Business Wire

Merz Therapeutics Presents New Phase 2 PaiNT Data in Peripheral Neuropathic Pain at IASP 2026

26.10.2026 08:00:00 CET | Business Wire | Press Release

Share

Merz Therapeutics, a leading player in neurology-focused specialty pharma, today announced the presentation of new clinical and translational research in peripheral neuropathic pain (PNP) at the International Association for the Study of Pain (IASP) 2026 World Congress in Bangkok, Thailand, taking place from 26 to 30 October. The research spans new Phase 2 findings on incobotulinumtoxinA in postherpetic neuralgia (PHN) and post-surgical/post-traumatic neuropathic pain (PS/PTNP), as well as preclinical studies exploring potential biological mechanisms involved in effects of incobotulinumtoxinA on PNP models, highlighting Merz Therapeutics’ growing presence in neuropathic pain.

In the PHN population of the Phase 2 PaiNT trial, results over 20 weeks favored incobotulinumtoxinA versus placebo treatment. In an exploratory analysis of average daily pain (ADP) intensity, the greatest difference between treatment groups was observed at Week 6 (adjusted mean difference, −1.14 points; p=0.0488). More weeks with ≥30% and ≥50% pain reduction were observed in the incobotulinumtoxinA group than in the placebo group. 1, However, the primary endpoint of the PaiNT trial, combining the outcome of the PHN and PS/PTNP population, did not significantly separate from placebo. In the PS/PTNP population, the heterogeneity of underlying diagnoses made the comparison with placebo inconclusive. 1,4

Most treatment-emergent adverse events were mild or moderate; treatment-related events were uncommon, and no serious treatment-related adverse events occurred. Tolerability was rated as good or very good for 72.7% of patients receiving incobotulinumtoxinA and 74.6% receiving placebo.2 In patients with PHN, incobotulinumtoxinA was also associated with stable emotional outcomes and improvements in pain-related interference with daily functioning.3

“Neuropathic pain is complex and often has a significant impact on patients’ daily lives,” said Stefan Albrecht, CSO, Merz Therapeutics.“The breadth of research we are presenting at IASP reflects our work to better understand both the clinical experience of patients and how incobotulinumtoxinA may act on biological pathways involved in neuropathic pain. Our broader research is helping us explore potential mechanisms and inform the next steps in our pain research program.”

Beyond PaiNT, Merz Therapeutics is presenting research exploring how botulinum neurotoxin type A (BoNT/A) may influence biological pathways involved in neuropathic pain. In human sensory-neuron models, BoNT/A reduced neuronal excitability, with findings pointing towards potential effects on sodium, calcium, and TRPV1 ion-channel pathways involved in neuropathic pain signaling.5 Complementary preclinical research demonstrated incobotulinumtoxinA effects on spinal glutamate levels and molecular targets associated with inflammation and pain signaling, providing further insights into potential mechanisms for future investigation.6,7

About the PaiNT trial

PaiNT was a Phase 2 proof-of-concept trial in adults with postherpetic neuralgia (PHN) or post-surgical/post-traumatic neuropathic pain (PS/PTNP). Participants received a single subcutaneous treatment with incobotulinumtoxinA, at a dose of up to 300 units across up to 60 injection sites within the painful area, or placebo, and were followed for 20 weeks.8,9

IncobotulinumtoxinA is not approved for the treatment of peripheral neuropathic pain. Its safety and efficacy for this investigational use have not been established.

About Merz Therapeutics

Merz Therapeutics GmbH is dedicated to delivering better outcomes for more patients. With science as its foundation and the patient experience as its focus, the company relentlessly pursues innovative treatments and partnerships to address unmet needs in movement disorders, neurodegenerative conditions, liver disease, and other health conditions that severely impact patients’ quality of life.

Merz Therapeutics is headquartered in Frankfurt am Main, Germany, and is active in more than 80 countries. Merz Therapeutics GmbH is part of the Merz Group, a privately held, family-owned company with more than 115-year legacy. With passion and purpose, Merz Therapeutics continues to advance care in specialty neurology in ways that benefit both patients and society.

Please visit www.merztherapeutics.com.

References

  1. Attal N, Bicker I, Pulte I, et al. IncobotulinumtoxinA in postherpetic neuralgia: sustained pain improvement in the PaiNT Phase 2 study. Presented at: IASP 2026; 2026.
  2. Attal N, Bicker I, Pulte I, et al. Understanding patient heterogeneity & placebo response in post-surgical/traumatic neuropathic pain: results from the PaiNT proof-of-concept Phase 2 trial. Presented at: IASP 2026; 2026.
  3. Viel E, Bicker I, Pulte I, et al. Safety and tolerability of subcutaneous incobotulinumtoxinA in peripheral neuropathic pain: findings from the PaiNT trial. Presented at: IASP 2026; 2026
  4. Baron R, Attal N, Bicker I, et al. Functional and psychosocial benefits of incobotulinumtoxinA in postherpetic neuralgia: patient-reported outcomes from the PaiNT trial. Presented at: IASP 2026; 2026.
  5. Oscar Sánchez-Carranza et al, Oscar Sanchez-Carranza, Claudia Jatzke, Andreas Gravius, Jens Nagel Botulinum Neurotoxin Type A Modulates Ion Channel Function in Human Sensory Neurons IASP, Bangkok. 2026
  6. Nagel, et al.Jens Nagel, Oscar Sanchez-Carranza, Andreas Gravius IncobotulinumtoxinA Attenuates Pathological Spinal Glutamatergic Overactivity in a Rat Model of Neuropathic PainIASP, Bangkok 2026
  7. Paulina Nunez Badinez, Oscar Sanchez-Carranza, Andreas Gravius, Jens Nagel Effects of IncobotulinumtoxinA in a Rat Model for Peripheral Neuropathic Pain IASP, Bangkok 2026
  8. Attal N, Bicker I, Pulte I, et al. Efficacy & Safety of IncobotulinumtoxinA in Patients with Postherpetic Neuralgia – Results from the PaiNT Proof-of-Concept Phase 2 Trial. Accepted for presentation at: European Academy of Neurology (EAN); June 27–30, 2026; Geneva, Switzerland.
  9. Attal N, Bicker I, Pulte I, et al. Understanding Patient Diversity & Placebo Response in Post-Surgical/Traumatic Neuropathic Pain – Results from the PaiNT Proof-of-Concept Phase 2 Trial. Accepted for presentation at: European Academy of Neurology (EAN); June 27–30, 2026; Geneva, Switzerland.

View source version on businesswire.com: https://www.businesswire.com/news/home/20261023526805/en/

Contacts

Media contact

Merz Therapeutics GmbH
Luke Anthony Mircea-Willats
Global Communications & Strategic Affairs
merztherapeutics@merz.com

(c) 2024 Business Wire, Inc., All rights reserved.

Business Wire, a Berkshire Hathaway company, is the global leader in multiplatform press release distribution.

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

BeOne Presents Compelling Data in Hard-to-Treat Liver and Lung Cancers at ESMO 202624.10.2026 10:15:00 CEST | Press Release

BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced new data from multiple differentiated investigational medicines across its priority solid tumor disease areas at the European Society for Medical Oncology (ESMO) Congress 2026 (October 23–27, Madrid). The presentations span gastrointestinal, lung, and breast cancers, and reflect the growing momentum of BeOne’s solid tumor franchise. Mark Lanasa, M.D., Ph.D., Chief Medical Officer, Solid Tumors at BeOne, said: “At ESMO, we are showing how our strategy of matching the right modality to disease biology is translating into meaningful clinical progress. Our GPC3 x 4-1BB bispecific antibody continues to be well tolerated and demonstrates durable activity with longer follow up in patients with heavily pre-treated hepatocellular carcinoma, while the first clinical data from our brain-penetrant PRMT5 inhibitor and CEA-targeting ADC expand our innovation in non-small cell lung cancer. Alongsi

Phase 3 RAINIER Results Supporting Best-in-Class Potential of Povetacicept in IgA Nephropathy Published in the New England Journal of Medicine and Presented at the American Society of Nephrology Kidney Week 202623.10.2026 19:42:00 CEST | Press Release

Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced the publication of Phase 3 RAINIER results for povetacicept in the New England Journal of Medicine (NEJM), presentation of these data at the American Society of Nephrology (ASN) Kidney Week 2026 in Denver, Colorado, and advancement of the povetacicept clinical research program in IgAN. Vertex will also host an investor event during ASN on October 23 at 6:15-7 p.m. MDT (8:15-9 p.m. EDT). Further details are below. Data being presented include a pre-specified Week 36 interim analysis of the ongoing Phase 3 RAINIER trial of povetacicept, an engineered fusion protein and dual inhibitor of the BAFF (B cell activating factor) and APRIL (a proliferation inducing ligand) cytokines, in immunoglobulin A nephropathy (IgAN). RAINIER met its primary endpoint, with povetacicept achieving a 52.0% reduction from baseline in proteinuria at Week 36 and a statistically significant and clinically meaningful 49.8% reduction versus placebo (

Lifezone Metals Confirms Advanced Negotiations with Orion CMC on Kabanga Nickel Project23.10.2026 16:19:00 CEST | Press Release

Lifezone Metals Limited (NYSE: LZM) notes comments made today by Oskar Lewnowski, Founder and Group Chief Executive of Orion Resource Partners, in an interview with Bloomberg Television regarding the Company’s Kabanga Nickel Project in Tanzania. In response to inbound inquiries from media outlets and investors following the interview, the Company can confirm that negotiations with Orion Critical Mineral Consortium (Orion CMC) regarding a significant equity investment into the Kabanga Nickel Project are at an advanced stage. The Orion CMC is a global investment platform launched by Orion Resource Partners in partnership with the U.S. International Development Finance Corporation (DFC) and Abu Dhabi's sovereign investor ADQ. As previously announced, the Company has been running a competitive process, led by Standard Chartered Bank, to secure a strategic investment into the Kabanga Nickel Project. Social Media LinkedIn | X | YouTube About Lifezone Metals Lifezone Metals (NYSE: LZM) is com

BeOne Medicines Reports Sustained Survival Benefit with TEVIMBRA-ZIIHERA Combination in First-Line HER2+ Gastroesophageal Cancer23.10.2026 16:15:00 CEST | Press Release

BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced new survival results from the planned second interim analysis (IA2) and final formal analysis of the Phase 3 HERIZON-GEA-01 trial, further confirming the benefit of TEVIMBRA® (tislelizumab) plus ZIIHERA® (zanidatamab) and chemotherapy as first-line treatment for patients with HER2-positive locally advanced or metastatic gastroesophageal adenocarcinoma (GEA). The results will be presented today as a late-breaking abstract during a rapid oral session at the European Society for Medical Oncology (ESMO) Congress 2026 in Madrid, Spain (LBA79). Mark Lanasa, M.D., Ph.D., Chief Medical Officer, Solid Tumors at BeOne, said: “Following the U.S. approval in August, these longer-term data provide further evidence supporting TEVIMBRA plus ZIIHERA and chemotherapy as the new standard of care in all first-line HER2-positive advanced gastroesophageal adenocarcinoma patients, regardless of PD-L1 sta

inDrive and Pony.ai Announce Collaboration to Explore Autonomous Mobility in Kazakhstan Built on NVIDIA Hyperion23.10.2026 15:00:00 CEST | Press Release

inDrive, the global mobility and delivery platform, today announced it has signed a memorandum of understanding (MOU) with NVIDIA and Pony.ai, a global leader in the large-scale commercialization of autonomous driving technology, to explore the future of autonomous ride-hailing. Kazakhstan will serve as the first test market. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20261023143469/en/ inDrive partners with Pony.ai and NVIDIA to explore autonomous mobility in Kazakhstan Kazakhstan was chosen first for its regulatory readiness following the creation of the country’s first structured legal framework for driverless transport, as part of its “Year of Digitalization and Artificial Intelligence.” Combined with Kazakhstan’s position as a leading Central Asian economy, this gives the companies a clear basis to assess autonomous ride-hailing in practice. The three companies will evaluate the technical, operational, regulatory and

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye