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GET A PIECE OF SCITECH DEVELOPMENT, L.L.C.

Advancing Cancer Treatment Through Safer Drug Delivery

SciTech Development is a Specialty Pharmaceutical Company dedicated to advancing breakthrough cancer treatments. We have developed a powerful, new Drug Delivery Platform (SDP) that will revolutionize how safe and promising, yet challenged drugs, can be delivered to kill cancer. SciTech has developed our first, patented drug, ST-001-nanoFenretinide that combines SDP and the drug fenretinide as a broadly applicable anticancer drug. SciTech’s innovations will impact our mission to develop cost-effective therapeutics that deliver transformative clinical outcomes. SciTech Development is in the pre-revenue clinical stage of development.

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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.
Company Image

$135,205.02 Raised

REASONS TO INVEST

Reasons Icon

SDP, our proprietary and revolutionary Drug Delivery Platform, has enormous potential to develop and deliver new and better drugs for incurable cancers.

Reasons Icon

ST-001 (SDP plus fenretinide) is patented and clinical trial ready, with an FDA guided accelerated trial plan. Fenretinide presents a low risk scenario since it has been shown to be safe and effective in both children and adults. ST-001 is an affordable, cost-effective cancer treatment.

Reasons Icon

The market potential for ST-001 is about $2B, with an additional $5B-25B+ market potential from other targeted cancer indications, ST-001 combination therapies and from using our Delivery Platform to engineer and patent new drugs.

TEAM

Earle Holsapple

Earle Holsapple • CEO, President & Co-Founder

Mr. Holsapple has extensive managerial experience spanning many decades in a wide host of industries. He has successfully served as CEO/COO of six profitable midsize industrial or consumer products companies ranging in size from $10M to $100M in sales. He has managed four corporate turnarounds restoring each company to financial health. As an entrepreneur, he has started four new companies ranging in focus from international trade to complex life science startups. He previously served his country as an air defense officer in the United States Marine Corps rising to the rank of Captain. 

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Andrew Stumpf

Andrew Stumpf • Chief Financial Officer (CFO)

Mr. Stumpf brings 20+ years of experience as a finance professional in private equity, investment banking, corporate finance, and public accounting. Mr. Stumpf serves on the board of directors of a public diversified holding company as a member on the audit, compensation and nominating committees. Mr. Stumpf is a partner with Storm Lake Capital, a private equity firm that invests in middle market companies. Mr. Stumpf also performs in a finance capacity for several portfolio companies with responsibilities including financial and strategic planning and budgeting, financial reporting and year-end audit and tax filings.

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Louis M. Scarmoutzos, Ph.D.

Louis M. Scarmoutzos, Ph.D. • Chief Operating Officer

Dr. Scarmoutzos has over 30 years of industrial experience in the biotech, chemistry, healthcare, medical device, pharmaceutical, and related industries. His hands-on industrial experience ranges from Bench Top Scientist to Vice President of R&D to President and CEO. He has founded several companies and is currently a Board Member of several small and emerging companies. Dr. Scarmoutzos received his B.S. cum laude in Chemistry from Boston College, a Ph.D. summa cum laude in Organic Chemistry from the Pennsylvania State University and was a Post-Doctoral Fellow in the Department of Chemistry and Chemical Biology at Harvard University. 

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We Are Making A Difference

Wouldn’t it be great if every patient could “Ring the Bell” to signify the end of their cancer journey?

We are SciTech Development, a Specialty Pharmaceutical Company with the goal of helping patients end their battle with cancer.


SciTech has developed a revolutionary new Drug Delivery Platform called “SDP” to safely deliver drugs that kill cancer cells. We have used our proprietary Delivery Platform to develop our first clinical drug candidate, ST-001 nano-Fenretinide, with potentially more to follow.


We initially brought our message to Big Pharma. Although excited, they said “Come back and see us when you have some clinical data”. So, we are bringing our message directly to you through StartEngine. Funding through StartEngine will help us start clinical trials.

