosing interval (Ctau) following repeat dose of GSK2140944

  Day 14, Day 15 and Day 16

• Pharmacokinetic parameter: Ro following repeat dose of GSK2140944

  Pharmacokinetic data will include accumulation ratio (Ro) following repeat dose of GSK2140944

  Day 14, Day 15 and Day 16

• Pharmacokinetic parameter: AUC(0-8) following single dose of GSK2140944

  Pharmacokinetic data will include area under the curve from time zero (pre-dose) to 8 hour post-dose (AUC\[0-8\]) following single dose of GSK2140944

  Day 1

Secondary Outcomes (9)

• To assess preliminary dose proportionality using PK parameter AUC(0-infinity) following single dose of GSK2140944

  Up to Day 3

• To assess preliminary dose proportionality using PK parameter Cmax following single dose of GSK2140944

  Up to Day 3

• To assess preliminary dose proportionality using PK parameter AUC(0-tau) following repeat doses of GSK2140944

  Day 14, Day 15 and Day 16

• To assess preliminary dose proportionality using PK parameter Cmax following repeat doses of GSK2140944

  Day 14, Day 15 and Day 16

• To examine extent of accumulation using PK parameter Ro using AUC(0-tau) following repeat doses of GSK2140944

  Day 14, Day 15 and Day 16

Study Arms (12)

Cohort 1 - GSK2140944 400 mg

EXPERIMENTAL

Subjects will be randomized in 6:2 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) BID oral doses) or placebo for approximately 15 days

Drug: GSK2140944

Cohort 1 - Placebo

PLACEBO COMPARATOR

Subjects will be randomized in 6:2 ratio to receive either GSK2140944 BID or matching placebo for approximately 15 days

Drug: Placebo

Cohort 2 - GSK2140944 800 mg

EXPERIMENTAL

Subjects will be randomized in 12:4 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) BID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 2 will be decided based on the safety and PK data from six subjects in Cohort 1

Drug: GSK2140944

Cohort 2 - Placebo

PLACEBO COMPARATOR

Subjects will be randomized in 12:4 ratio to receive either GSK2140944 BID or matching placebo for approximately 15 days

Drug: Placebo

Cohort 3 - GSK2140944 1500 mg

EXPERIMENTAL

Subjects will be randomized in 12:4 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) BID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 3 will be decided on the safety data and available PK data from at least 12 subjects dosed at the Cohort 2

Drug: GSK2140944

Cohort 3 - Placebo

PLACEBO COMPARATOR

Subjects will be randomized in 12:4 ratio to receive either GSK2140944 bid or matching placebo for approximately 15 days

Drug: Placebo

Cohort 4 - GSK2140944 2500 mg

EXPERIMENTAL

Subjects will be randomized in 12:4 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) BID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 4 will be decided on the safety data and available PK data from at least 12 subjects dosed at the Cohort 3

Drug: GSK2140944

Cohort 4 - Placebo

PLACEBO COMPARATOR

Subjects will be randomized in 12:4 ratio to receive either GSK2140944 bid or matching placebo for approximately 15 days

Drug: Placebo

Cohort 5 - GSK2140944 TBD

EXPERIMENTAL

Subjects will be randomized in 6:2 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) TID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 5 will be decided on the safety data and available PK data from at least 12 subjects dosed at the Cohort 4

Drug: GSK2140944

Cohort 5 - Placebo

PLACEBO COMPARATOR

Subjects will be randomized in 6:2 ratio to receive either GSK2140944 TID or matching placebo for approximately 15 days

Drug: Placebo

Cohort 6 - GSK2140944 TBD

EXPERIMENTAL

Subjects will be randomized in 6:2 ratio to receive either GSK2140944 (Day 1: Single oral dose Days 3 to 16: (14 Days) TID oral doses) or placebo for approximately 15 days. GSK2140944 dose in Cohort 5 will be decided on the safety data and available PK data from at least 6 subjects dosed at the Cohort 5

Drug: GSK2140944

Cohort 6 - Placebo

PLACEBO COMPARATOR

Subjects will be randomized in 6:2 ratio to receive either GSK2140944 TID or matching placebo for approximately 15 days

Drug: Placebo

Interventions

GSK2140944 DRUG

GSK2140944 will be available as immediate release capsules of dose strength 100 mg and 500 mg

Cohort 1 - GSK2140944 400 mg; Cohort 2 - GSK2140944 800 mg; Cohort 3 - GSK2140944 1500 mg; Cohort 4 - GSK2140944 2500 mg; Cohort 5 - GSK2140944 TBD; Cohort 6 - GSK2140944 TBD

Placebo DRUG

Matching placebo will be available

Cohort 1 - Placebo; Cohort 2 - Placebo; Cohort 3 - Placebo; Cohort 4 - Placebo; Cohort 5 - Placebo; Cohort 6 - Placebo

