Last updated: 11/04/2018 00:53:47
Pro-arrhythmic potential of GSK3039294 in healthy subjects
GSK study ID
208741
Clinicaltrials.gov ID
EudraCT ID
EU CT Number
Not applicable
Trial status
Withdrawn
Withdrawn
Trial overview
Official title: A randomised, double-blind, placebo controlled, repeat-dose, cross-over Phase I study to evaluate the pro-arrhythmic potential of GSK3039294 in healthy participants
Trial description: GSK3039294 has been developed to offer an orally available alternative to parenteral GSK2315698 (miridesap) for plasma serum amyloid P component (SAP) depletion prior to and following use of anti-SAP Monoclonal Antibody (mAb) in the treatment of systemic amyloidosis. The primary objectives of the study are to assess the cardiac arrhythmic potential of GSK3039294 and evaluate safety and tolerability of repeat doses of GSK3039294, in healthy subjects relative to placebo for the same duration. This study will consist of two parts, Part A and a conditional Part B. Part A is designed as a randomized double-blinded, 3 period, placebo-controlled, repeat-dose, crossover study. The decision to initiate Part B will be based on an evaluation of data from Part A, which will include an overall assessment of safety, pharmacokinetics (PK) and pharmacodynamics (PD). In Part A, there will be three treatment periods with 7 days of dosing in each and minimum 7-day washout period between each treatment session. Each subject will receive two dose levels of GSK3039294 and placebo. In Part B, there will be two treatment periods with 7 days of dosing in each and minimum 7-day washout period. Each subject will receive one dose level of GSK3039294 and placebo. In Part A, approximately 48 subjects will be recruited for an estimated total of 36 completers. In Part B, approximately 32 subjects will be recruited for an estimated total of 24 completers. The study will last up to approximately 10 weeks from screening to follow-up.
Primary purpose:
Treatment
Trial design:
Crossover Assignment
Masking:
Double (Participant, Investigator)
Allocation:
Randomized
Primary outcomes:
Number of subjects with benign arrhythmic events measured by Holter Electrocardiogram (ECG): Part A
Timeframe: Up to 44 days
Number of subjects with benign arrhythmic events measured by Holter ECG: Part B
Timeframe: Up to 27 days
Number of subjects with benign arrhythmic events as measured by cardiac telemetry: Part A
Timeframe: Up to 38 days
Number of subjects with benign arrhythmic events as measured by cardiac telemetry: Part B
Timeframe: Up to 23 days
Number of subjects with adverse events (AE) and serious adverse events (SAE): Part A
Timeframe: Up to 58 days
Number of subjects with AE and SAE: Part B
Timeframe: Up to 41 days
Number of subjects with abnormal hematology parameters: Part A
Timeframe: Up to 49 days
Number of subjects with abnormal hematology parameters: Part B
Timeframe: Up to 35 days
Number of subjects with abnormal clinical chemistry parameters: Part A
Timeframe: Up to 49 days
Number of subjects with abnormal clinical chemistry parameters: Part B
Timeframe: Up to 35 days
Number of subjects with abnormal urinalysis parameters: Part A
Timeframe: Up to 49 days
Number of subjects with abnormal urinalysis parameters: Part B
Timeframe: Up to 35 days
Number of subjects with abnormal results on core urine monitoring: Part A
Timeframe: Up to 52 days
Number of subjects with abnormal results on core urine monitoring: Part B
Timeframe: Up to 44 days
Number of subjects with abnormal vital sign parameters: Part A
Timeframe: Up to 58 days
Number of subjects with abnormal vital sign parameters: Part B
Timeframe: Up to 41 days
Number of subjects with abnormal 12-lead ECG findings: Part A
Timeframe: Up to 58 days
Number of subjects with abnormal 12-lead ECG findings: Part B
Timeframe: Up to 41 days
Number of subjects with abnormal cardiac telemetry findings: Part A
Timeframe: Up to 38 days
Number of subjects with abnormal cardiac telemetry findings: Part B
Timeframe: Up to 23 days
Secondary outcomes:
Plasma concentration of GSK3039294; Part A
Timeframe: Pre-dose, 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16 hours post-dose on Day 1; Pre-dose, 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16, 24 hours post-dose on Day 7; Pre-dose on Day 2, 3, 4, 5 and 6 and until follow-up
Plasma concentration of GSK3039294; Part B
Timeframe: Pre-dose, 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16 hours post-dose on Day 1; Pre-dose, 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16, 24 hours post-dose on Day 7; Pre-dose on Day 2, 3, 4, 5 and 6 and until follow-up
Plasma concentration of GSK2315698 (miridesap); Part A
Timeframe: Pre-dose, 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16 hours post-dose on Day 1; Pre-dose, 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16, 24 hours post-dose on Day 7; Pre-dose on Day 2, 3, 4, 5 and 6 and until follow-up
Plasma concentration of GSK2315698 (miridesap); Part B
Timeframe: Pre-dose, 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16 hours post-dose on Day 1; Pre-dose, 0.5, 1, 2, 3, 4, 6, 8, 10, 12, 16, 24 hours post-dose on Day 7; Pre-dose on Day 2, 3, 4, 5 and 6 and until follow-up
Plasma SAP levels; Part A
Timeframe: Up to 58 days
Plasma SAP levels; Part B
Timeframe: Up to 41 days
Interventions:
Drug: GSK3039294
Drug: Placebo
Enrollment:
0
Observational study model:
Not applicable
Primary completion date:
2018-25-07
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Amyloidosis
Product
GSK3039294
Collaborators
Not applicable
Study date(s)
July 2018 to July 2018
Type
Interventional
Phase
1
Participation criteria
Sex
Female & Male
Age
18 - 65 years
Accepts healthy volunteers
Yes
- Eligibility Criteria
- Inclusion Criteria:
Inclusion and exclusion criteria
Inclusion criteria:
- Eligibility Criteria Inclusion Criteria:
- 18 to 65 years of age inclusive at the time of signing the informed consent.
