Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06503380

Real-world Study on the Management of Hematological Toxicities Associated With Targeted Therapies for Breast Cancer

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Fudan University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This multicenter, real-world, observational study will retrospectively and prospectively collect real-world data related to the investigational drugs. We plan to observe 1000 patients and collect data on treatment cycles N and N+1 of the targeted therapies. Retrospective data collection is based on existing patient diagnosis and treatment records, collecting information on patients who have completed two treatment cycles before January 1, 2024. Prospective data collection is based on routine clinical treatment during the study period, collected until the end of the next cycle of treatment or early termination of the study. To observe the disease characteristics and management mode of hematological toxicity related to targeted therapies of breast cancer, and explore the possible related factors of hematological toxicity, such as age, disease subtype, cancer stage, targeted therapy regimens, etc. This study will respect the medication choices of researchers in the study, without specifying which medication to choose for treatment, dosage, mode of administration (including single drug, combination therapy, or sequential therapy), and duration of administration.

Conditions

Interventions

TypeNameDescription
OTHERNo intervenrion.This study will respect the medication choices of researchers in the study, without specifying which medication to choose for treatment, dosage, mode of administration (including single drug, combination therapy, or sequential therapy), and duration of administration.

Timeline

Start date
2024-07-15
Primary completion
2026-07-15
Completion
2027-06-10
First posted
2024-07-16
Last updated
2024-07-31

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06503380. Inclusion in this directory is not an endorsement.