Technology

Executive Summary

EyeCell is focused on development of microcurrent devices

EyeCell is focused on the development and sales of microcurrent devices for treating eye related diseases and disorders The company has developed and patented eight product lines:

  • Current of injury microcurrent devices for healing and pain management (3)
  • Current of injury microcurrent bandages.
  • Stem cell regeneration microcurrent device for regeneration, healing and improvement of blood flow.
  • Anti-angiogenic (stops over blood supply) signaling microcurrent device.
  • Stem cell growth factor cocktail compositions to be injected.
    Micropump for sustained delivery of eye repair agents over time.
  • Eye health vitamins for post procedure healing.
  • Microcurrent acupuncture point positioned eye patch.

The company has FDA 510K market clearance on three current of injury microcurrent products and one CE Mark for a wireless microcurrent stimulator working with selected vendors for OEM private label manufacturing.

The EyeCell microcurrent devices are designed to provide healing of injuries, reduce inflammation, reduce pain and risk of infection.

EyeCell collaborative researchers have treated nearly 3000 patients to date with 90% of them demonstrating improvement directly related to the microcurrent therapy.

Eye Regeneration by Bioelectric Controlled Protein Expression and Stem Cell Based Composition Micro Infusion

THE PROBLEMS

Wet Macular Degeneration

More than 20 million people worldwide suffer of wet macular degeneration related to leaky blood vessels within the eye.

Dry Macular Degeneration

Over 20 million people worldwide suffer of dry macular degeneration caused by local inflammation and oxidative stress as well as excessive accumulation of lipofuscin in the retinal pigment epitelium.

Retinal Degenerative Diseases

Over 10 million people worldwide suffer of retinal regenerative diseases

Diabetic retinopathy

is a complication of diabetes effecting more than 20 million people worldwide that causes damage to the blood vessels of the retina—the light-sensitive tissue that lines the back part of the eye, allowing you to see fine detail. There are generally 2 causes of vision loss from diabetic retinopathy: diabetic macular edema and proliferative diabetic retinopathy.

Solution

EyeCell’s treatment armamentarium is designed to (investigational use only):

Seal off leaky blood vessels.

  1. Reduce inflammation.
  2. Regenerate tissues healing.
  3. Stop over blood supply.
  4. Increase oxygenated blood supply when needed.
  5. Reduce infection risk.
  6. Reduce Pain.

Edward C. Kondrot, MD, our Executive Vice President of Clinical Studies and Co-Founder summarized three studies on the use of microcurrent for AMD:

1. A two-year study (1983 to 1985) involving 114 patients, conducted by Grace Halloran, PhD. The results of the study were as follows:

  • Eighteen patients had macular degeneration; 16 improved.
  • Seventy-eight patients had retinitis pigmentosa; 62 showed improvement.
  • Eighteen patients had other various retinopathies; 16 improved.
  • Of the patients who did not demonstrate any improvement, 14 stayed the same (although they otherwise would have been expected to lose vision); two continued to lose vision, although only slightly.

1. A 10-year clinical study was conducted by Drs. Jarding and Michael on the use of microcurrent to treat macular degeneration. Of the 400 eyes evaluated over the course of the study, the results were as follows:

  • Seventy-eight percent of the eyes showed from 1-9 lines of improvement in reading of a visual acuity chart.
  • Over 50 percent improved from 2-9 lines of improvement.
  • In the study, two patients suffered from retinal vein occlusion and swelling of the macula. Both had dramatic improvement in vision.

1. Damon Miller, MD, reviewed the results of using microcurrent stimulation in the treatment of Stargardt’s disease, retinitis pigmentosa and other degenerative retinal diseases. His results indicated the following:

  • Of the 120 patients treated, 83 percent showed improvement of greater than or equal to two lines of visual acuity in one or both eyes.

Mechanisms of Action:

Primary = Delivers stem cells growth factors directly to wound site and stimulates the over expression of the stem cell homing signal protein SDF-1 which is also a powerful arteriogenic agen.
2. Multiples recruited and delivered stem cells to greater quantities at wound site.
3. Increases blood flow at wound site 3X (from delivering and recruiting endothelial progenitor cells and increased expression of VEGF).
4. Decreases pain at wound sites.

Strategy

1. Add to current estate of patents.
2. Gain opinion leader support from leading institutions.
3. Get FDA AOK for specific indication of uses and reimbursement.
4. Grow to over $100 million in annual sales.
5. Auction company off to highest bidder on May 11th, 2018.

Management Team – A mix of proven medtech industry veterans and eye scientists and clinicians. Microcurrent therapy leaders.

6 focused executives on management team. Over 70 business mentors and board members

Business Model

Sell direct in the USA to physicians and hospitals. Sell through distributors overseas. Get opinion leaders to present data at major meetings. Attend over 20 cardiovascular meetings a year with showcase. Publish data.

Market for dry age-related macular degeneration

  • The current number of patients in the US and Europe is estimated to amount to 20 million.
  • Aging populations in the western world will lead to a significant increase in numbers. In 2020,about 30 million people are predicted to suffer from dry AMD.
  • The number of patients with wet AMD is comparable with the number of patients suffering from advanced dry AMD.

Competition

Dry Macular Degeneration

Although there are still very few development projects for the treatment of dry AMD, there is a handful of projects in advanced clinical stages of development.

  • Alimera Sciences glucocorticoid “Fluocinolone Acetonide” (Ph II)
  • Anti-Amyloid beta antibodies from Alzheimers research of GlaxoSmithKline and Pfizer (PhII and PhI)
  • Alexion pharmaceuticals C5 inhibiting antibody (Ph II)
  • Acucela’s visual cycle modulator ACU 4429 (Ph II)
  • Neurotech’s implant with genetically modified human cells (Ph II)
  • Stem Cell approaches by ACT (embryonic) and Stem Cells Inc. (central nervous system stem cells) (Ph I / II)
  • MacuClear’s and Succampos drugs for the improvement of coroidal blood flow (Ph II / III)

Wet Macular Degeneration

• Lucintis from Genentech Novartis

Note – Investment in this startup is only possible through the Cal-X Stars Business Accelerator, Inc. 506c Offering at this time. Please read completely the Private Placement Memorandum (PPM) via the link below and see all the warnings posted below and within the PPM. This offering is limited to accredited investors with > $1 million in assets or income > $200K a year or $300K as a couple past two years in a row.

ALL Cal-X Stars Business Accelerator, Inc. investors must verify their accredited status via Crowdentials, EarlyIQ or Healthiosxchange.

CIRCULATION on microcurrent improvement of blood flow – Click Here

• The securities may be sold only to accredited investors, which for natural persons, are investors who meet certain minimum annual income or net worth thresholds; > $200K individual income or $300K joint. > $1 million in assets excluding primary residence.
• The securities are being offered in reliance on an exemption from the registration requirements of the Securities Act and are not required to comply with specific disclosure requirements that apply to registration under the Securities Act;
• The Commission has not passed upon the merits of or given its approval to the securities, the terms of the offering, or the accuracy or completeness of any offering materials;
• The securities are subject to legal restrictions on transfer and resale and investors should not assume they will be able to resell their securities; and
• Investing in securities involves substantial high risk, and investors should be able to bear the loss of their investment

RISK WARNING: The Cal-X Stars Business Accelerator, Inc. portfolio of innovations and startup companies are all early stage. The investment risk is very high and investors should be in position to lose all their investment without hurting their financial security. This 506c offering is limited to accredited investors only with > $1 million in assets excluding their primary residence. The offering will be posted on authorized accredited investor only portal sites that verify accreditation qualification such as www.crowdfunder.com, www.healthiosxchange.com, www.equitynet.com and www.angelist.co These portals and other outside service providers assist in verifying with reasonable assurance the accredited status of any potential investor. Merriman Capital http://www.merrimanco.com/ has been hired as an advisory registered broker dealer for this offering. Any potential investor should review all risks published within our private placement memorandum that is available upon written request to email hleonhardt@aol.com or via the above mentioned password protected portals.
Note – New 506c regulations allow general advertising and up to 2000 shareholders while remaining private – http://www.sec.gov/rules/final/2013/33-9415.pdf

IMPORTANT LEGENDS (ANY POTENTIAL INVESTOR PLEASE READ)
Securities offered under Rule 506(c) may be purchased only by accredited investors = persons with > $1 million in assets excluding their home and vehicles or whom have income > $200,000 the past two years consecutively or > $300,000 income as a couple. Accreditation status must be verified via documentation of credible third parties in a position to provide accurate verification. Investors in this offering should have experience in making early stage investments.

Cal-X Stars Business Accelerator, Inc. develops early stage innovations and startups. By nature the risk is very high for these type of investments. Any investor should be fully prepared without reserve to lose all their investment. Our high focus on developing implantable devices and biologics for treating heart failure add exceptionally higher levels of risk as the products require multiple stages of clinical trials costing many millions of dollars and require high intellectual property protection to succeed commercially. The patent landscape in these areas of participation are wrought with potential for litigation. A high number of clinical trials in the heart failure space fail to prove greater safety and efficacy compared to currently available choices. A high number of early seed stage innovations fail to ever make it to market and even a smaller number become commercial successes. This type of investment is NOT appropriate for nest egg savings.

• The securities are being offered in reliance on an exemption from the registration requirements of the 150Securities Act and are not required to comply with specific disclosure requirements under the Securities Act; the Commission has not passed upon the merits of or given its approval to the securities, the terms of the offering, or the accuracy or completeness of any offering materials; the securities are subject to legal restrictions on transfer and resale and investors should not assume they will be able to resell their securities; and investing in securities involves risk and purchasers should be able to bear the loss of the entire investment. Private funds would be required to include a legend informing investors that the funds are not subject to the protections of the Investment Company Act.