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MIRA Pharmaceuticals Reports Mira-55 Shows No THC- or Rimonabant-Associated CNS Side Effects in Preclinical Studies

(Positive)
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MIRA (NASDAQ:MIRA) reported preclinical data showing Mira-55 produced morphine-comparable analgesia in a validated inflammatory pain model and did not produce THC- or rimonabant-like CNS side effects across behavioral assays at oral doses up to 100 mg/kg.

Findings support advancement toward IND-enabling studies for inflammatory pain and show a dose-dependent increase in open-arm time on the Elevated Plus Maze, without sedation, catalepsy, or motor impairment.

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Positive

  • Morphine-comparable analgesia in inflammatory pain model
  • No THC-like CNS side effects at tested doses up to 100 mg/kg
  • Dose-dependent anxiolytic signal (increased EPM open-arm time)
  • Data supports advancement toward IND-enabling studies for inflammatory pain

Negative

  • Data limited to preclinical models; human safety and efficacy unproven
  • IND submission and clinical development timelines not yet specified

News Market Reaction – MIRA

+22.28%
18 alerts
+22.28% Session close to close
+17.5% Peak in 2 hr 14 min
$48.14M Market Cap
1.2x Rel. Volume

In the Mar 23 session, MIRA gained 22.28%, reflecting a significant positive market reaction. Argus tracked a peak move of +17.5% during that session. Our momentum scanner triggered 18 alerts that day, indicating notable trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock surged +22.3% in the session following this news. A strong positive reaction aligns with M...
Analysis

The stock surged +22.3% in the session following this news. A strong positive reaction aligns with Mira-55’s expanding preclinical profile, now combining inflammatory pain efficacy with an absence of THC- or rimonabant-like CNS side effects. Past Mira-55 data in October 2025 drove a 36.36% gain, suggesting this program has been a key equity driver. Investors would still need to weigh financing history and at-the-market usage when assessing durability of any future upside.

Key Figures

Mira-55 dose: 10 mg/kg Mira-55 dose: 30 mg/kg Mira-55 dose: 100 mg/kg +5 more
8 metrics
Mira-55 dose 10 mg/kg Preclinical CNS safety and behavioral assays
Mira-55 dose 30 mg/kg Preclinical CNS safety and behavioral assays
Mira-55 dose 100 mg/kg Preclinical CNS safety and behavioral assays
Non-opioid pain market 2024 $45.3 billion Global non-opioid pain treatment market (Grand View Research 2024)
Non-opioid pain market 2030 $70.3 billion Projected global non-opioid pain market by 2030
Market CAGR 7.7% Projected 2024–2030 CAGR for non-opioid pain market
Price change -9.8% Move from prior close ahead of/around this article
Relative volume 2.68x Today’s volume vs 20-day average

Historical Context

5 past events · Latest: Mar 04 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Mar 04 Ketamir-2 Phase 1 complete Positive -1.6% Completed Phase 1 dosing of Ketamir-2 with clean safety in 56 volunteers.
Feb 03 Ketamir-2 Phase 1 update Positive -1.6% Initiated final MAD cohort for Ketamir-2 and outlined Phase 2a timing.
Oct 24 Ketamir-2 MAD start Positive -3.2% Started MAD Phase 1 trial for Ketamir-2 with encouraging preclinical efficacy data.
Oct 16 Mira-55 preclinical data Positive +36.4% Oral Mira-55 outperformed injected morphine in inflammatory pain and swelling.
Sep 30 SKNY acquisition Positive +2.3% Closed SKNY deal, adding SKNY-1 for obesity and nicotine addiction and securities.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

MIRA’s stock has often traded lower on positive clinical updates, with stronger upside historically tied to Mira-55 data and strategic transactions.

Recent Company History

Recent news flow highlights steady clinical and pipeline progress. Multiple positive Ketamir-2 Phase 1 updates in October 2025, February 2026, and March 2026 all saw modest share price declines over the following 24 hours. In contrast, Mira-55’s strong preclinical inflammatory pain data on October 16, 2025 produced a 36.36% gain, and the SKNY acquisition on September 30, 2025 added 2.26%. Today’s Mira-55 CNS safety data fits the pattern of program differentiation amid a volatile share base.

