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Vyome Therapeutics, Inc.; The Rise of Livechain, Inc (OTCMKTS: LICH)

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Livechain, Inc (OTCMKTS: LICH) has been rocketing up the charts in recent days hitting a high of $0.0598 earlier in the week and retracing some before the weekend. The stock is getting noticed after the Company filed their annual report on Friday which confirmed that Vyome Therapeutics, Inc is the new controlling shareholder of the Company with 70.08% of the companies issued and outstanding shares. At the time of transfer, Venkat Nelabhotla, Chief Executive Officer and Director of Vyome Therapeutics, Inc., also became Chief Executive Officer and Director of Livechain, Inc. 

Reverse Merger stocks (RM) are easily among the most exciting and explosive stocks in small caps rivaling only biotech’s in their ability to make historic gains. LICH is the perfect merger candidate; a clean shell with virtually no debt and the new Company Vyome Therapeutics is a clinical-stage company developing locally-acting, next generation therapeutics for immuno-inflammatory diseases. Vyome’s lead clinical drug candidate, VB-1953, is a first-in-class, topical, bactericidal small molecule with a novel mechanism of action in acne. In 2019, the acne treatment market was valued at nearly 11 billion U.S. dollars, according to market research company NMSC. However, until 2030 it is expected to increase to over 15 billion U.S. dollars. Regarding the global skin care market in total, the United States and Japan have the highest shares. 

Livechain, Inc (OTCMKTS: LICH) is a clean shell with just $64k in total liabilities operating out of Reno, Nevada. Management spent the summer of 2021 filing previous annual reports and the attorneys letter in June. The Company is now pink current with just 185,145,941 shares outstanding representing a total market valuation of $4,850,824. LiveChain, Inc. was originally formed as Eastern Star Mining Company, incorporated under the laws of the State of Idaho in 1906. In 1989 the predecessor merged into a newly-formed Nevada corporation as Eastern Star Mining, Inc. Immediately thereafter, the holder of a majority of the outstanding common stock transferred control of the corporation. After a number of incarnations, the name change to LiveChain, Inc. was approved by a majority of the shareholders of the Company on August 12, 2019 

On August 31, 2021, the board of directors, by consent entered a Stock Purchase agreement with Vyome Therapeutics, Inc., to sell to Vyome Therapeutics, Inc., 986,919 of the 996,919 of the company’s A-1 preferred shares. On the date of closing, Vyome Therapeutics, Inc., purchased 996,919 shares of Livechain, Inc.’s, A-1 proffered stock, assuming 70.08% of the companies issued and outstanding shares. At the time of transfer, Venkat Nelabhotla, Chief Executive Officer and Director of Vyome Therapeutics, Inc., also became Chief Executive Officer and Director of Livechain, Inc. 

Vyome Therapeutics is a clinical-stage company developing locally-acting, next generation therapeutics for immuno-inflammatory diseases with several drugs currently under development. Vyome works to treat inflammatory diseases using locally-acting, novel and next generation therapeutic solutions with validated mechanisms of action and effective formulations for site-targeted applications. With this approach to drug development, Vyome is working to develop safer and more effective alternatives to standards of care in multifactorial diseases of high unmet need which are underpinned by inflammation. 

Vyome’s lead clinical drug candidate, VB-1953, is a first-in-class, topical, bactericidal small molecule with a novel mechanism of action in acne. VB-1953 reduces inflammatory lesions in C. acnes by blocking inflammatory cytokine production through TLR-MD2 inhibition and has demonstrated the ability to treat antibiotic-resistant C. acnes strains. VB-1953 is the first bactericidal drug candidate to be tested for the treatment of C. acnes. VB-1953 is delivered topically with a microtechnology gel system that ensures the drug is retained at the site of infection and minimizes systemic exposure. Acne caused by antibacterial-resistant C. acnes currently poses an emerging and unmet need for patients worldwide, with a potential $2B market opportunity in the US alone. 

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Last year the Company reported positive data from its Phase 2 trial of VB-1953, a firstin-class topical bactericidal and TLR-MD2 inhibitor being developed for the treatment of moderate to severe inflammatory facial acne vulgaris. Results from the trial demonstrated a statistically significant difference in the primary endpoint, the mean absolute change in inflammatory lesions at week 12, for VB 1953, when applied once a day (QD) vs. combined vehicle group (p <0.012). In the comparison between the VB1953 QD arm versus vehicle QD, the mean absolute change in the inflammatory lesions at week 12 in the intent to treat (ITT) group showed 20.4 and 17.8 respectively, with p<0.003, and 20.4 and 16.6 respectively in per protocol group with p<0.001. In addition, VB-1953 exhibited an excellent safety profile and there were no drug related adverse or serious adverse events. “These results demonstrate that VB-1953, with its dual mechanism of action directly killing resistant and non-resistant C. acnes strains while blocking inflammation through TLR-MD2 inhibition, has the potential to become a safe and effective topical treatment for facial acne and an alternative to oral, systemic drugs,” said Dr. Shiladitya Sengupta, scientific co-founder of Vyome. 

