ALSEN Sensorion SAS

Sensorion Announces Two Presentations at AAO-HNSF 2019 in New Orleans

Regulatory News:

Sensorion (Paris:ALSEN) (FR0012596468 – ALSEN) a pioneering clinical-stage biopharmaceutical company which specializes in the development of novel therapies to restore, treat and prevent inner ear diseases such as hearing loss, tinnitus and vertigo, has contributed two presentations in the scientific poster session at the 2019 Annual Meeting of the American Academy of Otolaryngology, Head and Neck Surgery/Foundation (AAO-HNSF) held in New Orleans LA, the 15-18th of September, 2019.

The first poster is entitled “SENS-111 Maintains Cognitive Functions in Healthy Volunteers in Contrast to Meclizine”. The study has demonstrated that SENS-111 compared to placebo has no sedative effects and consequences on vigilance, cognition and working memory confirmed by both the VigTrack and Pepsy® tests battery. The data is further confirmed by patients’ self-assessed measures on the Stanford Sleepiness Scale (SSS). In contrast, Meclizine 50mg has been demonstrated to negatively impact vigilance and showed sedative effects. The most important and limiting side effect of sedation is counterproductive to normal functioning and the natural recovery process from vertigo occurring via central compensation. The impact of these findings on the long-term recovery from acute vertigo will need to be confirmed in clinical trials.

The presentation “Plasma Prestin and Distortion Product Otoacoustic Emission Correlations after Mild Noise-Induced Hearing Loss” demonstrated a strong correlation between the amplitude loss of Distortion Product OtoAcoustic Emissions (DPOAE) and changes in circulating Prestin levels in an animal model of variable and mild noise-induced hearing loss studied in collaboration with with Dr. Kourosh Parham at UCONN Health.

These results expand the successful collaboration with the group of Dr. Parham on the potential of the inner ear specific protein Prestin as a circulating biomarker, with promising results from a more severe model of noise-induced hearing loss published jointly in the peer-reviewed journal Hearing Research earlier this year (Parham, K et all: Noise-induced trauma produces a temporal pattern of change in blood levels of the outer hair cell biomarker Prestin, Hear Res, 371:98-104, 2019).

About Seliforant

Seliforant (formerly SENS-111) is the first representative candidate of the histamine type 4 receptor antagonist class to be tested for the symptomatic treatment of vertigo crises. Displaying a neuromodulation effect of the sensorineural inner ear cell function, Seliforant is a small molecule that can be taken orally or via a standard injection, and is currently in a separate Phase 2 clinical trial, being conducted in the United States, Europe, Israel and South Korea.

About Sensorion

Sensorion is a pioneering clinical-stage biopharmaceutical company, which specializes in the development of novel therapies to restore, treat and prevent inner ear diseases such as hearing loss, vertigo and tinnitus. Our clinical-stage portfolio includes two phase 2 products: Seliforant (SENS-111) under investigation for acute unilateral vestibulopathy and Arazasetron (SENS-401) for sudden sensorineural hearing loss (SSNHL). We have built a unique R&D technology platform to expand our understanding of the physiopathology and etiology of inner ear related diseases enabling us to select the best targets and modalities for drug candidates. We also identify biomarkers to improve diagnosis and treatment of these underserved illnesses. Sensorion is launching in the second half of 2019 two preclinical gene programs aiming to correct hereditary monogenic forms of deafness including Usher Type 1 and deafness caused by a mutation of the gene encoding for Otoferlin. We are uniquely placed through our platforms and pipeline of potential therapeutics to make a lasting positive impact on hundreds of thousands of people with inner ear related disorders; a significant global unmet need in medicine today.

Label: SENSORION

ISIN: FR0012596468

Mnemonic: ALSEN

Disclaimer

This press release contains certain forward-looking statements concerning Sensorion and its business. Such forward looking statements are based on assumptions that Sensorion considers to be reasonable. However, there can be no assurance that such forward-looking statements will be verified, which statements are subject to numerous risks, including the risks set forth in the ‘Document de référence’ registration document filed with the ‘Autorité des Marchés Financiers’ (AMF French Financial Market Authority) on September 7th, 2017 under n°R.17-062 and to the development of economic conditions, financial markets and the markets in which Sensorion operates. The forward-looking statements contained in this press release are also subject to risks not yet known to Sensorion or not currently considered material by Sensorion. The occurrence of all or part of such risks could cause actual results, financial conditions, performance or achievements of Sensorion to be materially different from such forward-looking statements.

