Kidney Cancer Clinical Trial

The HistoSonics Edison™ System for Treatment of Primary Solid Renal Tumors Using Histotripsy (#HOPE4KIDNEY)

Summary

The purpose of this trial is to evaluate the effectiveness and safety of the HistoSonics Edison System for the destruction of kidney tissue by treating primary solid renal tumors.

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Full Description

This trial is a prospective, multi-center, single-arm pivotal trial designed to evaluate the effectiveness and safety of the HistoSonics Edison System for the destruction of kidney tissue by treating primary solid renal tumors. Data through 90 days for all enrolled subjects will be summarized in a primary analysis to be submitted for Regulatory Submission to the FDA. Additionally, subjects will be followed for five (5) years post-index procedure, with evaluations at the 14-day, 30-day, 90-day, 180-day and annual time points.

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Eligibility Criteria

Inclusion Criteria:

Subject is ≥22 years of age.
Subject has signed the Institutional Review Board (IRB) approved trial Informed Consent Form (ICF) prior to any trial related tests/procedures and is willing to comply with trial procedures and required follow-up assessments.
Subject is diagnosed with only one (1) non-metastatic solid renal mass ≤3cm confirmed via CT or MRI ≤30 days prior to the index procedure date.
Subject has had a biopsy to determine the type of tumor, ≥14 days prior to the index procedure.
Subject can tolerate general anesthesia.
Subject has an Eastern Cooperative Oncology Group Performance Status (ECOG PS) grade 0-2 at baseline screening.

Subject meets all the following functional criteria at ≤14 days prior to the planned index procedure date:

White Blood Count (WBC) ≥3,000/mm3 (≥3 10*9/L)
Absolute Neutrophil Count (ANC) ≥1,200/mm3 (≥1.2 10*9/L)
Hemoglobin (Hgb) ≥9 g/dL
Platelet count ≥100,000/mm3 (≥100 10*9/L)
White Blood Count (WBC) ≤5 hpf via urinalysis
Albumin ≤300 mg/g via urinalysis
Subject has an eGFR (Glomerular filtration rate) ≥45mL/min, ≤14 days prior to the planned index procedure date.
The tumor selected for histotripsy treatment must be ≤3cm in longest diameter.
Subject has an adequate acoustic window to visualize targeted tumor using the HistoSonics Edison System.

Exclusion Criteria:

Subject is pregnant or planning to become pregnant or nursing (lactating) during the trial period.
Subject is being actively treated in another pharmaceutical or device trial ≤30 days prior to planned index procedure date that may interfere with the primary endpoint(s).
Subjects who have active cancers (not in remission for the last two years) other than non-melanomatous skin cancers.
In the Investigator's opinion, the subject has co-morbid disease(s) or condition(s) that would cause undue risk and preclude safe use of the HistoSonics Edison System.
Subject is on dialysis, being considered for dialysis or has acute renal failure.
Subject has not recovered to Common Terminology Criteria for Adverse Events (CTCAE) grade 2 or better from any adverse effects (except alopecia and neuropathy) related to previous therapy.
Subject has an International normalized ratio (INR) >1.5 or uncorrectable coagulopathy, (e.g., known von Willebrand disease, hemophilia, or on anticoagulants), on the planned index procedure date.
Subject is taking Aspirin (ASA) or NSAIDS ≤14 days prior to the planned index procedure date.
Subject has a life expectancy less than one (< 1) year.
In the investigator's opinion, histotripsy is not a treatment option for the subject.
Subject has a concurrent condition that could jeopardize the safety of the subject or compliance with the protocol.
Subject's targeted tumor has had prior locoregional therapy (e.g., ablation, embolization, radiation).
Subject's targeted tumor is not treatable by the HistoSonics Edison System's working ranges (refer to User Guide).
In the investigator's opinion, the anticipated risks of intervention outweigh the potential benefits of the intervention.
Subject has bilateral kidney tumors or has a single functioning kidney.

Subject has a genetic predisposition to kidney cancer such as:

Von Hippel Lindau (VHL)
Hereditary Papillary Renal Carcinoma (HPRC)
Birt-Hogg-Dubé Syndrome (BHD)
Tuberous Sclerosis Complex (TSC)
Hereditary Leiomyomata's Renal Cell Carcinoma (HLRCC)
Reed's Syndrome
Succinate Dehydrogenase B Deficiency (SDHB)
BRCA 1 associated protein -1 (BAP1) Renal Cell Carcinoma
MITF predisposed Renal Cell Carcinoma
The targeted tumor is an angiomyolipoma.
Subject has a known sensitivity to contrast media and cannot be adequately pre-medicated.
The targeted tumor is not clearly visible with ultrasound, MRI or CT.
Targeted tumor with adequate margin overlaps the renal pelvis, main renal vessel, ureter, or other vital structure.
The treatment of the tumor will not allow an adequate margin (as determined by the investigator).

Study is for people with:

Kidney Cancer

Estimated Enrollment:

68

Study ID:

NCT05820087

Recruitment Status:

Recruiting

Sponsor:

HistoSonics, Inc.

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There are 5 Locations for this study

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University of Southern California
Los Angeles California, 90089, United States More Info
Ileana Aldana
Contact
[email protected]
Monish Aron, MD
Principal Investigator
Michael Katz, MD
Sub-Investigator
Yale School of Medicine
New Haven Connecticut, 06510, United States More Info
Kristin DeFrancesco
Contact
[email protected]
David Madoff, MD
Principal Investigator
Sandeep Arora, MD
Sub-Investigator
AdventHealth Celebration
Celebration Florida, 34747, United States More Info
Tracy Rivera, RN
Contact
[email protected]
Michael McDonald, MD
Principal Investigator
Northwell Health
Lake Success New York, 11042, United States More Info
Sharon Choi
Contact
[email protected]
Arun Rai, MD
Principal Investigator
Manish Vira, MD
Sub-Investigator
Michael Schwartz, MD
Sub-Investigator
NYU Langone Health
New York New York, 10016, United States More Info
Dayna Leis
Contact
[email protected]
William Huang, MD
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Kidney Cancer

Estimated Enrollment:

68

Study ID:

NCT05820087

Recruitment Status:

Recruiting

Sponsor:


HistoSonics, Inc.

How clear is this clinincal trial information?

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