assignment
Not Yet Recruiting

A Phase II Study of Cell-Based Immunotherapy for the Treatment of Stage II and III Triple-Negative Breast Cancer

Trial ID
2023-506019-16-03
Protocol
aHyC-TNBC

Trial statistics

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Diseases & Conditions

Objectives

The primary objective is to evaluate the efficacy of cell-based immunotherapy in patients diagnosed with triple negative breast cancer at stages II and III. This investigation focuses on determining the therapeutic impact of the intervention on disease progression within these specific clinical stages.

Participants

The sponsor did not provide information regarding the total number of participants. The study population consists of patients diagnosed with triple negative breast cancer. The cohort includes both female and male individuals, including vulnerable populations. Based on the provided age range codes, the participants fall within specific developmental or geriatric categories.

Plans and Procedures

This clinical trial evaluates cell-based immunotherapy for the treatment of triple negative breast cancer in stages II and III. The research methodology utilizes a specific study design to assess the efficacy and safety of the intervention. The sequence of study activities begins with a screening visit to determine eligibility. Subsequent follow-up visits are scheduled to monitor clinical progress, concluding with an end-of-study visit. The total duration of the trial is estimated to span from March 2026 to March 2030. Early termination from the study may occur based on predefined clinical criteria.

Treatment

Please provide the source data containing the names of the medications, dosages, forms, and administration details. Once the source data is provided, the description will be generated according to your specific technical and structural requirements.

Efficacy

The assessment of efficacy in this clinical trial for triple negative breast cancer is not specified.

Trial Status by Country

Country Status Start of Recruitment Planned Patients
Slovenia SloveniaNot Yet Recruiting30 Mar 202682

Sites & Investigators

Conditions Studied in This Trial