Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06504719
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
None
First Post:
2024-04-09
Brief Title:
Safety and Efficacy Real-world Data of Trastuzumab Deruxtecan and Sacituzumab Govitecan
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Safety and Efficacy Real-world Data of Trastuzumab Deruxtecan and Sacituzumab Govitecan in Patients With Advanced Breast Cancer
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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
Detailed Description:
Antibody-drug conjugates ADCs have significantly changed the therapeutic landscape of advanced breast cancer Trastuzumab deruxtecan T-DXd a HER2-targeting ADC and sacituzumab govitecan SG a TROP-2-targeting ADC recently demonstrated superior efficacy over standard of care treatments depending on breast cancer subtype The study aims to evaluate real-world efficacy and toxicity data of treatment with T-DXd and SG in pretreated patients with advanced breast cancer
This study includes a retrospectiveprospective multicenter review of medical records of patients with advanced breast cancer who received treatment with T-DXd and SG at Departments of Oncology affiliated with the Hellenic Cooperative Oncology Group HeCOG
This study includes a retrospectiveprospective multicenter review of medical records of patients with advanced breast cancer who received treatment with T-DXd and SG at Departments of Oncology affiliated with the Hellenic Cooperative Oncology Group HeCOG
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None