TUB-010, a novel anti-CD30 antibody-drug conjugate based on Tub-tag technology, widens the therapeutic window by reducing toxicity while maintaining high efficacy

  • Mol Cancer Ther. 2025 Aug 20. doi: 10.1158/1535-7163.MCT-25-0062.
Marcus Gerlach  1 Saskia Schmitt  1 Philipp Cyprys  1 Marc-André Kasper  1 Isabelle Mai  1 Magdalena Klanova  2 Andreas Maiser  3 Heinrich Leonhardt  4 Christian P R Hackenberger  5 Günter R Fingerle-Rowson  6 Annette M Vogl  1 Dominik Schumacher  1 Jonas Helma  1
Affiliations
  • 1. Tubulis GmbH, Planegg-Martinsried, Bavaria, Germany.
  • 2. Charles University, Prague, Czech Republic.
  • 3. Faculty of Biology, Human Biology and Bioimaging, LMU Munich, Munich, Germany, Munich, Germany.
  • 4. LMU Munich, Munich, Germany.
  • 5. Leibniz-Forschungsinstitut für Molekulare Pharmakologie, Berlin, Germany.
  • 6. Tubulis GmbH, Cambridge, MA, United States.
Abstract

TUB-010 is a next-generation antibody-drug conjugate (ADC) targeting CD30 expressed on various hematopoietic malignancies such as Hodgkin lymphoma. Among the therapeutic options for patients with relapsed and refractory CD30-positive cancers is brentuximab vedotin (Adcetris), an MMAE-delivering anti-CD30 ADC with a mean drug-to antibody ratio (DAR) of 4. Adcetris exhibits a high response rate at the cost of significant toxicities, likely driven by the payload MMAE and instability of the maleimide conjugation chemistry. TUB-010 uses the same antibody and payload as Adcetris, but is based on the Tub-tag conjugation strategy, which stably attaches MMAE to the hydrophilic Tub-tag peptides on the light chains via chemoenzymatic conjugation. This new technology enables the generation of a homogenous and site-specific DAR 2 ADC with unique biophysical properties. TUB-010 demonstrates similar binding and lysosomal release characteristics as Adcetris, which translates into comparable in vitro cytotoxicity on CD30-positive cell lines when normalized to the MMAE concentration. Importantly, TUB-010 exhibits higher stability with neglectable premature deconjugation in circulation and reduced aggregation as well as lower non-specific cytotoxicity on target-negative cells compared to Adcetris. As a consequence, TUB-010 induces superior tumor control compared to Adcetris when dosed at equal MMAE concentrations in vivo and also lower toxicity and higher tolerability in rodents and non-human primates. Taken together, TUB-010 is a novel, potential best-in-class anti-CD30 ADC with improved biophysical properties designed to deliver MMAE with higher precision and a wider therapeutic window than Adcetris using Tub-tag technology. Therefore, TUB-010 may increase the clinical benefit of anti-CD30 ADC therapies.

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