NeuWire Medical Appoints Ramin Mousavi as Executive Chairman Following Stroke Journal Publication.

Company advances toward FDA pivotal study for post-stroke rehabilitation.

NeuWire PressReleaseCard May6 V1 03
NeuWire PressReleaseCard May6 V1 03
NeuWire Logo Principal positivo
NeuWire Logo Principal positivo

DALLAS–(BUSINESS WIRE)–NeuWire Medical, a medical device company advancing the development of a targeted plasticity therapy platform for individuals living with chronic ischemic stroke, today announced the appointment of Ramin Mousavi as Executive Chairman of the Board. His arrival marks an important step in the company’s next phase of growth as NeuWire Medical prepares to advance its clinical, regulatory, and financing strategy.

Ramin joins NeuWire Medical following his role as President, Chief Executive Officer, and board member of CathWorks, where he led the company through a strategic partnership, global co-promotion agreement, landmark clinical trial, and eventual acquisition by Medtronic.

NeuWire is developing a closed-loop neuromodulation therapy designed to improve functional recovery in stroke survivors living with chronic motor deficits. The company’s technology pairs vagus nerve stimulation with targeted rehabilitation exercises, using an ultra-miniaturized, wireless, battery-free implant and intelligent stimulation timing to support neuroplasticity during therapy.

“I am very excited to join NeuWire Medical at this important moment,” said Ramin Mousavi, Executive Chairman of NeuWire Medical. “The progress achieved by Rob Rennaker and the team over the past years is impressive, both scientifically and clinically. NeuWire Medical is addressing one of the largest unmet needs in rehabilitation, and I look forward to supporting the company as it steps into its next chapter.”

NeuWire Medical is led by Rob Rennaker, PhD, Co-Founder and CEO, who has been deeply involved in the research and development of the company’s technology for over a decade. His work, together with collaborators across the field, has helped establish the scientific and clinical foundation for NeuWire Medical’s closed-loop VNS approach in post-stroke recovery.

The announcement follows the publication in Stroke, the journal of the American Heart Association, of clinical results from the company’s pilot study. The double-blinded, randomized, sham-controlled study evaluated a miniaturized closed-loop VNS system in individuals with chronic ischemic stroke and residual upper limb deficits.

The published data reported a favourable safety and feasibility profile, and statistically significant improvements in upper limb motor function following active closed-loop VNS therapy. The authors concluded that the system merits evaluation in a larger study.

“These results are an important validation point for our company,” said Rob Rennaker, PhD, Co-Founder and CEO of NeuWire Medical. “Our goal is to help stroke survivors achieve greater recovery by combining rehabilitation with precisely timed neuromodulation at home and in the clinic. We are now focused on securing the financing required to execute the pivotal study required to bring this therapy closer to patients.”

Dr. Rennaker added: “We are thrilled to welcome Ramin as Executive Chairman at this time. With an exceptional history of turning vision into results, Ramin is the ideal Executive Chairman to guide our next chapter of growth and value creation for NeuWire Medical.”

NeuWire Medical is preparing to raise capital to support its FDA IDE pivotal clinical study, regulatory activities, manufacturing scale-up, and preparation for future commercialization.

About NeuWire Medical

NeuWire Medical is developing a next-generation closed-loop vagus nerve stimulation platform for post-stroke rehabilitation. The system uses a miniature, wireless implant that delivers stimulation during high-quality therapeutic movements. By pairing active rehabilitation with precisely timed neuromodulation, NeuWire aims to enhance targeted neuroplasticity and improve functional recovery for stroke survivors.

NeuWire Medical’s VNS implant system is an investigational device and has not been approved or cleared by the U.S. Food and Drug Administration. The device is limited by U.S. law to investigational use. No claims of safety or effectiveness are made or implied.

Contacts

Investors:

Robert L. Rennaker

[email protected]

Media:

Media Contact

[email protected]

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