Eligibility Criteria

• Age: 18 Years - 60 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase and bilirubin \<=1.5x upper limit of normal (ULN) (isolated bilirubin \>1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin \<35%).
• Healthy as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring. - A subject with a clinical abnormality or laboratory parameters outside the reference range for the population being studied may be included only if the Investigator and the GlaxSmithKline (GSK) Medical Monitor agree that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.
• Male or female between 18 and 60 years of age inclusive, at the time of signing the informed consent.
• A female subject is eligible to participate if she is of: Non-childbearing potential defined as pre-menopausal females with a documented tubal ligation or hysterectomy; or postmenopausal defined as 12 months of spontaneous amenorrhea. To confirm post-menopausal status, a blood sample for simultaneous follicle stimulating hormone (FSH) \>40 MlU/ml and estradiol \<40 pg/ml (\<147 pmol/L) is confirmatory. Male subjects with female partners of child-bearing potential must agree to use the contraception methods. This criterion must be followed from the time of the first dose of study medication until the final follow-up visit.
• Body weight \>=50 kg and body mass index (BMI) within the range 19 to 31 kg/m2 (inclusive).
• Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

You may not qualify if:

• A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening or positive Human Immunodeficiency Virus (HIV) antibody.
• Current or chronic history of liver disease, or known hepatic or biliary abnormalities.
• Any clinically significant central nervous system (e.g., seizures), cardiac, pulmonary, metabolic, renal, hepatic or gastrointestinal conditions or history of such conditions that, in the opinion of the investigator may place the subject at an unacceptable risk as a participant in this trial or may interfere with the absorption, distribution, metabolism or excretion of drugs.
• A screening or Day -2 urinalysis positive for protein or glucose (greater than "trace" findings of protein or glucose).
• A serum creatinine value between screening and Day -2 visit that is increased by more than 0.2 mg/dL (or 15.25 umol/L) changes.
• History of photosensitivity to quinolones and tendon rupture.
• Unwillingness to commit to avoid excessive exposure to sunlight which would cause a sunburn reaction from first dose up to and including the follow-up visit.
• A positive urine test for drugs of abuse or alcohol (or alcohol breath test) at screening or Day -2.
• History of drug abuse within 6 months of the study
• History of smoking or use of nicotine containing products within 3 months of screening, or a positive urine cotinine indicative of smoking at screening.
• History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of \>14 drinks for males or \>7 drinks for females. One drink is equivalent to 12 g of alcohol: 12 ounces (360 ml) of beer, 5 ounces (150 ml) of wine or 1.5 ounces (45 ml) of 80 proof distilled spirits.
• The subject has participated in a clinical trial and has received a drug or a new chemical entity within 30 days or 5 half-lives, or twice the duration of the biological effect of any drug (whichever is longer) prior to the first dose of current study medication.
• Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements within 7 days or 5 half-lives (whichever is longer) prior to the first dose of study medication, or use of St. John's Wort within 14 days prior to the first dose of study medication. By exception, the volunteer may take paracetamol or acetaminophen (\<=2 grams/day) up to 48 hours prior to the first dose of study medication. However, the Investigator and GSK study team can review medication on a case by case basis to determine if its use would compromise subject safety or interfere with the study procedures or data interpretation.
• History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.
• History of sensitivity to heparin or heparin-induced thrombocytopenia (if the clinical research unit uses heparin to maintain intravenous cannula patency).

Sponsors & Collaborators

• GlaxoSmithKline: lead

Study Sites (1)

GSK Investigational Site

Overland Park, Kansas, 66211, United States

Location

Related Publications (1)

• Tiffany C, Dumont EF, Hossain M, Srinivasan M, Swift B. Pharmacokinetics, safety, and tolerability of gepotidacin administered as single or repeat ascending doses, in healthy adults and elderly subjects. Clin Transl Sci. 2022 Sep;15(9):2251-2264. doi: 10.1111/cts.13359. Epub 2022 Jul 13.

  PMID: 35769034 DERIVED

Related Links

• Results for study 116778 can be found on the GSK Clinical Study Register.
• Researchers can use this site to request access to anonymised patient level data and/or supporting documents from clinical studies to conduct further research.

MeSH Terms

Conditions

Respiratory Tract Infections

Interventions

gepotidacin

Condition Hierarchy (Ancestors)

Infections; Respiratory Tract Diseases

Study Officials

• GSK Clinical Trials

  GlaxoSmithKline

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 11, 2012
• First Posted: October 15, 2012
• Study Start: October 17, 2012
• Primary Completion: December 13, 2013
• Study Completion: December 13, 2013
• Last Updated: May 9, 2017

Record last verified: 2017-05

Data Sharing

• IPD Sharing: Will share

Locations

US (1)