Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, 200032, China
NCT Number: NCT05571618
To investigate the efficacy and safety of ADC rechallenge
This study is active but is not currently recruiting participants.
Notify Me18 year and older
Female
Observational
Shanghai, Shanghai Municipality, 200032, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients with prior exposure to ADC (either in the adjuvant setting or metastatic disease are allowed).
Time frame: 6 weeks
Progression free survival
Time frame: 6 weeks
Objective Response Rate
Time frame: 6 weeks
Clinical Benefit Rate
Time frame: 6 weeks
Duration of Response
Time frame: 6 weeks
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time frame: 6 weeks
Overall Survival
Fudan University
Other
A Multicenter, Real-world Study of the Efficacy and Safety of Antibody-drug Conjugates (ADCs) Rechallenge in Patients with Prior Exposure to ADCs Metastatic Breast Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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