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PBMC (Peripheral Blood Mononuclear Cells) /Lymphocyte SPECT (Single Photon Emission Computerized Tomography) Imaging in Crohn's Disease

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ClinicalTrials.gov Identifier: NCT01051622
Recruitment Status : Completed
First Posted : January 18, 2010
Last Update Posted : June 2, 2014
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline

December 3, 2009
January 18, 2010
June 2, 2014
January 2010
February 2011   (Final data collection date for primary outcome measure)
Quantification of scintigraphic activity score for small bowel disease (for both PBMC and lymphocyte imaging methodologies) [ Time Frame: 1 day ]
Same as current
Complete list of historical versions of study NCT01051622 on ClinicalTrials.gov Archive Site
  • Tolerability endpoints including AEs [ Time Frame: Up to 3 weeks ]
  • Variability and reproducibility of the PBMC and lymphocyte imaging methodologies at visits 1 and 2. [ Time Frame: Up to 3 days ]
  • Rate of label accumulation in small bowel [ Time Frame: 1 day ]
  • Circulating PBMC and lymphocyte subpopulation cell counts and correlation with scintigraphic activity scores. [ Time Frame: 1 day ]
  • Correlation between CDAI, CRP, calprotectin, ASCA antibodies and SAS [ Time Frame: Up to 3 weeks ]
  • Variability and reproducibility of the PBMC and lymphocyte imaging methodologies at visits 1 and 2. [ Time Frame: Up to 3 days ]
  • Rate of label accumulation in small bowel [ Time Frame: 1 day ]
  • Circulating PBMC and lymphocyte subpopulation cell counts and correlation with scintigraphic activity scores. [ Time Frame: 1 day ]
  • Correlation between CDAI, CRP, calprotectin, ASCA antibodies and SAS [ Time Frame: Up to 3 weeks ]
  • Tolerability endpoints including AEs [ Time Frame: Up to 3 weeks ]
Not Provided
Not Provided
 
PBMC (Peripheral Blood Mononuclear Cells) /Lymphocyte SPECT (Single Photon Emission Computerized Tomography) Imaging in Crohn's Disease
An Exploratory SPECT Imaging Study to Assess the Utility of High-specific Activity 99mTc-HMPAO Labeling as a Tool to Detect PBMC and Lymphocyte Trafficking in the Small Bowel or Ileo-caecal Region of Crohn's Disease Patients

Using scintigraphic imaging including planar scintigraphy and SPECT, this study will evaluate the utility of two different ex vivo 99mTc-HMPAO labelled mononuclear cell populations in order to select the optimal methodology (using PBMC or purified lymphocyte subpopulations) for future drug intervention studies in Crohn's disease.

Two parallel exploratory approaches will be investigated to enrich for lymphocyte populations expressing leukocyte trafficking inhibitors. In the first, whole blood will be fractionated on a ficoll gradient to purify a heterogeneous population of all the peripheral blood mononuclear cells (PBMC) for labelling. Secondly, further enrichment will be attempted using depletion of PBMC fractions of monocytes and B cells.

This study is based on the established technology of scintigraphic 'white cell scanning', in which the leukocytes in a limited volume of patient's blood are radiolabeled with indium-111 or technetium-99m, re-introduced into the circulation, and their subsequent trafficking and accumulation in areas of active inflammation is visualised by scintigraphic imaging. This methodology is routinely used for diagnosis of inflammatory conditions and pharmacodynamic changes have been documented in the literature. As it is intended that this technology could be used in future drug intervention studies.

However, because this sub-population labelling methodology remains exploratory, this study will investigate the utility of such techniques for use in future clinical trials in Crohn's patients.

Two parallel exploratory approaches will be investigated to enrich for lymphocyte populations expressing leukocyte trafficking inhibitors. In the first, whole blood will be fractionated on a ficoll gradient to purify a heterogeneous population of all the peripheral blood mononuclear cells (PBMC) for labelling. Secondly, T lymphocytes will be further enriched by depletion of monocytes and B cells from PBMC fractions. In part A one scintigraphy scan will be performed in healthy volunteers to confirm that the purification and labelling procedure does not show abnormal biodistribution compared to the known physiological distribution of labelled mononuclear cells [Bennink, 2008].

In part B, Crohn's disease patients will then be recruited to undergo two scintigraphy scans 48-72 hours apart to establish intra-patient variability and feasibility of the repeated procedure that will be used in subsequent studies for therapeutic intervention. Analysis of SPECT images will be performed using a standardized scoring system.

