Clearmind Medicine Inc.

Clearmind Medicine Inc.

NNASDAQ:CMND
6.00
USD
+0.06
(+1.01%)
-14.88EPS
20.08MMarket Cap
2017 Y
2018 Y
2019 Y
2020 Y
2021 Y
2022 Y
2023 Y
2024 Y
2025 Y
TTM
Revenue per Share
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Basic EPS, GAAP
- -
-9.14
-4.93
-10.89
-21,151.58
-63,255.67
-4,094.03
-678.02
-303.48
-14.88
Free Cash Flow per Basic Share
- -
-11.12
-3.42
-7.24
-17,435.43
-34,220.71
-2,992.57
-626.92
-372.53
-14.03
Dividend per Share
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Book Value per Share
3.11
11.23
6.26
13.17
30,072.12
-10,146.77
467.05
291.46
75.45
8.72
Tangible Book Value per Share
3.11
11.23
6.26
13.17
28,831.87
-11,341.85
410.39
281.3
69.29
8.66
Basic Weighted Avg Shares
- -
- -
- -
- -
- -
- -
- -
- -
- -
1
Sales/Revenue/Turnover
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Operating Margin (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Depreciation Expense
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Net Income, GAAP
- -
- -
- -
- -
-2
-7
-6
-5
-4
-7
Effective Tax Rate (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Profit Margin (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Working Capital
- -
- -
- -
- -
3
-1
1
3
1
13
LT Debt
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Total Equity
- -
- -
- -
- -
3
-1
1
3
1
13
Return on Invested Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Return on Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Return on Common Equity (%)
- -
-127.48
-56.32
-129.78
-129.07
- -
- -
-275.36
-179.39
-106.98

Capital Structure

USD

•

in mil. unless spec.
Jan'26
Apr'26
Jul'26
ST Debt
- -
- -
2
LT Borrowings
- -
- -
- -
LT Finance Leases
- -
- -
- -
Preferred Equity and Hybrid Capital
- -
- -
- -
Shares Outstanding
- -
1
1
Market Capitalization
26
58
20

Working Capital

USD

•

in mil. unless spec.
Jan'26
Apr'26
Jul'26
Total Current Assets
11
14
17
Cash, Cash Equivalents & STI
10
14
16
Accounts Receivable, Net
- -
- -
- -
Inventories
- -
- -
- -
Total Current Liabilities
3
3
4
Payables & Accruals
1
1
1
ST Debt
- -
- -
2
Deferred Revenue
- -
- -
- -

Growth Rates

USD

•

in mil. unless spec.

(avg. rate of change)

10 years
5 years
1 year
Total Equity
- -
197.83%
-61.62%
Free Cash Flow
- -
240.95%
-2.56%
Net Income, GAAP
- -
201.45%
-26.6%
Sales/Revenue/Turnover
- -
- -
- -
Total Cash Common Dividend
- -
- -
- -

Quarterly Revenue

USD

•

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Quarterly Earnings Per Share

USD

•

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
-360.61
-111.67
-235.3
-82.97
-678.02
2025
-95.5
-62.27
-96.72
-47.62
-303.48
2026
-33.17
-6.78
-0.57
- -
- -

Quarterly Dividends Per Share

USD

•

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Company Description

CEO
Adi Zuloff-Shani
Full Time Employees
4
Sector
Non-energy minerals
Industry
Other metals/Minerals
Address
1220 West 6th Avenue Vancouver BC Canada V6H 1A5
IPO Date
Nov 15, 2022
Business
Clearmind Medicine Inc. is a clinical-stage pharmaceutical company that develops novel psychedelic-derived medicines aimed at treating widespread and under-served health problems. The company’s core product offerings include psychedelic-based therapeutics targeting alcohol use disorders, binge drinking, eating disorders, weight loss, obesity, metabolic syndrome, anxiety disorders, post-traumatic stress disorder, depression, and treatment-resistant depression. Its key products under development are the MEAI compound for treating alcohol use disorder, obesity, and metabolic disorders, including an alcohol substitute consumer product, and CM-CMND-001, currently in Phase I/IIa clinical trials for alcohol use disorder treatment. The company also explores combination treatments for obesity and metabolic syndrome through collaborations. Recent major changes include a strategic partnership with Dr. Glitter Pty Ltd to co-develop and commercialize an MEAI-based alcohol substitute using Dr. Glitter’s ActivCrystal™ technology, an innovative oral delivery format that enables flexible consumption by sprinkling the product onto food or beverages. This partnership aims to provide a safer alternative to traditional alcohol consumption, addressing alcohol misuse and related health risks. Additionally, Clearmind obtained final regulatory approval from Hadassah Medical Center in Jerusalem to expand its Phase 1/2a clinical trial for CMND-100, furthering its multinational studies that include leading medical centers such as Yale and Johns Hopkins. The company has also engaged JS First Sdn. Bhd to source global manufacturers and distributors, supporting its international expansion plans. Furthermore, Clearmind secured $10 million in a securities purchase agreement to advance strategic opportunities and has recently filed for patents related to novel non-hallucinogenic neuroplastogen treatments for depression. Operating primarily in the biotechnology and healthcare sectors, Clearmind Medicine targets mental health and metabolic disease markets worldwide. Founded in 2017, the company is headquartered in Vancouver, Canada. It maintains a collaborative research relationship with Yissum Research Development Company of the Hebrew University of Jerusalem for developing and commercializing compounds for PTSD and other conditions. The company was formerly known as Cyntar Ventures Inc. until its name change to Clearmind Medicine Inc. in March 2021. Clearmind’s broad clinical pipeline and strategic alliances position it as an innovator in psychedelic medicine development with a focus on transforming treatment options for alcohol-related and mental health disorders.

Company News

  • Clearmind: Charging Robotics Launches Next-Generation Automated EV-Charging Technology for Robotaxis and Autonomous Fleets

  • Clearmind Announces Patent Publication in Japan Covering Treatment for Neurological Movement Disorder

  • Clearmind Advances Dialogue with U.S. Federal Government on Psychedelic Therapies, Submitting Recommendations to FDA

  • NeuroThera Highlights Enhancement of U.S. Patent Portfolio Through Collaboration with Clearmind Covering LSD, Ketamine and Ibogaine Combinations

  • Clearmind Enhances U.S. IP Presence with Publication of Three Patent Applications Covering LSD, Ketamine and Ibogaine Combinations

  • Stickit Technologies Announces Corporate Update: Leadership Appointments, Capital Restructuring & Loan Acquisition, And Update Of Intellectual Property Portfolio

  • Clearmind Medicine Delivers Briefing to FDA Following Invitation to Historic Psychedelic Hearing in Washington, D.C.

  • Clearmind Enrolls First Patients with Alcohol Use Disorder in CMND-100 Clinical Trial

  • Clearmind Medicine Receives Yale IRB Approval, Enabling Patient Recruitment for Parts B and C of CMND-100 Phase I/II Trial, Following Positive Safety Results

  • Clearmind Medicine Stock Slides Friday: What's Happening?

  • Clearmind Medicine Signs Definitive Agreement to Acquire 51% Stake in Wireless Charging Company for Automated Parking and Robotaxis

  • Clearmind Reaches Key Milestone: CMND-100 Phase IIa now Underway for Alcohol Use Disorder Trial, One-Third of Part C Enrolled

  • Clearmind Advances MDMA-N-acylethanolamines IP for the Treatment of PTSD Amid Rising U.S. Federal Support for Psychedelic Innovation

  • NeuroThera-Clearmind Collaboration Advances MDMA-N-acylethanolamines IP for the Treatment of PTSD Amid Rising U.S. Federal Support for Psychedelic Innovation

  • Clearmind Medicine Makes Clinical Progress in Alcohol Addiction Treatment Trial

  • Clearmind Advances CMND-100 to Alcohol Use Disorder Patients After Achieving Primary Safety Endpoint

  • Clearmind Medicine Announces Positive Permeation Results for Intranasal MEAI Formulation, Supporting Enhanced Nasal Retention Without Compromising Drug Delivery

  • Clearmind Reaches Key Clinical Trial Milestone as DSMB Unanimously Clears Progression in AUD Study

  • Clearmind Medicine Signs Letter of Intent to Acquire 51% Majority Stake in EV Wireless Charging Solutions for Automated Parking Systems Company

  • Clearmind Announces Positive Safety Findings for CMND 100, Demonstrating Consistent Tolerability Throughout Full Dose Escalation in Part A of its FDA-Regulated Clinical Trial