AB Science announces that Health Canada has resumed its review of the New Drug Submission for masitinib in amyotrophic lateral sclerosis, following issuance of a screening acceptance letter
AB SCIENCE ANNOUNCES THAT HEALTH CANADA HAS RESUMED ITS REVIEW OF THE NEW DRUG SUBMISSION FOR MASITINIB IN AMYOTROPHIC LATERAL SCLEROSIS, FOLLOWING ISSUANCE OF A SCREENING ACCEPTANCE LETTER
Paris, 09 May, 2023, 6pm CET
AB Science SA (Euronext - FR0010557264 - AB) today announces that Health Canada has issued a screening acceptance letter for the application of masitinib in the treatment of amyotrophic lateral sclerosis (ALS), meaning that the information and materials submitted by AB Science in response to the Notice of Deficiency (NOD) previously issued by Health Canada have been screened and found acceptable for the New Drug Submission to resume.
This letter is an important step in the procedure and effectively marks the restart date of the application’s review by Health Canada. Indeed, once the Response to a NOD is screened and found acceptable for scientific review, a new review period begins immediately.
Under the NOC/c policy, Health Canada has a target of 200 calendar days maximum to review the application.
As a reminder, Health Canada issued in December 2022 a notice of deficiency (NOD) for the New Drug Submission of masitinib in the treatment of amyotrophic lateral sclerosis, meaning that Health Canada requested the provision of additional information. AB Science submitted its revised application in April 2023, which has now been found acceptable for scientific review.
The application includes new analysis, recently presented at the American Academy of Neurology (AAN) 2023 Annual Meeting in Boston, performed in ALS patients prior to any complete loss of physical function (corresponding to a score of 0 on any ALSFRS-R individual component and regardless of baseline progression rate and accounting for about 80% of the overall AB10015 study population), showing a statistically significant 18.4% relative benefit on the CAFS endpoint in favor of masitinib 4.5 mg/kg/day as compared with control (p=0.035). The composite endpoint of functioning and survival (CAFS) is recommended by FDA and Health Canada as a primary endpoint to evaluate efficacy in ALS trials.
Alain Moussy, co-founder and CEO of AB Science, said: “There is an urgent need expressed by ALS patients and their families in Canada to access masitinib treatment under NOC/c status and we will continue to work diligently with Health Canada to respond to this need.”
An estimated 3,000 Canadians are currently living with ALS. Each year approximately 1,000 Canadians die from ALS. A similar number of Canadians are diagnosed with ALS each year.
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:
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