The Phase 2 randomized, multicenter, double-blind, dose-ranging study was designed to evaluate the safety and efficacy of VB-1953 topical gel when applied once daily and twice daily for 12 weeks in subjects with moderate to severe inflammatory facial acne vulgaris. The Company enrolled 471 patients across 13 trial sites in the U.S.  Once daily (QD) application was found to be as effective as twice daily application in the mean absolute change in the inflammatory lesions. 

Venkat Nelabhotla, Chief Executive Officer of Vyome Therapeutics, said at the time: “We are very pleased to have met the primary endpoint of the study, and to demonstrate the continued safety of the molecule. Patients need a highly effective drug, and our data shows a very high response, which is encouraging as we plan to advance to Phase 3 with a once daily dose. We look forward to delivering a next-generation solution to patients.” 

Although the study was not powered to test for significance in secondary end points, the drug (VB 1953 QD group) achieved a 66.6% mean reduction in inflammatory lesions at week 12 with p<0.020 in ITT and p<0.004 per protocol group versus vehicle group, and a 49.6% successful improvement in the IGA score (minimum two-grade improvement and achieving clear or almost clear IGA score at week 12) with p<0.361 in ITT group and p<0.069 per protocol group versus vehicle group. 

Acne is a skin condition caused by a clogging of hair follicles with dead skin or oils. This condition is also known as acne vulgaris. Acne is a very common medical condition and a majority of the world’s population has been affected by acne in their life. There are a variety of treatment options and skin care products used for acne. Despite acne being a common skin condition, recent estimates indicate that acne treatment products contributed a small amount to the overall sales of skin care products globally.  In 2019, the acne treatment market was valued at nearly 11 billion U.S. dollars, according to market research company NMSC. However, until 2030 it is expected to increase to over 15 billion U.S. dollars. Regarding the global skin care market in total, the United States and Japan have the highest shares. 

 

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LICH has been rocketing up the charts recently hitting a high of $0.0598 earlier in the week and retracing some before the weekend. The stock is getting noticed after the Company filed their annual report on Friday which confirmed that Vyome Therapeutics, Inc is the new controlling shareholder of the Company with 70.08% of the companies issued and outstanding shares. At the time of transfer, Venkat Nelabhotla, Chief Executive Officer and Director of Vyome Therapeutics, Inc., also became Chief Executive Officer and Director of Livechain, Inc. Reverse Merger stocks (RM) are easily among the most exciting and explosive stocks in small caps rivaling only biotech’s in their ability to make historic gains. LICH is the perfect merger candidate; a clean shell with virtually no debt and the new Company Vyome Therapeutics is a clinical-stage company developing locally-acting, next generation therapeutics for immuno-inflammatory diseases. Vyome’s lead clinical drug candidate, VB-1953, is a first-in-class, topical, bactericidal small molecule with a novel mechanism of action in acne. In 2019, the acne treatment market was valued at nearly 11 billion U.S. dollars, according to market research company NMSC. However, until 2030 it is expected to increase to over 15 billion U.S. dollars. Regarding the global skin care market in total, the United States and Japan have the highest shares. LICH is currently under heavy accumulation and is starting to get noticed by some heavy hitters in small caps who are looking for a break over $0.0598 for confirmation of the next leg up. A break over and its blue skies ahead. We will be updating on LICH when more details emerge so make sure you are subscribed to Microcapdaily so you know what’s going on with LICH.

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Disclosure: we hold no position in LICH either long or short and we have not been compensated for this article.

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Organogenesis (NASDAQ: ORGO): Latest Developments and Future Growth Prospects

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Organogenesis Holdings (NASDAQ: ORGO), a top regenerative medicine company dedicated to advanced wound care, surgical, and sports medicine solutions, gains over 30% during intraday trading and after hours combined after their latest release. According to the release, three Medicare Administrative Contractors (MACs) decided to withdraw certain coverage rules that were meant to start on October 1. These rules related to products for treating diabetic foot ulcers (DFU) and venous leg ulcers (VLU).

More Background:

Organogenesis serves a range of clients, from hospitals and wound care centers to doctors’ offices. The MACs’ initial rules, set on August 9, caused concern. They specified that covered products must be particular types of skin substitutes. Unfortunately, this excluded five products from Organogenesis, impacting their financial outlook.

Fast forward, the MACs pulled back these rules just in time, preventing potential harm to Organogenesis. Even before these rules, the company was facing challenges. In the second quarter, revenue was slightly down compared to the same period last year. Despite this, the company is doing better than the previous year in a six-month comparison.

