Cardiovascular Contrast-enhanced Magnetic Resonance Imaging Using Polysaccharide Superparamagnetic Iron Oxide Injection in Diabetic Patients

• ClinicalTrials.gov Identifier: NCT06051565
• Recruitment Status: Completed
• First Posted: September 25, 2023
• Last Update Posted: September 29, 2023
• Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
• Information provided by (Responsible Party): Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Study Description

Brief Summary:

This is an open-label, single-center, single-dose study aims to evaluate the effect and safety of polymeric superparamagnetic iron oxide in cardiovascular magnetic resonance imaging for diabetic patients with concomitant chronic kidney disease.

Condition or disease	Intervention/treatment	Phase
Diabetes; Magnetic Resonance Imaging	Drug: Polysaccharide superparamagnetic iron oxide injection	Phase 1; Phase 2

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 12 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Diagnostic
• Official Title: Open-label, Single-dose Study of Polysaccharide Superparamagnetic Iron Oxide Injection for Contrast-enhanced Cardiovascular Magnetic Resonance Imaging in Patients With Type 2 Diabetes and Chronic Kidney Disease.
• Actual Study Start Date: November 6, 2021
• Actual Primary Completion Date: June 13, 2022
• Actual Study Completion Date: September 15, 2022

Arms and Interventions

Arm	Intervention/treatment
Experimental: Polysaccharide superparamagnetic iron oxide injection; Intravenous injected polysaccharide superparamagnetic iron oxide injection at 3 mg/kg dose	Drug: Polysaccharide superparamagnetic iron oxide injection; Polysaccharide superparamagnetic iron oxide injection can be used for the treatment of iron-deficiency anemia and for magnetic resonance imaging enhancement.

Outcome Measures

Primary Outcome Measures :

1. The number of vascular segments with lesions [ Time Frame: 0 hour after administration ]
   The number of vascular segments with lesions after administration
2. Lesion length [ Time Frame: 0 hour after administration ]
   Vascular lesion length
3. Degree of vascular stenosis [ Time Frame: 0 hour after administration ]
   Vascular stenosis degree

Secondary Outcome Measures :

1. Image quality scores [ Time Frame: 0 hour after administration ]
   Vascular image quality was scored on a 4-point scale. 1 = Vessels not assessable due to poor image quality; 2 = Vessels visualized but only gross features (size/patency) confidently assessable; 3 = Vessels well defined and evaluable for structural pathology with high confidence; 4 = Excellent vessel definition with sharp borders such that fine details can be evaluated with high confidence.
2. Myocardium T1 values [ Time Frame: 0 hour after administration ]
   Changes from baseline in the longitudinal relaxation value of myocardial tissue.
3. Signal-to-noise ratio [ Time Frame: 0 hour after administration ]
   The strength of a signal relative to the background noise.
4. Contrast-to-noise ratio [ Time Frame: 0 hour after administration ]
   The visibility and distinguishability of structures or features of interest in an image in the presence of noise.
5. Adverse event rate [ Time Frame: Baseline up to 24 hours after administration ]
   The occurrence of all adverse events (AEs), serious adverse events (SAEs) and treatment-related adverse events (TEAEs).
6. Serum iron [ Time Frame: Baseline up to 24 hours after administration ]
   Changes from baseline in the amount of circulating iron that is bound to transferrin and freely circulate in the blood.
7. Serum ferritin [ Time Frame: Baseline up to 30 days and 60 days after administration ]
   Changes from baseline in the concentration of plasma (or serum) ferritin.
8. Total iron-binding capacity [ Time Frame: Baseline up to 30 days and 60 days after administration ]
   Changes from baseline in the total amount of iron that can be bound by transferrin proteins in the blood.
9. Serum transferrin saturation [ Time Frame: Baseline up to 30 days and 60 days after administration ]
   Changes from baseline in the value of serum iron divided by the total iron-binding.

