Fact CheckerSign in

NCT06504719Completed

Safety and Efficacy Real-world Data of Trastuzumab Deruxtecan and Sacituzumab Govitecan

Safety and Efficacy Real-world Data of Trastuzumab Deruxtecan and Sacituzumab Govitecan in Patients With Advanced Breast Cancer

Source: ClinicalTrials.gov · Last updated 15 Sept 2025

Brief summary (registry, in English)

The study aims to evaluate real-world efficacy and toxicity data of treatment with Trastuzumab deruxtecan (T-DXd), a HER2-targeting ADC and sacituzumab govitecan (SG), a TROP-2-targeting ADC in pretreated patients with advanced breast cancer.

Status (registry)
Completed
Study type
Observational
Enrollment
312 (actual)
First submitted
9 Apr 2024
Start date
1 Jan 2023
Primary completion date
1 Jun 2024
Lead sponsor
Hellenic Cooperative Oncology Group
NCT number
NCT06504719

What you commit to

  • Study type: Observational
  • Participants enrolled: 312
  • From 1 Jan 2023 to the primary completion date, 1 Jun 2024
  • 1 site 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

  • NA

Who the study is looking for

  • Histologically confirmed metastatic/recurrent breast cancer
  • 18 years of age
  • Triple-negative (TNBC), HER2-positive and/or hormone receptor positive advanced breast cancer
  • Treatment with an ADC at any of line of treatment
  • Treatment with at least one cycle of T-DXd and/or SG

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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hellenic Cooperative Oncology Group
Coordinator of this site? Confirm its status
AthensGreeceUnknown status

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