Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Losatuxizumab vedotin is a second-generation antibody-drug conjugate (ADC) designed to target the epidermal growth factor receptor (EGFR). It consists of a chimeric/humanized IgG1 monoclonal antibody directed against EGFR, conjugated via a linker to the cytotoxic payload monomethyl auristatin E (MMAE), a microtubule inhibitor. The drug was developed for the treatment of EGFR-expressing solid tumors, including non-small cell lung cancer, head and neck squamous cell carcinoma, glioblastoma multiforme, colon cancer, and breast cancer. Its mechanism involves binding to EGFR on tumor cells; upon internalization, MMAE is released intracellularly to induce cell death by disrupting microtubule dynamics. Clinical development was halted in early-phase trials due to high rates of infusion-related reactions[1][2][3][5].
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 losatuxizumab vedotin.