July 16 (Reuters) - NICOX SA NCOX.PA :
* Q2 REVENUE EUR 700,000
* VYZULTA AND ZERVIATE PRESCRIPTIONS IN U.S. INCREASED BY
21% AND
712% RESPECTIVELY IN Q2 2021 COMPARED TO Q2 2020
* CASH OF EUR 36.5 MILLION ON JUNE 30, 2021 SUFFICIENT FOR
COMPANY
TO MEET ITS CURRENT REQUIREMENTS FOR NEXT TWELVE MONTHS
* AS OF JUNE 30, 2021, NICOX GROUP HAD FINANCIAL DEBT OF EUR
18.0
MILLION
* NCX 4251 TOP-LINE RESULTS EXPECTED IN SEPTEMBER 2021
* NEXT STEPS IN DEVELOPMENT OF NCX 4251, NOT CURRENTLY
FINANCED,
TO BE ANNOUNCED AFTER END-PHASE 2 MEETING WITH FDA, EXPECTED
START OF 2022
* NCX 470 IS CURRENTLY IN TWO MULTI-REGIONAL PHASE 3
GLAUCOMA
CLINICAL TRIALS, WITH TOP-LINE RESULTS FROM THE FIRST PHASE 3
CLINICAL TRIAL, MONT BLANC, EXPECTED IN Q2 2022
* NCX 470 : RESULTS FROM THE SECOND PHASE 3 TRIAL, DENALI,
ARE
EXPECTED IN 2023
* OUR MARKET RESEARCH SUGGESTS PEAK NET SALES POTENTIAL FOR
NCX
470 IN U.S. OF OVER $500 MILLION, IF APPROVED AND DEPENDING ON
RESULTS OF PHASE 3 CLINICAL TRIALS
Source text for Eikon: ID:nGNX8dTwXV
Further company coverage: NCOX.PA
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 7696600;))