Interventional
Phase 1
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Crohn's Disease
Other: Labeling Ceretec
Technetium-99m is used to radiolabel cells of interest i.e PBMC's
  • Experimental: PBMC Trafficking
    In part B, Patients undergo a blood draw (up to150 mL) and the PBMC's are separated and selected or 99mTc-HMPAO labeling. The purified and labelled cells will be re-introduced into the patient by intravenous infusion and one SPECT scan and up to 8 serial planar scintigraphy scans will initially be conducted over up to 6 hours within 1 scan session. All suitable patients showing evidence of cellular uptake in the ileo-caecal region and/or small bowel at Visit 1 will be progressed to an identical second cell labeling and scanning session at Visit 2 (48 hours later). Subjects showing no evidence of cellular uptake in the ileo-caecal region or small bowel at Visit 1 (negative scan) will be withdrawn from the study and proceed to the follow-up.
    Intervention: Other: Labeling Ceretec
  • Experimental: T Lymphocyte Trafficking

    In part B, Patients undergo a blood draw (up to150 mL) and the T lymphocyte cells are separated and selected or 99mTc-HMPAO labeling. The purified and labelled cells will be re-introduced into the patient by intravenous infusion and one SPECT scan and up to 8 serial planar scintigraphy scans will initially be conducted over up to 6 hours within 1 scan session. All suitable patients showing evidence of cellular uptake in the ileo-caecal region and/or small bowel at Visit 1 will be progressed to an identical second cell labeling and scanning session at Visit 2 (48 hours later). Subjects showing no evidence of cellular uptake in the ileo-caecal region or small bowel at Visit 1 (negative scan) will be withdrawn from the study and proceed to the follow-up.

    visit.

    Intervention: Other: Labeling Ceretec
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
13
10
February 2011
February 2011   (Final data collection date for primary outcome measure)

Inclusion

A subject will be eligible for inclusion in this study only if all of the following criteria apply:

Part A only:

  1. Healthy as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, vital signs, ECG, complete blood count and clinical chemistry. 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 GSK Medical Monitor agree that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.

    Part A and B:

  2. Male or female over 18 years of age inclusive, at the time of signing the informed consent.
  3. 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 [in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) > 40 MlU/ml and estradiol < 40 pg/ml (<140 pmol/L) is confirmatory]. Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to use one of the contraception methods in Section 8.1 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.

    Part B only:

  4. A history of CD for at least 3 months with a diagnosis confirmed by radiologic, endoscopic or histological assessment.
  5. Moderate to severe CD as evidenced by an elevated retrospective CDAI score (of

    ≥150) and 1 or more of the following:

    • CRP (of ≥5 mg/L); or
    • recent (within 4 weeks before the screening visit) evidence of active CD by CT scan, MRI scan or endoscopy. Scans must be part of the patients routine care and should not be conducted as a screening test for this study.
  6. Radiographic (barium, CT, MRI) or endoscopic evidence of small bowel involvement (if a patient has had a surgical intervention, evidence of small bowel involvement must have been obtained after the procedure).

Exclusion

A subject will not be eligible for inclusion in this study if any of the following criteria apply:

Part A and B:

  1. Known or positive infection with hepatitis B, hepatitis C or HIV.
  2. The subject has participated in a clinical trial and has received an investigational product within the following time period prior to Day 1 of the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
  3. Previous inclusion in a research and/or medical protocol involving nuclear medicine, PET or radiological investigations with significant radiation burden (a significant radiation burden being defined as ICRP category IIb or above: no more than 10 mSv in addition to natural background radiation, in the previous 3 years including the dose from this study).

    Part B only:

  4. Patients with active Crohn's disease with small bowel involvement who are not yet receiving treatment for whom it is judged inappropriate to defer initiating steroid or other treatment for up to 13 days (the maximum interval from screening to last imaging session).
  5. Patients who are corticosteroid dependent for whom it is judged inappropriate to defer increasing the dose of steroids or initiating other treatment for up to 13 days (the maximum interval from screening to last imaging session).
  6. Patients who are refractory to steroids or immunosuppressants or anti-TNFs for whom it is judged inappropriate to defer change of medical management or surgical intervention for up to 13 days (the maximum interval from screening to last imaging session).
  7. The subject is taking >20mg/day Prednisolone or a prednisolone equivalent during the 4 weeks prior to screening
  8. The subject received treatment natalizumab within 12 weeks prior to study entry;
  9. The subject has Hb<10 g/l or Lymphocyte count <10^9 /l
  10. Known C. difficile infection, or a clinical suspicion of a pathogenic bowel infection (including significant infection due to fistula).
  11. Suspected or diagnosed intra-abdominal abscess or bowel perforation
  12. The subjects has had bowel surgery (other than appendectomy) within 12 weeks prior to randomization or is likely to require abdominal surgery within 1 month of screening
  13. Concurrent illness, infection or disability (including malignancies or neoplastic disease of the bowel) that may affect the interpretation of clinical data, or otherwise contraindicates participation in this clinical study (e.g., an unstable cardiovascular, autoimmune, renal, hepatic, pulmonary, endocrine, metabolic, gastrointestinal, hematologic, psychiatric or neurological condition).
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
Belgium,   Netherlands
 
 
NCT01051622
113265
No
Not Provided
Not Provided
GlaxoSmithKline
GlaxoSmithKline
Not Provided
Study Director: GSK Clinical Trials GlaxoSmithKline
GlaxoSmithKline
May 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP