GlobeNewswire by notified

Major shareholder announcement – BlackRock, Inc.



Major shareholder announcement

Major shareholder announcement – BlackRock, Inc.

Pursuant to Section 30 of the Capital Markets Act, it is hereby announced that BlackRock, Inc. has informed ChemoMetec A/S that BlackRock Investment Management (UK) Limited on 13 May 2024, decreased its holding of voting rights attached to shares and voting rights in ChemoMetec A/S to below 10%, and that the holding thus is below the 10 per cent limit in section 38 of the Capital Markets Act.

The aggregate holding of shares and voting rights of BlackRock, Inc. in ChemoMetec A/S amounts to 14,07% of the total share capital and voting rights in ChemoMetec A/S.

Additional information

Niels Høy Nielsen, CFO
Telephone (+45) 2551 8724

About ChemoMetec A/S

ChemoMetec develops, manufactures and markets instruments for cell counting and a wide range of other measurements. ChemoMetec’s instruments are marketed to the pharmaceutical, biotech and agricultural industries worldwide.

ChemoMetec was founded in 1997 and is listed on Nasdaq OMX Copenhagen. For more information, go to

To view this piece of content from, please give your consent at the top of this page.
To view this piece of content from, please give your consent at the top of this page.

About GlobeNewswire by notified

GlobeNewswire by notified
GlobeNewswire by notified
One Liberty Plaza - 165 Broadway
NY 10006 New York

GlobeNewswire by notified is one of the world's largest newswire distribution networks, specializing in the delivery of corporate press releases financial disclosures and multimedia content to the media, investment community, individual investors and the general public.

Subscribe to releases from GlobeNewswire by notified

Subscribe to all the latest releases from GlobeNewswire by notified by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from GlobeNewswire by notified

Curium Announces First Commercial Doses in France of Pylclari® – an Innovative 18F-Psma Pet Tracer Indicated in Patients With Prostate Cancer30.5.2024 09:00:00 CEST | Press release

PARIS, May 30, 2024 (GLOBE NEWSWIRE) -- Curium, a world leader in nuclear medicine, today announced that earlier this month patients in France received the first doses of PYLCLARI® (INN: Piflufolastat (18F) also known as (18F)-DCFPyL) indicated for the detection of prostate-specific membrane antigen (PSMA) positive lesions with positron emission tomography (PET) in patients with prostate cancer in the following clinical settings: Primary staging of patients with high-risk prostate cancer prior to initial curative therapyTo localize recurrence of prostate cancer in patients with a suspected recurrence based on increasing serum prostate-specific antigen (PSA) levels after primary treatment with curative intent Today’s news follows earlier announcements by Curium of the first doses for Greece in November 2023, and for 2024 first doses for Italy in February, for the Netherlands in March, and for Germany in May. Benoit Woessmer, PET Europe CEO at Curium commented, “We are extremely pleased

Interim financial report for 1 January - 31 March 2024 for FirstFarms A/S30.5.2024 09:00:00 CEST | Press release

Satisfactory start of 2024 FirstFarms has had a satisfactory start to the year. A number of significant events will have a positive impact on the Group going forward. FirstFarms has in the accounting period Q1-2024 realised: · A turnover of 104 mDKK (2023: 109 mDKK) · An EBITDA of 36 mDKK (2023: 33 mDKK) · An EBIT of 22 mDKK (2023: 22 mDKK) · A pre-tax result of 14 mDKK (2023: 20 mDKK) EBITDA has improved by 3.0 mDKK compared to the same period last year. The decrease in turnover is due to lower sale of previous years’ crops compared to Q1 2023. The lower pre-tax result compared to the same period last year is primarily due to a higher interest rate level, but also completed investments in 2023. CEO of FirstFarms, Anders H. Nørgaard, is satisfied with the Q1 results: "Our animal production has got off to a good start, and we have increased the turnover of pigs and milk by a total of 9 mDKK compared to the same period last year. "The low crop prices have continued into 2024. This means

