NeuroOne® Reports Second Quarter Fiscal Year 2024 Financial Results and Provides Corporate Update

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NeuroOne Medical Technologies Corp
NeuroOne Medical Technologies Corp

EDEN PRAIRIE, Minn., May 14, 2024 (GLOBE NEWSWIRE) -- NeuroOne Medical Technologies Corporation (NASDAQ: NMTC) (“NeuroOne” or the “Company”), a medical technology company focused on improving surgical care options and outcomes for patients suffering from neurological disorders, today announces its operating results for the second quarter fiscal year 2024 ended March 31, 2024.

Second Quarter Fiscal Year 2024 and Recent Business Updates

Financial Highlights:

  • Product revenue of $1,377,000 in Q2 2024, compared to $466,000 in Q2 2023

  • Raised an additional $2.0 million using the ATM Program in Q2 2024

Evo® sEEG:

  • Zimmer Biomet continued to expand into new accounts

  • Product exhibited by Zimmer Biomet at the American Association of Neurological Surgeons (AANS) in May

OneRF Ablation System:

  • Completed site training and initiated limited commercial launch of the OneRF Ablation System in late March

  • Successfully implanted five patients

  • Completed initial manufacturing run for limited commercial launch

  • Presented ICD-10-PCS hospital inpatient code application to the Centers for Medicare and Medicaid Services (CMS) in March for the OneRF ablation procedure to support accurate data collection and processing of reimbursement claims by hospitals for the ablation procedure

  • Exhibited the OneRF Ablation System at the AANS meeting in May

Drug Delivery Program:

  • Completed feasibility bench top testing and animal study demonstrating the ability to deliver a therapeutic agent and provide recording capabilities using the sEEG drug delivery system

  • Continued discussions with potential strategic partners for use in clinical studies and research

Spinal Cord Stimulation Program:

  • Completed animal study to evaluate stimulation and battery performance using the Company’s spinal cord stimulation electrode technology

  • Led by our Spinal Cord Stimulation Advisory Board, completed cadaver study to further advance the development of the percutaneous implantation technique for NeuroOne’s thin-film paddle electrodes for spinal cord stimulation

  • Presented posters on pre-clinical experience with thin-film paddle leads at North American Neuromodulation Society (NANS) and Gordon Research Conference on Neuroelectronic Interfaces

Dave Rosa, CEO of NeuroOne, commented, “We made excellent progress this quarter across multiple fronts. Revenue growth continued regarding our sEEG product line as new customer sites were added by Zimmer Biomet. We also initiated the limited commercial launch of the OneRF™ Ablation System, an exciting accomplishment given we are the first company to receive FDA 510(k) clearance to market this novel technology in the United States. Customer interest has been strong and we believe the OneRF™ Ablation System, with combination diagnostic and therapeutic functionality, has the capability to create a paradigm shift in neurosurgical procedures. Moving forward, we will investigate other applications to leverage our ablation system. We continue to believe strongly in the market opportunity for our drug delivery system as we believe it has the potential to create a unique platform for both identifying the target area in the brain, delivering the pharmacologic agent and monitoring its performance.”