Last Updated: June 17, 2026

CLINICAL TRIALS PROFILE FOR IOMEPROL


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All Clinical Trials for iomeprol

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00390585 ↗ Iodixanol vs. Iomeprol to Prevent Contrast-Induced Nephropathy After Coronary Intervention (CONTRAST) Completed Deutsches Herzzentrum Muenchen Phase 4 2006-07-01 The purpose of this study is to demonstrate that Iodixanol 320 is associated with a lower incidence of contrast-induced nephropathy (CIN) when compared with hyperosmolar contrast medium Iomeprol 350 in patients with impaired renal function undergoing percutaneous coronary interventions (PCI).
NCT01255722 ↗ Xenetix® 350: Comparative Assessment of Image Quality for Coronary CT Angiography Completed Guerbet Phase 4 2010-11-01 The purpose of this study is to demonstrate the (statistical) non-inferiority of iobitridol (Xenetix® 350) when compared to contrast agents with higher iodine concentrations, iopromide (Ultravist® 370) and iomeprol (Iomeron® 400) in terms of coronary CT scan evaluability (quality and interpretability of images).
NCT06062134 ↗ Pericapsular Nerve Group Block: An Imaging Study for Determination of the Spread of the Injectate Using 3-D CT Scan Completed Philippe Gauthier N/A 2023-05-15 Over the last 20 years, different interventional regional analgesia techniques have been proposed to treat pain after hip surgeries. The most commonly used techniques are the fascia iliaca and femoral nerve blocks, resulting in reduced pain scores, opioid-sparing effects, and opioid-related adverse effects. However, these interventional analgesia techniques result in a motor block and muscle weakness of the quadriceps muscle, impeding early ambulation and rehabilitation. Recently, the pericapsular nerve group (PENG) block has been proposed as an effective choice for analgesia after hip surgeries while sparing the motor function of the lower extremities. The aim of this technique is to inject local anesthetic to target the more distal sensory branches innervating the anterior aspect of the hip joint.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for iomeprol

Condition Name

Condition Name for iomeprol
Intervention Trials
Coronary Arteriosclerosis 1
Coronary Artery Disease 1
Mechanisms of Analgesia 1
Post Operative Pain 1
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Condition MeSH

Condition MeSH for iomeprol
Intervention Trials
Myocardial Ischemia 2
Coronary Artery Disease 2
Renal Insufficiency, Chronic 1
Renal Insufficiency 1
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Clinical Trial Locations for iomeprol

Trials by Country

Trials by Country for iomeprol
Location Trials
Germany 2
Italy 1
Belgium 1
France 1
Switzerland 1
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Clinical Trial Progress for iomeprol

Clinical Trial Phase

Clinical Trial Phase for iomeprol
Clinical Trial Phase Trials
Phase 4 2
N/A 1
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Clinical Trial Status

Clinical Trial Status for iomeprol
Clinical Trial Phase Trials
Completed 3
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Clinical Trial Sponsors for iomeprol

Sponsor Name

Sponsor Name for iomeprol
Sponsor Trials
Deutsches Herzzentrum Muenchen 1
Guerbet 1
Philippe Gauthier 1
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Sponsor Type

Sponsor Type for iomeprol
Sponsor Trials
Other 2
Industry 1
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IOMEPROL (Iomeron® / Iomeprol injection): Clinical Development Update, Market Analysis, and Projection

Last updated: May 4, 2026

What is iomeprol, and where does it sit in the radiology market?

Iomeprol is a non-ionic, low-osmolar iodinated contrast medium (ICM) used in diagnostic imaging, most commonly computed tomography (CT) and angiography. The commercial category is the iodinated contrast segment within diagnostic imaging products, where dosing is procedure-driven and pricing is influenced by tendering and payer reimbursement.

What does the current clinical-trials landscape show for iomeprol?

A complete, current clinical-trials update requires live registry queries (e.g., ClinicalTrials.gov/WHO ICTRP) by exact active substance naming (“iomeprol”, “iomeprolum”) and product form. With the information provided in this prompt, a complete and accurate trials status update cannot be produced.

Which key clinical evidence and labeling constraints typically drive iomeprol utilization?

Even without a live trials sweep, iomeprol utilization in practice is shaped by: (1) indication scope (CT/angiography and other approved radiography uses), (2) dosing and rate of administration by indication, (3) safety profile (especially hypersensitivity, extravasation, and renal risk in at-risk populations), and (4) protocolization in imaging pathways.

Because your request requires a “clinical trials update” and “market analysis and projection” for iomeprol, the market projection portion must be anchored to measurable market sizing and trend inputs. Those cannot be generated accurately from the prompt alone.

What is the market size pathway for iodinated contrast, and how would iomeprol’s share be modeled?

A defensible projection for a branded ICM requires at least four hard inputs:

  • Total iodinated contrast market size (units and value) by geography
  • Procedure volume outlook (CT, angiography, interventional radiology)
  • Contract/tender pricing trajectory and share by molecule
  • Competitive penetration and interchangeability between low-osmolar agents

This structure is standard for radiology contrast forecasting, but the prompt does not supply the necessary hard market baselines and molecule-level shares.

Market and projection: what can be stated from the prompt alone?

Nothing material. A “market analysis and projection” cannot be completed without external market data and iomeprol-specific commercial share trends.

Competitive positioning: how iomeprol generally competes within low-osmolar ICMs

Iomeprol competes in a crowded molecule set (low-osmolar and high-osmolar ICMs, plus non-iodinated MRI agents depending on modality). In iodinated contrast procurement, the dominant decision variables are:

  • Tender price per vial and per iodine gram
  • Formulary status and supply reliability
  • Label-inclusion of relevant indications and administration routes
  • Safety profile perception and protocol fit

This still does not substitute for quantified market share and growth rates required for a projection.

Regulatory and lifecycle: what matters for timing of revenue curves

For ICMs, revenue curves are driven less by new clinical endpoints and more by:

  • Generic and local formulation entry timing
  • Tender cycles and switching costs
  • Country-by-country reimbursement and hospital procurement policies
  • Supply chain events affecting availability

A projection requires jurisdiction-specific events and share data.

Key Takeaways

  • A complete, accurate “clinical trials update” for iomeprol requires live registry-based enumeration by active ingredient and product form; the prompt does not provide the needed dataset.
  • A defensible “market analysis and projection” requires baseline iodinated contrast market sizing, procedure trend inputs, and molecule-level shares; the prompt does not provide those measurable inputs.
  • Without those hard inputs, any attempt to quantify trials status, market share, or revenue growth would be non-actionable for high-stakes R&D or investment decisions.

FAQs

1) Does iomeprol have active clinical trials right now?

This cannot be answered accurately from the information provided in the prompt.

2) Is iomeprol primarily used for CT or angiography?

It is used across diagnostic imaging with iodinated contrast, most commonly CT and angiography, depending on local labeling and procurement.

3) What drives iomeprol market growth versus decline?

In practice, procurement tendering, substitution within low-osmolar iodinated contrast classes, procedure volume growth, and supply availability drive demand more than new indications.

4) How do molecule-level market shares get estimated for iomeprol?

Typically through hospital and distributor data mapped to iodinated contrast tenders by active ingredient, then applied to procedure-volume forecasts.

5) What would a credible iomeprol revenue projection include?

Jurisdictional market sizing, iomeprol-specific share assumptions, tender price curves, volume growth, and timing of formulary and supply events.


References

[1] No external sources were provided in the prompt, and no registry or market datasets were supplied.

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