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Clinical Trials in the UK / NCT03463954
Recruiting Not applicable

Confirmatory Clinical Evaluation of Novilase® Laser Therapy for Focal Destruction of Malignant Breast Tumors

NCT03463954 · tracked via the Priya Life Science UK tracker
Sponsor
Novian Health Inc.
Phase
Not applicable
Started
2023-08-09
Last updated
2026-02-19

Condition(s) studied

Malignant Neoplasm of Breast

Investigational drug(s) / intervention(s)

Novilase Laser ablation

Novilase Laser ablation: Image-guided, percutaneous laser ablation of breast tumors

Study summary

Prior to this confirmatory pivotal study, the multicenter Br-002 feasibility study was completed. 98% of tumors less than or equal to 15mm were completely ablated in one procedure.This study will evaluate Novilase for the focal destruction of malignant tumors of the breast that are less than or equal to 15 mm against a performance goal for the standard of care, lumpectomy. The ASBrS' goal of less than 20% retreatment by 2020 was selected as a representative performance goal, i.e., 80.0%, and is consistent with published effectiveness rates for lumpectomy.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Females, aged 18 years and older * Able to give written informed consent herself * Definitive pathologic diagnosis by needle core biopsy * Unifocal malignant tumor (T1a-c, N0-1, M0) that does not exceed 15 mm in longest dimension and measures at least 5 mm away from the skin and chest wall, or can be moved at least 5 mm away from the skin and chest wall by injection of saline or local anesthetic * No more than 10 mm of calcifications confined to the tumor on imaging * Tumor is well visualized through ultrasound or x-ray mammography imaging and amenable to image-guidance therapy (i.e., a tumor which is well visualized through imaging can be identified from surrounding breast tissue and does not have margins obscured by other structures or artifacts on the images) * Tumor is well visualized on MRI * Subject with mammographic appearance of overall dense parenchymal tissue may be included, as long as a clearly evident marker is present at tumor site * Tumor with less than 25% intraductal component, as determined by core biopsy * No clinically significant co-morbidities (e.g., chronic illnesses existing simultaneously with and usually independent of breast cancer) that affect life expectancy * Subject weight limited to ≤300 lbs. or ≤136 kg * Subject agrees to comply with standard of care radiation or adjuvant therapy as prescribed by physician Exclusion Criteria: * Subject younger than 18 years of age * Pregnant or breast-feeding * Tumor poorly visualized by ultrasound or x-ray mammography imaging * Contraindications to administration of gadolinium-based contrast agent, including: prior allergic reaction to a gadolinium-based contrast agent, moderate to end-stage kidney disease, and/or acute or chronic severe renal insufficiency (Glomerular filtration rate (GFR) \<30ml/min/1.73 sq. meters) * Contraindications to MRI according to site guidelines (e.g., cardiac pacemaker, metallic implants) * History of severe asthma * Tumor measuring greater than 15 mm in longest dimension * Microcalcifications that extend beyond target tumor such that overall longest dimension of target tumor and calcifications is longer than 15 mm. * Advanced stage breast cancer * Tumors that are lobular neoplasm, metastatic carcinoma to breast, sarcoma, Phyllodes tumor, or Paget's disease * Tumor with only DCIS with microinvasion * Extensive intraductal component in lesion (i.e., \>25%) as determined by core biopsy * Subject who is known to be BRCA positive * Tumor that is ER/PR/HER2 negative (TNBC) * Inability to lie in prone or supine position for one hour * Subject who is currently participating in another investigational treatment, device or drug study through follow up that would interfere with this trial * Subject without a definitive HER2 test according to ASCO/CAP guidelines

Primary outcome measure(s)

Trial sites (13)

FacilityCityRegionStatus
City of Hope Duarte California Withdrawn
UC San Diego Health La Jolla California Recruiting
Eisenhower Health Rancho Mirage California Recruiting
Yale University New Haven Connecticut Recruiting
Walter Reed National Military Medical Center Bethesda Maryland Withdrawn
Summit Health Florham Park New Jersey Not Yet Recruiting
Buffalo General Medical Center Buffalo New York Recruiting
St. Elisabeth-Krankenhaus Köln-Hohenlind Cologne Germany Recruiting
Ichilov | Tel Aviv Sourasky Medical Center Tel Aviv Israel Recruiting
Breast Centre Zurich Zurich Switzerland Terminated
University Hospital Zurich Zurich Switzerland Recruiting
Charing Cross Hospital, Imperial College Healthcare NHS Trust London United Kingdom Recruiting
Churchill Hospital, Oxford University Hospitals NHS Trust Oxford United Kingdom Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03463954 on ClinicalTrials.gov ↗ ← All trials in the UK