Zanzalintinib
DrugAdministered as specified in the treatment arm.
Other names: XL092
NCT Number: NCT06943755
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Monash Health, Clayton, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Administered as specified in the treatment arm.
Other names: XL092
Administered as specified in the treatment arm.
Other names: Afinitor
Time frame: Up to 48 months
Time frame: Up to 48 months
Time frame: Up to 48 months
Time frame: Up to 60 months
Time frame: Up to 48 months
Time frame: Up to 48 months
Time frame: Up to 48 months
Time frame: Up to 48 months
Time frame: Up to 48 months
Contact information is provided by the study sponsor or research team.
Backup or International
CONTACT
Exelixis Clinical Trials
CONTACT
1-888-EXELIXIS (888-393-5494)
Exelixis
Industry
A Phase 2/3, Multicenter, Randomized Open-Label Study of Zanzalintinib vs Everolimus in Participants With Previously Treated, Unresectable, Locally Advanced or Metastatic Neuroendocrine Tumors
Acronym: STELLAR-311
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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