According to IQVIA, about 80% of the industry's drug development pipeline comes from emerging biopharma companies, which means small companies are overwhelmingly driving innovation and new drug products.

The first step to potentially curing cancer is to begin clinical trials of ST-001 for the treatment of lymphoma. Our intent is to expand the use of ST-001 in other cancers and develop additional new drugs so we can help the millions of patients that are battling cancer.

FDA approval of ST-001 would be a significant step towards becoming a revenue-generating company.


How It Works


*The above video contains computer generated demonstrations of the SciTech Drug Delivery Platform.

For more detailed technical info, visit our science-based website at  www.scitechdevelopment.com

THE PROBLEM


Cancer is an Escalating Worldwide Problem

Billions of dollars have been spent on developing new cancer therapies. And yet, there have been limited advancements in treatment and healthcare costs continue to rise.


There is an urgent need for therapies that can fight multiple cancers with high effectiveness, low side effects, and at an affordable cost. Many existing drugs are not able to achieve their full potential because they simply cannot effectively enter the cancer cell in sufficient amounts. Administering them in higher doses may not solve this problem without causing significant harm to the patient.


Patients suffering from cancer are often faced with the reality that there may be limited benefits from their existing treatment. Their cancer treatment is often fraught with long-lasting side effects from potentially harmful or toxic treatments with no cost-effective alternative therapies. Their struggle may be long and traumatic with no end in sight.


Help us try to make the struggle shorter, safer, and more cost-effective for those suffering from cancer. 



THE SOLUTION


An Effective Drug Delivery Platform for New Cancer Treatments 

We believe that ST-001 will provide hope to millions of cancer patients.



  • The SciTech Drug Delivery Platform or “SDP” is designed to safely deliver high concentrations of drugs to kill cancer cells.
  • SDP works by formulating drugs into very tiny spheres known as “nanovesicles”, which “trick” the cells into letting the drug inside, ultimately killing the cancer.
  • SDP can be engineered with other drugs, making them more effective and patentable.
  • ST-001 nanoFenretinide, our patented lead drug candidate, is a combination of the Delivery Platform and fenretinide, a drug with a well-documented safety profile.
  • ST-001 and newly engineered SDP drugs may be used alone or in combination with existing therapies.

THE MARKET


New Therapeutics for Broader and Better Clinical Outcomes

Oncology is the world’s largest pharmaceutical therapeutic area. The growing prevalence of cancer around the world will continue to spur opportunities for the oncology drug market. SciTech plans to engineer new cancer drugs for better clinical outcomes in more oncology areas and diseases.


Source


The immediate targeted market for ST-001 is estimated to be about $2 Billion.  
 
The market potential can be expanded to $5B-25B+ with ST-001 combination therapies, targeting other cancer indications, and from using our Delivery Platform to engineer and patent new drugs.  
 


According to Global Industry Analysts Inc., the global market for cancer therapies is projected to reach USD $204.2 billion by 2024 with a compounded annual growth rate (CAGR) of 9.7%. The U.S. represents the largest market for cancer therapies with an estimated 38.3% share of the total global market.

Our Traction


SciTech Anticipates a Rapid Path to Commercialization

Fenretinide: Safe with Great Promise in Previous Clinical Trials


ST-001 contains the active ingredient fenretinide, a drug with a well-documented safety profile in over 3000 patients. However, it does not easily dissolve in the body so it cannot get to the cancer cells in high enough doses to be effective, a problem solved by ST-001.


After achieving numerous milestones, our approved clinical trials are “Confirmatory” not “Exploratory”.  Our trial simply needs to confirm that ST-001 can transport the drug into the cancer cell safely, at the right dose, without toxic side effects, and provide beneficial patient outcomes.




Unlike other “typical” clinical trials, the FDA has provided SciTech with guidance to a much faster pathway requiring fewer patients.  Once the clinical trials are completed and with FDA approval SciTech will be able to commercialize ST-001.


