Clearmind Medicine Reports Safety Results for CMND-100 Clinical Trial
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Feb 09 2026
0mins
Should l Buy CMND?
Clearmind Medicine announced additional safety topline results from the second cohort of its ongoing FDA-approved Phase I/IIa clinical trial evaluating CMND-100, the Company's proprietary non-hallucinogenic MEAI-based oral drug candidate, for the treatment of Alcohol Use Disorder. These further safety data points, emerging following the successful completion of treatment in another six patients of the second cohort, previously announced January 14, 2026, continue to strengthen the encouraging safety and tolerability profile previously established in the first cohort. The results reinforce no serious adverse events and overall good tolerability, consistent with the favorable results reported from the first cohort, support the rapid progression enabled by the Company's Data and Safety Monitoring Board's unanimous approval to advance for the second cohort. The Phase I/IIa clinical trial is a multinational, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of CMND-100 in patients with moderate to severe AUD. The second cohort, conducted across leading sites, including Johns Hopkins University, Tel Aviv Sourasky Medical Center, and Hadassah Medical Center, achieved full treatment completion shortly after DSMB clearance, underscoring continued confidence in CMND-100's safety profile as a potential innovative therapy for AUD.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy CMND?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
Analyst Views on CMND
About CMND
Clearmind Medicine Inc. is a psychedelic pharmaceutical biotech company. The Company is focused on the discovery and development of novel psychedelic-derived therapeutics to solve widespread and underserved health problems, including alcohol use disorders. The Company researches and develops psychedelic-based compounds and attempts to commercialize them as regulated medicines, foods, or supplements. The Company’s intellectual portfolio consists of 19 patent families including 31 granted patents.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
Clearmind's MEAI Drug Breakthrough in Obesity Treatment
- Therapeutic Progress: Clearmind Medicine's MEAI drug has made significant strides in obesity treatment, with preclinical studies indicating a potential 20% weight reduction while prioritizing muscle preservation, showcasing its promise as a next-generation neuroplastogen that could transform obesity management.
- Innovative Mechanism: MEAI targets the brain's monoaminergic system to modulate reward and addiction pathways, addressing psychological roots of obesity such as compulsive eating and emotional overeating, potentially offering a more holistic treatment approach compared to traditional GLP-1 drugs, thereby enhancing long-term patient adherence.
- Market Potential: According to Goldman Sachs, the obesity market is projected to exceed $100 billion in the coming years, positioning Clearmind to potentially lead the next era of weight loss therapeutics if MEAI fulfills its promise, addressing the urgent global demand for effective weight loss solutions.
- Strategic Partnerships and Patents: Clearmind has recently filed new patent applications targeting obesity and metabolic disorders, collaborated with Polyrizon to develop an intranasal formulation for improved delivery, and is advancing its FDA-approved Phase I/IIa trial for alcohol use disorder, demonstrating its ongoing commitment to innovative drug development.
See More
Clearmind's MEAI Drug Breakthrough in Obesity Treatment
- Therapeutic Progress: Clearmind Medicine's MEAI drug has demonstrated approximately 20% weight reduction in preclinical studies while preserving lean mass, indicating its potential to provide a more effective alternative in obesity treatment, which is crucial in a multi-billion dollar market.
- Innovative Mechanism: MEAI targets the brain's monoaminergic system to disrupt rigid behavioral patterns and promote cognitive flexibility, potentially addressing psychological factors like binge eating and emotional overeating, thus offering a more holistic treatment approach for obesity.
- Market Potential: Goldman Sachs projects the obesity market to exceed $100 billion in the coming years, positioning Clearmind to potentially lead the next generation of weight loss therapeutics if MEAI fulfills its promise, thereby driving long-term growth for the company.
- Strategic Partnerships: Clearmind's collaboration with Polyrizon to develop an intranasal formulation aims to enhance MEAI's delivery, while its FDA-approved Phase I/IIa trial progresses smoothly, reflecting the company's ongoing advancements in obesity and metabolic disorders.
See More
Clearmind Medicine Reports Positive Clinical Trial Results
- Clinical Trial Progress: Clearmind Medicine Inc. announced additional positive safety topline results from the second cohort of its FDA-approved Phase I/IIa clinical trial for CMND-100, reinforcing the encouraging safety and tolerability profile established in the first cohort, indicating the drug's potential in treating Alcohol Use Disorder.
- Therapeutic Potential: CMND-100 is viewed as a potentially safe, non-hallucinogenic treatment that does not require adjunct psychotherapy, aiming to address significant unmet needs in the Alcohol Use Disorder space, potentially offering new options for patients.
- Market Reaction: In pre-market trading, CMND shares are priced at $1.36, up 0.76% from the previous trading day, reflecting market recognition of the company's positive clinical results, which may attract more investor interest.
- Future Plans: Backed by these positive clinical results, Clearmind Medicine plans to gather further evidence to support the safety and efficacy of CMND-100, thereby advancing its application in the treatment of Alcohol Use Disorder.
See More
Clearmind Reports Positive Safety Results for AUD Drug in Phase I/IIa Trial
- Clinical Trial Progress: Clearmind Medicine has completed treatment for six patients in the second cohort of its FDA-approved CMND-100 trial, further confirming the drug's safety and tolerability with no serious adverse events, indicating its potential as a treatment for Alcohol Use Disorder (AUD).
- Multicenter Study: The trial is conducted at leading institutions such as Johns Hopkins University and Tel Aviv Sourasky Medical Center, emphasizing CMND-100's global research capabilities and enhancing the company's competitiveness in the psychedelic pharmaceutical sector.
- Support from Data Monitoring Board: The unanimous approval from the Data and Safety Monitoring Board (DSMB) to advance the second cohort reflects confidence in CMND-100's safety and efficacy, potentially accelerating the progression to subsequent clinical phases.
- Intellectual Property Strategy: Clearmind currently holds 19 patent families and 31 granted patents, with plans to seek additional patents as needed, demonstrating the company's long-term strategic positioning and market competitiveness in psychedelic drug development.
See More
Cannabis Sector Update: Aurora's Strategic Shift Amid Record Medical Sales
- Aurora Financial Performance: Aurora Cannabis reported net revenue of $94.2 million for Q3 2026, a 7% year-over-year increase, with global medical cannabis sales reaching $76.2 million, accounting for over 80% of total sales, indicating strong growth potential in the high-margin medical market.
- Strategic Transformation Plan: Aurora announced plans to gradually exit select Canadian consumer cannabis markets to reduce sales and marketing costs, which is expected to significantly improve overall profit margins in the coming quarters.
- Canopy Growth Results: Canopy Growth reported net revenue of $90.4 million for Q3 2026, with a nearly 50% reduction in net loss despite weak international performance, reflecting positive progress in cost control and market integration.
- Cronos Brand Expansion: Cronos Group launched its premium Lord Jones brand in Israel, marking a significant step in its global expansion strategy aimed at meeting local market demands with high-quality products while enhancing brand recognition in international markets.
See More
Clearmind Regains Nasdaq Compliance with Share Price Above $1
- Compliance Restoration: Clearmind Medicine confirmed on December 30, 2025, that its common shares have maintained a closing price above $1 for the last 10 consecutive trading days, successfully regaining compliance with Nasdaq Listing Rule 5550(a)(2), indicating positive progress in stock price stability.
- Price Volatility Context: Previously, Clearmind was notified on December 4, 2025, of non-compliance due to its share price being below $1 for over 30 consecutive trading days, and this compliance restoration is expected to enhance investor confidence and attract more capital inflow.
- Market Reaction Expectations: With the restoration of compliance, Clearmind is likely to improve its market image and bolster investor confidence in its future growth potential, particularly in light of its commitment to developing novel psychedelic treatment solutions.
- Strategic Development Focus: Clearmind is currently focused on developing neuroplastic drugs targeting under-treated health issues and will continue to seek patent protection to enhance its intellectual property portfolio, further strengthening its competitiveness in the biotech sector.
See More
Clearmind's MEAI Drug Breakthrough in Obesity Treatment
- Therapeutic Progress: Clearmind Medicine's MEAI drug has made significant strides in obesity treatment, with preclinical studies indicating a potential 20% weight reduction while prioritizing muscle preservation, showcasing its promise as a next-generation neuroplastogen that could transform obesity management.
- Innovative Mechanism: MEAI targets the brain's monoaminergic system to modulate reward and addiction pathways, addressing psychological roots of obesity such as compulsive eating and emotional overeating, potentially offering a more holistic treatment approach compared to traditional GLP-1 drugs, thereby enhancing long-term patient adherence.
- Market Potential: According to Goldman Sachs, the obesity market is projected to exceed $100 billion in the coming years, positioning Clearmind to potentially lead the next era of weight loss therapeutics if MEAI fulfills its promise, addressing the urgent global demand for effective weight loss solutions.
- Strategic Partnerships and Patents: Clearmind has recently filed new patent applications targeting obesity and metabolic disorders, collaborated with Polyrizon to develop an intranasal formulation for improved delivery, and is advancing its FDA-approved Phase I/IIa trial for alcohol use disorder, demonstrating its ongoing commitment to innovative drug development.
See More
Clearmind's MEAI Drug Breakthrough in Obesity Treatment
- Therapeutic Progress: Clearmind Medicine's MEAI drug has demonstrated approximately 20% weight reduction in preclinical studies while preserving lean mass, indicating its potential to provide a more effective alternative in obesity treatment, which is crucial in a multi-billion dollar market.