Key Terms

Δ9-tetrahydrocannabinol (THC), CB1 receptor antagonist, central nervous system (CNS), Investigational New Drug (IND), +3 more
7 terms
Δ9-tetrahydrocannabinol (THC) medical
"differentiated from both Δ9-tetrahydrocannabinol (THC), the primary psychoactive component"
δ9-tetrahydrocannabinol (THC) is the primary psychoactive compound in cannabis that produces the “high” and many of the plant’s effects on mood, perception and appetite. Investors care because THC levels and legal status drive product demand, regulatory limits, labeling, clinical use and safety rules—similar to how alcohol content and laws shape the beer market—affecting sales, licensing, and risk for companies in cannabis, pharmaceutical and consumer goods sectors.
CB1 receptor antagonist medical
"differentiated from both Δ9-tetrahydrocannabinol (THC)... and the CB1 receptor antagonist rimonabant"
A CB1 receptor antagonist is a type of drug that blocks the brain’s CB1 “lock” used by natural or plant-derived cannabis-like chemicals, preventing those signals from taking effect. Think of it as putting a stopper in a pipe so the flow that drives appetite, mood and metabolism is reduced; that can shrink appetite or change metabolism but also carries risks to mood and behavior. Investors watch these drugs because they can create large markets for obesity, metabolic or addiction treatments, yet face safety concerns and strict regulatory review that affect commercial value.
central nervous system (CNS) medical
"did not produce cannabinoid-like central nervous system (CNS) side effects"
The central nervous system (CNS) is the part of the body that includes the brain and spinal cord, acting as the control center for processing information and directing actions. It is essential for coordinating all bodily functions, from movement to thinking. For investors, understanding the CNS is important because it illustrates how complex systems—like markets or organizations—rely on core components to operate smoothly.
Investigational New Drug (IND) regulatory
"advance Mira-55 toward an Investigational New Drug (IND) submission for inflammatory pain"
An investigational new drug (IND) is a drug or biologic that is being tested but has not yet been approved for general use; it is the application and formal status that allows a company to begin human clinical trials under regulator oversight. Investors care because an IND marks the transition from lab work to human testing — like getting a permit to run real-world experiments — which creates important milestones, costs, timelines and regulatory risk that drive a development-stage company's value.
Elevated Plus Maze (EPM) medical
"including:HypothermiaCatalepsyElevated Plus Maze (EPM)Open Field (OF)"
A standardized preclinical behavioral test in which a rodent explores a raised, plus-shaped platform with two open arms and two enclosed arms; more time spent in open arms is taken as a sign of reduced anxiety-like behavior. Investors care because EPM results are an early, widely accepted signal about a drug candidate’s potential to affect anxiety or central nervous system function—positive or negative readouts can change development plans, costs, timelines and perceived market value, like a dress rehearsal that shapes the next staging decisions.
nonsteroidal anti-inflammatory drugs (NSAIDs) medical
"Nonsteroidal anti-inflammatory drugs (NSAIDs), which may cause gastrointestinal, renal"
Nonsteroidal anti-inflammatory drugs (NSAIDs) are a class of widely used medicines that reduce pain, fever and inflammation without using steroid hormones. They include over-the-counter and prescription products and work on common body pathways to ease symptoms, like turning down the volume on an alarm. Investors care because NSAID sales, safety alerts, patent status, or regulatory changes can quickly affect a drugmaker’s revenue, costs and stock value.
CB2 receptor medical
"designed to modulate CB1 and CB2 receptor activity while minimizing CB1-mediated"
A CB2 receptor is a protein on the surface of certain cells—mainly immune and inflammatory cells—that acts like a lock for specific chemical “keys” produced by the body or developed as drugs. Investors watch CB2-targeting therapies because turning this lock can reduce inflammation, pain, or immune overreaction with less risk of mind‑altering effects than similar brain-targeted receptors, so successful drugs or clinical advances can drive patents, approvals, and market value.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Previously shown to deliver morphine-comparable pain relief without opioid-related risks in a validated inflammatory pain model, supporting planned IND submission for inflammatory pain