SciTech can now  begin its clinical trial at Rush University Medical Center in Chicago, IL.


how we're different


SciTech Can Develop a Robust Commercial Pipeline Using SDP, Our Proprietary Drug Delivery Platform


  • Our revolutionary new Drug Delivery Platform (SDP) has enormous potential in developing and delivering new drugs.
  • ST-001 is clinical trial ready with a rapid path to commercialization.
  • ST-001 is an affordable cancer therapy that can reduce treatment costs and improve outcomes.
  • SciTech has an exceptional leadership and scientific advisory team with vast industry experience.



THE BUSINESS MODEL


Milestone Driven With Multiple Exit Strategies

Our immediate goal is to commercialize ST-001 and develop strategic partnerships with companies in the pharmaceutical industry who are looking to expand their existing drug portfolio in oncology, target new diseases, or develop combination drug therapies.


ST-001 would be an ideal candidate for use in combination drug/therapy regimens. The emerging trend in cancer treatment is to combine new, targeted therapies with other drugs in order to increase their effectiveness and therapeutic benefit. Use of ST-001 in this manner would have a significant positive impact on revenue.



SciTech can develop a robust pipeline of new drug candidates using our Delivery Platform, potentially increasing the valuation of the company.


All potential exit strategies will be considered, based on the best outcome for our investors, the company, and the timing of these potential options.



Due to the COVID-19 pandemic, the company is currently working virtually. We have engaged a large-scale drug manufacturer to produce ST-001 and a clinical trial site to conduct our study.

WHY INVEST


Together, We Can Fight Cancer and Bring New Hope to Patients Around the World.

First and foremost, we believe that ST-001 may drastically improve the therapeutic options for cancer patients.  Whether it's you, a family member, or a friend, just about everyone has been touched by cancer. Too many of us have too many common stories of pain and sorrow.


SciTech’s Delivery Platform provides an opportunity to develop new cancer drugs and change the cancer treatment landscape.

FDA approval of ST-001 would be a significant step toward becoming a revenue-generating company.

With our science and your help, we can provide a brighter future for patients, our partners, and our investors.


Please join us in helping to give each and every cancer patient a fighting chance to “Ring the Bell’’!


Italic (⌘I)

ABOUT

HEADQUARTERS
P.O. Box 36927
Grosse Pointe Farms, MI 48236
WEBSITE
View Site
SciTech Development is a Specialty Pharmaceutical Company dedicated to advancing breakthrough cancer treatments. We have developed a powerful, new Drug Delivery Platform (SDP) that will revolutionize how safe and promising, yet challenged drugs, can be delivered to kill cancer. SciTech has developed our first, patented drug, ST-001-nanoFenretinide that combines SDP and the drug fenretinide as a broadly applicable anticancer drug. SciTech’s innovations will impact our mission to develop cost-effective therapeutics that deliver transformative clinical outcomes. SciTech Development is in the pre-revenue clinical stage of development.

TERMS

SciTech Development, L.L.C.
Overview
PRICE PER SHARE
$2.75
DEADLINE
Jul. 30, 2022 at 6:59 AM UTC
VALUATION
$63.93M
FUNDING GOAL
$10K - $5M
Breakdown
MIN INVESTMENT
$275
MAX INVESTMENT
$4,999,997.75
MIN NUMBER OF SHARES OFFERED
3,636
MAX NUMBER OF SHARES OFFERED
1,818,181
OFFERING TYPE
Equity
SHARES OFFERED
Units

Maximum Number of Shares Offered subject to adjustment for bonus shares

*Maximum Number of Units Offered subject to adjustment for bonus units. See Bonus info below.

Company Perks

Time-Based Bonuses*:

  • Invest within the 1st week and receive 20% bonus shares.
  • Invest within the 2nd week and receive 15% bonus shares.
  • Invest within the 3rd week and receive 10% bonus shares.
  • Invest within the 4th week and receive 5% bonus shares.

Volume Based Bonuses and Perks*:

Tier 1

  • Invest >$500, you will receive 5% bonus shares. 

Tier 2

  • If you invest >$1,500, you will receive 10% bonus shares.