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Gary S. Gillheeney, Sr., the head of Organogenesis, expressed deep gratitude for the MACs and the Centers for Medicare & Medicaid Services (CMS). He praised their thoughtful consideration of stakeholder concerns and putting patients first. This decision will positively affect the lives of many.

He also thanked the stakeholders, including doctors, patient advocacy groups, and various associations. Their unified support played a vital role in challenging these rules, considering the potential harm they could cause patients. Their advocacy shed light on the possible negative health outcomes and treatment disparities, especially for those with higher rates of diabetes and related conditions. Their collective efforts made a significant difference.

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Disclosure: We have not been compensated for this article/video. MicroCap Daily is not an investment advisor; this article/video does not provide investment advice. Always do your research, make your own investment decisions, or consult with your nearest financial advisor. This article/video is not a solicitation or recommendation to buy, sell, or hold securities. This article/video is our opinion, is meant for informational and educational purposes only, and does not provide investment advice. Past performance is not indicative of future performance.

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Vaccitech (NASDAQ: VACC) Gains Unprecedented Support—What’s Behind It?

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On September 25, 2023, Vaccitech (NASDAQ: VACC) experienced a jaw-dropping 90% surge in its stock price in just one day of trading. Now, this kind of jump usually happens when a company drops a major announcement or puts out a significant SEC filing. But, surprise, surprise—there was nothing of that sort this time .So naturally we did some digging, explored further online and guess what? Turns out retail traders were also not on a main reason for this rollercoaster ride. Curious to uncover what’s really behind this financial rollercoaster? Before we go any further, let’s get to know Vaccitech a bit better. There’s some pretty important aspects on the company you might like.

 

Background:

Vaccitech operates as a clinical-stage biopharmaceutical company, dedicated to discovering and developing innovative T cell immunotherapies. These therapies are crafted to leverage the immune system’s potency for treating conditions like chronic infectious diseases, cancer, and autoimmune disorders.

What sets Vaccitech apart is their distinctive, multi-platform approach, demonstrating the capacity to generate higher quantities of T cells compared to alternative technologies. This places Vaccitech in a unique position to cater to the needs of substantial, yet underserved patient populations. Their diverse clinical-stage pipeline includes potential treatments for severe diseases with limited available treatments, presenting significant public health risks.

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Among their lead product candidates are VTP-300, an immunotherapeutic designed to contribute to a potential functional cure for chronic hepatitis B viral (HBV) infection. Additionally, VTP-200 is a non-invasive, early-stage investigational treatment targeting persistent, high-risk human papillomavirus (HPV). VTP-850 stands out as a novel T cell investigational therapy aimed at prostate cancer, while VTP-1000, a preclinical T cell therapeutic candidate, focuses on reinstating immune tolerance in celiac disease.

Vaccitech possesses well-established expertise in drug development and scientific knowledge within the immunization realm. Notably, they co-developed a COVID-19 vaccine in collaboration with the University of Oxford. As many of you know, their vaccine has been successfully approved and holds an exclusive license worldwide with AstraZeneca.

What happened:

The one and only thing that happened today was Alliance Global Partners adding coverage of Vaccitech with a favourable buy recommendation.What’s truly eye-catching are the projections made, suggesting some pretty significant upside. The average one-year price target for Vaccitech is $12.24. Forecasts within this period have a bit of a spectrum, reaching from a low estimate of $7.07 to a high of $15.75. With that said, from today’s closing price that’s nearly 400% gain.

What’s The Big Deal?:

Alliance Global Partners giving the green light to cover Vaccitech is like a thumbs-up from a respected expert. It’s like a top-tier food critic saying, “This restaurant is a must-try.”

Think of it as Vaccitech stepping into the spotlight. It’s like a talented musician getting featured on a famous music blog—suddenly, more people start paying attention.

When a big player like Alliance Global Partners says, “Hey, this stock is a good buy,” it’s like a friend recommending a must-watch movie. You’re more likely to check it out based on that suggestion.

This kind of recommendation can also affect the stock price. It’s similar to when a popular influencer talks about a cool product—lots of people want to try it.

In a nutshell, this coverage is like a stamp of approval, making Vaccitech catch the attention of more potential investors and possibly giving the stock a boost. But it’s important to mention that just because a well established financial firm gives a price target, does not mean it’s accurate. In fact, tons of these projections are made daily with many being totally off the mark. Always do your own due diligence.

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Disclosure: We have not been compensated for this article/video. MicroCap Daily is not an investment advisor; this article/video does not provide investment advice. Always do your research, make your own investment decisions, or consult with your nearest financial advisor. This article/video is not a solicitation or recommendation to buy, sell, or hold securities. This article/video is our opinion, is meant for informational and educational purposes only, and does not provide investment advice. Past performance is not indicative of future performance.

