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Artelo Announces Peer-Reviewed Publication Supporting its FABP5 Inhibitor ART26.12 as a Novel Pain Treatment with a Potentially First-in-Class Profile

Key Takeaway: Artelo Biosciences, Inc. announced the publication of a peer-reviewed article highlighting ART26.12, its FABP5 inhibitor, as a potential first-in-class pain treatment. The article provides evidence that FABP5 inhibition can lead to analgesic effects across various pain models. Notably, the drug showed excellent safety in a Phase 1 study, with no adverse events reported. Artelo plans to advance ART26.12 into a multiple ascending dose study, building on its promising preclinical results.

Market Sentiment Analysis

POSITIVE FACTORS

  • ART26.12 demonstrated excellent safety with zero adverse events in the Phase 1 SAD study.
  • Peer-reviewed publication supports FABP5 as a promising target for non-opioid pain relief.
  • ART26.12 may redefine pain treatment and addresses significant unmet medical needs.

Full Press Release Details

Demonstrates ART26.12’s Differentiated Profile as a Promising Pain Treatment Ahead of Planned Multiple Ascending Dose Study This Year
Phase 1 SAD Study Exhibited Excellent Safety with Zero Adverse Events Attributed to ART26.12
SOLANA BEACH, Calif., April 20, 2026 (GLOBE NEWSWIRE) -- Artelo Biosciences, Inc. (Nasdaq: ARTL), a clinical‑stage pharmaceutical company focused on modulating lipid‑signaling pathways to develop treatments for people living with cancer, pain, dermatological, or neurological conditions, today announced the publication of a peer‑reviewed article titled “Evaluating fatty acid-binding protein 5 (FABP5) as a therapeutic target for pain management” in the European Journal of Pain, an internationally recognized journal in pain research.
The article discusses preclinical evidence showing that FABP5 inhibition produced analgesic effects across multiple pain models, including visceral, inflammatory, neuropathic, and joint pain. The publication also highlights evidence that FABP5 inhibition may influence several established pain-related pathways while reducing pro-inflammatory mediators, supporting its potential as a differentiated, non-opioid therapeutic approach.
These findings are supported by a broader body of evidence – specifically for ART26.12 – from seven prior preclinical studies in diabetic neuropathy, osteoarthritis, cancer bone pain, and peripheral neuropathy caused by chemotherapy. ART26.12 demonstrated consistent analgesic activity across each model and validated FABP5 as a novel lipid-signaling target for pain treatment.
“This peer-reviewed publication strengthens the scientific foundation for ART26.12 and reinforces our view that FABP5 inhibition represents a novel mechanism of action with the potential to redefine the treatment of pain,” stated Dr. Andrew Yates, Artelo’s Chief Scientific Officer. “Importantly, ART26.12 with a potentially first-in-class profile has demonstrated what we believe to be a highly differentiated approach for the treatment of pain. In our completed Phase 1 single ascending dose study, ART26.12 was well-tolerated, with no severe or serious drug-related adverse events presented for all doses evaluated. We believe ART26.12 has tremendous potential as an effective and well-tolerated therapy in a space where safety remains a critical limitation. We are now advancing ART26.12 into a planned multiple ascending dose study this year as the next step in its clinical development.”
Novel, non-opioid, and better tolerated pain treatments remain an area of significant unmet need, particularly for patients seeking alternatives to opioids and NSAIDs. According to the CDC, 24.3% of U.S. adults experienced chronic pain in 2023, while the FDA has highlighted the serious risks associated with opioid analgesics, including misuse, addiction, overdose, and death.
“Preclinical data across multiple pain modalities strongly support FABP5 as a promising target for non‑opioid and non‑steroidal pain relief,” said Dr. William George Warren, Principal Scientist at Artelo and lead author of the publication. “These findings strengthen the rationale for advancing selective FABP5 inhibitors, such as ART26.12, toward clinical development for the treatment of pain.”
Artelo continues to advance a diversified portfolio of selective, dual, and pan FABP inhibitors – including programs targeting FABP5 – to pursue therapeutic opportunities in pain and other indications driven by dysregulated lipid signaling.
About Artelo Biosciences
Artelo Biosciences, Inc. is a clinical-stage pharmaceutical company dedicated to the development and commercialization of proprietary therapeutics that modulate lipid-signaling pathways, with a diversified pipeline addressing significant unmet needs in anorexia, cancer, anxiety, dermatologic conditions, pain, inflammation, and diseases of the eye. Led by an experienced executive team collaborating with world-class researchers and technology partners, Artelo applies rigorous scientific, regulatory, and commercial, discipline to maximize stakeholder value. More information is available at www.artelobio.com and X: @ArteloBio.
Forward-Looking Statements
This press release contains certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, as amended, including statements regarding the Company's plans and expectations. These statements involve known and unknown risks, uncertainties, and other factors that may cause actual results to differ materially from those expressed or implied by such statements, including market and other conditions. All statements that are not historical facts are forward-looking statements, including but not limited to, statements regarding: the use of proceeds from the offering and the potential exercise of the warrants. For a discussion of risks and uncertainties, please refer to the Company's filings with the Securities and Exchange Commission, including its most recent Annual Report on Form 10-K. The Company undertakes no obligation to publicly update any forward-looking statement, except as required by applicable securities laws.
Investor Relations Contact:
Crescendo Communications, LLC

Frequently Asked Questions

What is ART26.12's mechanism for pain management?

ART26.12 targets FABP5, showing potential as a non-opioid pain treatment.

What were the results of ART26.12's Phase 1 study?

The Phase 1 study showed excellent safety, with no adverse events reported.

What types of pain models did preclinical studies of ART26.12 include?

Preclinical studies included models for visceral, inflammatory, neuropathic, and joint pain.

What is the next step for ART26.12's development?

ART26.12 is advancing into a planned multiple ascending dose study this year.

Why is FABP5 inhibition significant for pain treatment?

FABP5 inhibition may redefine pain therapy by reducing inflammatory mediators.

Last updated: Apr 20, 2026