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Pipeline

From discovery to treatment

Coretag’s most advanced clinical candidates, CyanTag® and CyanCore®, have physical half-lives of approximately 1 hour and 9 hours, respectively. Each compound is composed by a cyanine conjugated to a chelator (like DOTA or DOTAGA). The therapeutic radioisotope being used is Lutetium-177, which has a half-life of 6.7 days and emits β-particles with a most abundant energy of 0.5 MeV and an average energy of 0.1 MeV. The ranges of these β-particles in tissue are 1.8 mm and 0.5 mm, respectively. Additionally, Lutetium-177 emits photons at 113 and 208 keV, allowing for imaging, biodistribution studies, and absorbed-dose calculations.

Asset
Indication
Discovery / Preclinical
Phase I
Phase II
Phase III
Next Milestone
CyanTag®
Solid Tumors
Discovery / Preclinical
Phase I
Phase II
Phase III
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FIH: Q1 2026
CyanCore®
Solid Tumors
Discovery / Preclinical
Phase I
Phase II
Phase III
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FIH: Q1 2026
HQ4
Solid Tumors
Discovery / Preclinical
Phase I
Phase II
Phase III
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Undisclosed
Solid Tumors
Discovery / Preclinical
Phase I
Phase II
Phase III
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Undisclosed
Solid Tumors
Discovery / Preclinical
Phase I
Phase II
Phase III
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  • CyanTag is selected to get developed as the Theranostics Step1, NC-Scan®
  • CyanCore is selected to get developed as the Theranostics Step2, CyanCoreTherapy®.
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