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Amoéba: final phase for marketing authorisation of AXPERA
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Amoéba: final phase for marketing authorisation of AXPERA
Amoeba
Tue, February 24, 2026 at 7:17 PM GMT+9 4 min read
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Amoeba
Chassieu, Feb. 24, 2026 (GLOBE NEWSWIRE) –
Chassieu (France), 23 February 2026 – 6:00 pm - Amoéba (FR0011051598 - ALMIB), industrial greentech specialised in the development of natural microbiological solutions based on the patented use of amoebae, announces that the ANSES (French Agency for Food, Environmental and Occupational Health & Safety) has initiated the final phase of its assessment of the marketing authorisation application for the biocontrol product AXPERA, submitted in March 2025.
One final step before obtaining marketing authorisation on the French market
In 2025, Amoéba initiated the procedure in Europe to apply for marketing authorisation for its AXPERA biocontrol product in priority Member States. France agreed to act as the rapporteur Member State (zRMS) for all of these countries (see press releases dated 15 January 2025 and 22 April 2025). As such, the ANSES, the French competent authority, is currently finalising its assessment of the authorisation application submitted in March 2025.
The procedure includes a final stage for comments on the draft assessment report (“draft Registration Report”), open to both the applicant (Amoéba) and the other Member States concerned. This comment phase, which began in February, will end on 6 March 2026. It will be followed by the final phase of signing and official publication of the marketing authorisation in France. This administrative phase may take several weeks.
At this stage of the draft Registration Report, Amoeba considers that there are no obstacles to the marketing authorisation of the product. The requested uses (culture/disease combinations) have all been deemed acceptable, and the product’s safety profile has been confirmed.
On the basis of the ANSES final assessment report and the French authorisation, the other Member States concerned will then initiate the national authorisation procedure for AXPERA in their territories.
New derogatory marketing authorisations to come in order to meet demand from the agricultural sectors for AXPERA
Given the uncertainty regarding the timing of this final phase, the agricultural sectors in France and Italy have initiated procedures to obtain exceptional marketing authorisations for the use of AXPERA in certain situations presenting phytosanitary emergencies, similar to the authorisation granted in 2025 for the use of AXPERA against downy mildew in vineyards in France (see press release of 22 April 2025). The aim is therefore to enable agricultural producers to use AXPERA from the start of the production season.
Furthermore, following on from the exceptional authorisation granted in 2025 by the Dutch authorities, Amoéba has submitted a new application for exceptional authorisation for large-scale trials in the Netherlands to use AXPERA on several crops, including the possibility of consuming the harvests.
Provided they are granted, which was the case in 2025, these derogatory authorisations would allow AXPERA to be marketed for the uses concerned, regardless of the final timetable for obtaining marketing authorisation.
**About Amoéba: **
Founded in 2010, Amoéba is a green tech company based in Chassieu (Lyon, France) that aims to become a major player in microbiological risk treatment through the patented use of amoebae in the plant protection and cosmetics sectors.
With unique expertise protected by numerous patents, Amoéba is currently the only company authorised to use the Willaertia amoeba industrially for biocontrol and cosmetic applications. To the Company’s knowledge, it is also the only company capable of producing it on an industrial scale in volumes compatible with commercial applications, in order to offer a viable alternative to the chemical products widely used today.
Amoéba is currently focusing on the global biocontrol market for plant protection and the cosmetics market. As the marketing of plant protection products is subject to obtaining local regulatory approvals, the Company has taken the necessary regulatory steps and submitted applications for approval in Europe and the United States. The active substance has already been approved in the United States in 2022 and received a positive and final report from the EFSA in Europe. Product registration was obtained in 2025 for the United States and is expected in 2026 in France and then in other targeted European countries.
The cosmetic application does not require prior approval from a competent authority in Europe or the United States. The cosmetic ingredient is already listed on the INCI (International Nomenclature of Cosmetic Ingredients) list, paving the way for its commercialisation worldwide, except in China, where local approval is required.
Amoéba is listed on Euronext Growth (ALMIB). The company is a member of the Bpifrance Excellence network and is eligible for the PEA-PME scheme. For more information, visit www.amoeba-nature.com.
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Disclaimer
This press release contains certain forward-looking statements concerning Amoéba which are based on its own assumptions and estimates and on information that is currently available to us. However, Amoéba gives no assurance that the estimates contained in such forward-looking statements will be verified, with these estimates subject to numerous risks, including the risks set forth in Amoéba’s universal registration document filed with the French Financial Markets Authority (Autorité des Marchés Financiers) on April 17, 2025 under number D.25-0281 and available on the Amoéba website (www.amoeba-nature.com). The forward-looking statements contained in this press release are also subject to risks not yet known to Amoéba or not currently considered material by Amoéba. The occurrence of all or part of such risks could cause Amoéba’s actual results, financial conditions, performance, or achievements to be materially different from such forward-looking statements.
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