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NCT06678919Recruiting

AGMT Metastatic Colorectal Cancer Registry (mCRC) Third Line and Beyond

Source: ClinicalTrials.gov · Last updated 10 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Colorectal cancer (CRC) is the second leading cause of cancer-related death in the United States and Europe. Although selected patients with oligometastatic CRC undergo systemic therapy and surgery/local ablative therapy in curative intent, the treatment approach for the majority of metastatic CRC (mCRC) patients remains palliative with a median overall survival (OS) ranging between 9-38 months depending on various prognostic and predictive factors. Particularly in advanced stages (in the third line of therapy and beyond), interesting and promising results have recently been achieved with various treatment approaches. The aim of this registry is to establish a disease-specific registry to evaluate the treatment landscape of patients with mCRC who have already received at least two lines of therapy.

Status (registry)
Recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
6 Nov 2024
Start date
31 Oct 2024
Primary completion date
Dec 2034
Lead sponsor
Arbeitsgemeinschaft medikamentoese Tumortherapie
NCT number
NCT06678919

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 31 Oct 2024 to the primary completion date, Dec 2034
  • 7 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Due to the non-interventional design of this registry, there are no specific exclusion criteria

Who the study is looking for

  • patients ≥ 18 years with tissue-based diagnosis of mCRC
  • ≥ 2 prior lines of palliative systemic therapy including 5-FU, irinotecan, oxaliplatin, anti-VEGF, anti-EGFR (in case of RAS/BRAF wildtype), anti-PD1- therapy (in case of MSI/MMRd) . (Exception: Patients who have received mFOLFOXIRI +/- anti-VEGF or anti- EGFR- 1L therapy or patients with ineligibility to receive 5-FU, oxaliplatin or irinotecan can be included after 1st line.)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Ordensklinikum Linz, BHS - Interne I
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LinzAustriaRecruiting
KUK Linz - Med Campus III.: Univ.-Klinik für Hämatologie und Internistische Onkologie
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LinzAustriaRecruiting
LKH Feldkirch: Innere Medizin II/ Interne E (Hämatologie und Onkologie)
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RankweilAustriaRecruiting
Department of Internal Medicine III, Paracelsus Medical University Salzburg
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SalzburgAustriaRecruiting
Klinikum Steyr: Innere Medizin II: Onkologie, Gastroenterologie, Angiologie
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SteyrAustriaRecruiting
Klinikum Wels: Abteilung für Innere Medizin IV
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WelsAustriaRecruiting
KH Zams: Innere Medizin Internistische Onkologie und Hämatologie
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ZamsAustriaRecruiting

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This page is information, not medical advice. Discuss any trial with your doctor.