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MiNK Therapeutics’ (NASDAQ: INKT) Breakthrough Treatment: Unveiling the Potential of agenT-797 for Immunocology

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MiNK Therapeutics, Inc. (NASDAQ: INKT) experienced a significant surge in its stock shares, soaring by an additional 22% on June 22, 2023. Although there was no specific press release or news filing directly responsible for this recent gain, it appears that the company’s growing success is attracting heightened investor attention. MiNK Therapeutics’ positive clinical data on their leading asset, allo-iNKTs (agenT-797), in the context of COVID-19 associated Acute Respiratory Distress Syndrome (CARDS), seems to be a contributing factor to this increased investor interest.

Patients with severe respiratory distress who were treated with agenT-797 had a 5% chance of survival, which is quite low. However, the treatment showed some positive outcomes. It improved lung function, significantly reduced inflammation, and helped prevent secondary infections.

“The encouraging activity, tolerability, and ease of administration seen with allogeneic iNKT cells in patients with CARDS suggests the important role that cellular based therapies could play in infectious, inflammatory diseases, and autoimmunity,” said Dr. Terese C. Hammond, Medical Director, Providence Saint John’s Health Center and Sound Physicians. “Addressing immune system dysfunction is essential to improving outcomes in critical illness. I believe these results illuminate how novel immune cell interventions can have an impactful role in treating acute critical illness.”

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Delving Deeper: Insights into the agenT-797 clinical trial:

The clinical trial involved 20 patients with moderate to severe ARDS, including 4patients who received venovenous extracorporeal membrane oxygenation (VV ECMO) therapy. These patients were given a single dose of agenT-797. The results showed a significant survival benefit and manageable safety profile, including the following findings:

  • Patients on VV ECMO who received agenT-797 had a 75% survival rate at 90 days, compared to only 30% survival among the control group treated in the hospital.
  • The administration of agenT-797 at a dosage of 1 billion cells was well-tolerated and did not lead to oxygenation failure or other major adverse events like cytokine release syndrome (CRS).
  • A patient on VV ECMO support showed improved lung function (according to radiologic measurements) and significant anti-inflammatory changes within 24 hours after receiving agenT-797.
  • Overall, the study indicated a reduction in secondary infections with agenT-797, including an impressive over 80% decrease in pneumonia cases in the group receiving a dose of 1 billion cells. In one patient on VV ECMO, bacterial pneumonia cleared 12 days after receiving agenT-797.

 

https://twitter.com/BioStockAnalyst/status/1672001843545755655?s=20

 

These findings underscore the value of cellular-based therapies, particularly allogeneic invariant natural killer T (iNKT) cell therapies, in addressing immune system dysfunction in infectious and inflammatory diseases. Notably, patients on venovenous extracorporeal membrane oxygenation (VV ECMO) therapy showed a remarkable 75% survival rate at 90 days with agenT-797 treatment, compared to the control group. 

The treatment exhibited a manageable safety profile without significant adverse events, such as oxygenation failure or cytokine release syndrome (CRS). Moreover, agenT-797 induced rapid anti-inflammatory changes and improved lung function within 24 hours of administration, particularly in patients receiving VV ECMO support. 

Additionally, there was a substantial reduction in secondary infections, including an impressive over 80% decrease in pneumonia cases among those receiving a specific dosage. These findings provide valuable insights into the potential of agenT-797 as a therapeutic option for COVID-19 associated ARDS, furthering the development of immune cell interventions to improve critical illness outcomes and advance immune-mediated disease treatments.

https://twitter.com/CapitalJc/status/1669428813745344542?s=20

 

Key Players Utilizing The Potential of Invariant Natural Killer T (iNKT) Cells:

Allogeneic invariant natural killer T (iNKT) cells are a specialized subset of immune cells that hold great promise in the field of immunotherapy. These unique cells play a crucial role in regulating the immune system by swiftly responding to various infections and diseases. What sets iNKT cells apart is their ability to recognize specific molecules known as lipid antigens, which they detect through a receptor called the T-cell receptor (TCR). This distinctive feature allows iNKT cells to mount rapid and targeted immune responses.

The potential of iNKT cells in immunotherapy has captured the attention of several large pharmaceutical companies, recognizing the therapeutic opportunities they present. One notable example is Bristol Myers Squibb (BMS), a leading pharmaceutical company that has made significant investments in the development of iNKT cell therapies. BMS has been actively involved in research collaborations to explore the therapeutic applications of iNKT cells, with a particular focus on cancer treatment. Their aim is to leverage the unique immunomodulatory properties of iNKT cells to enhance the body’s natural anti-tumor responses and improve patient outcomes.

Juno Therapeutics, a subsidiary of Bristol Myers Squibb, is another pharmaceutical company at the forefront of utilizing iNKT cells. Juno Therapeutics specializes in developing innovative immunotherapies, including chimeric antigen receptor (CAR) T-cell therapies. They are actively investigating the potential of incorporating iNKT cells into CAR-T therapies to enhance their effectiveness and broaden their applicability in treating various diseases. By combining the unique capabilities of iNKT cells with the precision targeting of CAR-T cell therapies, Juno Therapeutics aims to create powerful and tailored treatment options for patients.

The efforts of these pharmaceutical companies, among others, demonstrate the growing recognition of the therapeutic potential of iNKT cells. By harnessing the unique properties of these cells, they seek to advance the field of immunotherapy and improve patient outcomes in a wide range of diseases, particularly in the realm of cancer treatment. Through ongoing research and development, these companies are paving the way for the future application of iNKT cell-based therapies in clinical practice.

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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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BioPharma

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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BioPharma

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.

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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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