Tier 3

  • If you invest >$5,000, you will receive 15% bonus shares.

Tier 4

  • If you invest >$10,000, you will receive 20% bonus shares and an in-person** or virtual meeting with the leadership team.

*Investors cannot qualify for both bonuses in any single investment. If an investor qualifies for two bonuses the higher of the two bonuses will be applied. All perks occur after the offering is completed.

**Travel Not Included

*All perks occur when the offering is completed.

The 10% StartEngine Owners' Bonus

SciTech Development LLC will offer 10% additional bonus Units for all investments that are committed by investors that are eligible for the StartEngine Crowdfunding Inc. OWNer's bonus.

This means eligible StartEngine members will receive a 10% bonus for any units they purchase in this offering. For example, if you buy 100 Units at $2.75/unit, you will receive 110 Units, meaning you'll own 110 shares for $275. Fractional Units will not be distributed and unit bonuses will be determined by rounding down to the nearest whole unit.

This 10% Bonus is only valid during the investors eligibility period. Investors eligible for this bonus will also have priority if they are on a waitlist to invest and the company surpasses its maximum funding goal. They will have the first opportunity to invest should room in the offering become available if prior investments are cancelled or fail.

Investors will only receive a single bonus, which will be the highest bonus rate they are eligible for.

Insider Investment Notice

Officers, directors, executives, and existing owners with a controlling stake in the company (or their immediate family members) may make investments in this offering. Any such investments will be included in the raised amount reflected on the campaign page.

Irregular Use of Proceeds

The Company might incur Irregular Use of Proceeds that may include but are not limited to the following over $10,000: Vendor payments. Salary payments made to one’s self, a friend or relative. Any expense labeled “Travel and Entertainment”. Inter company debt or back payments.

ALL UPDATES

08.05.22

Your StartEngine SciTech Development Investment

07.30.22

Thank You

07.29.22

LAST CHANCE – ONLY HOURS LEFT TO INVEST!

Don’t miss out on this opportunity! 

Invest in SciTech at startengine.com/scitechdevelopment

Follow us on LinkedIn, Facebook and Twitter!

07.28.22

Fenretinide as a Potential Treatment for Brain Cancer

A recent publication suggests a combination therapy (which includes fenretinide) as a potential treatment for DIPG (diffuse intrinsic pontine glioma), a type of childhood brain cancer that is always fatal (https://bit.ly/3vk0u9T).

An earlier Phase 2 clinical study of fenretinide in adults with brain cancer showed that fenretinide was inactive at the dosage used in that clinical trial. The authors of the study further relay that additional studies are warranted based on the tolerability of the agent and the potential for activity at a higher fenretinide dosage, as suggested in the trial (https://bit.ly/3RYhnjU).

The impact of a brain cancer diagnosis is significant and can affect the quality of life through disease progression as well as by the effects of the treatment. Current treatment primarily includes surgery, radiation therapy and chemotherapy, with low survival rates (https://bit.ly/3vlUgpX).

Famous people who have succumbed to brain cancer include John McCain, Ted Kennedy, Lou Rawls, Pete Rozelle, Celia Cruz, Mary Shelley, Slim Pickens, Bobby Bonds, Gene Siskel (of Siskel & Ebert fame), Ethel Merman, and George Gershwin to name a few (https://bit.ly/3PY0x2N).

SciTech’s ST-001 nanoFenretinide drug candidate offers the potential of a bioavailable, non-toxic, and affordable treatment for brain cancer.

Visit www.SciTechSDP.com to learn more about ST-001 nanoFenretinide and SciTech’s proprietary technology.

Follow SciTech on LinkedIn, Facebook and Twitter!

07.28.22

One Day Left to Invest in SciTech

There’s so little time left to join our Investor Family – but you can still do it!

Make your investment at startengine.com/scitechdevelopment

Visit www.SciTechSDP.com to learn more about SciTech.

Follow Us on LinkedIn, Facebook and Twitter!

07.27.22

Only Two Days Left to Invest in SciTech

Right now is the perfect time for you to make your best decision of the day... with an investment in SciTech!

Only 2 days left in our crowdfunding campaign at startengine.com/scitechdevelopment

Visit www.SciTechSDP.com to learn more about SciTech.

Follow Us on LinkedIn, Facebook and Twitter!

07.26.22

Fenretinide Treatment for Obesity and Type 2 Diabetes – 3 Days Left to Invest –

A recent publication demonstrated that fenretinide can prevent obesity and improve insulin sensitivity in mice. The authors of the publication discuss the beneficial effects of fenretinide's multiple mechanisms of action. However, despite all the beneficial effects of fenretinide, they did observe increased atherosclerosis in their LDLR-/- mutated mouse models, models for studying familial (genetic) hypercholesterolemia (high cholesterol). https://doi.org/10.1101/2022.07.22.500933

An earlier publication demonstrated that fenretinide and metformin exhibited positive individual and synergistic effects when administered to treat diabetes in a rat model. https://doi.org/10.1080/26895293.2020.1732483

The recent publications suggest that SciTech's ST-001 nanoFenretinide technology may present additional out-licensing opportunities.

Follow SciTech on LinkedIn, Facebook and Twitter!

07.26.22

You Only Have The Next Three Days To Invest

Hurry! There are only three (3) days left to invest in SciTech.

Invest what you can at startengine.com/scitechdevelopment

Visit www.SciTechSDP.com to learn more about SciTech and its proprietary technology.

Follow Us on LinkedIn, Facebook and Twitter!

07.25.22

Only Four Days Left to Invest

Keep calm - only four (4) days left to invest in SciTech at startengine.com/scitechdevelopment

Visit www.SciTechSDP.com to learn more about SciTech and its proprietary technology.

Follow Us on LinkedIn, Facebook and Twitter!

07.25.22

Only Five Days Left to Invest

Only five (5) days left to invest in our crowdfunding campaign on StartEngine.

Don't miss your chance to be part of our investor community! Invest Now at startengine.com/scitechdevelopment

Visit www.SciTechSDP.com to learn more about SciTech and its proprietary technology.

Follow Us on LinkedIn, Facebook and Twitter!

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).

JOIN THE DISCUSSION

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EH
Earle Holsapple

3 years ago

A special thanks to those investors who have contributed to this wonderful cause and opportunity or those who have been following us. SciTech is on track to test its promising drug in humans in Q4. Your help in enabling that trial is greatly appreciated. As we close this campaign, keep following us at SciTechsdp.com. Regards, Earle Holsapple, President

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Salvador Avalos

3 years ago

How does the prevalence of Statin medications impact your delivery platform? Could you provide details on your approach regarding Statins?

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EH
Earle Holsapple

SciTech Development, L.L.C.

3 years ago

The prevalence of statin medications should have no impact on our SDP drug delivery platform. As you know, statins are widely prescribed to lower high cholesterol; and, we are unaware of any human data regarding the combined effect of fenretinide and statins. Our FDA-approved clinical protocol does not prohibit patients that are on statins from enrolling in our clinical trial and requires patient disclosure of all prescriptions, including statins. Lou

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JI
Jerry Irwin

3 years ago

when does your raise close?

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DS
David Schaffer

3 years ago

Jerry, Thank you for the question. All of Start Engine's Reg CF raises are 60 days in length and can be extended based on hitting certain milestones. Additionally, there is also a 30-day extension that Start Engine can grant for meeting certain conditions. SciTech’s current 60-day window is Jun 30, and as indicated, can be extended. Thank you for your interest and support of our campaign. Please don’t hesitate to ask further questions. David

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Steve Mills

3 years ago

From recent update: "..since sophisticated, accredited investors are willing to invest larger sums of money." For myself and all my fellow 'rube' investors on Start Engine, I say, "Ouch!" : )

