Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Ab-vcMMAE refers to an antibody-drug conjugate (ADC) platform or benchmark construct consisting of a monoclonal antibody (Ab) conjugated to the microtubule inhibitor monomethyl auristatin E (MMAE) through a cathepsin-cleavable valine-citrulline (vc) linker. This specific configuration is one of the most widely utilized ADC technologies, characterized by a stable linker in systemic circulation that releases the potent cytotoxic payload upon internalization into the lysosomal compartment of target cells. In the context of preclinical oncology research, "Ab-vcMMAE" is often employed as a reference or benchmark molecule to compare the anti-tumor activity of novel antibodies or alternative payload classes (such as Topoisomerase I inhibitors) against a standard-of-care ADC architecture. In specific studies, such as those conducted by Biocytogen, it is used as a benchmark targeting Cadherin-3 (CDH3) to evaluate the relative potency of new therapeutic candidates.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Ab-vcMMAE.