Current report No. 13K– Conclusion of a licence agreement with Glenmark Pharmaceuticals Ltd. – correction

Current reports March 3, 2021

Legal basis: Article 17 section 1 of the Market Abuse Regulation (MAR) - confidential information.
Time: 3:36 PM

Content of the report:   

The Management Board of Celon Pharma S.A. hereby presents a correction of a clerical error that appeared in the content of current report No. 13/2021 of March 2, 2021, concerning the indication of one of the markets that is covered by the licence agreement – it was written: “Canary Islands”, whereas it should be written “Caribbean Islands”. The corrected content of the current report No. 13/2021 is as follows:

The Management Board of Celon Pharma S.A. (the “Company”) hereby informs that on March 2, 2021, it signed a licence agreement with Glenmark Pharmaceuticals Ltd with its registered seat in India (“Glenmark") to cooperate in the registration, sale and distribution of a product that constitutes a combination of fluticasone and salmeterol in a dry powder inhaler (sold in Poland under the name Salmex) on the following markets: Saudi Arabia, United Arab Emirates, Kuwait, Qatar, Bahrain, Oman, Libya, Algeria, Morocco, Iraq, South Africa, Mexico, Peru, Ecuador, Argentina, the Caribbean Islands, Philippines, Malaysia, Thailand, Singapore and Hong Kong.

The agreement was concluded for a period of 10 years from the date of sales commencement in the respective markets, with the possibility of extension. The agreement gives Glenmark the exclusive right to sell the product in the above markets and the Company only the right to manufacture the product for sale in the above markets.

The Company informed about the cooperation with Glenmark Pharmaceuticals Europe Ltd. with its registered seat in the UK regarding the licensing agreement, with respect to 15 European countries, for the aforementioned product in the prospectus approved by the Polish Financial Supervision Authority on August 29, 2016.