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Renal Adjuvant MultiPle Arm Randomised Trial

Study acronym: RAMPART
StatusRecruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗
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.

Record History

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  1. Notable Primary completion date: Dec 1, 2023 to Jul 1, 2024v3 Show 4 more changesShow less
    • Study sites: 5 to 35
    • Study completion date: Dec 1, 2037 to Dec 1, 2034
    • Eligibility criteria expanded, about 94 words
    • Collaborators: 2 to 3
  2. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Dec 1, 2017 to Jul 19, 2018
    • Study sites: 0 to 5
    v2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT03288532
Lead Sponsor University College, London
Collaborators: AstraZeneca, Kidney Cancer UK, Cancer Research UK
Conditions
(from sponsor)
Renal Cell Carcinoma
Related terms Carcinoma, Renal Cell
Enrollment 1,750 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov