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Clinical Trials/JPRN-UMIN000050067
JPRN-UMIN000050067
Recruiting
Phase 2

A Phase II study of the efficacy and safety of Perflubutane for predicting highly Tumor Infiltrating Lymphocytes in early breast cancer (AppTIL study) - A Phase II study of the Perflubutane for predicting TILs in EBC (AppTIL study)

Hiroshima University Hospital0 sites100 target enrollmentJanuary 18, 2023

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Hiroshima University Hospital
Enrollment
100
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 18, 2023
End Date
January 1, 2024
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. Patients undergoing preoperative treatment for breast cancer 2\. Patients with a history of breast cancer on the affected side 3\. Patients with a history of hypersensitivity to perflubutane 4\. Patients with allergy to eggs or egg products 5\. Patients with arteriovenous shunts in the heart or lungs 6\. Patients with serious cardiac or pulmonary disease 7\. Patients deemed inappropriate by the principal investigator or subinvestigator

Outcomes

Primary Outcomes

Not specified

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