CURAsight

Targeting uPAR

One target. Multiple aggressive cancers. Curasight is developing uPAR-targeted radiopharmaceuticals designed to characterize and treat aggressive cancer biology.

Curasight is a clinical-stage radiopharmaceutical company developing radiopharmaceuticals targeting uPAR, a cell-surface target associated with tumor invasion, angiogenesis and metastasis across multiple solid tumors. The portfolio is organized through two platforms: uTRACE® for imaging and diagnostic development and uTREAT® for therapeutic development.

Seeing cancer. Treating cancer.

Seeing cancer

uTRACE®

uTRACE® provides the human imaging and diagnostic evidence base for uPAR.

uTRACE uPAR-PET imaging
uTREAT radioligand therapy
Treating cancer

uTREAT®

uTREAT® comprises clinical stage glioblastoma program and next-generation uPAR targeting ligand program designed for modular alpha and beta payloads to support separate radionuclide-specific therapeutic product candidates. In the glioblastoma clinical trial 64Cu-DOTA-AE105 is used for imaging and dosimetry to evaluate regional delivery, biodistribution and dosimetry and to inform a separate 177Lu therapeutic product candidate.

Therapy
Diagnostics

uPAR Theranostics

What you see is what you treat.

Curasight pipeline

Our pipeline

Curasight's pipeline is organized around one biological target, uPAR. uTRACE® is the imaging and diagnostic platform and provides the human imaging evidence base and uTREAT® is the therapeutic development platform comprising glioblastoma clinical program and the next-generation uPAR targeting ligand designed for modular alpha and beta payload for additional distinct therapeutic products across multiple solid tumors.

Pipeline Overview
From human target validation to therapeutic development
View the pipeline

Latest press releases

Jul 27

Curasight announces protocol update for the Phase I uTREAT® trial in aggressive brain cancer (glioblastoma)

A protocol amendment to the ongoing Phase I uTREAT® trial in glioblastoma, intended to optimize the clinical study design, has been submitted for regulatory approval.

Therapeutic programs

“The proposed amendments are intended to strengthen the scientific value of the study.”

Ulrich Krasilnikoff
CEO, Curasight
Jun 22

Curasight A/S has successfully completed a directed issue of shares of approximately DKK 20 million

Curasight has raised approximately DKK 20 million before transaction costs through a directed issue of 1,120,605 shares at DKK 17.80 per share.

Share information

The proceeds support the continued clinical development of uTRACE® and uTREAT® programs through the end of H1 2027.

Curasight A/S
Press release
Sep 14

Major shareholding notification – ownership restructuring – related party transaction

Following an internal restructuring, Curacap Holding ApS, jointly controlled by Andreas Kjær and Ulrich Krasilnikoff, now holds 27.68% of the shares and votes in Curasight.

Share information

The restructuring is of a technical nature, with no change to the underlying economic ownership at the individual shareholder level.

Curasight A/S
Company announcement
Jul 27

Curasight announces protocol update for the Phase I uTREAT® trial in aggressive brain cancer (glioblastoma)

A protocol amendment to the ongoing Phase I uTREAT® trial in glioblastoma, intended to optimize the clinical study design, has been submitted for regulatory approval.

Therapeutic programs

“The proposed amendments are intended to strengthen the scientific value of the study.”

Ulrich Krasilnikoff
CEO, Curasight
Oct 5

Curasight resumes patient enrolment in Phase 1 glioblastoma study following approval of protocol amendment

The protocol amendment for the ongoing Phase 1 uTREAT® study in glioblastoma has been approved, and patient enrolment resumes. Top-line data are expected in H1 2027.

Clinical studies

“We are very pleased that the amended protocol has now been approved and that patient enrolment can resume.”

Ulrich Krasilnikoff
CEO, Curasight
Sep 14

Major shareholding notification – ownership restructuring – related party transaction

Following an internal restructuring, Curacap Holding ApS, jointly controlled by Andreas Kjær and Ulrich Krasilnikoff, now holds 27.68% of the shares and votes in Curasight.

Share information

The restructuring is of a technical nature, with no change to the underlying economic ownership at the individual shareholder level.

Curasight A/S
Company announcement
Aug 27

Curasight publishes Interim Report Q2 2026

The second quarter was led by the encouraging preliminary readout from the Phase 1 uTREAT® trial in glioblastoma and a directed share issue of approximately DKK 20 million.

Financial reports

“The encouraging preliminary uTREAT® data represent an important milestone for Curasight and reinforce our confidence in the potential of our uPAR-targeted approach.”

