At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Zanzalintinib (drug), Everolimus (drug)
- How long the study runs
- Study runs about 47 months (dates as stated)
- About the drug or intervention
- Zanzalintinib — drug: Administered as specified in the treatment arm. · Everolimus — drug: Administered as specified in the treatment arm.
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 440
- Started
- 2025-07-21
- Last checked
- 2026-09
Plain English Summary
What is this study?
- • Testing a new treatment for pancreatic neuroendocrine tumor (pnet)
- • Phase2/Phase3 - 440 participants
- • The primary purpose of this study is to assess the effectiveness of zanzalintinib compared to everolimus in participants with previously treated, unresectable, locally advanced or metastatic neuroendocrine tumors
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with pancreatic neuroendocrine tumor (pnet)
Where?
- • Birmingham - University Hospitals Birmingham NHS Foundation Trust
- • Cardiff - Velindre Cancer Center
- • Glasgow - NHS Greater Glasgow and Clyde
- • Liverpool - The Clatterbridge Cancer Centre
- • +6 more UK sites
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
The primary purpose of this study is to assess the effectiveness of zanzalintinib compared to everolimus in participants with previously treated, unresectable, locally advanced or metastatic neuroendocrine tumors.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
What the study is looking for
- ✓confirmed by a biopsy, that has grown locally/unresectable or that has spread, well-differentiated Grade 1, 2, or 3 NETs of...
- ✓Allowed previous treatments, based on the site of NET and functional status.
- ✓cancer that can be measured on scans according to (standard scan measurements) as determined by the Investigator.
Who cannot take part
- ✗Prior treatment with a vascular endothelial growth factor receptor (VEGFR) -targeting tyrosine kinase inhibitor or a...
- ✗Systemic drug treatment and any liver-directed or other ablative therapy within 4 weeks before randomization.
- ✗Systemic radionuclide therapy within 6 weeks before randomization.
- ✗radiotherapy for bone metastases within 2 weeks, any other radiotherapy, except as indicated above, within...
- ✗Note: Other protocol defined Inclusion/Exclusion criteria may apply.
See the full criteria
Where Is This Study? (10 UK sites)
University Hospitals Birmingham NHS Foundation Trust
Birmingham B15 2GW, United Kingdom
Velindre Cancer Center
Cardiff CF14 2TL, United Kingdom
NHS Greater Glasgow and Clyde
Glasgow G12 0YN, United Kingdom
The Clatterbridge Cancer Centre
Liverpool L7 8YA, United Kingdom
Guy's and St Thomas' NHS Foundation Trust
London SE1 9RT, United Kingdom
King's College Hospital NHS Foundation Trust
London SE5 9RS, United Kingdom
Oxford University Hospitals NHS Foundation Trust
Oxford OX3 7LE, United Kingdom
Sheffield Teaching Hospitals NHS Foundation Trust
Sheffield S10 2SJ, United Kingdom
The Royal Marsden NHS Foundation Trust
Sutton SM2 5PT, United Kingdom
Swansea Bay University Health Board
Swansea SA2 8QA, United Kingdom
How to Get in Touch
Exelixis Clinical Trials
Sponsor contactCONTACT
Backup or International
Sponsor contactCONTACT
