The purpose of this study is to evaluate the safety and efficacy of SYD985 in recurrent,
advanced or metastatic endometrial cancer.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT04205630.
This is an open-label, single-arm study in patients with HER2-expressing recurrent,
advanced or metastatic endometrial carcinoma. HER2-expression is defined as a 1+, 2+ or
3+ score on immunohistochemistry (IHC) or positive by in situ hybridization (ISH).
Eligible patients for this study should have progressed on or after first line
platinum-based chemotherapy. Patients who have had two or more lines of chemotherapy for
advanced/metastatic disease are not eligible.
Eligible patients will receive SYD985 until disease progression or unacceptable toxicity.
Patients who have stopped study treatment for other reasons than disease progression will
continue their tumor evaluations in an observation period until disease progression or
start of a new anticancer therapy.
Lead OrganizationByondis B.V.