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Octopus Clinical Trial Biorepository

Population Size

323

People

Population Size statistic card

Years

2023

Years statistic card

Associated BioSamples

Serum

Plasma

Associated BioSamples statistic card

Geographic coverage

London

Cardiff

...see more

Geographic coverage statistic card

Lead time

Variable

Lead time statistic card

Summary

A biorepository of longitudinal samples (Serum, plasma, DNA) collected from individuals registered to the Octopus clinical trial for progressive MS. The OCTOPUS trial presents a unique opportunity for collection of biospecimens. The valuable cohort includes people at more advanced stages of disability, a placebo arm for comparison, and long duration of expected follow-up. The collection of samples from study participants is an optional activity.

Documentation

A biorepository of samples from individuals recruited to the OCTOPUS clinical trial for progressive-MS. Samples (serum, plasma, DNA) were collected longitudinally every 6 months (W0, W26, W52, W78), alongside MRI and measurements of disability progression.

Biomarkers that are predictive of a) long-term disability in MS and b) responses to medication/ therapy (whether a broad therapy response or a response to a specific medication) are needed for people with MS. While new data suggest that several potential biomarkers may portend a worse long-term prognosis for MS, the interpretation of these results may be limited by the fact that the data were generated from either observational, non-randomised cohorts or from clinical trials, in which people with MS were chosen based on a certain degree of recent disease activity. Hence, there is a need to evaluate such novel biomarkers in a prospective, less biased study to assess its true clinical applicability and generalisability. The OCTOPUS trial presents a unique opportunity for collection of biospecimens.

Dataset type

Health and disease, Treatments/Interventions

Dataset population size

323

Keywords

Observations

Observed Node

Disambiguating Description

Measured Value

Measured Property

Observation Date

Persons

Participants recruited to Octopus who have provided samples for the biorepository

323

Participants recruited to Octopus who have provided samples for the biorepository

01 Mar 2026

Events

Number of individual sample aliquots stored in the Cardiff biorepository

9589

sample aliquot

01 Mar 2026

Events

Number of DNA samples available

230

sample aliquot

01 Mar 2026

Events

Number of Serum samples available

6261

sample aliquot

01 Mar 2026

Events

Number of Plasma samples available

3098

sample aliquot

01 Mar 2026

Persons

Persons providing Randomisation (Baseline / Week 0) samples

305

Participants recruited to Octopus who have provided samples for the biorepository

01 Mar 2026

Persons

Persons providing Week 26 samples

231

Participants recruited to Octopus who have provided samples for the biorepository

01 Mar 2026

Persons

Persons providing Week 52 samples

172

Participants recruited to Octopus who have provided samples for the biorepository

01 Mar 2026

Persons

Persons providing Week 78 samples

108

Participants recruited to Octopus who have provided samples for the biorepository

01 Mar 2026

Provenance

Purpose of dataset collection

Research cohort, Study, Trial, Care

Source of data extraction

Other

Collection source setting

Cohort, study, trial

Patient pathway description

  1. Participants with a confirmed diagnosis of MS
  2. A diagnosis of Secondary progressive stage (SPMS) or Primary Progressive MS (PPMS)
  3. Steady progression as assessed by the treating clinician
, rather than relapse must be the major cause of increasing disability in the preceding 2 years. Progression can be evident from either an increase of at least 1 point if on the Expanded Disability Status Scale (EDSS) score or an increase of 0.5 point if EDSS score,

and/or clinical documentation of increasing disability

  1. EDSS 4.0 - 8.0 (inclusive) as assessed at the time of randomisation by the assessing clinician
  2. Aged 25 - 70 years old inclusive on the day of randomisation
  3. Willing and able to have MRI scans

Image contrast

Not stated

Biological sample availability

Serum,Plasma,DNA

Structural Metadata

Details

Publishing frequency

Other

Version

1.0.0

Modified

05/03/2026

Distribution release date

01/01/2027

Citation Requirements

tbc

Coverage

Start date

01/02/2023

Time lag

Variable

Geographic coverage

London, Cardiff, Edinburgh, Belfast, UK

Minimum age range

25

Maximum age range

70

Follow-up

1 - 10 Years

Accessibility

Language

en

Alignment with standardised data models

LOCAL

Controlled vocabulary

LOCAL

Format

text

Data Access Request

Dataset pipeline status

Not available

Access rights

Please contact www.mrcctu.ucl.ac.uk to discuss access to samples / data.

Time to dataset access

Variable

Access request cost

An indicative cost will be provided to applicants upon application. Charges will be based on workload associated with the application. Discussions surrounding costs to access material should be initiated prior to funding applications being made.

Access method category

Varies based on project

Access service description

Please contact www.mrcctu.ucl.ac.uk to discuss access to samples / data.

Jurisdiction

UK

Data use limitation

Research-specific restrictions

Data use requirements

Project-specific restrictions,Collaboration required

Data Controller

MRC Clinical Trials Unit at UCL

Data Processor

MRC Clinical Trials Unit at UCL

Dataset Types: Health and disease, Treatments/Interventions

Dataset Sub-types: Neurological, Therapeutic


Collection Sources: Cohort, study, trial