Actively Recruiting

Age: 18Years +
FEMALE
NCT05804578

Using a Blood Test to Monitor Metastatic Breast Cancer Treatment

Led by Dr. Christopher Mueller · Updated on 2025-07-25

150

Participants Needed

2

Research Sites

127 weeks

Total Duration

On this page

Sponsors

D

Dr. Christopher Mueller

Lead Sponsor

C

Canadian Institutes of Health Research (CIHR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to assess the effectiveness of the mDETECT breast cancer blood test at monitoring treatment response in women with metastatic breast cancer undergoing treatment.

CONDITIONS

Official Title

Using a Blood Test to Monitor Metastatic Breast Cancer Treatment

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult women (≥ 18 years of age) with a confirmed diagnosis of breast adenocarcinoma
  • Evidence of recurrent or metastatic breast cancer not suitable for surgery or radiation with curative intent
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Kingston Health Sciences Centre - Cancer Centre of Southeastern Ontario

Kingston, Ontario, Canada, K7L 5P9

Actively Recruiting

2

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada, M4N 3M5

Actively Recruiting

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Research Team

C

Christopher R Mueller, Ph.D.

CONTACT

K

Keira Frosst

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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