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MyMD Pharmaceuticals, Inc. - MYMD STOCK NEWS

Welcome to our dedicated page for MyMD Pharmaceuticals news (Ticker: MYMD), a resource for investors and traders seeking the latest updates and insights on MyMD Pharmaceuticals stock.

MyMD Pharmaceuticals, Inc. (DE) (NASDAQ: MYMD) is a clinical-stage biopharmaceutical company that focuses on extending healthy lifespan through the development of innovative therapeutic platforms. The company is committed to addressing serious autoimmune and inflammatory diseases as well as age-related conditions.

Core Therapeutic Platforms:

  • MyMD-1: This is a small molecule drug platform that aims to regulate the immunometabolic system by controlling tumor necrosis factor-alpha (TNF-α) and other pro-inflammatory cytokines. MyMD-1 is being developed to treat autoimmune diseases such as multiple sclerosis, diabetes, rheumatoid arthritis, and inflammatory bowel disease. Additionally, it targets age-related illnesses, including frailty and sarcopenia. The drug’s oral administration is a significant advantage over existing TNF-α inhibitors, which require injectable forms.
  • Supera-CBD: This drug platform is based on a novel synthetic derivative of cannabidiol (CBD) that targets key receptors, including CB2 and opioid receptors, and inhibits monoamine oxidase. Supera-CBD is designed to cater to the rapidly expanding CBD market, addressing conditions such as epilepsy, pain, and anxiety/depression.

Recent Achievements and Current Projects:

MyMD Pharmaceuticals has made significant strides in its clinical trials, particularly with MyMD-1. In a recently completed phase 2 clinical trial, MyMD-1 successfully met its primary endpoints by reducing biomarkers common in chronic inflammatory diseases, such as TNF-α, IL-6, and sTNFR1. The drug also met all secondary endpoints related to safety and tolerability standards. Full study results are expected to be released in 2024.

The company has already submitted and received approval for three Investigational New Drug Applications for MyMD-1, which is now advancing in clinical programs for conditions like sarcopenia, rheumatoid arthritis, and Hashimoto's disease. With a unique oral dosing method, MyMD-1 offers a promising alternative to current TNF-α inhibitors, which typically require infusion or injection.

Partnerships and Future Outlook:

Through strategic partnerships and ongoing research, MyMD Pharmaceuticals aims to pioneer the development of therapies that not only manage symptoms but also extend the healthy lifespan of patients. With its robust pipeline and innovative approaches, MyMD Pharmaceuticals is well-positioned to make a significant impact in the field of autoimmune and age-related disease treatment.

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MyMD Pharmaceuticals has entered into a material transfer agreement with Bascom Palmer Eye Institute to explore the use of MYMD-1 in treating traumatic optic neuropathy (TON). TON affects vision due to optic nerve injury, occurring in 1.5% to 4% of head trauma cases. The study is fully funded by Bascom Palmer, ranked #1 eye hospital in the U.S. for 20 consecutive years. MyMD’s MYMD-1, originally developed for autoimmune diseases, is positioned as a potential treatment for various conditions due to its novel mechanism.

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MyMD Pharmaceuticals (NASDAQ: MYMD) announced progress in its Phase 2 clinical trial for MYMD-1, aimed at delaying aging and chronic inflammation in individuals over 65. All trial sites are now actively enrolling patients, with efficacy data anticipated in the second half of 2022. Previous Phase 1 results indicated a significant decrease in TNF-alpha levels in treated subjects. The aging treatment market is projected to exceed $600 billion by 2025, with no other FDA-approved drugs targeting aging disorders currently available.

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MyMD Pharmaceuticals aims to transform the $31 billion rheumatoid arthritis (RA) market with its drug candidate MYMD-1. New preclinical data indicates MYMD-1 exhibits a 30-70% greater anti-inflammatory effect than leading TNF-alpha inhibitors. The company plans to submit an Investigational New Drug (IND) application and protocols for a Phase 2 RA study in H2 2022. MYMD-1's advantages include smaller molecular size, selective TNF-alpha inhibition, minimal side effects, and ease of oral administration. The drug also targets other conditions like multiple sclerosis and diabetes.

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MyMD Pharmaceuticals has announced an acceleration in patient dosing for its Phase 2 clinical trial of MYMD-1, a potential therapy for aging-related conditions. The study involves participants aged 65 and older and aims to assess the drug's efficacy and safety. MYMD-1 selectively modulates the immune response to address chronic inflammation, a significant factor in aging. With no FDA-approved treatments for aging disorders, the market could exceed $600 billion by 2025. Initial results from the trial are expected in the first half of 2022.

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MyMD Pharmaceuticals, Inc. (Nasdaq: MYMD) announced that Dr. Adam Kaplin, Chief Scientific Officer, will appear on Cheddar News Network's "Cheddar Innovates" on March 24, 2022, at 11:50 AM ET. He will discuss the Company's Phase 2 clinical trial of MYMD-1, aimed at delaying aging and expanding healthspan, as well as insights into the projected $600 billion market. The episode will be available for replay on MyMD's website after airing.

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MyMD Pharmaceuticals has initiated patient enrollment in a Phase 2 clinical trial for MYMD-1, a drug aimed at delaying aging and enhancing healthy lifespan. The trial's primary goal is to lower inflammatory proteins TNF-α and IL-6. Following successful Phase 1 results showing significant TNF-α reduction, the company anticipates efficacy data in the first half of 2022. With a growing market for aging treatments projected at $600 billion by 2025, MyMD aims to capitalize on this opportunity while exploring MYMD-1's potential in treating autoimmune diseases.