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DS
David Schaffer

3 years ago

Hi Steve – I want to thank you for bringing this to our attention. We never intended to offend anyone, especially our StartEngine supporters. In our exuberance to share, what we felt would be information that would validate a decision to invest in SciTech on the StartEngine platform – we should have chosen our words more carefully and for that we apologize. The advancement of clinical stage medicines like ST-001 requires significant amounts of capital. In many cases those numbers can reach well into the billions of dollars. Because of the data in over 3000 previous patients that exists with regards to our underlying drug fenretinide, SciTech anticipates being able to advance ST-001 into commercialization for less than $50 million. StartEngine provides individuals with an opportunity to review and analyze companies with solid ideas and growth potential which is why we chose them as the platform to launch the SciTech opportunity. Previously, only accredited investors were presented with these offerings and the retail investors had been left out. StartEngine changed that for individuals like you and me. We had hoped that sharing this news would be reassuring to our community of supporters and that it would bolster the confidence of those who were still evaluating the opportunity. I hope you can accept our apology and our promise to do better in the future… Sincerely, the entire SciTech Team

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Anne Oshman

3 years ago

I do not see anyone listed as an employee of the company involved in this study of nanofenretinide. "Orienti, I., Francescangeli, F., De Angelis, M.L. et al. A new bioavailable fenretinide formulation with antiproliferative, antimetabolic, and cytotoxic effects on solid tumors. Cell Death Dis 10, 529 (2019). https://doi.org/10.1038/s41419-019-1775-y." What involvement, if any, did the company have with this study?

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David Schaffer

3 years ago

Thanks for your questions, Anne. There have been numerous studies done and papers written on fenretinide relating to efficacy, safety and its potential as a cancer fighting drug. Although SciTech was not involved in this particular study, we felt it was worthy of reporting on as a basis to further substantiate the value that we believe ST-001 offers patients.

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Anne Oshman

3 years ago

Does the company own the patent to the SDP delivery system? Are there any royalty payments due to any third parties? Likewise, does the company own the patent for ST-001? Are there any royalty payments due to any third parties for use of the underlying fenretinide?

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David Schaffer

3 years ago

Another great question… SciTech co-owns and licenses the patent, which covers both ST-001 and the nanoparticle delivery platform (SDP) with Wayne State University (WSU). Our license agreement with WSU has us making industry standard milestone and royalty payments. To answer the last part of your question regarding the underlying drug fenretinide – there are no royalties to be paid for its use. Fenretinide itself has been off-patent for decades and as you may be aware once a drug is off patent it can be manufactured and used as a generic “as is” or in other formulations. SciTech merely has to acquire the drug for use in ST-001.

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JK
Joseph Kraus

3 years ago

Just curious- given that the campaign has just been live for only a few weeks, why does the company dashboard indicate your campaign has "14 Days Left" when it seems as though you have just begun? Doesn't make sense to me. Thanks.

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David Schaffer

3 years ago

Joe, thank you for addressing an issue likely on most observers’ minds. SciTech’s latest fiscal year ended on December 31, 2021. Under SEC Reg CF rules, the company is required to provide an audited financial statement within 120 days of that date. The 14-day countdown indicates that the company must provide the audit within that time-period, or the campaign will stop. The company has generated the required financial statement and it is presently under review by the auditors for anticipated submission within the required timeline. Once this requirement is fulfilled, we presume the “Days Left” metric will be adjusted accordingly. We are committed to ensuring the success of this campaign and our unique oncology drug platform.

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David Schaffer

3 years ago

SciTech would like to thank all of the early investors for joining us on this mission to fight and defeat cancer. We are very appreciative of the early investor support and confidence in this significant opportunity that has enabled the Start Engine offering to achieve its first funding milestone surpassing $45k raised on the platform. Our sights are now set on toppling the next milestone of $75k. Thank you!!!! again!

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alex boosalis

3 years ago

On Page 29 of the Offering Memorandum, you mention Trillium and its 128mm Valuation at pre phase 1 trial (which is the same spot you are in now) . How is your “therapeutics” similar to Trillium....