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 80 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Aged ≥ 18 years, ≤ 80 years.
• Patients who have been diagnosed with chronic kidney disease (CKD) according to diagnostic criteria, meeting at least one CKD diagnostic criterion.

• Patients with a confirmed history of atherosclerosis and/or chronic venous disease (including deep vein thrombosis, thrombotic venous inflammation, lower limb varicose veins, etc.) either in their medical history or diagnosed during hospital admission, and within the past year, at least one imaging examination has confirmed the presence of at least one of the following vascular abnormalities in at least one vascular bed:

  1. ≥50% vascular stenosis;
  2. Arterial aneurysm;
  3. Arterial dissection;
  4. Arteriovenous malformation;
  5. Arteriovenous fistula;
  6. Vascular developmental abnormalities;
  7. Varicose veins, etc. For details, please refer to the inclusion criteria section.
• Patients capable of self-care in daily life.
• Patients who voluntarily agree to participate in this study, sign an informed consent form, have a full understanding of the trial's content, procedures, and potential adverse reactions, and demonstrate good compliance.
• Patients who are unwilling to sign an informed consent form for the exploratory research can still be enrolled in the main study.
• Subjects who have no plans for pregnancy for at least 2 weeks before self-administration of the investigational drug and for at least 6 months after the last use of the investigational drug and voluntarily agree to adopt effective contraceptive measures.

Exclusion Criteria:

• Patients who have undergone stent implantation for vascular treatment in the target vascular bed.
• Patients who have had or currently have malignant tumors within the last 3 years.
• Serum ferritin > 1000 μg/L.
• Patients who are planned to undergo magnetic resonance imaging (MRI) examination for various reasons during the trial.
• Blood donation or significant blood loss (> 450 ml) within the two months before medication.
• Patients with a history of substance abuse involving psychotropic drugs and are unable to quit or have psychiatric disorders.

• Patients with any severe and/or uncontrolled diseases, including:

  1. Outpatients diagnosed through medical history; inpatients diagnosed based on past medical history and current medical history indicating ≥ Grade 2 myocardial ischemia or myocardial infarction, ≥ Grade 2 congestive heart failure (New York Heart Association (NYHA) classification).
  2. Active or uncontrolled severe systemic infections (≥ Common Terminology Criteria for Adverse Events (CTCAE) 5.0 Grade 2).
• Infectious diseases such as cirrhosis, active hepatitis*, syphilis, human immunodeficiency virus (HIV), etc. *Reference for hepatitis B: hepatitis B surface antigen (HBsAg) positive and Hepatitis B Virus (HBV) DNA test value exceeds the upper limit of normal; Reference for hepatitis C: Hepatitis C Virus (HCV) antibody positive and HCV viral titer test value exceeds the upper limit of normal.
• History of immunodeficiency, acquired or congenital immunodeficiency diseases, or organ transplantation.
• Pregnancy or currently breastfeeding or planning to breastfeed during the study.
• Presence of metal objects in the body (dentures, contraceptive rings, metal implants, metal clips, etc.) and claustrophobia.
• Allergic reactions to the investigational drug, its metabolites, or excipients.
• Use of the investigational drug or participation in drug clinical trials within the two months before medication.
• Difficulty with or intolerance to MRI scans.
• Subjects who cannot or will not comply with the hospital management regulations.
• According to the investigator's judgment, patients with accompanying diseases that pose a serious risk to patient safety or may interfere with the completion of the study, or patients deemed unsuitable for inclusion for other reasons.

Contacts and Locations

Locations

China, Beijing

Beijing Luhe Hospital, Capital Medical University

Beijing, Beijing, China, 101149

Sponsors and Collaborators

Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

More Information

• Responsible Party: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
• ClinicalTrials.gov Identifier: NCT06051565
• Other Study ID Numbers: DJTCSCYHT-I-03
• First Posted: September 25, 2023
• Last Update Posted: September 29, 2023
• Last Verified: October 2021

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No