Last updated: 07/29/2020 13:10:05
A proof of mechanism study with GSK2126458 in patients with Idiopathic Pulmonary Fibrosis (IPF)
Clinicaltrials.gov ID
EudraCT ID
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: A randomised, placebo-controlled, double-blind, repeat dose escalation study with GSK2126458 in patients with Idiopathic Pulmonary Fibrosis (IPF)
Trial description: This is a dose escalation/dose finding, double-blind, placebo-controlled, parallel study of GSK2126458 in subjects with IPF. The study is designed to explore a number of doses of GSK2126458 for engagement of pharmacology after short term dosing. It is anticipated that approximately 24 subjects will be enrolled in this study. Actual number of cohorts in this study could vary up to a maximum of 6 cohorts (n=4/cohort; 3 on active and 1 on placebo).Each cohort will consist of four subjects who will be randomised to receive GSK2126458 (three subjects) or placebo (one subject) for approximately 8 days (7 to 10 days). On Day 1 they will receive their first dose of GSK2126458 (or placebo) and safety, tolerability and PK/PD in the blood will be measured for up to 8 hours post-dose. Subjects will then be discharged from the site with study drug until the last day of dosing. They will also receive hand held spirometers and instructions on action to be taken in case of deterioration in pulmonary function or any other adverse events (AEs). On the last day of dosing they will return to the site for a repeat of the Day 1 procedures.A bronchoalveolar lavage (BAL) and [18F]-fluoro-deoxyglucose (FDG)- positron emission tomography / computed tomography (PET/CT) scan will be conducted twice during the study; once, at least 2 days before dosing commences and again during the course of the dosing period.After the final subject in each cohort has completed dosing, a dose escalation meeting will take place. Safety and tolerability and PK data will be reviewed during this meeting and decisions made may include but are not limited to: escalate the dose, decrease the dose or repeat the same dose in the next cohort; stop the study.
Primary purpose:
Treatment
Trial design:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Allocation:
Randomized
Primary outcomes:
Pharmacodynamic (PD) endpoints pAKT/AKT in platelet-rich plasma and BAL cells, [18F]-FDG-PET/CT
Timeframe: Baseline, Day 1, mid-study BAL visit (Day 5-9) and final dosing day (Day 7, 8, 9 or 10) for each cohort
Area under the curve (AUC) in blood for GSK2126458
Timeframe: Day 1, mid-study PET visit (Day 4-8), mid-study BAL visit (Day 5-9) and final dosing day post-dose (Day 7, 8, 9 or 10) for each cohort
Maximum observed concentration (Cmax) in blood for GSK2126458
Timeframe: Day 1, mid-study PET visit (Day 4-8), mid-study BAL visit (Day 5-9) and final dosing day post-dose (Day 7, 8, 9 or 10) for each cohort
Pre-dose (trough) concentration at the end of the dosing interval (Ctrough) in blood for GSK2126458
Timeframe: Day 1, mid-study PET visit (Day 4-8), mid-study BAL visit (Day 5-9) and final dosing day post-dose (Day 7, 8, 9 or 10) for each cohort
Concentration of GSK2126458 in bronchoalveolar lavage fluid (BALF)
Timeframe: Baseline BAL visit and mid-study BAL visit (Day 5-9).
Secondary outcomes:
Safety and tolerability of GSK2126458 as assessed by number of subjects with adverse events (AE)s
Timeframe: Baseline up to final dosing day (Day 7, 8, 9 or 10) for each cohort
Safety and tolerability of GSK2126458 as assessed by change from baseline in vital signs
Timeframe: Day 1, final dosing day (Day 7, 8, 9 or 10) and follow-up (10-14 days post last dose), for each cohort
Safety and tolerability of GSK2126458 as assessed by change from baseline in clinical laboratory parameters
Timeframe: Day 1, mid-study BAL visit (Day 5-9), final dosing day (Day 7, 8, 9 or 10) and follow-up (10-14 days post last dose) for each cohort
Safety and tolerability of GSK2126458 as assessed by change from baseline in pulmonary function
Timeframe: Recorded daily from screening until final dosing day (Day 7, 8, 9 or 10) for each cohort
Safety and tolerability of GSK2126458 as assessed by change from baseline in electrocardiogram (ECG)
Timeframe: Screening, Day 1 and final dosing day (Day 7, 8, 9 or 10) for each study cohort
Assessment of subject’s breathlessness using MRC dyspnoea scale
Timeframe: Day 1 and final dosing day (Day 7, 8, 9 or 10) for each study cohort
Assessment of FEV1 and FVC using daily hand-held spirometry
Timeframe: Recorded daily from screening until final dosing day (Day 7, 8, 9 or 10) for each cohort
Investigate the effect of GSK2126458 on the frequency and or severity of chronic cough using Leicester Cough Questionnaire (LCQ) in IPF subjects
Timeframe: Day 1 and final dosing day (Day 7, 8, 9 or 10) for each cohort
Interventions:
Drug: GSK2126458
Drug: Placebo
Enrollment:
17
Observational study model:
Not applicable
Primary completion date:
2016-12-07
Time perspective:
Not applicable
Clinical publications:
P T Lukey, S Harrison, S Yang, Y Man, B F Holman, A Rashidnasab, G Azzopardi, M Grayer, J K Simpson, P Bareille, L Paul, H Woodcock, R Toshner, P Saunders, P L Molyneaux, K Thielemans, F J Wilson, P F Mercer, R C Chambers, A M Groves, W A Fahy, R P Marshall, T M Maher. RESUBMISSION of Pi3KPAN-1MS-00026641 A Randomised, Placebo-Controlled Study of Omipalisib (PI3K/mTOR) in Idiopathic Pulmonary Fibrosis. Eur Respir J. 2019;53(2)
DOI: 10.1183/13993003.01992-2018
PMID: 30765508
Medical condition
Idiopathic Pulmonary Fibrosis
Product
omipalisib
Collaborators
No
Study date(s)
March 2013 to July 2016
Type
Interventional
Phase
1
Participation criteria
Sex
Female & Male
Age
45+ years
Accepts healthy volunteers
No
- Diagnosis of IPF as determined by a responsible and experienced chest physician and based on established criteria defined by the American Thoracic Society/European Respiratory Society: American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias.
- FVC greater than (>) 40% predicted and Diffusing capacity of the Lung for Carbon Monoxide (DLCO) >30% predicted
- Current IPF exacerbation
- History of acute coronary syndromes, atrial fibrillation, coronary angioplasty, or stenting within the past 24 weeks.
Inclusion and exclusion criteria
Inclusion criteria:
- Diagnosis of IPF as determined by a responsible and experienced chest physician and based on established criteria defined by the American Thoracic Society/European Respiratory Society: American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias.
- FVC greater than (>) 40% predicted and Diffusing capacity of the Lung for Carbon Monoxide (DLCO) >30% predicted
- Alanine aminotransferase (ALT) less than (<) 2x upper limit of normal (ULN); alkaline phosphatase and bilirubin less than or equal to (<=) 1.5xULN.
- QTcB <450 milliseconds (msec) and QTc interval <=480 msec; or QTc <480 msec in subjects with Bundle Branch Block.
- Male over 45 years of age inclusive, or female over 50 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 amenorrhoea. Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to use one of the contraception, if they wish to continue their HRT during the study. Otherwise, they must discontinue HRT to allow confirmation of post-menopausal status prior to study enrolment. For most forms of HRT, at least 2 to 4 weeks should elapse between the cessation of therapy and the blood draw; this interval depends on the type and dosage of HRT. Following confirmation of their post-menopausal status, they can resume use of HRT during the study without use of a contraceptive method.
- Male subjects with female partners of child-bearing potential must agree to use one of the contraception methods. This criterion must be followed from the time of the first dose of study medication until the follow-up contact.
- Body weight >=40 kilogram (kg) (female), >=50 kg (male), and body mass index (BMI) between 20 and 35 kg/meter squared (m^2) inclusive.
- Subjects must have left ventricular ejection fraction (LVEF) >=50 % as demonstrated by a recent echocardiogram (at screening or within 3 months prior to screening).
Exclusion criteria:
- Current IPF exacerbation
- History of acute coronary syndromes, atrial fibrillation, coronary angioplasty, or stenting within the past 24 weeks.
- Class II, III, or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system
- Uncontrolled hypertension or a history of conditions which could increase the risk of complications from hypertension
- Current upper or lower respiratory tract infection
- Repeated systolic BP >=160 millimeters of mercury (mmHg) and/or diastolic BP >=90 mmHg unless they are diabetic, in which case subjects with repeated systolic BP >=145 mmHg and/or diastolic >=85 mmHg
- Poorly controlled diabetes (HbA1c [glycated hemoglobin (hemoglobin A1c)] >7.5%).
- Clinically significant laboratory assessment outside the reference range unless the Investigator considers that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures
- A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
- Current or chronic history of liver disease, or known hepatic or biliary abnormalities
- Previous exposure to ionising radiation >5 millisievert (mSv) in the 3 years prior to enrolment
- History of regular alcohol consumption within 6 months of the study defined as: an average weekly intake of >21 units for males or >14 units for females. One unit is equivalent to 8 g of alcohol: a half-pint (approximately 240 milliliters [mL]) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits
- 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).
- Exposure to more than four new chemical entities within 12 months prior to the first dosing day
- Currently taking Pirfenidone or have received Pirfenidone within the previous 30 days
- Unable to refrain from the use of prohibited prescription or non-prescription drugs, unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety
- History of sensitivity to any of the study medications, or components there of or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation
- Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period
- History of sensitivity to heparin or heparin-induced thrombocytopenia
Trial location(s)
Study documents
Clinical study report
Available language(s): English
Protocol
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
Recruitment status
Completed
Actual primary completion date
2016-12-07
Actual study completion date
2016-12-07
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
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Additional information
Results for study 116711 can be found on the GSK Clinical Study Register.
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