UV1
DrugUV1 (300 microgram)
NCT Number: NCT03538314
UV1 is a therapeutic cancer vaccine that has been explored in prostate and lung cancers, and in combination with ipilimumab in malignant melanoma. This study will explore the safety, tolerability and efficacy of UV1 administered with GM-CSF in melanoma patients who are also receiving pembrolizumab.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
John Wayne Cancer Center, Santa Monica, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Exclusion criteria
UV1 (300 microgram)
GM-CSF (37,5 or 75 microgram)
Time frame: Up to week 29
Frequency and severity of adverse events
Time frame: Up to week 52
RECIST and iRECIST
Time frame: up to 2 years
Overall survival
Ultimovacs ASA
Industry
A Phase I, Open-label, Multicenter Study Investigating the Tolerability and Efficacy of UV1 Vaccine in First-line Malignant Melanoma Patients Planned for Treatment With Pembrolizumab
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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