- Innovative Mechanism: MEAI targets the brain's monoaminergic system to disrupt rigid behavioral patterns and promote cognitive flexibility, potentially addressing psychological factors like binge eating and emotional overeating, thus offering a more holistic treatment approach for obesity.
- Market Potential: Goldman Sachs projects the obesity market to exceed $100 billion in the coming years, positioning Clearmind to potentially lead the next generation of weight loss therapeutics if MEAI fulfills its promise, thereby driving long-term growth for the company.
- Strategic Partnerships: Clearmind's collaboration with Polyrizon to develop an intranasal formulation aims to enhance MEAI's delivery, while its FDA-approved Phase I/IIa trial progresses smoothly, reflecting the company's ongoing advancements in obesity and metabolic disorders.
See More
Clearmind Medicine Reports Positive Clinical Trial Results
- Clinical Trial Progress: Clearmind Medicine Inc. announced additional positive safety topline results from the second cohort of its FDA-approved Phase I/IIa clinical trial for CMND-100, reinforcing the encouraging safety and tolerability profile established in the first cohort, indicating the drug's potential in treating Alcohol Use Disorder.
- Therapeutic Potential: CMND-100 is viewed as a potentially safe, non-hallucinogenic treatment that does not require adjunct psychotherapy, aiming to address significant unmet needs in the Alcohol Use Disorder space, potentially offering new options for patients.
- Market Reaction: In pre-market trading, CMND shares are priced at $1.36, up 0.76% from the previous trading day, reflecting market recognition of the company's positive clinical results, which may attract more investor interest.
- Future Plans: Backed by these positive clinical results, Clearmind Medicine plans to gather further evidence to support the safety and efficacy of CMND-100, thereby advancing its application in the treatment of Alcohol Use Disorder.
See More
Clearmind Reports Positive Safety Results for AUD Drug in Phase I/IIa Trial
- Clinical Trial Progress: Clearmind Medicine has completed treatment for six patients in the second cohort of its FDA-approved CMND-100 trial, further confirming the drug's safety and tolerability with no serious adverse events, indicating its potential as a treatment for Alcohol Use Disorder (AUD).
- Multicenter Study: The trial is conducted at leading institutions such as Johns Hopkins University and Tel Aviv Sourasky Medical Center, emphasizing CMND-100's global research capabilities and enhancing the company's competitiveness in the psychedelic pharmaceutical sector.
- Support from Data Monitoring Board: The unanimous approval from the Data and Safety Monitoring Board (DSMB) to advance the second cohort reflects confidence in CMND-100's safety and efficacy, potentially accelerating the progression to subsequent clinical phases.
- Intellectual Property Strategy: Clearmind currently holds 19 patent families and 31 granted patents, with plans to seek additional patents as needed, demonstrating the company's long-term strategic positioning and market competitiveness in psychedelic drug development.
See More
Cannabis Sector Update: Aurora's Strategic Shift Amid Record Medical Sales
- Aurora Financial Performance: Aurora Cannabis reported net revenue of $94.2 million for Q3 2026, a 7% year-over-year increase, with global medical cannabis sales reaching $76.2 million, accounting for over 80% of total sales, indicating strong growth potential in the high-margin medical market.
- Strategic Transformation Plan: Aurora announced plans to gradually exit select Canadian consumer cannabis markets to reduce sales and marketing costs, which is expected to significantly improve overall profit margins in the coming quarters.
- Canopy Growth Results: Canopy Growth reported net revenue of $90.4 million for Q3 2026, with a nearly 50% reduction in net loss despite weak international performance, reflecting positive progress in cost control and market integration.
- Cronos Brand Expansion: Cronos Group launched its premium Lord Jones brand in Israel, marking a significant step in its global expansion strategy aimed at meeting local market demands with high-quality products while enhancing brand recognition in international markets.
See More
Clearmind Regains Nasdaq Compliance with Share Price Above $1
- Compliance Restoration: Clearmind Medicine confirmed on December 30, 2025, that its common shares have maintained a closing price above $1 for the last 10 consecutive trading days, successfully regaining compliance with Nasdaq Listing Rule 5550(a)(2), indicating positive progress in stock price stability.
- Price Volatility Context: Previously, Clearmind was notified on December 4, 2025, of non-compliance due to its share price being below $1 for over 30 consecutive trading days, and this compliance restoration is expected to enhance investor confidence and attract more capital inflow.
- Market Reaction Expectations: With the restoration of compliance, Clearmind is likely to improve its market image and bolster investor confidence in its future growth potential, particularly in light of its commitment to developing novel psychedelic treatment solutions.
- Strategic Development Focus: Clearmind is currently focused on developing neuroplastic drugs targeting under-treated health issues and will continue to seek patent protection to enhance its intellectual property portfolio, further strengthening its competitiveness in the biotech sector.
See More