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MyMD Pharmaceuticals announced positive results from a Phase 1 study of MYMD-1, demonstrating a statistically significant reduction in TNF-α levels, a key driver of aging, in healthy subjects. The study met its primary endpoints, confirming MYMD-1's efficacy. The FDA has approved TNF-α reduction as a primary endpoint for an upcoming Phase 2 trial, anticipated to start in the first half of 2022. With a growing market for aging therapies projected to exceed $600 billion by 2025, MYMD-1 may offer a distinct profile compared to existing TNF-α blockers.

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MyMD Pharmaceuticals (NASDAQ: MYMD) has expanded its intellectual property for MYMD-1, now covering three additional U.S. patents, bringing the total to 16. These patents protect MYMD-1's use in treating sarcopenia, a condition affecting 40% of the elderly, linked to severe health issues. The company is launching a Phase 2 trial for MYMD-1 targeting sarcopenia, with the U.S. market for aging-related disorders expected to exceed $600 billion by 2025. MyMD aims for MYMD-1 to become a leading drug in delaying aging and managing related diseases.

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MyMD Pharmaceuticals has announced that its investment company, Oravax Medical, signed a Cooperation and Purchase Agreement with Vietnam's Tan Thanh Holdings for an initial pre-order of 10 million doses of an oral COVID-19 vaccine currently under development. The deal also allows for significant follow-on orders. Oravax's vaccine targets less mutable proteins and has benefits in logistics due to simplified storage requirements. MyMD holds a 13% stake in Oravax, along with a 2.5% royalty on future net sales. This agreement may boost revenue potential for both companies in the ASEAN region.

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MyMD Pharmaceuticals (Nasdaq: MYMD) announced participation in two upcoming investor conferences in December 2021. At the Benchmark Company Discovery Conference on December 2 and the Benzinga Global Small Cap Conference on December 8-9, executives will discuss its drug candidates, MYMD-1 and Supera-CBD. MYMD-1 aims to slow aging and treat autoimmune conditions while Supera-CBD targets anxiety and neurodegeneration. Both drugs are positioned to tap significant market opportunities in their respective therapeutic areas.

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FAQ

What is the current stock price of MyMD Pharmaceuticals (MYMD)?

The current stock price of MyMD Pharmaceuticals (MYMD) is $1.82 as of July 23, 2024.

What is the market cap of MyMD Pharmaceuticals (MYMD)?

The market cap of MyMD Pharmaceuticals (MYMD) is approximately 4.3M.

What is MyMD Pharmaceuticals, Inc.?

MyMD Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company focused on extending healthy lifespan through the development of innovative therapeutic platforms for autoimmune and age-related diseases.

What are the main therapeutic platforms developed by MyMD Pharmaceuticals?

MyMD Pharmaceuticals is developing two main therapeutic platforms: MyMD-1, a small molecule drug for autoimmune and age-related diseases, and Supera-CBD, a synthetic derivative of CBD targeting various receptors and enzymes.

What is MyMD-1?

MyMD-1 is a drug platform that regulates the immunometabolic system to control TNF-α and other pro-inflammatory cytokines. It targets autoimmune diseases like multiple sclerosis and age-related conditions such as sarcopenia.

What is Supera-CBD?

Supera-CBD is a novel synthetic derivative of cannabidiol (CBD) developed by MyMD Pharmaceuticals. It targets key receptors, including CB2 and opioid receptors, and aims to treat conditions like epilepsy, pain, and anxiety/depression.

What recent achievements has MyMD Pharmaceuticals made?

MyMD Pharmaceuticals recently completed a phase 2 clinical trial for MyMD-1, meeting its primary and secondary endpoints for reducing biomarkers of chronic inflammatory diseases and demonstrating safety and tolerability.

What conditions is MyMD-1 being developed to treat?

MyMD-1 is being developed to treat autoimmune diseases such as multiple sclerosis, diabetes, rheumatoid arthritis, and inflammatory bowel disease, as well as age-related conditions like frailty and sarcopenia.

How is MyMD-1 administered?

MyMD-1 is administered orally, which is a significant advantage over existing TNF-α inhibitors that require injection or infusion.

What are the potential benefits of Supera-CBD?

Supera-CBD aims to cater to the expanding CBD market and address conditions such as epilepsy, pain, and anxiety/depression through its effects on various receptors and enzymes.

Has MyMD Pharmaceuticals received any regulatory approvals?

Yes, MyMD Pharmaceuticals has received approval for three Investigational New Drug Applications for MyMD-1, which is advancing in clinical programs for conditions like sarcopenia, rheumatoid arthritis, and Hashimoto's disease.

What is the future outlook for MyMD Pharmaceuticals?

With its innovative therapeutic platforms and ongoing clinical trials, MyMD Pharmaceuticals is well-positioned to make significant advancements in the treatment of autoimmune and age-related diseases, potentially extending healthy lifespans.

MyMD Pharmaceuticals, Inc.

Nasdaq:MYMD

MYMD Rankings

MYMD Stock Data

4.31M
2.37M
6.61%
6.62%
11.12%
Biotechnology
In Vitro & in Vivo Diagnostic Substances
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United States of America
BALTIMORE