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Aeterna Zentaris Starts Preclinical Development of Macimorelin as a Potential Treatment for ALS
americanpharmaceuticalreview
May 18, 2021
Aeterna Zentaris Inc. has announced the commencement of the previously announced preclinical program to qualify macimorelin for clinical development as a potential treatment option for amyotrophic lateral sclerosis (ALS; Lou Gehrig's disease).
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Aeterna Zentaris signs agreement to evaluate oral Covid-19 vaccine
pharmaceutical-technology
February 04, 2021
Aeterna Zentaris has signed an exclusive option agreement with the Julius-Maximilians-University Wuerzburg, Germany, to analyse the latter’s preclinical potential Covid-19 vaccine.
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Aeterna Zentaris Announces Strategic Review and Engagement of Financial Advisor
firstwordpharma
March 13, 2019
Aeterna Zentaris Inc. (NASDAQ:AEZS) (TSX: AEZS) announced today that its board of directors has formed a special committee of independent directors (the “Special Committee”) to review strategic options available to Aeterna Zentaris.
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Aeterna Zentaris Announces ZoptEC Phase 3 Clinical Study of Zoptrex Misses Primary Endpoint
americanpharmaceuticalreview
May 02, 2017
Aeterna Zentaris announced the ZoptEC Phase 3 clinical study of Zoptrex in women with locally advanced.
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Aeterna Zentaris Intends to File NDA with Respect to Macrilen in Third Quarter of 2017
drugs.com
April 06, 2017
Aeterna Zentaris Inc. (NASDAQ: AEZS) (TSX: AEZS) (the “Company”) today announced that, following its meeting with the U.S. Food and Drug Administration (the “FDA” or the “Agency”) on March 29, 2017.
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Aeterna Zentaris Announces Plans to Pursue FDA Registration of Macrilen™
americanpharmaceuticalreview
February 15, 2017
Eli Lilly and Company and Incyte Corporation announced that the European Commission has granted marketing authorization for Olumiant® (baricitinib) 4 mg and 2 mg film-coated tablets in Europe for the treatment of moderate-to-severe active rheumatoid arthr
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Aeterna Zentaris Announces Plans to Pursue FDA Registration of Macrilen
drugs.com
February 14, 2017
Aeterna Zentaris Inc. announced it concluded that Macrilen™ demonstrated performance supportive of achieving registration with the U.S. Food and Drug Administration.