Abstract CT285: Design and rationale of DOMISOL, a first-in-human Phase I/II study of DT-7012 (NCT06819735) in advanced solid tumors

Abstract Background: CCR8 has recently emerged as a promising target in the treatment of solid tumors. DT-7012, a novel anti-CCR8 monoclonal antibody, distinguishes itself from competitors through its binding properties and optimized effector functions. These characteristics suggest that DT-7012 has the potential to effectively modulate the tumor microenvironment and improve clinical outcomes. Based on its differentiated mechanism, DT-7012 has advanced into first-in-human evaluation. Objectives: To describe the design and scientific rationale of the ongoing Phase I/II trial (NCT06819735) assessing the safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of DT-7012 in patients with advanced solid tumors. Methods: This multicenter and open-label DOMISOL study comprises a dose-escalation phase followed by indication-specific expansion cohorts. Adaptive Bayesian dose-escalation will identify the recommended Phase II dose (RP2D) based on safety, pharmacokinetics, and biomarker readouts (CCR8 + Treg depletion, cytokine modulation). Expansion cohorts will evaluate antitumor activity as monotherapy and in combination with anti-PD-1 therapy. Paired tumor biopsies and peripheral blood analyses will enable translational assessment of immune modulation. Results: The trial is actively enrolling across multiple centers. The design incorporates real-time translational endpoints and stringent safety monitoring to optimize dose selection and patient benefit. Preclinical data predict a favorable therapeutic window and synergy with checkpoint blockade. Conclusions: This Phase I/II study is designed to rigorously characterize DT-7012’s safety profile and biological activity in patients with solid tumors. The integration of adaptive design and translational biomarkers aims to accelerate clinical validation of this novel CCR8-depleting antibody. Citation Format: Andrew Parsonson, Vineet Kwatra, Prachi Bhave, Azim Khan, Samira El-Farouk, Anne Quesnel, Carolina Duarte, Claire Jouffroy-Zeller, Hélène Muller, David Allman, Abdelkrim Taamma, Ikrame Sahmoudi, Hélène Lelièvre, Mélanie Frauli, Stephan Schann, Nathalie Lenne, Jean-Marie Cuillerot, Vinod Ganju. Design and rationale of DOMISOL, a first-in-human Phase I/II study of DT-7012 (NCT06819735) in advanced solid tumors [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(8_Suppl):Abstract nr CT285.

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Cancer Research
Published
2026-04-17
DOI
https://doi.org/10.1158/1538-7445.am2026-ct285
Primary Topic
Chemokine receptors and signaling
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article
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article

Abstract CT285: Design and rationale of DOMISOL, a first-in-human Phase I/II study of DT-7012 (NCT06819735) in advanced solid tumors

Vineet Kwatra, Claire Jouffroy-Zeller, Nathalie Lenne, Stéphan Schann et al.
Cancer Research
Chemokine receptors and signaling
article

Abstract CT285: Design and rationale of DOMISOL, a first-in-human Phase I/II study of DT-7012 (NCT06819735) in advanced solid tumors

Vineet Kwatra, Claire Jouffroy-Zeller, Nathalie Lenne, Stéphan Schann, A. Taamma, Jean-Marie Cuillerot, Azim Khan, Mélanie Frauli, Prachi Bhave, Helene Lelievre, A. Parsonson, Samira El-Farouk, Anne Quesnel, David Allman, Carolina Duarte, Hélène Muller, Vinod Ganju, Ikrame Sahmoudi
article en

Abstract

Abstract Background: CCR8 has recently emerged as a promising target in the treatment of solid tumors. DT-7012, a novel anti-CCR8 monoclonal antibody, distinguishes itself from competitors through its binding properties and optimized effector functions. These characteristics suggest that DT-7012 has the potential to effectively modulate the tumor microenvironment and improve clinical outcomes. Based on its differentiated mechanism, DT-7012 has advanced into first-in-human evaluation. Objectives: To describe the design and scientific rationale of the ongoing Phase I/II trial (NCT06819735) assessing the safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of DT-7012 in patients with advanced solid tumors. Methods: This multicenter and open-label DOMISOL study comprises a dose-escalation phase followed by indication-specific expansion cohorts. Adaptive Bayesian dose-escalation will identify the recommended Phase II dose (RP2D) based on safety, pharmacokinetics, and biomarker readouts (CCR8 + Treg depletion, cytokine modulation). Expansion cohorts will evaluate antitumor activity as monotherapy and in combination with anti-PD-1 therapy. Paired tumor biopsies and peripheral blood analyses will enable translational assessment of immune modulation. Results: The trial is actively enrolling across multiple centers. The design incorporates real-time translational endpoints and stringent safety monitoring to optimize dose selection and patient benefit. Preclinical data predict a favorable therapeutic window and synergy with checkpoint blockade. Conclusions: This Phase I/II study is designed to rigorously characterize DT-7012’s safety profile and biological activity in patients with solid tumors. The integration of adaptive design and translational biomarkers aims to accelerate clinical validation of this novel CCR8-depleting antibody. Citation Format: Andrew Parsonson, Vineet Kwatra, Prachi Bhave, Azim Khan, Samira El-Farouk, Anne Quesnel, Carolina Duarte, Claire Jouffroy-Zeller, Hélène Muller, David Allman, Abdelkrim Taamma, Ikrame Sahmoudi, Hélène Lelièvre, Mélanie Frauli, Stephan Schann, Nathalie Lenne, Jean-Marie Cuillerot, Vinod Ganju. Design and rationale of DOMISOL, a first-in-human Phase I/II study of DT-7012 (NCT06819735) in advanced solid tumors [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(8_Suppl):Abstract nr CT285.

Cancer ResearchVol. 86(8_Supplement)
South Australia Pathology (AU), Danone (France) (FR), Cabrini Hospital (AU), CEA Le Ripault (FR), Domain Therapeutics (France) (FR), Nishida Hospital (JP), Forest and Wood Products (Australia) (AU), Macquarie University (AU)
Openalex Percentile: Top 20%
Chemokine receptors and signaling
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