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GET A PIECE OF RECOMBINANT TECHNOLOGIES

Revolutionary Alzheimer's Treatment

Recombinant Technologies is developing a revolutionary treatment for Alzheimer's Disease. By designing an injection of a molecule treatment to reduce the plaque buildup that causes dementia, we have successfully improved memory in mice and are ready to move toward human trials.

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This Reg CF offering is made available through StartEngine Capital, LLC. This investment is speculative, illiquid, and involves a high degree of risk, including the possible loss of your entire investment.
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REASONS TO INVEST

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There are an estimated 5,500,000 people in the U.S. who have Alzheimer’s disease, and we have developed an innovative treatment that addresses the cause of the disease rather than the symptoms. By this treatment strategy, we are addressing a significant unmet medical need and opportunity.

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Our patented technology was developed over a decade with the support of $4.5 million in grants and has successfully improved memory in mice in our proof of concept trials.

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Our team is comprised of top experts in their fields, including our founder who trained at Yale School of Medicine for about a decade prior to founding this company.

TEAM

Pazhani Sundaram PhD

Pazhani Sundaram PhD • President, Chief Executive Officer, Interim-CFO, and Chairman of the Board

Dr. Pazhani Sundaram has a Ph.D. in Biochemistry and Molecular Biology. He is the founder of Recombinant Technologies, a pre-clinical stage biotechnology company [www.recombtech.com]. Dr. Sundaram has strong experience in protein expression technologies, molecular biology, biochemistry, peptidomimetics, and in drug delivery systems. Prior to starting Recombinant Technologies in 1998, he was trained at Yale School of Medicine for about a decade. At Yale, Dr. Sundaram contributed to the research and development of a vaccine to treat the human papillomavirus in a rabbit model. This work formed the basis for Merck in developing the vaccine for HPV 16, which was marketed as 'Gardasil'. Dr. Sundaram's research is acknowledged on Merck's patent for the above vaccine.

Dr. Sundaram's focus for the past 19 years has been to develop a viable drug to treat Alzheimer's Disease. He has been awarded multiple SBIR grants and matching grants to perform this task. He is also an inventor of the patented drug called 'Amytrap' to treat Alzheimer's Disease. Current research focuses on the safety/toxicology assessment of this drug with the support of a recent phase 2 SBIR grant award. Efforts are underway to join forces with investors from multiple platforms to expedite the preclinical development activities. Immediate efforts are focused on developing a device called 'Amytrapper' to trap amyloid from circulation utilizing the proprietary API molecule. This research is also supported by a peer-reviewed grant from NIA. 

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Amrit Dhawan

Amrit Dhawan • Secretary

Amrit is responsible for corporate transactions/projects for the efficient administration of the company, particularly with regards to meetings and financial transactions. She has provided support and advice on a managerial and professional level to Yale University for about 19 years. 

Amrit's primary occupation is working for Yale University. She serves as a part-time Secretary for Recombinant Technologies, working 5 hours per week.

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Treating the Root Cause of Alzheimer’s Disease


We have developed a patented molecule (AmyTrap) with demonstrated success in animal-model proof of concept studies to remove amyloid-beta, which is the physiological cause behind the plaque buildup in the brain associated with Alzheimer's Disease. 



Incorporating that same molecule, we designed and developed two types of extracorporeal devices, called AmyTrappers, for treatments. These proposed innovative devices trap amyloid from circulation (just like dialysis to remove urea in patients with kidney failure) which may lead to achieving a novel treatment strategy that improves the lives of patients with AD.


We are excited about the promising results AmyTrapper has shown up to this point, and are now ready to bring our technology to the next level through new research that will result in the initiation of human trials.

The problem


Current Alzheimer’s Disease Treatments Fall Short


Alzheimer’s Disease (AD) is a common disease leading to dementia affecting millions of people worldwide.  


One of the many targets in treatment for AD is amyloid-beta plaque buildup. However, currently there are no treatments that address amyloid-beta as the underlying pathophysiology behind Alzheimer’s. Instead, most current drugs work to alleviate symptoms or marginally slow disease progression. Recently,  Biogen’s Aduhelm(Adecanumab) was accepted by the FDA  as the first treatment that targets reduction of amyloid- beta plaque in the brain. This underscores the significance of amyloid- beta plaque removal strategies as a key against Alzheimer’s . 


