MIRA Pharmaceuticals Reports Successful Formulation Results Supporting Development of MIRA-55 as a Non-Opioid Oral Therapy for Chronic Inflammatory Pain
Rhea-AI Summary
MIRA Pharmaceuticals (NASDAQ:MIRA) reported positive preclinical results for optimized oral formulations of MIRA-55, its non-opioid candidate for chronic inflammatory pain. A lead oral formulation was selected after comparison with an intravenous reference, demonstrating favorable oral bioavailability, sustained systemic exposure, and reproducible distribution to brain and liver tissue.
According to MIRA, brain and peripheral tissue exposure supports MIRA-55’s proposed central and anti-inflammatory mechanisms. Prior preclinical studies showed oral MIRA-55 normalized pain and reduced inflammation in a validated model, outperforming injected morphine, with a differentiated pharmacological profile and anxiolytic activity distinct from THC. The company plans further preclinical development.
AI-generated analysis. How Rhea-AI works. Not financial advice.
Positive
- Lead oral formulation selected with favorable bioavailability and sustained systemic exposure in preclinical study
- Reproducible brain and liver distribution following oral administration supports central and peripheral pain mechanisms
- Preclinical efficacy: oral MIRA-55 normalized pain and reduced inflammation, outperforming injected morphine in a validated inflammatory pain model
- Differentiated from THC: showed anxiolytic activity, lacked characteristic THC CNS effects, and interacts with the cannabinoid system via a distinct mechanism
Negative
- None.
News Market Reaction – MIRA
On the day this news was published, MIRA gained 0.49%, reflecting a mild positive market reaction. Our momentum scanner triggered 4 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $189K to the company's valuation, bringing the market cap to $38.66M at that time.
Data tracked by StockTitan Argus on the day of publication.
Historical Context
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| Mon 06 | Preclinical data update | Positive | +1.1% | Positive preclinical pharmacokinetic results for SKNY-1 oral formulation. |
| Thu 25 | Preclinical data update | Positive | -0.3% | New preclinical data on Mira-55’s differentiated mechanism and anxiolytic activity. |
| Wed 17 | Clinical trial planning | Positive | +3.0% | Submission of Phase 2a Ketamir-2 trial protocol to the FDA for CIPN. |
| Thu 04 | License agreement | Positive | +5.0% | Amended license securing worldwide exclusive rights to MIRA-55 and SKNY-1. |
| Wed 27 | License agreement | Positive | +18.6% | Expansion of Ketamir-2 rights to worldwide coverage across 10 major markets. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Recent MIRA pipeline and licensing news has more often been followed by modestly positive next‑day price moves, with one small negative reaction.
Key Terms
oral bioavailability medical
pharmacokinetic medical
central nervous system medical
mechanism of action medical
cannabinoid system medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
Optimized Oral Formulation Demonstrates Favorable Oral Bioavailability Together with Robust Brain and Liver Distribution Following Oral Administration
MIAMI, FL / ACCESS Newswire / July 10, 2026 / MIRA Pharmaceuticals, Inc. (NASDAQ:MIRA) ("MIRA" or the "Company"), a clinical-stage pharmaceutical company, today announced positive results from preclinical studies evaluating optimized oral formulations of MIRA-55, the Company's oral drug candidate being developed as a non-opioid therapy for chronic inflammatory pain.
Following evaluation of multiple oral formulations, the Company selected a lead formulation demonstrating favorable oral bioavailability together with sustained systemic exposure and reproducible distribution into both brain and liver tissue following oral administration. Collectively, these findings support the continued development of MIRA-55 as an orally administered therapy for chronic inflammatory pain.
"Patients deserve safer and more effective non-opioid treatment options for chronic inflammatory pain," said Erez Aminov, Chief Executive Officer of MIRA Pharmaceuticals. "These formulation and pharmacokinetic findings represent another important step in advancing MIRA-55 as a differentiated oral therapy designed to address that need."
The objective of the study was to optimize the oral formulation of MIRA-55 by comparing multiple formulations in a preclinical pharmacokinetic study. An intravenous reference arm was included to characterize absolute oral bioavailability and support selection of the lead formulation based on its overall pharmacokinetic profile.
