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Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
TUB-010, a Novel Anti-CD30 Antibody-Drug Conjugate Based on Tub-Tag Technology, Widens the Therapeutic Window by
Marcus Gerlach1, Saskia Schmitt1, Philipp Cyprys1
1Tubulis GmbH, Planegg-Martinsried, Germany.
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), a monomethyl auristatin E (MMAE)-delivering anti-CD30 ADC with a mean drug-to-antibody ratio of 4. Adcetris exhibits a high response rate at the cost of significant toxicities, likely driven by the payload MMAE and the 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 homogeneous and site-specific drug-to-antibody ratio 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 negligible premature deconjugation in circulation and reduced aggregation, as well as lower nonspecific cytotoxicity on target-negative cells compared with Adcetris. As a consequence, TUB-010 induces superior tumor control compared with Adcetris when dosed at equal MMAE concentrations in vivo and also lower toxicity and higher tolerability in rodents and nonhuman 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.
Insights
TUB-010, a novel antibody-drug conjugate (ADC), offers improved stability and reduced toxicity compared to brentuximab vedotin for CD30-positive cancers. This next-generation ADC demonstrates superior tumor control and tolerability, potentially enhancing patient outcomes.
Area of Science:
- Oncology
- Pharmacology
- Biotechnology
Background:
- Relapsed/refractory CD30-positive hematologic malignancies present treatment challenges.
- Brentuximab vedotin (Adcetris) is an anti-CD30 antibody-drug conjugate (ADC) but exhibits significant toxicities.
- Adcetris's toxicities may stem from payload (MMAE) release and unstable maleimide conjugation chemistry.
Purpose of the Study:
- To evaluate TUB-010, a novel anti-CD30 ADC utilizing Tub-tag chemoenzymatic conjugation.
- To compare the efficacy, stability, and safety of TUB-010 against brentuximab vedotin (Adcetris).
Main Methods:
- TUB-010 was developed using the same antibody and payload (MMAE) as Adcetris but with Tub-tag conjugation.
- Generated a homogeneous, site-specific DAR 2 ADC with improved biophysical properties.
- Assessed binding, lysosomal release, in vitro cytotoxicity, stability, aggregation, off-target toxicity, in vivo tumor control, and tolerability in preclinical models.
Main Results:
- TUB-010 demonstrated comparable binding and in vitro cytotoxicity to Adcetris (normalized for MMAE).
- TUB-010 exhibited enhanced stability, reduced premature deconjugation, lower aggregation, and decreased non-specific cytotoxicity.
- In vivo studies showed superior tumor control and improved tolerability for TUB-010 compared to Adcetris at equal MMAE doses.
Conclusions:
- TUB-010 is a potential best-in-class anti-CD30 ADC with superior biophysical properties.
- Tub-tag technology enables precise MMAE delivery, offering a wider therapeutic window than Adcetris.
- TUB-010 may significantly improve clinical outcomes for patients with CD30-positive malignancies.
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