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Second Sight Announces First Age-Related Macular Degeneration Patient Receives the Argus II Retinal Prosthesis System as Part of Groundbreaking Study Five Patients to be Implanted with the Argus II to Evaluate the Feasib

Key Takeaway: Sight Announces First Age-Related Macular Degeneration Patient Receives the Argus II Retinal Prosthesis System as Part of Groundbreaking Five Patients to be Implanted with the Argus II to Evaluate the Feasibility of the Device in Patients with Dry Age-Related Macular Degenerati

Full Press Release Details

Sight Announces First Age-Related Macular Degeneration Patient Receives the Argus II Retinal Prosthesis System as Part of Groundbreaking
Five Patients to be Implanted with the
Argus II to Evaluate the Feasibility of the Device in Patients with Dry Age-Related Macular Degeneration
SYLMAR, Calif.--(BUSINESS WIRE)-- Second Sight Medical Products,
Inc. (Nasdaq:EYES) ("Second Sight" or "the Company"), a developer, manufacturer and marketer of implantable
visual prosthetics that restore some useful vision to blind patients, today announced the first implant and successful activation
of the Argus II Retinal Prosthesis System (Argus II) in a dry age-related macular degeneration (AMD) patient.
The implant is part of a feasibility study which aims to evaluate
the safety and utility of the Argus II System in individuals with late-stage Dry AMD, a condition that severely affects their central
vision. The implant was performed at the Manchester Royal Eye Hospital in the United Kingdom by Dr. Paulo Stanga MD, Consultant
Ophthalmologist & Vitreoretinal Surgeon at the Manchester Royal Eye Hospital, Professor of Ophthalmology and
Retinal Degeneration at The University of Manchester. The device was activated approximately two weeks after implantation, and
initial reports confirm that the subject is receiving some useful vision from the Argus II system. The Argus II has already been
tested and approved in the United States and Europe for individuals with Retinitis Pigmentosa (RP) and Outer Retinal Degeneration,
"The difference between RP and Dry AMD is that RP
primarily affects the peripheral vision whereas AMD primarily affects the central vision. Retinal implants for individuals with
AMD may restore some useful vision in their central visual field, which is non-functional due to degeneration of the photoreceptors.
The goal in restoring this central vision is to provide individuals with AMD more natural vision and ultimately improve their
independence and quality of life," says Dr. Paulo Stanga, MD. "This is totally groundbreaking research, where positive
results from the study could provide advanced Dry AMD patients with a new alternative treatment."
Eligibility for this study includes patients 25 to 85 years
of age with advanced dry AMD, some residual light perception, and a previous history of useful form vision. Study subjects will
be followed for three years to evaluate safety and utility of the Argus II system on visual function. Pending positive study results,
the Company plans to conduct a larger study to support market approvals. It is estimated that two million individuals worldwide
are legally blind due to AMD and 375,000 people are blinded by RP.
Second Sight Chief Executive Officer, Dr. Robert Greenberg,
said, "We are very excited to begin such an important study for this patient population and to have the opportunity to help
a great deal more people living with blindness. Though it is obviously still early in this clinical trial, we are very encouraged
by these initial results."
Recently, a story about the first AMD patient to receive the
Argus II appeared on a BBC News broadcast throughout the United Kingdom generating much interest in the technology. A link to
the story can be found on http://www.bbc.com/news/health-33612558.
The launch of this study is another step toward Second Sight's
mission to enable blind people to achieve greater independence. Earlier this year, the first Orion I Visual Cortical Prostheses
were implanted in animals to evaluate fit, form, stability, and biocompatibility. Human trials for the Orion I are planned to commence
by Q1 2017. If successful, the Orion I has the potential to address nearly all forms of blindness.
About Dry Age-Related Macular Degeneration
Dry AMD is more common than the wet' type, affecting
85% of AMD patients. Dry AMD usually develops slowly and causes gradual loss of central vision. While Dry AMD also affects the
peripheral vision over time, it rarely results in loss of vision across the entire visual field. There are currently very limited
approved treatment options for Dry AMD.
About the Argus II Retinal Prosthesis System
Second Sight's Argus II System provides electrical stimulation
that bypasses the defunct retinal cells and stimulates remaining viable cells inducing visual perception in individuals with severe
to profound Retinitis Pigmentosa (RP). The Argus II works by converting images captured by a miniature video camera mounted on
the patient's glasses into a series of small electrical pulses, which are transmitted wirelessly to an array of electrodes implanted
on the surface of the retina. These pulses are intended to stimulate the retina's remaining cells, resulting in the perception
of patterns of light in the brain. The patient then learns to interpret these visual patterns, thereby regaining some visual function.
The system is controlled by software and is upgradeable, which may provide improved performance as new algorithms are developed
and tested. The Argus II is the first artificial retina to receive widespread approval, and is offered at approved centers in Austria,
Canada, France, Germany, Italy, Netherlands, Saudi Arabia, Spain, Switzerland, Turkey, United Kingdom and the United States.
Second Sight's mission is to develop, manufacture and market
innovative implantable visual prosthetics to enable blind individuals to achieve greater independence. Second Sight has developed,
and manufactures, the Argus II Retinal Prosthesis intended to provide some useful vision to individuals with outer-retinal
degenerations such as Retinitis Pigmentosa (RP). Second Sight is also developing the Orion I Visual Cortical Prosthesis
to restore some vision to individuals who are blind due to causes other than preventable or treatable conditions. U.S. Headquarters
are in Sylmar, CA, and European Headquarters are in Lausanne, Switzerland. For more information, visit www.secondsight.com.
This press release contains forward-looking statements within
the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange and Exchange Act
of 1934, as amended, which are intended to be covered by the "safe harbor" created by those sections. All statements
in this release that are not based on historical fact are "forward looking statements." These statements may be identified
by words such as "estimates," "anticipates," "projects," "plans," or "planned,"
"seeks," "may," "will," "expects," "intends," "believes," "should,"
"could" and similar expressions or the negative versions thereof and which also may be identified by their context. All
statements that address operating performance or events or developments that Second Sight expects or anticipates will occur in
the future are forward-looking statements. While management has based any forward looking statements included in this release on
its current expectations, we operate in a complex and changing domestic and international regulatory environment where new and
unanticipated risks may arise, and consequently the information on which such expectations were based may change. Forward-looking
statements involve inherent risks and uncertainties which could cause actual results to differ materially from those in the forward-looking
statements as a result of various factors, including those risks and uncertainties described in the Risk Factors and in Management's
Discussion and Analysis of Financial Condition and Results of Operations sections of our Annual Report on Form 10-K as filed on
March 17, 2015 and our other reports filed from time to time with the Securities and Exchange Commission. We urge you to consider
those risks and uncertainties in evaluating our forward-looking statements. We caution readers not to place undue reliance upon
any such forward-looking statements, which speak only as of the date made. Except as otherwise required by the federal securities
laws, we disclaim any obligation or undertaking to publicly release any updates or revisions to any forward-looking statement contained
herein (or elsewhere) to reflect any change in our expectations with regard thereto or any change in events, conditions or circumstances
on which any such statement is based.
Last updated: Jul 24, 2015