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Business Alliances4572Carna Biosciences,Inc.Pharmaceuticals

Notice of Entering into a Clinical Trial Agreement (CTA) with The University of Texas MD Anderson Cancer Center for an Investigator-Initiated Clinical Trial of monzosertib

A formal clinical trial agreement (CTA) was executed for a Phase 1b investigator-initiated clinical trial of monzosertib, following the non-binding memorandum of understanding (MOU) with MD Anderson Cancer Center. Carna Biosciences will supply the investigational drug and bear the trial-related costs.

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Agreements reached under this partnership

Business Alliances
4572Carna Biosciences,Inc.
Alliance partnerThe University of Texas MD Anderson Cancer Center (テキサス大学MDアンダーソンがんセンター)
Details of the alliance
  1. 1

    Abhishek Maiti, MD, of the Department of Leukemia at MD Anderson Cancer Center, will lead the trial as Principal Investigator.

  2. 2

    The Company will supply the monzosertib required for the trial.

  3. 3

    The Company will bear the trial-related costs under the agreement.

  4. 4

    The trial will be conducted as a Phase 1b study in patients with relapsed/refractory AML to evaluate the safety, tolerability and efficacy of monzosertib monotherapy and triple-combination therapy with AZA/VEN.

These are items that the documents state the two companies will work on. The lines above and below represent arrangements between the two companies.

About the partner
Business DescriptionOne of the world's leading cancer research and treatment institutions. It also leads the development of numerous innovative treatments in the AML field.
LocationTexas, USA
Impact on Business Performance

This matter will have no impact on the consolidated earnings forecast for the fiscal year ending December 2026.

Contract Date5 October 2026Alliance start datePreparations for patient enrollment are expected to proceed.
Agreements reached under this partnership
ItemDetails
Name of alliance partnerThe University of Texas MD Anderson Cancer Center (テキサス大学MDアンダーソンがんセンター)
Alliance partner's business activitiesOne of the world's leading cancer research and treatment institutions. It also leads the development of numerous innovative treatments in the AML field.
Alliance partner's locationTexas, USA
Type of allianceBusiness Alliances
Details of the allianceAbhishek Maiti, MD, of the Department of Leukemia at MD Anderson Cancer Center, will lead the trial as Principal Investigator., The Company will supply the monzosertib required for the trial., The Company will bear the trial-related costs under the agreement., The trial will be conducted as a Phase 1b study in patients with relapsed/refractory AML to evaluate the safety, tolerability and efficacy of monzosertib monotherapy and triple-combination therapy with AZA/VEN.
Contract Date5 October 2026
Alliance start datePreparations for patient enrollment are expected to proceed.
Impact on Business PerformanceThis matter will have no impact on the consolidated earnings forecast for the fiscal year ending December 2026.
Items this document does not state (15)
Alliance partner's capitalAlliance partner's net salesAlliance partner's operating incomeNumber of shares acquiredAcquisition priceShareholding ratioOverview of the joint ventureOwnership ratioDispatch of directors and officersContract PeriodNumerical targets under the allianceShareholding PolicyDate of board resolutionShare Acquisition Date and Payment DateChange in major shareholders

These are items the company does not state in this document. We do not leave them blank, nor fill them in from other sources or by inference.

The reasons the company gives

The company's own explanation, not something inferred from the numbers.

The parties agreed on the terms of the clinical trial. The aim is to obtain insights into the clinical utility of monzosertib through the trial and accumulate data to support future development strategies.

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Notice of Entering into a Clinical Trial Agreement (CTA) with The University of Texas MD Anderson Cancer Center for an Investigator-Initiated Clinical Trial of monzosertib | Carna Biosciences,Inc. (4572) timely disclosure | Komori