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Intellectia

ANGO News

AngioDynamics Receives FDA Approval for NanoKnife Study

Jun 18 2026NASDAQ.COM

AngioDynamics Receives FDA Approval for IRE Study

Jun 17 2026Newsfilter

Palmetto GBA Medicare Coverage Update for NanoKnife IRE

May 28 2026Newsfilter

AngioDynamics Reports Strong Revenue Growth in Med Tech Segment

Apr 02 2026Yahoo Finance

AngioDynamics Reports Strong Q3 FY2026 Earnings Growth

Apr 02 2026seekingalpha

AngioDynamics Reports Wider Loss in Q3 Earnings

Apr 02 2026NASDAQ.COM

AngioDynamics Reports Sixth Consecutive Quarter of Double-Digit Growth

Apr 02 2026Newsfilter

AngioDynamics Q3 Earnings Exceed Expectations

Apr 02 2026seekingalpha

ANGO Events

06/17 09:30
AngioDynamics Receives FDA Approval to Initiate RELIEF Study
AngioDynamics announced that the U.S. Food and Drug Administration, FDA, has approved the Company's Investigational Device Exemption, IDE, application to initiate the RELIEF study. RELIEF is a feasibility study evaluating irreversible electroporation, IRE, the non-thermal ablation technology delivered by the Company's NanoKnife System, for the treatment of lower urinary tract symptoms in men with benign prostatic hyperplasia.
05/13 09:10
AngioDynamics Announces Two-Year Results for NanoKnife System
AngioDynamics announced two-year results from the PRESERVE pivotal trial demonstrating durable oncologic control and a sustained safety profile for the NanoKnife System in the focal ablation of intermediate-risk prostate cancer. The data will be discussed by Izak Faiena, M.D., of Columbia University at the 2026 American Urological Association Annual Meeting on Sunday, May 17 in Washington, D.C. The PRESERVE trial is a prospective, single-arm pivotal IDE study evaluating focal irreversible electroporation using the NanoKnife System in 121 patients with Gleason Grade Group 2-3 intermediate-risk prostate cancer, conducted across 17 U.S. clinical centers in collaboration with the Society of Urologic Oncology Clinical Trials Consortium. Primary 12-month results, published in European Urology in July 2025, demonstrated an 80% freedom-from-treatment-failure rate among protocol-biopsied patients. At 24 months, the updated findings confirm durability of outcomes: 94.4% of analysis-eligible patients (68 of 72) completed the 24-month assessment, reflecting strong cohort retention; No new treatment failures were identified among patients with available follow-up at 24 months; One patient (1.5%) underwent a clinically indicated biopsy, which was negative for any cancer; 97% of patients (66 of 68) had a PSA at 24 months below their baseline value; No new device- or procedure-related adverse events were reported between the 12- and 24-month assessments. The 24-month PRESERVE data complement an international long-term evidence base for focal IRE, including median five-year outcomes from a 2023 international multi-institutional cohort demonstrating sustained oncologic control and preservation of functional outcomes.

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ANGO Earnings Analysis

Strong Growth in Med Tech Drives AngioDynamics' Q2 2025 Earnings - Intellectia AI™
1 years ago
AngioDynamics Inc Reports First Quarter Fiscal Year 2025 Financial Results
1 years ago

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