Clinical Trial

Renal Adjuvant MultiPle Arm Randomised Trial

Study acronym: RAMPART
Recruiting Phase 3
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Record status
This record was last updated September 7, 2020 (before its estimated July 1, 2024 completion). Its status may not reflect the trial's current state.
Summary
RATIONALE: The current global standard of care after nephrectomy for localised RCC therefore remains active monitoring (i.e., observation by clinical and radiological means). 30-40% patients with initially localised RCC develop metastatic disease following nephrectomy. Need for adjuvant therapy is most marked in the high risk population where outcomes are predictably poor. However, the risk of recurrence in patients who are of intermediate risk of recurrence is not insignificant. Unfortunately, despite showing efficacy in advanced RCC, the results in the adjuvant setting, so far, are inconclusive. AIM: RAMPART is a phase III Multi-Arm Multi-Stage randomised controlled platform trial, initiated with three arms. The trial is assessing if durvalumab monotherapy or the combination of durvalumab and tremelimumab can improve Disease Free Survival (DFS) or Overall Survival (OS) compared to the current global standard-of-care (active monitoring). At the start of recruitment, patients with Leibovich scores 3 to 11 will be eligible for randomisation. Accrual of intermediate risk patients (Leibovich scores 3 5) will stop after 3 years or when intermediate risk patients contribute 25% of the total accrual target, whichever is earlier. Recruitment of patients with Leibovich scores 6 to 11 will continue until the accrual target is reached.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2017-09-18; most recent amendment 2020-09-03.
Status change: Not Yet Recruiting → Recruiting 2018-09-06
Trial Details
NCT Number NCT03288532
Lead Sponsor University College, London
Collaborators: AstraZeneca, Kidney Cancer UK, Cancer Research UK
Conditions Renal Cell Carcinoma
Enrollment 1,750 participants
Start Date 2018-07-19
Primary Completion 2024-07-01 (estimated)
Study Completion 2034-12-01 (estimated)
Updated on ClinicalTrials.gov 2020-09-07