Delårsrapport for 1. januar - 31. marts 2024 for FirstFarms A/S30.5.2024 09:00:00 CEST | pressemeddelelse

Tilfredsstillende start på 2024 FirstFarms har fået en tilfredsstillende start på året. En række væsentlige begivenheder får positiv betydning for koncernen fremadrettet. FirstFarms har i regnskabsperioden Q1-2024 realiseret: · En omsætning på 104 mDKK (2023: 109 mDKK) · Et EBITDA på 36 mDKK (2023: 33 mDKK) · Et EBIT på 22 mDKK (2023: 22 mDKK) · Et resultat før skat på 14 mDKK (2023: 20 mDKK) EBITDA er forbedret med 3,0 mDKK sammenlignet med samme periode sidste år. Faldet i omsætning skyldes lavere salg af tidligere års afgrøder i forhold til Q1 2023. Det lavere resultat før skat i forhold til samme periode sidste år, skyldes primært et højere renteniveau men også gennemførte investeringer i 2023 Administrerende direktør i FirstFarms, Anders H. Nørgaard, er tilfreds med Q1-resultatet: ”Vores animalske produktion er kommet godt fra start, og vi har løftet omsætningen på grise og mælk med samlet 9 mDKK i forhold til samme periode sidste år. ”De lave afgrødepriser er fortsat ind i 2024.

Samsung Bioepis to Present Post-hoc Analysis of Phase 3 Study for EPYSQLI™ (SB12; Eculizumab Biosimilar), at the European Hematology Association (EHA) Congress 202430.5.2024 08:30:30 CEST | Press release

Post-hoc analysis of Phase 3 study to highlight transfusion avoidance results of SB12 compared to reference eculizumab-treated groups INCHEON, Korea, May 30, 2024 (GLOBE NEWSWIRE) -- Samsung Bioepis Co., Ltd. today announced that a post-hoc analysis of the Phase 3 clinical study results for EPYSQLI™ (SB12), a biosimilar to Soliris1 (eculizumab), will be presented at the 29th European Hematology Association 2024 (EHA2024) Hybrid Congress held in Madrid, Spain and virtually, from June 13 to 16, 2024. SB12 has shown equivalent efficacy with reference eculizumab (ECU) by lactate dehydrogenase (LDH) and comparable safety, pharmacokinetics, pharmacodynamics, and immunogenicity profiles in paroxysmal nocturnal hemoglobinuria (PNH) through the pivotal Phase 3 study.2 The post-hoc analysis of SB12 pivotal Phase 3 study presented at EHA2024 compared the proportion of patients remaining transfusion-free (“transfusion avoidance”) among those treated with SB12 or ECU, respectively. Eculizumab is kn

Combined General Meeting of June 20, 2024 - Availability of the preparatory documents30.5.2024 08:30:00 CEST | Press release

Daix (France), Long Island City (New York, United States), May 30, 2024 – Inventiva (Euronext Paris and Nasdaq: IVA), a clinical-stage biopharmaceutical company focused on the development of oral small molecule therapies for the treatment of metabolic dysfunction-associated steatohepatitis (“MASH”), also known as non-alcoholic steatohepatitis (“NASH”), and other diseases with significant unmet medical needs, today announced the availability of the preparatory documents for the Combined General Meeting of June 20, 2024. Shareholders are invited to participate in the Combined General Meeting that will be held on June 20, 2024 at 9 a.m. at Hôtel Castel Burgond, 3 route de Troyes, 21121 Daix (France). The preliminary notice of meeting comprising the agenda and the draft resolutions, as well as information on how to attend and vote at the Combined General Meeting, was published in the Bulletin des Annonces Légales Obligatoires (BALO) n°58 of May 13, 2024 and a translation was filed with the

HiddenA line styled icon from Orion Icon Library.Eye