Study #2024-0338
A first-in-human open label phase Ia/Ib, multicenter/multiregional, dose escalation study of BI 765883 administered as monotherapy and in combination with gemcitabine and nab-paclitaxel in unselected patients with metastatic pancreatic ductal adenocarcinoma (mPDAC) or patients with PDAC who have relapsed after post-surgery adjuvant therapy
MD Anderson Study Status
Enrolling
Treatment Agent
BI 765883, gemcitabine, nab-paclitaxel
Description
This study is open to adults with advanced pancreatic cancer for whom previous treatment was not successful or no treatment exists. The purpose of this study is to find the highest dose of BI 765883 that people with advanced pancreatic cancer can tolerate when taken alone or together with chemotherapy. Another purpose is to check whether BI 765883 helps people with advanced pancreatic cancer. In this study, BI 765883 is given to humans for the first time. Participants receive either BI 765883 alone or BI 765883 in combination with chemotherapy. Participants can stay in the study as long as they benefit from treatment and can tolerate it. At study visits, doctors collect information on any health problems of the participants and check the severity of participants' cancer.
Resources and Links
Phone Number: 1-877-MDA-6789
Information and next steps
Disease:
Pancreatic Ductal Adenocarcinoma
Study phase:
Phase I
Physician name:
Shubham Pant
Department:
Gastrointestinal Medical Oncology
For general questions about clinical trials:
1-833-642-1954
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