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CORONADO (Circulating tumOur pROtein quaNtification cApillary blooD cOvid-19)

I

Institute of Cancer Research, United Kingdom

Status

Unknown

Conditions

Multiple Myeloma

Treatments

Other: n/a - samples collected along routine care samples only

Study type

Observational

Funder types

Other

Identifiers

NCT04659252
CCR5361

Details and patient eligibility

About

The coronavirus (COVID-19) pandemic has brought severe challenges for myeloma patients. Myeloma patients are considered ultra-high risk for COVID-19 and fall into the strictest group for shielding. When on treatment, but also during times of active surveillance, patients have to regularly and frequently leave shielding and visit the hospital for blood tests to monitor their disese. This is specifically for quantification of circulating tumour protein biomarker tests for paraprotein (PP) and/or serum free light chains (sFLCs) by specialised biochemistry units.

This research aims to evaluate the potential use of an at-home patient administered technique to sample blood. The purpose of the blood sampling technique is to monitor your disease status. We want to test if it is possible to monitor a patient's disease status using this alternative blood collection method when compared to monitoring disease status using the traditional blood collection methods (venous blood sampling).

The new VAMS method is not intended to be used interchangeably or will not replace the current method. This study is to evaluate an alternative sample type that may be used to improve the patient pathway, especially during these uncertain times.

Enrollment

70 estimated patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. A diagnosis of a B-cell dyscrasia
  2. Measurable disease by serum free light chain assay
  3. Signed informed consent

Exclusion criteria

  1. Patients <21 years of age
  2. Cognitive impairment
  3. Non-B Cell Dyscrasia patients

Trial contacts and locations

1

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Central trial contact

Haemato-oncology Research Team; Chloe Burrows

Data sourced from clinicaltrials.gov

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