ClinicalTrials.gg
Enrolling by invitationNCT06856122PISCESUpdated Jul 14, 2025

Pharmacogenomics to Improve Supportive Care Symptoms.

An observational study in Palliative Care and Supportive Care, sponsored by Norfolk and Norwich University Hospitals NHS Foundation Trust. Enrolling by invitation at 2 sites in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-07-14.

Sponsored by Norfolk and Norwich University Hospitals NHS Foundation Trust · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2026, 7 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
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Study summary

To understand the clinical utility of multi-gene pharmacogenetic testing in patients receiving palliative and supportive care across palliative care settings (inpatient hospital, outpatient), specifically to calculate a drug-gene interaction ratio, based on extant prescriptions paired with an individual's pharmacogenetic results.

Read the detailed description

This is a prospective, observational cross-sectional study of patients with serious and/or life limiting condition conditions, such as incurable cancer undergoing palliative or supportive care treatment at a University Teaching Hospital in England, UK. Participants will be recruited at point of referral to in-patient or outpatient palliative care services (i.e. at point of presentation with symptom control issues).

All participant study activities:

All participants will undergo testing of a panel of genetic variants relevant to drugs used in symptom control (see https://cpicpgx.org/genes-drugs/ ). This will involve collecting a 5mL blood sample (the intervention) from individuals. All participants will be consented to examination of their records within local hospitals and/or primary care to extract study relevant data (described below).

The start of follow-up will be from the date of the blood sample (the intervention). Standard demographic information including ethnicity will be collected at baseline.

Participation in study will be for the duration of being under palliative care treatment, up to a maximum of 90days from recruitment date.

All participant sample will be stored and genetic analysis will take place after the end of recruitment and health data collection.

The study team will then calculate a drug-gene interaction ratio (DGI) (i.e. The total number of genetic variation results that pair with a relevant prescribed medication for that same individual, divided by total number of individuals tested).

02

Conditions studied

  • Palliative Care
  • Supportive Care

Keywords

  • Pharmacogenomics
  • pharmacogenetics
  • palliative
  • supportive care
03

In context

Lead sponsor

Norfolk and Norwich University Hospitals NHS Foundation Trust is the lead sponsor of 30 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population will be from Norfolk and Norwich University Hospitals NHS Foundation Trust

Eligibility criteria

Inclusion Criteria: Aged 18 or older; incurable, life limiting condition, clinical care provided at NNUH.

Exclusion Criteria: Lacking capacity to consent to research (unless there is an appropriate consultee)

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Study participants

    Patients with serious and/or life limiting condition conditions, such as incurable cancer undergoing palliative or supportive care treatment. They will have a 5mL blood sample collected.

06

What researchers measure

Primary outcomes

  1. Drug-gene interaction ratio (DGI)

    The total number of genetic variation results that pair with a relevant prescribed medication for that same individual, divided by total number of individuals tested.

    Time frame: This will be calculated for all current medications prescribed at the point of recruitment.

Secondary outcomes

  1. Frequency of changes in prescription medication that are potentially affected by drug-gene interaction

    Number of participants who have a change in prescribed medication (dose or formulation) during 90 day follow up period that could be theoretically paired to possession of a clinically relevant drug-gene interaction

    Time frame: from enrolment until 90 days post blood test

07

Study locations

2 sites
  • Norfolk and Norwich University Hospitals NHS Foundation Trust
    Norwich, Norfolk NR4 7UY, United Kingdom
  • The Manchester Centre for Genomic Medicine
    Manchester, M13 9WL, United Kingdom
08

References and documents

Publications

  • Barry C, Patel M. Pharmacogenomics and symptom management in palliative and supportive care: A scoping review. BMJ Support Palliat Care. 2025 Feb 26;15(2):158-167. doi: 10.1136/spcare-2024-005205. PubMed 39805678 ↗
  • Patel M, McDermott J, Newman W, Barry C. Pharmacogenomics to Improve Supportive Care Symptoms. A Prospective Observational Study Protocol. NIHR Open Res. 2026 Apr 10;5:125. doi: 10.3310/nihropenres.14182.2. eCollection 2025. PubMed 42022754 ↗
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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started May 2025 (actual). Primary completion is estimated for Apr 2026, 10 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 5, 2025
First posted
Mar 4, 2025
StartActual
May 9, 2025
Primary completionEst.
Apr 1, 2026
CompletionEst.
Oct 1, 2026
Last update
Jul 14, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 14, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06856122
Lead sponsor
Norfolk and Norwich University Hospitals NHS Foundation Trust
Collaborators
Manchester Centre for Genomic Medicine - St. Mary's Hospital University of Manchester
Responsible party
Sponsor
First posted
Mar 4, 2025
Start date
May 9, 2025
Primary completion
Apr 1, 2026 (estimated)
Completion
Oct 1, 2026 (estimated)
Last update
Jul 14, 2025

Study contacts

Dr Martyn Patel
principal investigator · Clinical Research and Trials Unit (Norfolk & Norwich University Hospital, UK)
Dr Caroline Barry
principal investigator · Clinical Research and Trials Unit (Norfolk & Norwich University Hospital, UK)

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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