MIAMI, FL / ACCESS Newswire / March 23, 2026 / MIRA Pharmaceuticals, Inc. (NASDAQ:MIRA) ("MIRA" or the "Company"), a clinical-stage pharmaceutical company developing novel therapies for neurologic, neuropsychiatric, and metabolic disorders, today announced new preclinical data demonstrating that Mira-55 did not produce cannabinoid-like central nervous system (CNS) side effects across a comprehensive battery of validated behavioral assays. The observed profile was differentiated from both Δ9-tetrahydrocannabinol (THC), the primary psychoactive component of cannabis, and the CB1 receptor antagonist rimonabant.

These findings build on previously reported preclinical data demonstrating that Mira-55 delivered morphine-comparable pain relief in a validated model of inflammatory pain, without opioid-related risks. Collectively, these data support the Company's ongoing efforts to advance Mira-55 toward an Investigational New Drug (IND) submission for inflammatory pain.

Study Overview and Key Findings

The study, conducted in collaboration with Pharmaseed, evaluated Mira-55 at oral doses of 10, 30, and 100 mg/kg and compared its behavioral effects to THC and rimonabant using established assays commonly employed to assess cannabinoid-related CNS and behavioral effects, including:

  • Hypothermia

  • Catalepsy

  • Elevated Plus Maze (EPM)

  • Open Field (OF)

Key Observations:

  • No cannabinoid-like psychogenic effects were observed at any tested dose of Mira-55

  • No evidence of sedation, catalepsy, or motor impairment, differentiating Mira-55 from CB1-active compounds such as rimonabant

  • No anxiogenic effects were observed, in contrast to rimonabant, which demonstrated anxiety-like behavioral changes

  • In the Elevated Plus Maze (EPM), Mira-55 showed a dose-dependent increase in time spent in open arms, consistent with reduced anxiety-like behavior

  • In Open Field testing, Mira-55-treated groups were comparable to vehicle controls, indicating no detectable adverse behavioral effects. Rimonabant-treated groups demonstrated reduced time spent in the center of the open field, a commonly used indicator of anxiety-like behavior, supporting the sensitivity of the experimental model.

Integrated Preclinical Profile

The CNS safety findings complement previously reported preclinical efficacy data demonstrating that Mira-55:

  • Reduced pain sensitivity and restored thresholds to near-baseline levels in inflammatory pain models

  • Demonstrated morphine-comparable analgesic effects in a validated inflammatory pain model

  • Did not produce sedation or opioid-like adverse effects

  • Did not induce inflammatory swelling, supporting a differentiated profile versus certain comparator agents

While these findings are based on preclinical models, they support a differentiated pharmacological profile for Mira-55.

Differentiation from THC and Historical Cannabinoid Therapies

Cannabinoid therapies that significantly activate CB1 receptors have historically been associated with central nervous system effects, including psychoactivity and psychiatric adverse events.

Mira-55 is a next-generation cannabinoid analog designed to modulate CB1 and CB2 receptor activity while minimizing CB1-mediated central nervous system effects. This differentiated pharmacological profile may enable therapeutic activity without the CNS liabilities that have historically limited cannabinoid-based drug development.

Leadership Commentary

"The challenge in cannabinoid drug development has never been the biology-it's been separating it from CNS side effects. We believe Mira-55 may represent an important step in that direction as we advance toward clinical development in inflammatory pain."
- Erez Aminov, Chairman and CEO of MIRA

Dr. Itzchak Angel, Chief Scientific Advisor, added:
"The consistency observed across multiple validated behavioral assays supports Mira-55's differentiated pharmacological profile and its separation from known CB1-related effects."

IND Strategy and Market Opportunity

MIRA is advancing Mira-55 toward regulatory IND-enabling studies for inflammatory pain, an area with significant unmet medical need.