- Non-smokers only (defined as a non-smoker during the last 3 months prior to screening).
- Body weight > 50 kilograms and body mass index (BMI) and <=30 kilograms/meter square.
- Male subjects and women of non-child bearing potential only will be eligible.
- Male subjects with female partners of childbearing potential must comply with one of the following contraception requirements from the time of first dose of study medication until completion of the follow-up visit.
- Vasectomy with documentation of azoospermia.
- Male condom plus partner use of one of the contraceptive options: Contraceptive sub dermal implant that meets the effectiveness criteria of a <1% rate of failure per year, as stated in the product label; Intrauterine device or intrauterine system that meets the standard operating procedure (SOP) effectiveness criteria including a <1% rate of failure per year, as stated in the product label; Oral Contraceptive, either combined or progestogen alone; Contraceptive vaginal ring; Occlusive cap (female diaphragm or cervical/vault cap) with a vaginal spermicide (foam, gel, cream or suppository).
- Capable of giving signed informed.
- 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 parameter(s) which is/are not specifically listed in the inclusion or exclusion criteria, outside the reference range for the population being studied may be included only if the investigator in consultation with the Medical Monitor if required agree and document that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.
- Aspartate aminotransferase, Alanine aminotransferase, Alkaline phosphatase and bilirubin <=1.5 ULN (Upper Limit of Normal) (isolated bilirubin >1.5 ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%). Exclusion Criteria:
- History or presence of/significant history of or current cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study treatment; or interfering with the interpretation of data.
- Clinically significant blood pressure as determined by the investigator.
- Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
- QT interval corrected for heart rate according to Fridericia’s formula (QTcF)>450 milliseconds.
- Screening 12-lead ECG with any of the following: second/third degree atrioventricular block (AVB); significant pathological Q-waves (defined as Q-wave > 40 milliseconds or depth greater than 0.4-0.5 millivolts); ventricular pre-excitation; complete left bundle branch block (LBBB); bradycardia as defined by sinus rate <= 35 beats per minute (BPM).
- Any clinically relevant abnormality on the screening medical assessment laboratory examination or ECG.
- A personal history of corrected QT interval (QTc) prolongation, symptomatic cardiac arrhythmias or cardiac arrest.
- Sinus bradycardia <= 35 BPM or junctional arrhythmia > 60 BPM for 10 seconds or longer on run-in Holter or pre-dose inpatient telemetry.
- Non-sustained supraventricular tachycardia (NSVT) or more than 30 Ventricular Premature Depolarization (VPD)/hour on run-in Holter or pre-dose inpatient telemetry.
- Atrial tachycardia > 100 BPM for 3 seconds or longer or more than 40 Atrial Premature Depolarization (APD)/hour on run-in Holter or pre-dose inpatient telemetry.
- Unable to refrain from the use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John’s Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and GlaxoSmithKline (GSK) Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.
- Participation in the study would result in loss of blood or blood products in excess of 500 milliliters within 56-day period.
- Exposure to more than 4 new chemical entities within 12 months prior to the first dosing day.
- The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
- Presence of Hepatitis B surface antigen (HBsAg) at screening Positive Hepatitis C antibody test result at screening.
- Positive Hepatitis C Ribonucleic acid (RNA) test result at screening or within 3 months prior to first dose of study treatment.
- Positive pre-study drug/alcohol screen.
- Positive human immunodeficiency virus (HIV) antibody test.
- Regular use of known drugs of abuse.
- Regular alcohol consumption within six months prior to the study defined as: For United Kingdom (UK) sites an average weekly intake of >21 units for males or >14 units for females. One unit is equivalent to 8 grams of alcohol: a half-pint (equivalent to 240 milliliters) of beer, one glass (125 milliliters) of wine or one (25 milliliters) measure of spirits.
- Urinary cotinine levels indicative of smoking/history/regular use of tobacco/nicotine-containing products within 3 months prior to screening.
- Sensitivity to heparin or heparin-induced thrombocytopenia.
- Sensitivity to any of the study treatments, or components thereof, or drug or other allergy that, in the opinion of the investigator or medical monitor, contraindicates participation in the study.
Trial location(s)
Study documents
No study documents available.
Results overview
Study Results yet to be posted
Recruitment status
Withdrawn
Actual primary completion date
2018-25-07
Actual study completion date
2018-25-07
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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