UnknownCancerNIHR-supported projectDigestion, Kidneys & Other Organs
A multi-centre, open label Phase I/ randomised Phase II study of VP-002, a C-C motif chemokine receptor 1 (CCR1) inhibitor, given orally in combination with nab-paclitaxel and gemcitabine (nPG) to patients with advanced pancreatic ductal adenocarcinoma
Recipient organisationNIHR Royal Free Clinical Research Facility
NIHR supportRecorded as supported by this research centre
PeriodJan 2025 — Ongoing
In plain English
AI plain-English summary
A new drug, VP-002, is being tested in combination with standard chemotherapy to see if it can extend survival for people with metastatic pancreatic cancer. This matters because pancreatic cancer is notoriously difficult to treat, and current chemotherapy alone offers limited survival gains. The tumour's microenvironment—the surrounding tissue and immune cells—often shields it from treatment. VP-002 targets a receptor called CCR1 on immune cells, aiming to alter that microenvironment and make the tumour more vulnerable to chemotherapy. If the trial succeeds, it could provide a new treatment option for a cancer with few effective therapies. The study is split into two phases: Phase I will test safety and find the right dose in about 30 patients; Phase II will compare survival, tumour response, and quality of life in 96 patients receiving the combination versus chemotherapy alone. The research is directly translational—it tests a specific drug in humans, with the immediate goal of improving outcomes for patients who currently have very poor prognoses.
View original technical description
The CRISTAL-APC study,led by Cambridge University Hospitals and the University of Cambridge,is a two-phase clinical trial investigating the safety,tolerability,and efficacy of VP-002 in combination with standard chemotherapy (nPG) for metastatic pancreatic cancer. Phase I aims to determine the optimal dose of VP-002 by assessing its safety and side effects. Phase II will evaluate the impact of this combination on overall survival compared to standard chemotherapy alone. The study hypothesizes that targeting the CCR1 receptor will alter the tumor microenvironment,enhancing anti-cancer effects. Approximately 30 patients will participate in Phase I,and 96 in Phase II,with recruitment facilitated through hospital multidisciplinary teams. Patients will provide informed consent after discussions and a screening process to confirm eligibility. The trial seeks to improve the tolerability of a new combination and to assess whether it results in any improvements in survival,tumor response,and quality of life for patients with metastatic pancreatic cancer.
Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.
Is something wrong? Let us know