The selected formulation demonstrated reproducible distribution into both brain and liver tissue following oral administration. Brain exposure may support modulation of central pain-processing pathways, while peripheral distribution may contribute to the anti-inflammatory activity previously observed in MIRA's preclinical efficacy studies. Together, these findings demonstrate that the optimized formulation successfully delivers MIRA-55 to pharmacologically relevant tissues associated with both central and peripheral mechanisms of chronic inflammatory pain.
"Formulation optimization is far more than a pharmaceutical exercise-it is what enables a molecule to consistently engage its intended biological targets," said Itzchak Angel, Ph.D., Chief Scientific Advisor of MIRA Pharmaceuticals. "The combination of favorable oral exposure together with reproducible brain and peripheral tissue distribution provides important support for MIRA-55's proposed mechanism of action and its continued development as an oral therapy for chronic inflammatory pain."
Today's pharmacokinetic findings build upon MIRA's previously reported preclinical studies demonstrating that oral MIRA-55 normalized pain and reduced inflammation in a validated inflammatory pain model, outperforming injected morphine, while also exhibiting a differentiated pharmacological profile relative to THC. In separate mechanistic and behavioral studies, MIRA-55 demonstrated anxiolytic activity, did not produce the characteristic central nervous system effects associated with THC, and was shown to interact with the cannabinoid system through a mechanism distinct from THC. Collectively, these efficacy, behavioral, mechanistic, and pharmacokinetic findings continue to strengthen the overall development package supporting MIRA-55 as a differentiated oral therapeutic candidate for chronic inflammatory pain.
The Company plans to continue evaluating the relationship between tissue exposure, pharmacodynamic activity, and therapeutic efficacy as MIRA-55 advances through additional preclinical development.
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 developing novel oral small-molecule therapeutics for neurologic, inflammatory, metabolic, and neuropsychiatric disorders. The Company's pipeline includes Ketamir-2, an investigational oral therapy that successfully completed a Phase 1 clinical trial and for which the Company has submitted a Phase 2a protocol to the U.S. Food and Drug Administration (FDA) under its active U.S. Investigational New Drug (IND) application for chemotherapy-induced peripheral neuropathy (CIPN); MIRA-55, a preclinical oral drug candidate being developed for chronic inflammatory pain; and SKNY-1, a preclinical oral drug candidate being developed for obesity and addiction-related disorders.
Cautionary Note Regarding Forward-Looking Statements
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements generally can be identified by the use of words such as "anticipate," "expect," "plan," "can," "could," "would," "may," "will," "believe," "estimate," "forecast," "goal," "project," "guidance," "potential," "intend," "seek," "target" and other words of similar meaning, although not all forward-looking statements include these words. Forward-looking statements may include, but are not limited to, statements regarding the development of SKNY-1; its potential efficacy, safety, tolerability, pharmacokinetic profile, tissue distribution, mechanism of action, and therapeutic benefits; the potential advantages of SKNY-1 compared to existing treatment options; the potential for once-daily oral dosing; the preservation of lean body mass; future preclinical studies; future clinical development; regulatory interactions; intellectual property protection; strategic partnership opportunities; and the future development and commercialization of SKNY-1. Forward-looking statements are based on current expectations, estimates, forecasts, and projections, as well as management's beliefs and assumptions, and are subject to significant risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements.
These risks and uncertainties include, among others, risks related to preclinical and clinical development; the ability to obtain regulatory approvals; the outcome of future studies; reliance on third parties; intellectual property protection; financing needs; market conditions; and the other risks identified under the heading "Risk Factors" contained in the Company's Annual Report on Form 10-K and the Company's other filings with the U.S. Securities and Exchange Commission ("SEC"). Forward-looking statements contained in this press release speak only as of the date hereof, and the Company undertakes no obligation to update or revise such statements, whether as a result of new information, future events, or otherwise, except as required by applicable law.
We caution investors not to place undue reliance on the forward-looking statements contained in this press release. Investors are encouraged to review the Company's filings with the SEC, available at www.sec.gov, and in the Investors section of the Company's website at www.mirapharma.com, for a discussion of these and other risks and uncertainties.
Contact
Krystina Quintana
MIRA Pharmaceuticals, Inc.
info@mirapharma.com
(786) 432-9792
SOURCE: MIRA Pharmaceuticals
View the original press release on ACCESS Newswire