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Taking people in DenmarkNo phase

Studies biomarkers and outcomes in lung or breast cancer patients

Observes patients with lung or breast cancer, linking biomarkers to their outcomes.

Plain-language title generated from the registry record
Registry title: Copenhagen Master Observational Trial

Key facts

Where
Copenhagen, DenmarkSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with non-small cell lung cancer or breast cancer who get treatment in the clinic and can give consent and have whole-genome sequencing done.

Age
18 years and older
Sex
All sexes can join
Disease stage
Non-small cell lung cancer or breast cancer that can be treated with medicine or radiation, either to remove all of the disease or to ease symptoms
Biomarker or test result
Willing and able to complete data collection including whole-genome sequencing (WGS)

Main reasons for not taking part

  • Breast cancer where adjuvant systemic therapy is starting
  • Life expectancy of fewer than 3 months at the time of diagnosis, in the investigator's judgment
  • Cannot read and understand Danish

Read by machine on 9 November 2026.

Where in Denmark

  • RigshospitaletCopenhagen, DenmarkTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Copenhagen University Hospital, Rigshospitalet
Trial code
NCT05145244
Record updated
12 August 2026
Original description
The primary objectives of this prospective non-interventional study (NIS) are to assess and describe outcomes in relation to biomarkers, including whole-genome sequencing (WGS) in patients with non- small cell lung cancer (NSCLC) or breast cancer receiving treatment offered in the clinic (standard of care or included in clinical trials).Read full original descriptionShow less

Copenhagen Master Observational Trial (C-MOT): A Prospective Investigator-initiated Observational Study to Study Biomarkers in Relation to Clinical Outcome in Patients With Non-Small Cell Lung Cancer or Breast Cancer

The primary objectives of this prospective non-interventional study (NIS) are to assess and describe outcomes in relation to biomarkers, including whole-genome sequencing (WGS) in patients with non- small cell lung cancer (NSCLC) or breast cancer receiving treatment offered in the clinic (standard of care or included in clinical trials).

Inclusion: Patients (≥ 18 years of age) with diagnosis of NSCLC or breast cancer amenable to medical or radiation therapy with curative or palliative intent; Evidence of a personally signed and dated informed consent form document indicating that the patient has been informed of all pertinent aspects of the study; Able to read and understand Danish; Willing and able to complete collection of data including WGS.

Exclusion: Patient with breast cancer initiating adjuvant systemic therapy; In the judgment of the investigator, the patient's life expectancy is fewer than 3 months at the time of diagnosis of NSCLC or breast cancer.

ClinicalTrials.gov NCT05145244

Under construction, not live – Copenhagen Master Observational Trial (NCT05145244) – Frontlight Research