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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Daiichi Sankyo Contact for Clinical Trial Information
9089926400
CTRinfo@dsi.com
Carcinoma Prostatic Neoplasms Melanoma Stomach Neoplasms Head and Neck Neoplasms Uterine Cervical Neoplasms Urinary Bladder Neoplasms Endometrial Neoplasms Ovarian Neoplasms Carcinoma, Ovarian Epithelial Pancreatic Neoplasms
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
This is a proof-of-concept study designed to investigate HER3-DXd monotherapy in locally advanced or metastatic solid tumors. The study is enrolling cohorts of participants with melanoma \[cutaneous/acral\], squamous cell carcinomas of the head and neck (SCCHN), and HER2-negative gastric cancerovarian carcinoma, cervical cancer, endometrial cancer, bladder cancer, esophageal carcinoma, pancreatic carcinoma, and prostate cancer.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
You can take part if:
You may not be able to take part if:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Daiichi Sankyo Contact for Clinical Trial Information
9089926400
CTRinfo@dsi.com
The study is sponsored by Daiichi Sankyo and is in collaboration with Merck Sharp & Dohme LLC.
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.