STRIDE
DrugTremelimumab 300 mg as a single dose administered in combination with durvalumab 1500 mg at Cycle 1/Day 1, followed by durvalumab monotherapy every 4 weeks.
NCT Number: NCT07607769
Italian multicenter observational study to evaluate time to clinical hepatic decompensation, quality of life, effectiveness, and safety of tremelimumab plus durvalumab in patients with advanced or unresectable hepatocellular carcinoma who have received no prior systemic treatment.
Interested in participating?
Request Info18 year–100 year
All sexes
Observational
Research Site, Ancona, Italy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Tremelimumab 300 mg as a single dose administered in combination with durvalumab 1500 mg at Cycle 1/Day 1, followed by durvalumab monotherapy every 4 weeks.
Time frame: From index date to first hepatic decompensation/study completion, up to 30 months
time from index date (start of new treatment) to the first occurrence of events such as ascites of any grade according to the European Association for the Study of the Liver (EASL) classification, hepatic encephalopathy of any grade according to West Haven classification, variceal hemorrhage, or jaundice (total bilirubin >3 mg/dL).
In Child-Pugh (CP)-A participants with a score of 6 at index date, TTDec is defined as the time from index date to any worsening in ascites, hepatic encephalopathy, variceal hemorrhage, or jaundice (defined as an increase in total bilirubin to greater than 3 mg/dL or a worsening of more than 1.0 mg/dL from index date).
At the time of decompensation (± 30 days) a CT scan should be performed to exclude worsening of liver function due to tumor progression.
Time frame: Baseline and every 8 weeks during treatment, up to 30 months
Time To Worsening (TTWors) based on the EORTC QLQ-C30 and QLQ-HCC18 PROs within the first 18 months of treatment. TTWors is the time from first treatment to first clinically meaningful deterioration confirmed at a subsequent visit/assessment or death from any cause. A clinically meaningful change (deterioration or improvement) is defined as an absolute change ≥ 10 points in total score from index date.
Time frame: From index date through study completion, up to 30 months
time from first treatment to death
Time frame: From index date until tumor progression, assessed until study completion, up to 30 months
time from first treatment to radiologic evidence of tumor progression or death based on investigator assessment (RECIST v1.1).
Time frame: From index date until objective tumor progression, assessed until study completion, up to 30 months
proportion of participants with a complete response (CR) or partial response (PR) per RECIST v1.1.
Time frame: From index date until objective tumor progression or date of death, assessed until study completion, up to 30 months
proportion of participants with a CR, PR, or stable disease (SD) per RECIST v1.1. (stable disease needs to be maintained for a minimum of 8 weeks to be included in the DCR).
Time frame: From index date until study completion, up to 30 months
Proportion of participants who undergo liver transplant following downstaging with the STRIDE regimen
Time frame: From index date until study completion, up to 33 months
Adverse events: severity, seriousness, causality, action taken with durvalumab, and outcome.
Time frame: From index date to first hepatic decompensation/study completion, up to 30 months
defined for the primary outcome within the first 18 months of treatment by:
Contact information is provided by the study sponsor or research team.
AstraZeneca Clinical Study Information Center AstraZeneca Clinical Study Information Center
CONTACT
+1877240 ext. 9479
AstraZeneca
Industry
MONTEROSA Italian Multicenter Observational Study to Evaluate Time to Clinical Hepatic Decompensation, Quality of Life, Effectiveness, and Safety of Tremelimumab Plus Durvalumab in Patients With Advanced or Unresectable Hepatocellular Carcinoma Who Have Received no Prior Systemic Treatment. (Real World Observational Study of STRIDE Regimen for Advanced HCC)
Acronym: MONTEROSA
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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