Current treatment options include:

  • Opioids, which are associated with risks of dependence, tolerance, and overdose

  • Nonsteroidal anti-inflammatory drugs (NSAIDs), which may cause gastrointestinal, renal, and cardiovascular adverse effects

According to Grand View Research (2024), the global non-opioid pain treatment market was estimated at approximately $45.3 billion in 2024 and is projected to reach $70.3 billion by 2030, growing at a compound annual growth rate (CAGR) of 7.7%.

About Mira-55

Mira-55 is a next-generation cannabinoid analog designed to modulate cannabinoid receptor activity, including CB1 and CB2 pathways, while minimizing CB1-related psychoactivity. Following scientific review, the U.S. Drug Enforcement Administration (DEA) determined that Mira-55 is not classified as a controlled substance.

About MIRA Pharmaceuticals, Inc.

MIRA Pharmaceuticals, Inc. (NASDAQ: MIRA) is a clinical-stage pharmaceutical company focused on the development of novel therapies for neurologic, neuropsychiatric, and metabolic disorders. Its pipeline includes Mira-55 for inflammatory pain, Ketamir-2 for neuropathic pain, and SKNY-1 targeting obesity and smoking cessation. The Company is headquartered in Miami, Florida.

Cautionary Note Regarding Forward-Looking Statements

This press release and the statements of MIRA's management related thereto contain "forward-looking statements," which are statements other than historical facts made pursuant to the safe harbor provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements may be identified by words such as "aims," "anticipates," "believes," "could," "estimates," "expects," "forecasts," "goal," "intends," "may," "plans," "possible," "potential," "seeks," "will," and variations of these words or similar expressions that are intended to identify forward-looking statements. Any statements in this press release that are not historical facts may be deemed forward-looking. Any forward-looking statements in this press release are based on MIRA's current expectations, estimates, and projections only as of the date of this release and are subject to a number of risks and uncertainties (many of which are beyond MIRA's control) that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements, including related to MIRA's potential merger with SKNY Pharmaceuticals, Inc. These and other risks concerning MIRA's programs and operations are described in additional detail in the Annual Report on Form 10-K for the year ended December 31, 2024, and the Form 14A filed by MIRA on June 18, 2025, and other SEC filings, which are on file with the SEC at www.sec.gov and on MIRA's website at https://www.mirapharmaceuticals.com/investors/sec-filings. MIRA explicitly disclaims any obligation to update any forward-looking statements except to the extent required by law.

Contact:
Krystina Quintana
info@mirapharma.com
(786) 432-9792

SOURCE: MIRA Pharmaceuticals



View the original press release on ACCESS Newswire

FAQ

What did MIRA (MIRA) report about Mira-55's pain relief in March 2026?

Mira-55 produced morphine-comparable analgesia in a validated inflammatory pain model. According to the company, preclinical tests showed restoration of pain thresholds near baseline without opioid-like adverse effects, supporting IND-enabling plans for inflammatory pain.

Did Mira-55 show cannabinoid-like CNS side effects in the preclinical study for MIRA?

No, Mira-55 did not produce cannabinoid-like CNS side effects at tested doses. According to the company, behavioral assays including hypothermia, catalepsy, EPM, and open field found no THC- or rimonabant-associated adverse central effects.

What doses of Mira-55 were evaluated in MIRA's March 23, 2026 preclinical study?

The study evaluated oral Mira-55 at 10, 30, and 100 mg/kg. According to the company, these doses were compared against THC and rimonabant across validated behavioral assays to assess CNS safety and behavior.

Does MIRA plan to seek regulatory clearance for Mira-55 after these preclinical results?

Yes, MIRA is advancing Mira-55 toward IND-enabling studies for inflammatory pain. According to the company, the preclinical efficacy and CNS safety profile support ongoing efforts toward an IND submission.

What are the limitations of MIRA's Mira-55 data announced March 23, 2026?

The results are limited to preclinical models and do not establish human safety or efficacy. According to the company, clinical trials will be required to confirm translation of analgesic and CNS safety findings to patients.