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Advancing Medical Frontiers: Elutia Inc.’s(NASDAQ: ELUT) Strategic Vision in a $600 Million Market

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Elutia Inc (NASDAQ: ELUT) shares bolstered a whopping 33% today as the company recently shared that they’ve secured about $10.5 million in funding through a private investment round. If all the warrants are cashed in as part of this funding, the total could go up to $26.2 million.

Latest Changes:

Just last week, Aziyo Biologics changed its name to Elutia Inc. Following this change, Elutia made an announcement about selling its Orthobiologics business unit to Berkeley Biologics, a subsidiary of GNI Group Ltd. This move is set to bring in a substantial amount of cash, totalling up to $35 million for Elutia. This sum includes a notable upfront payment of $15 million, plus additional potential earnings of up to $20 million over five years. The deal is expected to be finalized in the fourth quarter of 2023.

This sale is a big step for Elutia, especially in the realm of drug-eluting biomatrix technology (DEB). Elutia is actively seeking approval from the FDA for their main product, CanGaroo RM. This product utilizes innovative biomatrix technology with antibiotics rifampin and minocycline (RM), providing long-term protection for cardiac pacemakers and defibrillators. This tackles a huge market estimated to be worth around 600 million. Elutia is aiming to introduce CanGaroo RM to the market in the first half of 2024.

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Standard Of Care:

Medtronic (NYSE: MDT) stands as the exclusive provider of the antibiotic envelope within the current market. This envelope is crafted using synthetic mesh infused with antibiotics. Back in 2014, Medtronic acquired this technology, making a strategic investment of up to $200 million. Primarily intended for Cardiac Implantable Electronic Device (CIED) revision procedures, this product boasts estimated annual sales in the range of $250 to $300 million.

However, despite its market presence and revenue generation, the Medtronic antibiotic envelope has notable limitations. While it effectively combats infections, its synthetic composition renders it less effective in supporting wound healing. Moreover, it poses challenges in accommodating larger devices like Subcutaneous Implantable Defibrillators (SCID).

Drug-eluting biomatrix (DEB):

Drug-eluting biomatrix (DEB) involves a specialized approach to drug delivery using a biomatrix as a carrier or platform. In simple terms, it’s a technique where a biomaterial matrix, often a biocompatible polymer or similar substance, is used to release drugs in a controlled and targeted manner.

The biomatrix acts as a support structure that can hold and gradually release drugs or therapeutic agents at a specific site in the body, typically over an extended period. This is particularly useful in medical applications where a localized and sustained delivery of medication is necessary.

For instance, in the context of Elutia’s CanGaroo RM, a biomatrix incorporating antibiotics rifampin and minocycline is used to provide prolonged protection for cardiac pacemakers and defibrillators. The biomatrix slowly releases these antibiotics at the surgical site, preventing infections and promoting healing.

DEB technology is gaining traction because it enhances treatment efficiency by ensuring the drug is delivered directly to the target area, minimizing side effects, and optimizing therapeutic outcomes. It’s a promising approach in the field of medical advancements, especially in areas like cardiology, oncology, and orthopedics.

Post-mastectomy Breast Reconstruction:

On top of this, the company also has plans to develop an RM version of its SimpliDerm biomatrix tailored for breast reconstruction procedures. The rate of infections after this surgery is quite high, more than 10%, highlighting a big medical need in a market valued at over $500 million. Elutia is stepping up to address this issue by developing SimpliDerm® RM, which incorporates their unique DEB technology. The funds raised through the private investment round (PIPE) and the sale of the Orthobiologics business unit will not only boost Elutia’s efforts in advancing their drug-eluting biomatrix products for the cardiac pacemaker and defibrillator market, but also for post-mastectomy breast reconstruction.

What’s next:

As mentioned earlier, their biomatrix platform serves two major markets. CanGaroo RM, their upcoming product, is slated for a 1H of 2024 market release and is poised to be a pioneer in a $600 million market. Furthermore, their SimpliDerm RM product utilizes the same proprietary antibiotic-eluting technology found in CanGaroo RM, which serves a 1.6B market according to their presentation deck. They aim to secure an IDE by Q4 2024, and upon achieving these milestones, they plan to venture into neurostimulator markets, particularly in pain management, to further drive their growth.

We will update you on ELUT when more details emerge, subscribe to Microcapdaily to follow along!

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Disclosure: We have not been compensated for this article/video. MicroCap Daily is not an investment advisor; this article/video does not provide investment advice. Always do your research, make your own investment decisions, or consult with your nearest financial advisor. This article/video is not a solicitation or recommendation to buy, sell, or hold securities. This article/video is our opinion, is meant for informational and educational purposes only, and does not provide investment advice. Past performance is not indicative of future performance.

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