← Eichor
Study identifier: NCT04106115 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

DURvalumab in Combination With S-488210/S-488211 vAccine in Non-muscle Invasive Bladder CancEr

Condition: Bladder Cancer  ·  Sponsor: University College, London

PhasePhase 1/Phase 2
Planned participants52
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

DURANCE is a two part, phase Ib/II, multi-centre study to assess the safety and activity of S-488210/S-488211 in combination with durvalumab, in patients with non-muscle invasive bladder cancer (NMIBC).

This description comes directly from the study's public registry record.

Talk to the study team

Madison Williams  ·  02076799514  ·  ctc.durance@ucl.ac.uk

Rubina Begum  ·  02076799514  ·  rubina.begum@ucl.ac.uk

Always discuss trial participation with your own doctor first.

Locations (7)

Cambridge University NHS FTCambridge, United KingdomRecruiting
Guy's and St Thomas' NHS Foundation TrustLondon, United KingdomRecruiting
Royal Free London NHS FTLondon, United KingdomRecruiting
The Royal Marsden NHS Foundation TrustLondon, United KingdomRecruiting
University College London Hospital NHS Foundation TrustLondon, United KingdomRecruiting
The Christie NHS Foundation TrustManchester, United KingdomRecruiting
University Hospital Southampton NHS Foundation TrustSouthampton, United KingdomRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04106115