The Rechallenge of ADCs in MBC Patients

NCT ID: NCT05571618

Last Updated: 2024-10-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-09-01

Study Completion Date

2025-03-01

Brief Summary

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To investigate the efficacy and safety of ADC rechallenge

Detailed Description

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Conditions

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Breast Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Group1

ADC

Intervention Type DRUG

Patients with prior exposure to ADC (either in the adjuvant setting or metastatic disease are allowed).

Interventions

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ADC

Patients with prior exposure to ADC (either in the adjuvant setting or metastatic disease are allowed).

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* age \> 18 years old.
* Diagnosed with Metastatic Breast Cancer.
* Patients with prior exposure to ADC (either in the adjuvant setting or metastatic disease are allowed).
* Patients plan to or have received ADCs for the second or more time.
* Complete medical history was available.

Exclusion Criteria

* Medical history was incomplete
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Fudan University

OTHER

Sponsor Role lead

Responsible Party

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Biyun Wang, MD

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Site Status

Countries

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China

Other Identifiers

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YOUNGBC-23

Identifier Type: -

Identifier Source: org_study_id

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