This press release and the information that it contains do not constitute an offer to sell or subscribe for, or a solicitation of an offer to purchase or subscribe for, Sensorion shares in any country. The communication of this press release in certain countries may constitute a violation of local laws and regulations. Any recipient of this press release must inform oneself of any such local restrictions and comply therewith.

EN
17/09/2019

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on Sensorion SAS

 PRESS RELEASE

Sensorion présente ses résultats pour l’exercice 2024, fait le point s...

MONTPELLIER, France--(BUSINESS WIRE)-- Regulatory News : Sensorion (FR0012596468 – ALSEN), société pionnière de biotechnologie au stade clinique, spécialisée dans le développement de nouvelles thérapies pour restaurer, traiter et prévenir les troubles de la perte auditive, publie aujourd’hui ses résultats pour l’exercice 2024, fait le point sur ses activités et annonce la mise à disposition du rapport annuel. « L'année écoulée a été une période exceptionnelle de progression sur les fronts du développement clinique et de l'entreprise », a commenté Nawal Ouzren, Directrice Générale de Sensorio...

 PRESS RELEASE

Sensorion Reports Full-Year 2024 Results, Provides Corporate Update an...

MONTPELLIER, France--(BUSINESS WIRE)-- Regulatory News: Sensorion (FR0012596468 – ALSEN) a pioneering clinical-stage biotechnology company specializing in the development of novel therapies to restore, treat and prevent hearing loss disorders, today reported its full-year 2024 results, provided a corporate update, and announced the availability of the full-year report. “This past year has been an exceptional period of progress on clinical and corporate development fronts,” commented Nawal Ouzren, Chief Executive Officer of Sensorion. “Our portfolio of next generation treatments for hearing l...

 PRESS RELEASE

Sensorion annonce la fin du recrutement des patients dans NOTOXIS, son...

MONTPELLIER, France--(BUSINESS WIRE)-- Regulatory News: Sensorion (FR0012596468 – ALSEN), société pionnière de biotechnologie au stade clinique, spécialisée dans le développement de nouvelles thérapies pour restaurer, traiter et prévenir des troubles de la perte auditive, annonce aujourd'hui le recrutement du dernier patient dans son essai clinique NOTOXIS de Phase 2a (Preuve de Concept) du SENS-401 pour la prévention de l’ototoxicité induite par le cisplatine (CIO). L'essai NOTOXIS (ClinicalTrials.gov ID : NCT05628233) évalue l'efficacité du SENS-401 dans la prévention de l’ototoxicité indu...

 PRESS RELEASE

Sensorion Announces the End of Patient Inclusion in NOTOXIS Phase 2a C...

MONTPELLIER, France--(BUSINESS WIRE)-- Regulatory News: Sensorion (FR0012596468 - ALSEN), a pioneering clinical-stage biotechnology company specializing in the development of novel therapies to restore, treat and prevent hearing loss disorders, today announced the enrollment of the last patient in its NOTOXIS Proof of Concept (POC) Phase 2a clinical trial of SENS-401 for the prevention of Cisplatin-Induced Ototoxicity (CIO). The NOTOXIS trial (ClinicalTrials.gov ID: NCT05628233) evaluates the efficacy of SENS-401 in preventing CIO in adult patients with neoplastic disease, four weeks after c...

 PRESS RELEASE

Sensorion Receives Positive Recommendation from Data Monitoring Commit...

MONTPELLIER, France--(BUSINESS WIRE)-- Regulatory News: Sensorion (FR0012596468 – ALSEN) a pioneering clinical-stage biotechnology company specializing in the development of novel therapies to restore, treat and prevent hearing loss disorders, today announced that the Data Monitoring Committee (DMC) recommended the continuation of the Audiogene Phase 1/2 clinical trial of SENS-501, the Company’s gene therapy program being developed to treat a specific form of congenital deafness linked to mutations in the OTOF (otoferlin) gene. Nawal Ouzren, Chief Executive Officer of Sensorion commented: “O...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch