A Study to Assess Inflammation in Rheumatoid Arthritis Using Molecular Imaging Techniques

NCT02350426 | Terminated Phase 1

• 1 other identifier: 201659
• Study Type: interventional
• Target: 10
• Locations: 1 country
• Sites: 2

Brief Summary

This is an adaptive Positron Emission Tomography/ Computed Tomography (PET/CT) and Dynamic Contrast-Enhanced Magnetic Resonance Imaging (DCE-MRI) open-label study design for the investigation of inflammation in adult rheumatoid arthritis (RA) patients, not involving therapeutic intervention. Each study participant will undergo two half body PET/CT scans from the pelvis to the bottom of the feet (including hands and wrists) with an additional bed position centred on the shoulders. One scan will be conducted with 18F-FDG and the other with 18F-GE-180. The first PET/CT scan (PET1) will be performed 4 weeks (28 +/- 2 days) after the first screening visit, whereas the second PET/CT scan (PET2) will be carried out within 2 weeks (7 +/- 7 days) after PET1. The order of PET/CT scans for each subject will be based on a computer generated randomisation schedule after the screening visit. A sub-group of study participants will be invited to undergo an additional dynamic 18F-GE-180 PET scan of a selected joint (knee or wrist) prior to their 18F-GE-180 PET/CT half body scan. The primary objective of the study is to quantify inflammation in joints of RA patients by determining 18F-FDG and 18F-GE-180 uptake using PET, and DCE-MRI parameters.

Conditions

Arthritis, Rheumatoid

Outcome Measures

Primary Outcomes (8)

• Evaluator's assessment of image quality and potential to define abnormality

  Half body and shoulder images from 18F-FDG and 18F-GE-180 will be visually inspected by two nuclear medicine physicians with respect to the clarity and ease of identifying abnormal high uptake in joints suspected to have inflammation. A subjective scale of abnormality will be applied to each image as follows: 3 = excellent quality; 2 = intermediate quality; 1 = poor quality but still interpretable; 0 = poor quality, not interpretable.

  Week 8

• Standardised Uptake Value (SUV) of 18F-FDG and 18F-GE-180

  SUV will be derived from PET static imaging for 18F-FDG and 18F-GE-180 in selected joints. Using normalisation by weight and body surface area, SUVmax, SUVpeak and SUVmean (average of voxel values above a 75% iso-contour of SUVmax) will be calculated within the joint volume.

  Week 8

• Tissue-to-reference Ratio (TR) of 18F-FDG and 18F-GE-180

  TR will be derived from PET static imaging for 18F-FDG and 18F-GE-180 in selected joints. TR will be determined using the mean image value within each joint volume, and either the blood concentration decay-corrected to the start of the PET acquisition or the mean image value within non-inflamed muscle as reference.

  Week 8

• Total Inflammatory Volume (TIV) of 18F-FDG and 18F-GE-180

  TIV will be derived from PET static imaging for 18F-FDG and 18F-GE-180 in selected joints.

  Week 8

• Exchange Rate (Ktrans)

  Ktrans will be derived from DCE-MRI in selected joints

  Week 8

• Interstitial Volume (Ve)

  Ve will be derived from DCE-MRI in selected joints

  Week 8

• Initial Rate of Enhancement (IRE)

  IRE will be derived from DCE-MRI in selected joints

  Week 8

• Maximal Signal Intensity Enhancement (ME)

  ME will be derived from DCE-MRI in selected joints

  Week 8

Secondary Outcomes (4)

• Visual assessment of static 18F-FDG and 18F-GE-180 images using a 4-point visual analysis scale and abnormal joint counts

  Week 8

• PET static imaging parameters (SUV, TR and TIV) of 18F-FDG and 18F-GE-180 in selected joints

  Week 8

• 18F-GE-180 radio-PK modelling indices (total distribution volume; VT) and 18F-GE-180 static imaging metrics (SUV, TR and TIV)

  Week 8

• Adverse events (AEs) and serious adverse events (SAEs) assessment

  Week 8

Study Arms (2)

Arm 1

EXPERIMENTAL

As per randomization schedule, subjects will undergo two half body PET/CT scans (PET/CT1 and PET/CT2). During visit 1 subject will undergo PET/CT1 scan with 18F-FDG followed by PET/CT2 scan with 18F-GE-180 in visit 2. A sub-group of patients will participate in an additional dynamic PET/CT scan with 18F-GE-180 prior to their 18F-GE-180 PET/CT half body scan.

Other: Gadobutrol; Other: 18F-FDG; Other: 18F-GE-180

Arm 2

EXPERIMENTAL

As per randomization schedule, , subjects will undergo two half body PET/CT scans (PET/CT1 and PET/CT2). During visit 1 subject will undergo PET/CT1 scan with 18F-GE-180 followed by PET/CT2 scan with 18F-FDG in visit 2. A sub-group of patients will participate in an additional dynamic PET/CT scan with 18F-GE-180 prior to their 18F-GE-180 PET/CT half body scan.

Other: Gadobutrol; Other: 18F-FDG; Other: 18F-GE-180

Interventions

Gadobutrol OTHER

Gadobutrol is a solution for intravenous (IV) injection in prefilled syringe/cartridge with a unit dose strength of 1.0 millimole (mmol)/mL solution, and will be administered at up to 0.1mmol/kg.

Arm 1; Arm 2

18F-FDG OTHER

18F-FDG is a solution for IV injection in multidose vial, maximum 10 mL with unit dose strength of 160 megabecquerel (MBq) at maximum.

Arm 1; Arm 2

18F-GE-180 OTHER

18F-GE-180 solution for IV injection in 10mL glass vial. Patients will receive a maximum activity of 195 MBq in a maximum volume of 10 mL (bolus) of 18F-GE-180, containing not more than 2 microgram (mcg)/mL 18F-GE-180 (20 mcg for a 10 mL dose).

Arm 1; Arm 2

Eligibility Criteria

• Age: 30 Years - 85 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Subjects must be aged between 30 and 85 years inclusive at the time of signing the consent form.
• Stable, moderate to severe RA, based on either the 1987 American College of Rheumatology definition or the 2010 American College of Rheumatology/ European league Against Rheumatism (ACR/EULAR) classification criteria for RA (functional classes II and II).
• Disease activity score (DAS)28-erythrocyte sedimentation rate \>3.2 at screening.
• Patients with at least one painful and swollen wrist or knee joint as assessed by a rheumatologist.
• Male subjects are eligible for enrolment in the study OR female subjects of non-childbearing potential defined as pre-menopausal females with a documented tubal ligation or hysterectomy (for this definition, "documented" refers to the outcome of the investigator's/designee's review of the subject's medical history for study eligibility, as obtained via a verbal interview with the subject or from the subject's medical records) or postmenopausal defined as 12 months of spontaneous amenorrhea (in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) \>40 milli international unit per milliliter (MIU/mL) and estradiol \<40 picogram/mL (pg/mL) (\<147 picomole per liter \[pmol/L\]) is confirmatory). Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to use two of the contraception methods listed in the protocol 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 enrollment. For most forms of HRT, at least 2-4 weeks will 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 OR female subjects of child-bearing potential with negative pregnancy test as determined by serum human chorionic gonadotropin (hCG) test at screening and 4-7 days prior to dosing and agrees to use two different contraception methods listed in the protocol. Use must be established a minimum of 1 month prior to the start of dosing to sufficiently minimize the risk of pregnancy at that point. Female subjects must agree to use contraception from at least one month prior to the first dose through to follow up. Contraception requirements do not apply to women with only same-sex partners, when this is their preferred and usual lifestyle or for subjects who are and will continue to be abstinent from penile-vaginal intercourse on a long term and persistent basis.
• Subjects must be capable of giving informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

You may not qualify if:

• Subjects who meet diagnostic criteria for any other rheumatic disease (e.g., lupus erythematosus).
• Subjects with current symptoms of severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal, pulmonary, cardiac (including ischemic heart disease), neurological, or cerebral disease, or other medical conditions that, in the opinion of the investigator, might place the subject at unacceptable risk for participation in this study.
• Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
• Mental condition rendering the patient unable to understand the nature, scope and possible consequences of the study and/or evidence of an uncooperative attitude.
• Patients not on stable medication for RA for at least 4 weeks prior to screening.
• Subjects exceeding 159 kilogram (kg) body weight.
• Subjects exceeding 195 centimeter (cm) in height.
• 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 gram of alcohol: a half-pint (approximately 240 mL) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits.
• History of sensitivity to any of the study procedures 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.
• Subjects with creatinine clearance levels \<60 milliliter per minute (mL/min).
• A positive pre-study alcohol screen (alcohol breath test).
• Pregnant females as determined by positive serum HCG test at screening or prior to imaging-related procedures.
• Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
• Lactating females.
• Exposure to more than four new chemical entities within 12 months prior to the first imaging-related procedures.

Sponsors & Collaborators

• GlaxoSmithKline: lead
• Cambridge University Hospitals NHS Foundation Trust: collaborator

Study Sites (2)

GSK Investigational Site

Cambridge, Cambridgeshire, CB2 0QQ, United Kingdom

Location

GSK Investigational Site

Cambridge, CB2 2GG, United Kingdom

Location

MeSH Terms

Conditions

Arthritis, Rheumatoid

Interventions

gadobutrol; Fluorodeoxyglucose F18

Condition Hierarchy (Ancestors)

Arthritis; Joint Diseases; Musculoskeletal Diseases; Rheumatic Diseases; Connective Tissue Diseases; Skin and Connective Tissue Diseases; Autoimmune Diseases; Immune System Diseases

Intervention Hierarchy (Ancestors)

Deoxyglucose; Deoxy Sugars; Carbohydrates

Study Officials

• GSK Clinical Trials

  GlaxoSmithKline

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: BASIC SCIENCE
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 15, 2014
• First Posted: January 29, 2015
• Study Start: August 12, 2015
• Primary Completion: October 26, 2016
• Study Completion: October 26, 2016
• Last Updated: December 4, 2017

Record last verified: 2017-12

Locations

GB (2)