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Completed

NCT Number: NCT02542371

Use of 99mTc Tilmanocept for Imaging Arterial Inflammation

The purpose of this study is to measure arterial 99mTc-Tilmanocept uptake using single photon emission computed tomography (SPECT/CT) scanning in HIV infected subjects known to have subclinical coronary atherosclerosis as assessed by contrast-enhanced coronary computed tomography angiography (CCTA).

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

About this study

Detailed Description:

Patients with HIV have been shown to have increased atherosclerotic risk compared to age-matched controls, and this risk is thought to be related to increased systemic immune activation. Specifically, systemic immune activation may contribute to destabilizing coronary atherosclerotic plaque, leading to plaque rupture and myocardial infarction. This study is intended to measure arterial uptake of the macrophage specific marker 99mTc-Tilmanocept using single photon emission computed tomography, applied initially to a group of HIV-infected patients with known subclinical coronary atherosclerosis on CCTA. Moreover, traditional markers of CVD risk and inflammatory markers will be assessed in relation to CV imaging outcomes. Positive findings in the index HIV group with known subclinical atherosclerosis will prompt subsequent study of three comparison groups, as above.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

HIV infected subjects with known subclinical atherosclerosis:

Inclusion criteria

  • men and women, ages 18+, with documented HIV infection
  • current use of antiretroviral therapy (ART), with no changes to regimen within last 3 months
  • history of subclinical atherosclerosis on CCTA

Exclusion criteria

  • pregnancy or breastfeeding
  • known active opportunistic infection requiring ongoing medical therapy (not including Hepatitis B/C)
  • CD4 count < 50 cells/mm3
  • history of angina, myocardial infarction, acute coronary syndrome, or coronary artery stenting or surgery
  • recent and/or current treatment with prescription, systemic steroids or anti-inflammatory/immune suppressant medical therapies
  • current use of statin or use of statin for > 1 month within the last 6 months
  • known allergy to dextrans and/or DPTA and/or radiometals and/or iodinated contrast media
  • eGFR < 60 ml/min/1.73 m2 calculated by CDK-EPI
  • contraindications to beta blockers or nitroglycerin
  • significant radiation exposure (>2 CT angiograms) received within the past 12 months
  • BMI > 35 kg/m2 or waist circumference > 70 cm (scanner limitations)

HIV infected subjects without known subclinical atherosclerosis:

Inclusion criteria

  • men and women, ages 18+, with documented HIV infection
  • current use of antiretroviral therapy (ART), with no changes to regimen within last 3 months
  • history of clean aorta/ coronaries on CCTA

Exclusion criteria

  • Same as exclusion criteria for HIV infected subjects with known subclinical atherosclerosis

HIV negative subjects with known subclinical atherosclerosis:

Inclusion criteria

  • men and women, ages 18+, without documented HIV infection
  • history of subclinical atherosclerosis on CCTA

Exclusion criteria

  • pregnancy or breastfeeding
  • history of angina, myocardial infarction, acute coronary syndrome, or coronary artery stenting or surgery
  • recent and/or current treatment with prescription, systemic steroids or anti-inflammatory/immune suppressant medical therapies
  • current use of statin or use of statin for > 1 month within the last 6 months
  • known allergy to dextrans and/or DPTA and/or radiometals and/or iodinated contrast media
  • eGFR < 60 ml/min/1.73 m2 calculated by CDK-EPI
  • contraindications to beta blockers or nitroglycerin
  • significant radiation exposure (>2 CT angiograms) received within the past 12 months
  • BMI > 35 kg/m2 or waist circumference > 70 cm (scanner limitations)

HIV negative subjects without known subclinical atherosclerosis:

Inclusion criteria

  • men and women, ages 18+, without documented HIV infection
  • history of clean aorta/coronaries on CCTA

Exclusion criteria

  • Same as exclusion criteria for HIV negative subjects with known subclinical atherosclerosis

Treatment and study plan

Arterial Imaging

Other

Primary outcomes

  1. Aortic 99mTc-Tilmanocept uptake on SPECT/CT scanning in HIV Patients

    Time frame: within 6 weeks of screening visit

Secondary outcomes

  1. Aortic plaque burden and morphology on CCTA in HIV Patients

    Time frame: within 6 weeks of screening visit

  2. Traditional markers of cardiovascular disease (CVD) risk and inflammatory markers in relation to cardiovascular imaging outcomes

    Time frame: within 6 weeks of screening visit

  3. Imaging assessments in the coronary vasculature in HIV patients

    Time frame: within 6 weeks of screening visit

  4. Comparison of imaging assessments b/ HIV patients w/ known subclinical atherosclerosis, HIV patients w/o known subclinical atherosclerosis, non HIV patients w/ known subclinical atherosclerosis and non HIV patients w/o known subclinical atherosclerosis

    Time frame: within 6 weeks of screening visit

  5. 99mTc-Tilmanocept uptake on SPECT/CT in regions other than the aorta

    Time frame: within 6 weeks of screening visit

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • Havard University Center for AIDS Research
  • Navidea Biopharmaceuticals

Registry information

Important dates

Study start
2015
Primary completion
2021
Study completion
2021
First posted
Sep 7, 2015
Registry last updated
Apr 6, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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