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David Schaffer

3 years ago

Alex, this is a great question, and we applaud you for reading the Offering Memorandum in such detail. The Trillium comparable is very exciting to the SciTech team and its investors because its IND and Orphan drug designation are for the same indication as SciTech's, T Cell Non-Hodgkin's lymphoma. In addition, Pfizer later acquired Trillium for $2.3bb after they completed their successful phase 1 safety study. SciTech's lead drug candidate, ST-001 nano-fenretinide, has been shown in the lab to have great potential as both a monotherapy and combination therapy with existing approved drugs, as did Trillium's lead drug candidate, Ontorpacept. The market valuation expressed for Trillium reflects the same stage of development that ST-001 currently reflects; notably, entering Phase 1 clinical trials Below is a comparison of the two technologies: SciTech Development Trillium Therapeutics Drug Candidate ST-001 nanoFenretinide TTI-621 Common Name Fenretinide Ontorpacept Type Small molecule, synthetic Protein, recombinant fusion Stability 6+ months (refrigerated) 1 month (refrigerated) Mechanisms of Action Multiple Dual IND Approved (NHL) Approved (NHL) Orphan Drug FDA Designated (NHL) FDA Designated (NHL) Administration Intravenously Intravenously Prerequisites – i.e., Must Be Present None CD47*

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Barend Venter

3 years ago

I would like to understand why this delivery method kills cancer cells and not other cells. Is there a reference you can add to your pitch that will clear this up?

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DS
David Schaffer

3 years ago

Barend, That’s an excellent question; thank you for asking it, as it may help others who are considering an investment in SciTech. The active drug in ST-001 is fenretinide which has been proven safe (non-harmful to normal cells) and effective (killing cancer cells) in clinical trials in over 3,000 patients. Historically, the problem with fenretinide has been its bioavailability. SciTech believes it has solved this problem through its proprietary delivery platform – SDP. There is much more in-depth and technical explanation on the SciTech Development website, which can be found on our homepage at https://www.scitechdevelopment.com/ with associated references. Background info on fenretinide, including its history, properties and use can be found on our site at https://www.scitechdevelopment.com/fenretinide. Thanks again for the question.

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With Regulation A+, a non-accredited investor can only invest a maximum of 10% of their annual income or 10% of their net worth per year, whichever is greater. There are no restrictions for accredited investors.

With Regulation Crowdfunding, non-accredited investors with an annual income or net worth less than $124,000 are limited to invest a maximum of 5% of the greater of those two amounts. For those with an annual income and net worth greater than $124,000, they are limited to investing 10% of the greater of the two amounts.

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Please keep in mind that a company can conduct a series of “closes” or withdrawals of funds throughout the duration of the campaign. If you are included in that withdrawal period, you will be emailed your countersigned subscription agreement and proof of purchase immediately following that withdrawal.

StartEngine assists companies in raising capital, and once the offering is closed, we are no longer involved with whether the company chooses to list shares on a secondary market or what occurs thereafter. Therefore, StartEngine has no control or insight into your investment after the close of the live offering. In addition, we are not permitted to provide financial advice. You may want to contact a financial professional to discuss possible investment outcomes.

For Regulation Crowdfunding, investors are able to cancel their investment at any point throughout the campaign up until 48 hours before the closing of the offering. Note: If the company does a rolling close, they will post an update to their current investors, giving them the opportunity to cancel during this timeframe. If you do not cancel within this 5-day timeframe, your funds will be invested in the company, and you will no longer be able to cancel the investment. If your funds show as ‘Invested’ on your account dashboard, your investment can no longer be canceled.

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Refunds that are made through ACH payments can take up to 10 business days to clear. Unfortunately, we are at the mercy of the bank, but we will do everything we can to get you your refund as soon as possible. However, every investment needs to go through the clearing process in order to be sent back to the account associated with the investment.

Both Title III (Regulation Crowdfunding) and Title IV (Reg A+) help entrepreneurs crowdfund capital investments from unaccredited and accredited investors. The differences between these regulations are related to the investor limitations, the differing amounts of money companies are permitted to raise, and differing disclosure and filing requirements. To learn more about Regulation Crowdfunding, click here, and for Regulation A+, click here.