The solution


AmyTrap Treats the Cause, Not Just the Symptoms


Our prototype, AmyTrap, is designed to reduce disease-causing amyloid-beta plaque burden, improving memory by addressing the physiological cause behind Alzheimer’s Disease.


*Image is a computer-generated demo version. Product is still currently under development.


Use of the technology will slow disease progression in individuals at high risk of developing Alzheimer’s disease, increasing the duration of their independence and lessening third-party payor outlay for symptomatic treatments and caregiving.

The market


Meeting a Growing Need in Alzheimer’s Treatment


We estimate the total market size to be approximately $570,000,000 at the growth rate of 17.5% in 2018. 5,500,000 people in the U.S. have Alzheimer’s disease, and 5% of these patients have early-onset Alzheimer’s disease due to genetic or other factors.


Source

The niche therefore consists of 285,000 patients, and at $2000 per year in treatment, that amounts to a $570,000,000 total potential market. We believe that Amytrapper will be one of the few devices in the immediate future to address this unmet medical need by treating this subset population. 

our traction


Promising Early Results and Patented Technology


We have established proof of concept through our animal model, where we saw improved memory and behavior in model mice after treatment. In addition, toxicity and safety assessments in rats and dogs have been completed. Amytrap, the underlying molecule, was found to be safe and non toxic. Further, Amytrapper animal testing is in progress. 



We have achieved Intellectual Property protection in the form of a patent issued by USPTO which has been issued to Recombinant Technologies LLC. We have also won multiple small business innovation grants from the National institutes of Health through a rigorous peer-review process.

what we do


Clearing Plaque Buildup to Improve Memory

AmyTrap is a patented molecule composed of polymer-bound short peptides with the capacity to capture beta-amyloid (Aβ) peptide. Amytrap binds and sequesters Aβ from the circulation, leading to the depletion of amyloid plaques from the brain in model mice. 



Our preliminary studies in animal models suggest that AmyTrap does not enter the brain. Undetectable levels of AmyTrap and reduction of the Aβ burden in the brain suggest that the AmyTrap possibly exerts its therapeutic activity by acting as a peripheral sink for circulatory Aβ. Based on these observations it has been hypothesized that Aβ exists in equilibrium between the brain and in circulation. Sequestration of the circulatory Aβ in the periphery creates an imbalance in this equilibrium driving efflux of Aβ from the brain into the circulation.


The business model


Working with Established Partners to Reach High-Risk Patients


Currently, we are pre-commercialization and looking to perform additional research to perfect our product. 


When we are ready for commercialization, our strategy will initially be aimed at therapy towards individuals at highest risk, in particular those with familial or genetic predisposition for onset of Alzheimer’s disease. We plan to partner with established organizations with a substantial footprint in the marketplace to implement our treatment. 


*Likely to increase overtime


We estimate the cost per treatment to be approximately $500. Four treatments per patient per year are proposed, which would generate revenue of $2000 per patient per year. We are the only player in this market as of now.



How we are different


Our Technology Stops Alzheimer’s at the Source


According to our research, AmyTrapper devices are among the first of their kind in their focus on the depletion of beta amyloid from the brain prior to memory deterioration. Rather than functioning as an anti-beta amyloid antibody, our treatment specifically binds to the critical region of beta amyloid necessary for aggregation.





We expect this breakthrough to significantly improve the living condition of people with Alzheimer’s Disease, especially with its focus on early intervention. 

the vision


Developing a Life-Changing Treatment


We see our technology as an opportunity to improve the lives of the many patients suffering from Alzheimer’s Disease and related dementia. 


Our goal is to complete the studies to get FDA approval of the device within two to three years. Upon this milestone, we plan to exit by outright sale or license the technology out on a milestone and royalty reimbursement model.



our leadership


Experts in Science, Medicine, and Finance


Dr. Pazhani Sundaram, the Founder-President has wide experience in research and development. He was trained at Yale School of Medicine for about a decade prior to founding this company. He has successfully performed a clinical trial on a cholesterol-lowering Indian herbal medicine and commercialized it in the Indian pharmaceutical market.



Our team represents decades of experience across scientific research, biopharmaceuticals, and finance. We believe strongly that this technology will fill an unmet medical need and change many people’s lives for the better. 

why invest


A Unique Treatment for a Better World


In 2021, treatment of patients with Alzhemier’s Disease and dementia will cost the nation $355 billion, and this cost is likely to increase to $1.1 trillion by 2050. We need to change the way we are approaching the problem. 



Through our technological innovation, we believe we can stop beta amyloid plaque build-ups before they happen in the brain, rather than simply treating the symptoms. Our promising proof of concept trial results alongside our patented technology have us well prepared to move into the next phase of trials. 


ABOUT

HEADQUARTERS
1090 Meriden Waterbury Tpke, Suite 1
Cheshire, CT 06410
WEBSITE
View Site
Recombinant Technologies is developing a revolutionary treatment for Alzheimer's Disease. By designing an injection of a molecule treatment to reduce the plaque buildup that causes dementia, we have successfully improved memory in mice and are ready to move toward human trials.

TERMS

Recombinant Technologies
Overview
PRICE PER SHARE
$1
DEADLINE
Feb. 12, 2022 at 7:59 AM UTC
VALUATION
$35M
FUNDING GOAL
$10K - $1.07M
Breakdown
MIN INVESTMENT
$200
MAX INVESTMENT
$107,000
MIN NUMBER OF SHARES OFFERED
10,000
MAX NUMBER OF SHARES OFFERED
1,070,000
OFFERING TYPE
Equity
SHARES OFFERED
Common Stock

Maximum Number of Shares Offered subject to adjustment for bonus shares

*Maximum number of shares offered subject to adjustment for bonus shares. See Bonus info below.

Voting Rights of Securities Sold in this Offering

Each Subscriber shall appoint the Chief Executive Officer of the Company (the “CEO”), or his or her successor, as the Subscriber’s true and lawful proxy and attorney, with the power to act alone and with full power of substitution, to, consistent with this instrument and on behalf of the Subscriber, (i) vote all Securities, (ii) give and receive notices and communications, (iii) execute any instrument or document that the CEO determines is necessary or appropriate in the exercise of its authority under this instrument, and (iv) take all actions necessary or appropriate in the judgment of the CEO for the accomplishment of the foregoing. The proxy and power granted by the Subscriber pursuant to this Section are coupled with an interest. Such proxy and power will be irrevocable. The proxy and power, so long as the Subscriber is an individual, will survive the death, incompetency and disability of the Subscriber and, so long as the Subscriber is an entity, will survive the merger or reorganization of the Subscriber or any other entity holding the Securities. However, the Proxy will terminate upon the closing of a firm-commitment underwritten public offering pursuant to an effective registration statement under the Securities Act of 1933 covering the offer and sale of Common Stock or the effectiveness of a registration statement under the Securities Exchange Act of 1934 covering the Common Stock.

Investment Incentives*

Time-Based:

Friends and Family Early Birds

Invest within the first 48 hours and receive additional 20% bonus shares.

Super Early Bird Bonus

Invest within the first week and receive additional 15% bonus shares.

Early Bird Bonus

Invest within the first two weeks and receive an additional 10% bonus shares.

Amount-Based:

$500+ | Tier 1

Invest $500 and receive 2% bonus shares. 

$1,000+ | Tier 2

Invest $1,000 and receive 5% bonus shares.

$2,500+ | Tier 3

Invest $2,500 and receive 7% bonus shares.

$5,000+ | Tier 4

Invest $5,000 and receive 10% bonus shares.

$10,000+ | Tier 5

Invest $10,000 and receive 15% bonus shares.

*All perks occur when the offering is completed.

Irregular Use of Proceeds

Example - The Company might incur Irregular Use of Proceeds that may include but are not limited to the following over $10,000: Vendor payments and salary made to one's self, a friend or relative; Any expense labeled "Administration Expenses" that is not strictly for administrative purposes; Any expense labeled "Travel and Entertainment"; Any expense that is for the purposes of inter-company debt or back payments.

PRESS

Article Image
'Amytrapper', a Novel Immobilized Sepharose API Matrix, Removes Amyloid-β from Circulation in vitro

Recombinant Technologies LLC (RTL) has developed and studied its proprietary Amytrap peptide to remove Aβ from circulation which in turn depletes brain Aβ in a clinically relevant mouse model of AD. The results provide a proof of concept for our proposed prototype design for an Amytrapper device.

Article Image
Pre-Clinical Safety and Efficacy Evaluation of Amytrap, a Novel Therapeutic to Treat Alzheimer's Disease

Efficacy evaluations were performed on model mice. Pharmacokinetics and safety toxicology were assessed. Post treatment, mice showed significant improvements in cognition. Efficacy and safety features make Amytrap a promising candidate for treating or modulating AD.

ALL UPDATES

02.11.22

Last Chance to invest in this game-changing Alzheimer's Therapeutic/Device

Take Advantage of this last day opportunity before the campaign closes. As for updates we have the following in the pipeline:

1. Two NIH grant proposals are under review

2. Two investment firms and a private high net worth investor are in the process of doing due diligence to get involved with our patented molecule based technologies to treat Alzheimer's Disease. 

3. The valuation potentially could increase many fold if the FDA approves the device within 2-3 years. 

We want the SE community to get the best of this campaign opportunity. So get excited and get involved by investing at the following link


https://investment.startengine.com/recombinant-technologies


The information included above is forward-looking information. Please refer to our risk factors section in our Form C and to our Forward-Looking Information Legend included in our Terms section on this page.

02.08.22

Final few days to close out this campaign

Only Three Days Left before the campaign closes

You have a very short period of time before the current campaign closes on the SE platform. Get in early and participate in the growth and history of a great disease modifying therapy to treat Alzheimer's and other amyloidosis. Let us join together to make their (AD patients) living better !!!


Here's the link to invest !  

https://investment.startengine.com/recombinant-technologies




02.05.22

Exciting Development

Great News ! We are proud to announce that there are some private clients interested to invest about $ 5 million in our company. This goes to show the confidence from these clients on our technology. We are hoping to finalize the transaction by signing a definitive agreement. This may occur after this offering closes. Once this happens, we will keep the investors and potential investors from start engine posted with details. In addition, I would like to take take this opportunity to thank the current investors for your confidence in our company.  I also encourage all of  you to take advantage  and invest to increase your value along with the company's. You have a very short period of time before the current campaign closes on the SE platform. Here's the link to invest !  

https://investment.startengine.com/recombinant-technologies


The information included above is forward-looking information. Please refer to our risk factors section in our Form C and to our Forward-Looking Information Legend included in our Terms section on this page.

01.12.22

Campaign updated to allow more investors

We are happy to share the exciting news! To those who were worried about missing the boat. In order to accommodate more investors,  Start Engine has extended this campaign by one month. So, get in and be part of the history ! join us in this exciting journey to invest and to help find a possible cure for Alzheimer's Disease !!  Use the link below.

https://www.startengine.com/recombinant-technologies


Besides this campaign Recombinant is working to raise private capital via other partners and through grant applications worth about $ 1.8M are under review at the National Institute on Aging,  National institutes of Health. 

01.12.22

Notice of Material Change in Offering

[The following is an automated notice from the StartEngine team].

Hello! Recently, a change was made to the Recombinant Technologies offering. Here's an excerpt describing the specifics of the change:


Campaign is extending by 30 days.


When live offerings undergo changes like these on StartEngine, the SEC requires that certain investments be reconfirmed. If your investment requires reconfirmation, you will be contacted by StartEngine via email with further instructions.

01.07.22

Limited time before the campaign closes

Only a few weeks to get involved before this campaign ends ! Participate in this exciting opportunity to help those affected by Alzheimer's disease. Take a look at this video illustration:

 https://www.youtube.com/watch?v=KySn7kg0l2E

12.21.21

Update from Founder-President

We are thankful for your support. As we enter the new year we have reached a major milestone of $ 75,000 in our campaign raise. With respect to our research front, we are initiating a key animal model testing study in January 2022. Additional research funding (in multimillion dollar grant applications that are in review) is also sought from the National Institute on Aging, NIH. We anticipate positive results in 2022. With your continued help, we hope to able to kickstart the FDA application/approval process for our device, in 2022. Please join us and invest to participate in this exciting journey. 

https://www.startengine.com/recombinant-technologies

Have a safe and happy new year. 



10.15.21

Brand new Scientific Publication

https://www.heraldopenaccess.us/article_pdf/10/novel-api-coated-catheter-removes-amyloid-beta-from-plasma-of-patients-with-alzheimer-s-disease.pdf


We're excited to get this publication  out there and hope you'll join us on this journey. Invest today! Invest now and participate in our success. 



10.01.21

Notice of Funds Disbursement

[The following is an automated notice from the StartEngine team].

Hello!

As you might know, Recombinant Technologies has exceeded its minimum funding goal. When a company reaches its minimum on StartEngine, it's about to begin withdrawing funds. If you invested in Recombinant Technologies be on the lookout for an email that describes more about the disbursement process.


This campaign will continue to accept investments until its indicated closing date.


Thanks for funding the future.

-StartEngine

09.30.21

Press Releases for Recombinant Technologies

Recombinant has been talked about in various press releases (yahoo finance, marketwatch, Benzinga and seeking alpha).


We have press coverage from various publications this week! 

"Their patented technology was developed over ten years and has successfully improved memory in mice and proof of concept trials."

"Going beyond conventional modalities that only address the symptoms, Recombinant Technologies is focused on treating the root cause of Alzheimer's Disease delivering a huge improvement in the quality of life of those afflicted."


We're excited to get this technology out there and hope you'll join us on this journey. Invest today!


REWARDS

Multiple investments in an offering cannot be combined to qualify for a larger campaign reward.
Venture Club

Venture Club

Venture Club Members earn 10% bonus shares on top of this and all eligible investments for an entire year. Not a member? Sign up at checkout ($275/year).

$500

Tier 1

Invest $500 and receive 2% bonus shares.

$1,000

Tier 2

Invest $1,000 and receive 5% bonus shares.

$2,500

Tier 3

Invest $2,500 and receive 7% bonus shares.

$5,000

Tier 4

Invest $5,000 and receive 10% bonus shares.

$10,000

Tier 5

Invest $10,000 and receive 15% bonus shares.

JOIN THE DISCUSSION

0/2500

MN
Michael Nadler

3 years ago

Pazhani, if the private investors invest recently after this closing, what valuations are being discussed? Would that be a down round from this $35 pre money cap?

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MN
Michael Nadler

3 years ago

Pazhani, from your previous answers to my questions, what's to believe that the company will have enough capital to survive let alone grow given your burn rate? Profitability in 2-3 years potentially, and who knows when or how much grant money you'll receive? Convince me otherwise. I like the company and idea, but don't see enough capital funding to grow this business to scale to profitability.

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0

MN
Michael Nadler

3 years ago

Pazhani, thanks for all your insight. Are you closing this round tonight? How many hours are left on this round or are you extending it?

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2

0

MN
Michael Nadler

3 years ago

I'm interested in investing in the company, and have a concern about the amount raised with your monthly burn at 60K. When do you see needing to raise more cash? Or are you going to be collecting more of the outstanding grant money? How long do you expect grant money to last for 2-3 years? When do you expect profitability or is that not in the near future i.e. within 5 years? Is profitability seen shortly after you clear FDA approval in 2-3 years? Please get back to me with this insight before the closing of this round. Thanks.

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MN
Mario Nacinovich

3 years ago

The amyloid-β (Aβ) pathway at the center of Alzheimer’s disease (AD) pathophysiology. https://www.nature.com/articles/s41380-021-01249-0

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TJ
Thomas Johnson

4 years ago

Alzheimer's medications such as solanezumab and bapineuzumab succeeded in reducing amyloid plaques, but these medications did not significantly slow down cognitive decline. https://www.nejm.org/doi/full/10.1056/NEJMoa1705971 https://www.alzforum.org/therapeutics/bapineuzumab Also, some Alzheimer's medications succeeded in reducing amyloid plaques, and the reduction in the plaques had some bad side effects (such as brain hemorrhage and brain swelling). https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693547/ So, even if your Amytrap works to reduce amyloid plaques, will that be enough to significantly slow down cognitive decline? And will the reduction in amyloid plaques cause side effects like brain hemorrhage and brain swelling? When you tested the Amytrap on mice, did you test the mice for brain hemorrhage or brain swelling?

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BM
Barbara Morris

4 years ago

I'm not convinced plaques in the brain cause AD. I believe nutrition and exercise over a lifetime play a role in the formation of plaques but plaques alone are not the cause. I wish you well.

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MN
Michael Nadler

4 years ago

Very interested in the company and idea, why has no one ever thought of this before or if they have, then what is it about your company that you've been able to improve memory in mice that no one in the world has been able to do before? Can you explain more about what the patent is- it protects the chemical composition of AmyTrap molecule?

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AS
Andrius Steponavicius

4 years ago

Bill did raise some relevant questions, some of which you ignored answering. 5 million is a tiny investment for potentially blockbuster drug. Why would you seek investment here vs deep pocketed partner who could not only provide money but also expertise, facilities, etc? You could also structure a deal to get paid for milestones which would offer you nice paydays along the way. Maybe I am missing something but going this route makes no sense.

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BE
Bill Evers

4 years ago

Hello, Dr. Sundaram. I have a couple of questions for you. 1) You, your secretary Ms. Dhawan, and your consultant Dr. Ranjini Sundaram have strong ties to Yale University. Also, your research was used by the pharmaceutical giant Merck to create the Gardasil vaccine. So, you have strong ties to Merck as well. You have said that you will need to raise $5 million to get FDA approval for Amytrap. For Yale and Merck, $5 million is a very small amount of money. Why don't you ask Yale and Merck to fund Amytrap? Why are you raising money from average people on StartEngine? 2) As I just mentioned, your research was used by Merck to create Gardasil. Unfortunately, there have been problems with Gardasil, and Merck has been sued because of these problems. Here is an example of that: https://www.baumhedlundlaw.com/prescription-drugs/gardasil-lawsuit/ So, what went wrong with the creation of Gardasil? Was your research faulty to begin with? Or did Merck screw something up in using your research to create Gardasil? And, if your research was faulty, what are you doing to make sure that your research for Amytrap is not equally faulty?

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VALUATION
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StartEngine Marketplace (“SE Marketplace”) is a website operated by StartEngine Primary, LLC (“SE Primary”), a broker-dealer that is registered with the SEC and a member of FINRA and the SIPC.

StartEngine Secondary (“SE Secondary”) is our investor trading platform. SE Secondary is an SEC-registered Alternative Trading System (“ATS”) operated by SE Primary that matches orders for buyers and sellers of securities. It allows investors to trade shares purchased through Regulation A+, Regulation Crowdfunding, or Regulation D for companies who have engaged StartEngine Secure LLC as their transfer agent. The term “Rapid,” when used in relation to transactions on SE Marketplace, specifically refers to transactions that are facilitated on SE Secondary, This is because, unlike with trades on the StartEngine Bulletin Board (“SE BB”), trades on SE Secondary are executed the moment that they are matched.

StartEngine Bulletin Board (“SE BB”) is a bulletin board platform on which users can indicate to each other their interest to buy or sell shares of private companies that previously executed Reg CF or Reg A offerings not necessarily through SE Primary. As a bulletin board platform, SE BB provides a venue for investors to access information about such private company offerings and connect with potential sellers. All investment opportunities on SE BB are based on indicated interest from sellers and will need to be confirmed. Even if parties express mutual interest to enter into a trade on SE BB, a trade will not immediately result because execution is subject to additional contingencies, including among others, effecting of the transfer of the shares from the potential seller to the potential buyer by the issuer and/or transfer agent. SE BB is distinct and separate from SE Secondary. SE Secondary facilitates the trading of securities by matching orders between buyers and sellers and facilitating executions of trades on the platform. By contrast, under SE BB, SE Primary assists with the facilitation of a potential resulting trade off platform including, by among other things, approaching the issuer and other necessary parties in relation to the potential transaction. The term “Extended”, when used in relation to transactions on SE Marketplace denotes that these transactions are conducted via SE BB, and that these transactions may involve longer processing times compared to SE Secondary for the above-stated reasons.

Even if a security is qualified to be displayed on SE Marketplace, there is no guarantee an active trading market for the securities will ever develop, or if developed, be maintained. You should assume that you may not be able to liquidate your investment for some time or be able to pledge these shares as collateral.

The availability of company information does not indicate that the company has endorsed, supports, or otherwise participates with StartEngine. It also does not constitute an endorsement, solicitation or recommendation by StartEngine. StartEngine does not (1) make any recommendations or otherwise advise on the merits or advisability of a particular investment or transaction, (2) assist in the determination of the fair value of any security or investment, or (3) provide legal, tax, or transactional advisory services.