Welcome to our dedicated page for Clearmind Medicine Common Shares news (Ticker: CMND), a resource for investors and traders seeking the latest updates and insights on Clearmind Medicine Common Shares stock.
Clearmind Medicine Inc. (NASDAQ: CMND, FSE: CWY0) is a clinical-stage psychedelic pharmaceutical biotech company dedicated to the discovery and development of innovative psychedelic-derived therapeutics. The company focuses on addressing widespread and under-treated health issues, particularly alcohol use disorder (AUD).
Currently, Clearmind's flagship compound, CMND-100, is in the spotlight. This MEAI-based (5-methoxy-2-aminoindane) formula has shown promising pre-clinical results in disrupting binge drinking behaviors without inducing hallucinations. The Israeli Ministry of Health has recently approved a Phase I/IIa clinical trial for CMND-100, marking a significant milestone in its development.
Clearmind's intellectual property portfolio is robust and growing, comprising eighteen patent families and 27 granted patents. Recent developments include nine new patent applications filed with the USPTO, highlighting compositions for treating alcohol use disorder, cocaine addiction, and obesity-related metabolic disorders. These efforts reflect the company's commitment to expanding and protecting its IP assets.
Collaborations play a crucial role in Clearmind's strategy. The company has entered exclusive licensing agreements with institutions such as the Hebrew University of Jerusalem, further enriching its portfolio with generation 3.0 psychedelic compounds aimed at treating addiction and mental health disorders. Additionally, Clearmind has initiated a groundbreaking partnership with Yissum Research Development Company for PTSD treatments.
Another key project is Clearmind's proprietary MEAI-based alcohol substitute beverage program. This ethanol-free alternative aligns with the growing global trend towards no- and low-alcohol consumption, offering a health-focused option for consumers.
Clearmind Medicine Inc. continues to execute its intellectual property and development strategies, positioning itself at the forefront of psychedelic-based medical treatments. The company’s shares are traded on Nasdaq under the symbol 'CMND' and on the Frankfurt Stock Exchange under 'CWY0'.
For more information, please visit their official website at www.clearmindmedicine.com or contact Investor Relations at invest@clearmindmedicine.com.
Clearmind Medicine Inc. (Nasdaq: CMND) has successfully manufactured batches of its MEAI-based molecule, CMND-100, for its first in-human clinical trial targeting Alcohol Use Disorder (AUD). This milestone indicates readiness to proceed with clinical testing. The drug was produced under Good Manufacturing Practices to meet FDA standards, aligning with the company's goal to develop psychedelic-derived therapeutics. Clearmind holds seven patent families and aims to expand its intellectual property portfolio as it advances its clinical program.
Clearmind Medicine Inc. (CMND) announced promising pre-clinical trial results for its drug candidate MEAI, aimed at treating obesity and metabolic syndrome. Conducted at the Hebrew University of Jerusalem, the trials demonstrated a 20% weight loss in rodents, improved insulin sensitivity, and reduced liver fat. MEAI treatment also decreased sucrose preference, indicating potential applications in addiction treatment. The global obesity drug market was valued at $1.9 billion in 2021, with further growth projected. Clearmind's progress underscores the drug's potential to address significant health issues.
Clearmind Medicine Inc. (NASDAQ:CMND) announces a new interview featuring CEO Dr. Adi Zuloff-Shani, discussing the company's innovative approach using non-hallucinogenic psychedelic compounds to address addiction and mental health issues. Clearmind's lead candidate, CMND-100, derived from MEAI, aims to treat alcohol use disorder and is set for clinical trials in early 2023. The company holds seven patent families and has received a patent for using MEAI as an alcohol substitute. The interview addresses the significant market need for effective treatments and outlines plans for an IND application to the FDA for clinical trials.
Clearmind Medicine Inc. (CMND) held its shareholder meeting on December 28, 2022, where all proposed matters were approved. This includes the company's rolling stock option plan and an increase in options and restricted share units available for issuance. Clearmind focuses on developing psychedelic-derived therapeutics for under-treated health issues, holding seven patent families and planning further acquisitions of intellectual property. The company aims to commercialize its products as regulated medicines, foods, or supplements.
Clearmind Medicine Inc. (CMND) announced its first first-in-human clinical trial in Israel for the MEAI-based CMND-100 compound targeting alcohol use disorder (AUD). The agreement with the IMCA center in Ramat Gan will be led by Prof. Mark Weiser. CMND plans to establish a similar agreement in the U.S.. AUD affects nearly 28 million adults in the U.S., with significant public health implications. The global AUD treatment market is projected to grow from $564 million in 2021, at an annual rate of 8.8% by 2032.
Clearmind Medicine has received a new patent from the U.S. Patent and Trademark Office for its proprietary MEAI as a substitute for alcoholic beverages. This patent complements similar patents granted in Europe and India, marking a significant milestone in a rapidly growing market for non-alcoholic options, valued at $395 million in the U.S. with a year-on-year growth of +20.6%. The company believes that this innovative compound can generate substantial revenue outside the pharmaceutical sector. The appointment of Nicholas Kadysh bolsters regulatory navigation for this product.
Clearmind Medicine Inc. (Nasdaq: CMND) updates shareholders on its progress towards FDA approval for its proprietary compound CMND-100, a treatment for Alcohol Use Disorder (AUD). The company has completed required non-clinical studies and is nearing its first human clinical trial. Clearmind is also exploring MEAI's potential for cocaine addiction and other mental health issues. The firm completed a $7.5 million U.S. IPO and uplisted to Nasdaq, enhancing its market presence. Future plans include advancing its IP portfolio and targeting new drug candidates for unmet medical needs.
Clearmind Medicine Inc. (CMND) has completed IND-enabling studies for its lead compound, CMND-100, targeting Alcohol Use Disorder (AUD). The company is preparing to submit an Investigational New Drug application to the FDA and the Israeli Ministry of Health, paving the way for its first human clinical trial. The compound is anticipated to significantly reduce alcohol consumption, addressing a critical global health issue that costs the U.S. $250 billion annually. Clearmind holds patents for CMND-100 in various regions, indicating strong intellectual property backing.
Clearmind Medicine (Nasdaq: CMND) has appointed Nicholas Kadysh, a former executive at Red Bull Canada and Juul Labs Canada, as a special advisor for the development of MEAI as an alcohol substitute. Kadysh brings extensive experience in regulatory issues, which is crucial as Clearmind conducts safety studies for its innovative drug candidate. The non-alcoholic beverage market is expanding, with U.S. sales growing by 21% over the past year, indicating a strong market opportunity for MEAI. Clearmind aims to develop MEAI as a therapeutic solution for addiction and an alternative to alcohol.
Clearmind Medicine Inc. (Nasdaq: CMND) has initiated the production of clinical batches for its psychedelic-derived drug candidate, CMND-100, aimed at treating Alcohol Use Disorder (AUD). The production follows successful synthesis development and complies with FDA GMP standards. This milestone supports their upcoming first-in-human clinical trial. Clearmind's non-clinical data suggests CMND-100 could address addiction challenges. The firm has also completed a pre-IND meeting with the FDA, indicating strong regulatory engagement.
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