AB Science is providing a summary of the live webcast held on May 30, 2024, giving an update on the application for conditional marketing authorization of masitinib in ALS

AB Science

Fri, May 31, 2024, 7:30 AM 5 min read

Regarding the conditional approval of masitinib in ALS with EMA, AB Science presented the CHMP trend vote position, concluding that the safety of masitinib is deemed acceptable but outstanding issues remain preventing a favorable benefit assessment. These issues and main justifications presented by AB Science are detailed in the presentation. The EMA decision will be made public during the next CHMP meeting to be held on June 24-27, 2024.

As a next step, AB Science indicated that it has the option to request a re-examination, and that it would liaise with the EMA to define the appropriate pathway to registration. In case of re-examination, a new Rapporteur and new Co-Rapporteur are appointed to assess the dossier, and a Scientific Advisory Group) can be appointed to provide recommendations on key points. Such key points could include: Application of EMA guideline on the Good Clinical Practices (GCP), application of EMA guideline on subgroup, application of the two recommendations for handling of missing data, and whether excluding Fast progressors from primary analysis is justified.

Regarding the conditional approval of masitinib in ALS with Health Canada, AB Science presented the main clinical objections raised by Health Canada, which were slightly different from the ones raised by EMA.

Finally, AB Science clarified that a distinction was to be made between the conditional marketing authorization that requires very compelling evidence from a single study, and the available preclinical and clinical data from masitinib program, that are robust and will support full approval, provided a confirmatory study is positive.

Masitinib has a validated mechanism of action, targeting the innate immune system, via modulation of mast cells and microglia. Masitinib exerts a protective effect on the central nervous system and on the peripheral nervous system. In addition, Masitinib has demonstrated its ability to lower blood levels of neurofilament light (NfL) in a neurodegenerative disease model (EAE model).
Study AB10015 is a 48-week study, which is stronger evidence than a 24-week study, and is same time point as the confirmatory study. In addition, study AB10015 demonstrated a significant treatment effect in the primary analysis population.
Data are exceptionally strong in the population close to the confirmatory study and that could be the claim, with a significant benefit on functional score, a significant benefit on quality of life, and a significant benefit of plus 12 months on long-term overall survival.

AB Science has asked to Euronext Paris to resume listing of its shares from the opening of trading on Monday June 03, 2024.

About AB Science
Founded in 2001, AB Science is a pharmaceutical company specializing in the research, development and commercialization of protein kinase inhibitors (PKIs), a class of targeted proteins whose action are key in signaling pathways within cells. Our programs target only diseases with high unmet medical needs, often lethal with short term survival or rare or refractory to previous line of treatment.
AB Science has developed a proprietary portfolio of molecules and the Company’s lead compound, masitinib, has already been registered for veterinary medicine and is developed in human medicine in oncology, neurological diseases, inflammatory diseases and viral diseases. The company is headquartered in Paris, France, and listed on Euronext Paris (ticker: AB).
Further information is available on AB Science’s website:
www.ab-science.com.

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