Breast Neoplasm Malignant Female

4

Review clinical trials related to Breast Neoplasm Malignant Female. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Step Count and Treatment Response in Neoadjuvant Breast Cancer

This prospective multicenter observational study (NEOBRE-STEP) investigates the impact of daily step counts, measured by Huawei Fit 2 smartwatches, on treatment response in patients with non-metastatic Human Epidermal Growth Factor Receptor 2 (HER2)-negative breast cancer undergoing neoadjuvant systemic therapy. Patients will wear smartwatches to continuously record step counts, activity intensity, sleep, and heart rate. Patient-reported outcomes, including sleep quality (Pittsburgh Sleep Quality Index, PSQI) and quality of life (European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30, EORTC QLQ-C30), will be assessed at baseline and after treatment. The primary outcomes are pathological complete response (pCR) and Miller-Payne score. Secondary outcomes include sleep quality, quality of life, perioperative outcomes, and feasibility of smartwatch monitoring.

Participants needed: 82
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Ankara Etlik City HospitalUpdated: Feb 20, 2026Locations: 2
Eligibility criteria

Female patients aged ≥18 years. [+4]

Metastatic breast cancer at diagnosis. [+6]

Status: Recruiting

Omission of Local Therapies in Women Patients With HER2-positive or Triple-negative Breast Cancer

HER2-positive and Triple-negative are subtypes of breast cancer more sensitive to systemic therapies, where the complete pathological response rate may be higher than 50%. This gave rise to doubts about the usefulness of traditional local treatments for such responders. Omission of surgery after vacuum assisted breast biopsy (VABB) as well omission of radiotherapy after conservative surgery would now seem to be reasonable alternatives to standard care for highly selected patients, in whom systemic treatments have provided the maximum response.

Participants needed: 152
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Fondazione IRCCS Istituto Nazionale dei Tumori, MilanoUpdated: Sep 15, 2025Locations: 1
Eligibility criteria

Women ≥ 18y. [+5]

One of the inclusion criteria missed. [+5]

Status: Available

Expanded Access Protocol for Subjects Previously Treated With Gedatolisib in B2151009

Continued access to treatment for subjects who continue benefit from therapy with gedatolisib in combination with palbociclib, and fulvestrant or letrozole.

Trial details
Age: 18+Biological sex: FemaleType: Expanded AccessSponsor: Celcuity IncUpdated: Mar 21, 2025Locations: 5
Eligibility criteria

Currently enrolled in the B2151009 clinical study and benefiting from treatment... [+3]

Permanently discontinued from treatment in Study B2151009, or discontinued from... [+1]

Status: Recruiting

Safety and Performance of REGENERA Breast Implant in Women Affected by Malignant Breast Lesion Treated by Lumpectomy

The goals of this clinical trial are: * demonstrate the safety of REGENERA breast implant in patients undergoing lumpectomy of malignant breast lesions * demonstrate the safety and performance of REGENERA in terms of investigator's satisfaction, potential interference with current standard-of-care imaging techniques and occurrence of device-related serious adverse events.

Participants needed: 92
Trial details
Age: 40-70Biological sex: FemaleType: InterventionalSponsor: Tensive SRLUpdated: Nov 22, 2024Locations: 3
Eligibility criteria

Female adult subject aged 40-70 years. [+11]

Subject with actual concomitant benign breast lesion (B2 and B3), unless present... [+19]