Addex Therapeutics Reports 2025 Financial Results and Strategic Developments
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 1 hour ago
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Should l Buy ADXN?
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- R&D Progress: Addex Therapeutics' GABAB PAM chronic cough candidate demonstrated robust anti-tussive activity across multiple disease models, indicating its potential for clinical application and possibly opening new revenue streams for the company.
- Strategic Collaboration: The exclusive licensing agreement with Sinntaxis aims to leverage mGlu5 NAM for brain injury recovery, further enhancing Addex's competitive edge in the neurological disorder treatment space.
- Financial Position: As of December 31, 2025, cash reserves stood at CHF 1.6 million, significantly down from 2024, reflecting the company's cash burn in R&D and investment activities, which may impact future operational flexibility.
- Loss Overview: The net loss for 2025 reached CHF 6.7 million, a stark contrast to a net profit of CHF 7.1 million in 2024, primarily due to reduced revenues from the Neurosterix transaction, highlighting financial pressures on the company.
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About ADXN
Addex Therapeutics Ltd is a Switzerland-based clinical-stage pharmaceutical company. The Company focuses on development and commercialization of orally available small molecule drugs known as allosteric modulators for neurological disorders. The Company’s clinical programs pipeline include dipraglurant (mGlu5 NAM), which is Phase 2a placebo-controlled clinical trial for Parkinson's disease levodopa-induced dyskinesia (PD-LID), and is being prepared to enter registration trials for PD-LID, and ADX71149 (mGlu2 positive allosteric modulator or PAM), which is being developed in collaboration by its partner Janssen Pharmaceuticals, Inc to treat schizophrenia and anxious depression. It also is advancing several preclinical programs, including GABABPAM for pain, overactive bladder and other disorders, mGlu7 NAM for post-traumatic stress disorder, mGlu2 NAM for mild neurocognitive disorders, mGlu4 PAM for Parkinson’s disease and mGlu3 PAM for neurodegenerative disorders.
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.
- R&D Progress: Addex Therapeutics' GABAB PAM chronic cough candidate demonstrated robust anti-tussive activity across multiple disease models, indicating its potential for clinical application and possibly opening new revenue streams for the company.
- Strategic Collaboration: The exclusive licensing agreement with Sinntaxis aims to leverage mGlu5 NAM for brain injury recovery, further enhancing Addex's competitive edge in the neurological disorder treatment space.
- Financial Position: As of December 31, 2025, cash reserves stood at CHF 1.6 million, significantly down from 2024, reflecting the company's cash burn in R&D and investment activities, which may impact future operational flexibility.
- Loss Overview: The net loss for 2025 reached CHF 6.7 million, a stark contrast to a net profit of CHF 7.1 million in 2024, primarily due to reduced revenues from the Neurosterix transaction, highlighting financial pressures on the company.
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- Promising Preclinical Data: Addex Therapeutics announced that its GABAB positive allosteric modulator demonstrated significant antitussive activity in a bleomycin-induced idiopathic pulmonary fibrosis chronic cough model, indicating potential for improving patient quality of life.
- Efficacy and Safety Profile: In studies involving non-human primates, the compound exhibited robust antitussive efficacy without significant changes in respiratory rate or body temperature throughout the treatment, supporting its safety for chronic administration.
- Improved Lung Pathology: Compared to untreated animals, the treatment group showed significant reductions in Ashcroft scores and affected lung tissue percentages at both Day 7 and Day 28, indicating a positive impact on fibrosis and further validating its clinical application prospects.
- Strong Market Demand: Chronic cough remains a significant unmet medical need among patients with idiopathic pulmonary fibrosis, and Addex's research findings could provide new treatment options in this area, enhancing its competitive position in the market.
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- Clinical Trial Progress: Addex Therapeutics announced that the Phase 1 trial for NTX-253 targeting schizophrenia is expected to conclude by Q2 2026, demonstrating the company's ongoing commitment to mental health research and development.
- Drug Mechanism: NTX-253 is a potent, selective, orally available positive allosteric modulator that reduces psychotic symptoms by modulating dopamine signaling while avoiding movement disorders associated with other dopamine antagonists, potentially enhancing its market competitiveness.
- Trial Design: The Phase 1 trial consists of single ascending dose (SAD) and multiple ascending dose (MAD) parts, with the SAD part evaluating the impact of food on NTX-253 pharmacokinetics, while the MAD part assesses safety and tolerability in schizophrenia patients, ensuring clinical application safety.
- Equity Structure: Addex retains a 20% equity interest in Neurosterix, which is advancing a portfolio of allosteric modulator programs for schizophrenia, psychosis, and mood-related disorders, indicating Addex's strategic positioning in the mental health sector.
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- Clinical Study Progress: Addex Therapeutics' spin-out Neurosterix is on track to complete its Phase 1 clinical study of NTX-253, targeting schizophrenia, by Q2 2026, focusing on safety and pharmacokinetics.
- Innovative Study Design: The study features a multi-part, ascending-dose design that integrates data from both healthy adults and stable schizophrenia patients, aiming to efficiently characterize NTX-253's clinical profile and mitigate risks for subsequent studies.
- Mechanism of Action Advantage: NTX-253, as a selective positive allosteric modulator, may reduce psychotic symptoms by indirectly modulating dopamine signaling while avoiding the movement disorders and metabolic complications associated with traditional dopamine antagonists, demonstrating a favorable safety profile.
- Financing Background: Neurosterix was spun out from Addex in April 2024, raising $65 million in funding, with Addex retaining a 20% equity stake, reflecting confidence in its future development prospects.
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- Significant Drug Efficacy: Addex Therapeutics' novel GABAB positive allosteric modulator demonstrated robust anti-tussive activity in a non-human primate chronic cough model, significantly reducing citric acid-induced cough frequency with efficacy comparable to baclofen, but with fewer side effects, indicating a wider therapeutic margin and improved tolerability.
- Supporting Preclinical Research: Previous studies in guinea pigs also showed reductions in cough frequency and increased cough latency without signs of tolerance after repeated dosing, further validating the candidate's potential in chronic cough treatment.
- Importance of Therapeutic Context: Chronic cough is a challenging condition with limited approved therapies, and Addex's PAM aims to deliver the therapeutic benefits of baclofen while enhancing selectivity, tolerability, and durability by targeting an allosteric site of the GABAB receptor, which holds significant clinical implications.
- Optimistic Company Outlook: CEO Tim Dyer emphasized that the new primate data, combined with prior preclinical findings, supports the therapeutic potential of the GABAB PAM program, indicating that the company is expanding its portfolio of small-molecule allosteric modulators for neurological and psychiatric disorders.
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- Clinical Trial Results: Addex Therapeutics demonstrated robust anti-tussive activity of its GABAB positive allosteric modulator in a non-human primate chronic cough model, significantly reducing citric acid-induced cough frequency, indicating its potential as a once-daily treatment option for chronic cough patients.
- Efficacy Comparison: The drug candidate's antitussive efficacy was comparable to baclofen in the chronic cough model, and it outperformed nalbuphine, baclofen, and codeine in guinea pig models, suggesting a competitive edge in addressing the urgent need for novel therapeutics in this area.
- Tolerability Advantage: The GABAB PAM candidate exhibited better tolerability and a wider therapeutic margin compared to baclofen and codeine, which may attract more patients to this treatment option, thereby enhancing Addex's market share in the biopharmaceutical sector.
- Strategic Development Focus: Addex is advancing its independent GABAB PAM program for chronic cough while collaborating with Indivior to develop the drug for substance use disorders, showcasing its broad application potential in neurological disorders and strategic positioning in the market.
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