Clinical trial Recruiting at 12 sites Observational Ages 14 to 100

Genomics-guided precision medicine for metastatic breast cancer

Official title: Comprehensive Assessment of Clinical Features and Biomarkers to Identify Patients With Advanced or Metastatic Breast Cancer for Marker Driven Trials in Humans (CATCH)

Run by German Cancer Research Center · NCT05652569 · Data updated 2026-11-12

This study is testing whether using genetic information from tumors and blood samples can help doctors create personalized treatment plans for people with metastatic breast cancer.

More Metastatic Breast Cancer trials

Quick facts

Study typeObservational
Ages14 Years to 100 Years
SexAll
Enrollment5000 (estimated)
SponsorGerman Cancer Research Center
Academic / other
Locations12 sites (Augsburg and 11 other locations)
StatusRecruiting
StartedJune 12, 2017
Main results expectedDecember 31, 2030
Study endsDecember 31, 2030
Registry record updatedJanuary 28, 2026
Trial IDNCT05652569 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults with advanced or metastatic breast cancer, regardless of gender or molecular subtype.

Probably not a fit

Patients with early-stage breast cancer or those unable to provide a tissue biopsy may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

CATCH is an observational study that aims to implement genomics-guided precision medicine for patients with metastatic breast cancer. It involves collecting tumor and blood samples from patients at the time of diagnosis or disease progression to conduct genomic and transcriptomic profiling. This profiling helps identify biomarkers and potential drug targets, guiding personalized therapeutic interventions. The study seeks to integrate these precision oncology workflows into clinical practice to improve treatment outcomes.

Why it matters

Potential benefit: If successful, this approach could lead to more effective, personalized treatment options for patients with metastatic breast cancer.

How similar studies have gone: Other studies have shown promise in using genomics-guided approaches for cancer treatment, indicating that this method has potential for success.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Female and male breast cancer patients ≥ 18 or if the legal guardian has agreed to the respective informed consent form (ICF)
* Patients with advanced or metastatic breast cancer (irrespective of clinical parameters such as TNM, subgroups, therapy lines)
* Patients, who agreed to and were able to sign the informed consent form.

Exclusion Criteria:

* Early breast cancer
* Inability to take a tissue bioptic sample due to reasons such as physical location of the lesion or health of the patient
* Any physical or mental handicap or severe comorbidities that would hamper the adequate cooperation with the patient.

Where it's running

  • University Hospital Augsburg
    Augsburg, Germany
    Recruiting
  • Charité
    Berlin, Germany
    Recruiting
  • University Hospital Köln
    Cologne, Germany
    Recruiting
  • Medical Faculty and University Hospital Carl Gustav Carus
    Dresden, Germany
    Recruiting
  • University Hospital Erlangen
    Erlangen, Germany
    Recruiting
  • University Hospital Essen
    Essen, Germany
    Recruiting
Show 6 more locations
  • National Center for Tumor Diseases
    Heidelberg, Germany
    Recruiting
  • Caritas Hospital St. Josef
    Regensburg, Germany
    Recruiting
  • Robert-Bosch-Krankenhaus Stuttgart
    Stuttgart, Germany
    Recruiting
  • University Hospital Tübingen
    Tübingen, Germany
    Recruiting
  • University Hospital Ulm
    Ulm, Germany
    Recruiting
  • University Hospital Würzburg
    Würzburg, Germany
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.