Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsN/A

Understanding immunE-related toXicities by multifACeT Profiling

Sponsor: Royal Marsden NHS Foundation Trust

NCT ID: NCT05331066

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 72 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
200
Started
2022-04-06
Last checked
2025-09

Plain English Summary

What is this study?

  • • Testing a new treatment for oncology
  • • Clinical study - 200 participants
  • • A prospective observational cohort study of patients undergoing CPI therapy in which translational research is the fundamental aspect of the study

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with oncology

Where?

  • • Chelsea - Royal Marsden NHS Foundation Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

A prospective observational cohort study of patients undergoing CPI therapy in which translational research is the fundamental aspect of the study.

More detail

The study aims to enroll and obtain samples of investigational interest from 200 patients over a 36-month recruitment period. Blood and/ or stool samples will be taken at baseline, in context of irAE development / during CPI treatment and during follow-up. Skin samples may also be taken upon development of organspeciifc irAEs. Further assessments at baseline or during the course of or following treatment will be conducted in accordance with standard institutional practice and will be clinically driven. Clinical data, samples and results from archival, current or prospective diagnostic or therapeutic procedures will be used for research purposes within EXACT. IrAE clinical monitoring will be conducted in accordance with standard institutional practice and will be clinically driven.

Oncology

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Written agreement to take part
  • ✓Age 18 years or older
  • ✓Confirmed diagnosis of any form of solid cancer with a clinical indication and appropriate treatment plan to...

Who cannot take part

  • ✗Medical or psychological condition that would preclude agreement to take part
  • ✗Planned participation in a drug trial receiving investigational agents
  • ✗Subjects who have previously commenced immune checkpoint inhibitor therapy prior to study entry.
  • ✗Subjects unable to comply with the study or sample schedule.
See the full criteria
Inclusion Criteria: * Written informed consent * Age 18 years or older * Confirmed diagnosis of any form of solid malignancy with a clinical indication and appropriate treatment plan to commence immune checkpoint inhibitor therapy Exclusion Criteria: * Medical or psychological condition that would preclude informed consent * Planned participation in a drug trial receiving investigational agents * Subjects who have previously commenced immune checkpoint inhibitor therapy prior to study entry. * Subjects unable to comply with the study or sample schedule.

Where Is This Study? (1 UK site)

Royal Marsden NHS Foundation Trust

Chelsea SW3 6JJ, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Laura Boddy

Sponsor contact

CONTACT

020 7352 8171 exact@rmh.nhs.uk

Arjun Modi

Sponsor contact

CONTACT

exact@rmh.nhs.uk
Data sourced from ClinicalTrials.gov · Last verified: 2025-09