Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsPhase2/Phase3

Zanzalintinib Versus Everolimus in Participants With Locally Advanced or Metastatic Neuroendocrine Tumors

Sponsor: Exelixis

NCT ID: NCT06943755

View on ClinicalTrials.gov ↗

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.

Pancreatic Neuroendocrine Tumor (pNET)Extra-Pancreatic Neuroendocrine Tumor (epNET)

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

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
Key Inclusion Criteria: * Histologically confirmed, locally advanced/unresectable or metastatic, well-differentiated Grade 1, 2, or 3 NETs of pancreatic origin or extra-pancreatic origin. * Allowed prior lines of therapy, based on the site of NET and functional status. * Documented radiographic disease progression per RECIST 1.1, as assessed by the Investigator based on imaging assessments (computed tomography \[CT\] or magnetic resonance imaging \[MRI\]) within 12 months before randomization. * Measurable disease according to RECIST 1.1 as determined by the Investigator. * Archival tumor tissue is required, if available. If archival tumor tissue is not available, a fresh biopsy may be submitted if it can be safely and feasibly obtained. Every attempt should be made to provide tumor tissue. Key Exclusion Criteria: * Histologically confirmed neuroendocrine carcinomas (including small cell lung cancer), medullary thyroid cancer, pheochromocytoma, paraganglioma, Merkel cell carcinoma, and mixed neuroendocrine non-neuroendocrine neoplasm (MiNEN). * Prior treatment with a vascular endothelial growth factor receptor (VEGFR) -targeting tyrosine kinase inhibitor or a mammalian target of rapamycin (mTOR) inhibitor. * Systemic chemotherapy and any liver-directed or other ablative therapy within 4 weeks before randomization. * Systemic radionuclide therapy within 6 weeks before randomization. * Radiation therapy for bone metastases within 2 weeks, any other radiation therapy, except as indicated above, within 4 weeks before randomization. Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Where Is This Study? (10 UK sites)

University Hospitals Birmingham NHS Foundation Trust

Birmingham B15 2GW, United Kingdom

Recruiting
Hospital R&D contact (matched)

Sarah Pountain Head of Research Governance

R&D@uhb.nhs.uk0121 371 4185

Velindre Cancer Center

Cardiff CF14 2TL, United Kingdom

Recruiting
Hospital R&D contact (matched)

Sarah Townsend

Velindre.R&Doffice@wales.nhs.uk02920 196165

NHS Greater Glasgow and Clyde

Glasgow G12 0YN, United Kingdom

Recruiting
Hospital R&D contact (matched)

Radek Penar

radoslaw.penar@nhs.scotn/a

The Clatterbridge Cancer Centre

Liverpool L7 8YA, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Maria Maguire

maria.maguire2@nhs.net0151 556 5321

Guy's and St Thomas' NHS Foundation Trust

London SE1 9RT, United Kingdom

Recruiting
Hospital R&D contact (matched)

Main Email: gstt.research.rbhh@nhs.net

gstt.research.rbhh@nhs.netn/a

King's College Hospital NHS Foundation Trust

London SE5 9RS, United Kingdom

Recruiting
Hospital R&D contact (matched)

Jasmine Palmer

kch-tr.research@nhs.net0203 299 1980

Oxford University Hospitals NHS Foundation Trust

Oxford OX3 7LE, United Kingdom

Recruiting
Hospital R&D contact (matched)

Shahista Hussain

ouhtma@ouh.nhs.uk---

Sheffield Teaching Hospitals NHS Foundation Trust

Sheffield S10 2SJ, United Kingdom

Recruiting
Hospital R&D contact (matched)

Alessia Dunn

STH.ResearchAdministration@nhs.net0114 2712550

The Royal Marsden NHS Foundation Trust

Sutton SM2 5PT, United Kingdom

Recruiting
Hospital R&D contact (matched)

Mark Brandon-Grove

research.development@rmh.nhs.uk020 3186 5416

Swansea Bay University Health Board

Swansea SA2 8QA, United Kingdom

Recruiting
Hospital R&D contact (matched)

Jemma Rogers

Jemma.Rogers@wales.nhs.uk01792 530890

How to Get in Touch

Exelixis Clinical Trials

Sponsor contact

CONTACT

1-888-EXELIXIS (888-393-5494) druginfo@exelixis.com

Backup or International

Sponsor contact

CONTACT

650-837-7400
Data sourced from ClinicalTrials.gov · Last verified: 2026-09