Ulrich Krasilnikoff
CEO, Curasight
Jun 22

Curasight A/S has successfully completed a directed issue of shares of approximately DKK 20 million

Curasight has raised approximately DKK 20 million before transaction costs through a directed issue of 1,120,605 shares at DKK 17.80 per share.

Share information

The proceeds support the continued clinical development of uTRACE® and uTREAT® programs through the end of H1 2027.

Curasight A/S
Press release

Why Curasight. Why uPAR. Why now.

  • More than 500 patients imaged with uPAR PET in nine prospective Ph2 trials across eight solid tumor types.
  • Current Phase 1 glioblastoma study sits within the uTREAT® platform and uses 64Cu-DOTA-AE105 for imaging and dosimetry to evaluate delivery, biodistribution and dosimetry, providing the human bridge toward subsequent therapeutic dosing with a separate 177Lu product candidate.
  • Within uTREAT®, an additional next-generation uPAR targeting ligand designed for modular alpha and beta payload is being advanced for additional distinct therapeutic products depending on the cancer biology.
  • uTRACE® prostate cancer indication licensed to Curium.
  • An extensive family of granted patents and pending applications in major jurisdictions, with remaining exclusivity beyond 2043 varying by product, patent family and jurisdiction.
Our Purpose

To target the biology that makes cancer aggressive.

Curasight A/S
Copenhagen
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uPAR Theranostics
FAQ

Frequently Asked Questions

Key facts about Curasight, uPAR and the company’s development programs.

What is Curasight?

Curasight is a Copenhagen-based clinical-stage radiopharmaceutical company developing uPAR-targeted imaging, diagnostic and radioligand therapy products. The company is listed on Spotlight Stock Market under ticker CURAS.

What is uPAR?

uPAR is the urokinase-type plasminogen activator receptor, a cell-surface receptor associated with tumor invasion, angiogenesis and metastasis. Curasight targets uPAR with peptide-based radiopharmaceuticals.

Are uTREAT® and uTRACE® approved for routine use?

None of the product candidates within the uTREAT® or uTRACE® platforms are currently approved for commercial use (marketing authorization). The relevant product candidates are investigational.

What is uTREAT®?

uTREAT® is Curasight’s uPAR-targeted therapeutic development platform. It can encompass multiple ligands and distinct radionuclide-specific product candidates, including imaging and dosimetry constructs used specifically to enable therapeutic development. In the glioblastoma program, the current Phase 1 study uses 64Cu-DOTA-AE105 at imaging and dosimetry activity within uTREAT®, while a separate 177Lu product is intended for therapeutic dosing.

What is uTRACE®?

uTRACE® is Curasight’s uPAR-targeted imaging and diagnostic platform. Individual imaging agents within the platform are defined by their specific ligand, chelator, radionuclide and intended use. The accumulated uTRACE® evidence supports the broader uPAR strategy. The prostate cancer indication currently in phase 2 is licensed to Curium.

How are uTRACE® and uTREAT® related?

They share the same biological target, uPAR, and can draw on related ligand chemistry and human imaging evidence, but they are separate platforms. uTRACE® includes imaging and diagnostic agents, while uTREAT® includes therapeutic product candidates. A clinical program may use a uTRACE® imaging agent to inform development of a uTREAT® therapeutic product, but that does not make the products identical or require one-to-one pairing. uTRACE® will also be used as a target confirmation tool for selection of patients suited for uTREAT® therapy.

Why is glioblastoma the lead therapeutic indication?

Glioblastoma is an aggressive cancer with high unmet need and published human imaging evidence showing uPAR-positive disease in grade 4 gliomas. Within the uTREAT® program, Curasight is using regional super-selective intra-arterial administration (SIACI) of 64Cu-DOTA-AE105 at imaging and dosimetry activity to measure tumor delivery, biodistribution and dosimetry before therapeutic dosing is introduced through a separate 177Lu product in a subsequent study.

What are Curasight’s next-generation programs?

Within the uTREAT® platform, Curasight is advancing a next-generation uPAR-targeting ligand for systemic radioligand therapy. The ligand architecture is designed to support separate radionuclide-specific (alpha or beta emitters) product candidates, where biology and dosimetry support them. Candidate selection is based on binding, stability, biodistribution, dosimetry and manufacturability.

Where is Curasight listed?

Curasight A/S is listed on Spotlight Stock Market under ticker CURAS.

Where can I find the latest company information?

Material company developments are published through Curasight’s press releases and investor pages. Investors should rely on the latest published market disclosures and financial reports.