RAISED
$135,205.02
INVESTORS
97
MIN INVEST
$275
VALUATION
$63.93M

Important Message

IN MAKING AN INVESTMENT DECISION, INVESTORS MUST RELY ON THEIR OWN EXAMINATION OF THE ISSUER AND THE TERMS OF THE OFFERING, INCLUDING THE MERITS AND RISKS INVOLVED. INVESTMENTS ON STARTENGINE ARE SPECULATIVE, ILLIQUID, AND INVOLVE A HIGH DEGREE OF RISK, INCLUDING THE POSSIBLE LOSS OF YOUR ENTIRE INVESTMENT.

www.StartEngine.com is a website owned and operated by StartEngine Crowdfunding, Inc. (“StartEngine”), which is neither a registered broker-dealer, investment advisor nor funding portal.

Unless indicated otherwise with respect to a particular issuer, all securities-related activity is conducted by regulated affiliates of StartEngine: StartEngine Capital LLC, a funding portal registered here with the US Securities and Exchange Commission (SEC) and here as a member of the Financial Industry Regulatory Authority (FINRA), or StartEngine Primary LLC (“SE Primary”), a broker-dealer registered with the SEC and FINRA / SIPC. You can review the background of our broker-dealer and our investment professionals on FINRA’s BrokerCheck here. StartEngine Secondary is an alternative trading system (ATS) regulated by the SEC and operated by SE Primary. SE Primary is a member of SIPC and explanatory brochures are available upon request by contacting SIPC at (202) 371-8300.

StartEngine facilitates three types of primary offerings:

1) Regulation A offerings (JOBS Act Title IV; known as Regulation A+), which are offered to non-accredited and accredited investors alike. These offerings are made through StartEngine Primary, LLC (unless otherwise indicated). 2) Regulation D offerings (Rule 506(c)), which are offered only to accredited investors. These offerings are made through StartEngine Primary, LLC. 3) Regulation Crowdfunding offerings (JOBS Act Title III), which are offered to non-accredited and accredited investors alike. These offerings are made through StartEngine Capital, LLC. Some of these offerings are open to the general public, however there are important differences and risks.

Any securities offered on this website have not been recommended or approved by any federal or state securities commission or regulatory authority. StartEngine and its affiliates do not provide any investment advice or recommendation and do not provide any legal or tax advice concerning any securities. All securities listed on this site are being offered by, and all information included on this site is the responsibility of, the applicable issuer of such securities. StartEngine does not verify the adequacy, accuracy, or completeness of any information. Neither StartEngine nor any of its officers, directors, agents, and employees makes any warranty, express or implied, of any kind whatsoever related to the adequacy, accuracy, or completeness of any information on this site or the use of information on this site.

Investing in private company securities is not suitable for all investors. An investment in private company securities is highly speculative and involves a high degree of risk. It should only be considered a long-term investment. You must be prepared to withstand a total loss of your investment. Private company securities are also highly illiquid, and there is no guarantee that a market will develop for such securities. Each investment also carries its own specific risks, and you should complete your own independent due diligence regarding the investment. This includes obtaining additional information about the company, opinions, financial projections, and legal or other investment advice. Accordingly, investing in private company securities is appropriate only for those investors who can tolerate a high degree of risk and do not require a liquid investment. See additional general disclosures here.

By accessing this site and any pages on this site, you agree to be bound by our Terms of use and Privacy Policy, as may be amended from time to time without notice or liability.

Canadian Investors

Investment opportunities posted and accessible through the site will not be offered to Canadian resident investors. Potential investors are strongly advised to consult their legal, tax and financial advisors before investing. The securities offered on this site are not offered in jurisdictions where public solicitation for offerings is not permitted; it is solely your responsibility to comply with the laws and regulations of your country of residence.

California Investors Only – Do Not Sell My Personal Information (800-317-2200). StartEngine does not sell personal information. For all customer inquiries, please write to contact@startengine.com.

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.