Month: August 2022

LONDRES, 31 août 2022 (GLOBE NEWSWIRE) — Meco Limited (Mecobit) a dévoilé le très attendu Ultimate Solar Power System (un système d’énergie solaire avec des sauvegardes incroyables et des mineurs de cryptomonnaies) lors d’un événement de lancement d’élite au Hong Kong Technology Bureau en août 2020.

Le kit de panneaux solaires pour station solaire compacte (complet) Solar Array M4000 met en avant l’un des équipements cryptographiques à énergie solaire les plus marquants au monde. Des équipements essentiels qui aident à continuer à fonctionner ou affectent les équipements tels que les appareils électroménagers, les séchoirs, les siphons de piscine ou les chargeurs de voitures électriques, ou même les équipements de minage de cryptomonnaie. Nous recherchons une façon de résoudre les problèmes mondiaux des sous-produits de combustibles fossiles, des niveaux élevés de consommation d’électricité. « Cela améliore la façon dont nous abordons l’imagination et la planification. De plus, cela rend ces progrès raisonnables pour le client », a déclaré B. FRANCI, PDG de MECO LIMITED.

Avec la partie axée sur le solaire du taux de hachage contrôlé apparemment facile à développer, beaucoup voient le potentiel d’utilisation durable de l’électricité dans le minage de Bitcoin comme un « cycle vertueux » – Mecobit stimule considérablement le minage de cryptomonnaies en permettant à la mission d’utiliser une électricité durable. L’électricité la moins chère imaginable encouragera davantage de tâches à se concentrer exclusivement sur des sources respectueuses de l’environnement telles que l’énergie solaire.

Principales caractéristiques de nos mineurs :

⦁ Rack Meco :

Capacité : BTC-4850 TH/s, ETH/ETC-20000 MH/s

Calcul : SHA256, Ethash

8 x Nvidia RTX 3090 (garantie incluse)

2 x cadre/étagère de minage

3 alimentations 930W 110-220V entièrement modulaires.

⦁ Miner M100 :

Taux de hachage : BTC 450 TH/s, ETH/ETC 200 MH/s

Puissance : 1 400 watts

Calcul : SHA256, Ethash

Connexion : Ethernet/sans fil

⦁ Mineur M200

Taux de hachage : BTC 650 TH/s, ETH/ETC 2300 MH/s

Puissance : 1 800 watts

Calcul : SHA256, Ethash

Connexion : Ethernet/sans fil

À propos de Mecobit

Elle a été lancée en 2015 avec la détermination de créer et de démontrer au monde une mine de monnaies numériques alimentée par l’énergie solaire ; les innovations Ethash, SHA-256 ou Scrypt peuvent être utilisées en fonction de l’inclination du mineur. L’organisation affirme qu’il s’agit du tout premier projet de minage de cryptomonnaies à énergie solaire sur Terre. « Nous devons perturber le secteur des chargeurs solaires en fournissant plus d’énergie à un coût plus raisonnable que ce que l’on pensait récemment être le cas. » – B. Franci (fondateur). Basée à Chiswick High Road à Londres, au Royaume-Uni, Mecobit possède des sites dans diverses communautés urbaines du monde entier, y compris les États-Unis. De plus amples informations sur l’organisation et ses projets sont disponibles sur le site web de l’organisation : www.mecobit.com

Contact : Ben Lukas, ben.lukas@mecobit.com, 852-3001 1453

• Myriad Genetics’ EndoPredict test accurately identified premenopausal women with ER+, HER2- breast cancer who could safely avoid adjuvant chemotherapy

SALT LAKE CITY, Aug. 31, 2022 (GLOBE NEWSWIRE) — Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in genetic testing and precision medicine, announced today Clinical Cancer Research, a journal of the American Association for Cancer Research, published a study ¹ that shows the EndoPredict^® breast cancer prognostic test significantly predicted distant recurrence in premenopausal women with ER+, HER2- early-stage breast cancer. This newly published study represents the first clinical validation of EndoPredict in a solely premenopausal population.

The study — first presented in an abstract at the 2021 ASCO Annual Meeting by Anastasia Constantinidou et al² — examined tumor samples from 385 premenopausal women with ER+, HER2- primary breast cancer who had not received chemotherapy. The results show EndoPredict accurately identified premenopausal women with and without affected lymph nodes who could safely avoid adjuvant chemotherapy as part of their treatment plans due to a very low recurrence risk.

“This important publication on the new EndoPredict data demonstrates our ongoing commitment to advance precision medicine for patients with breast cancer,” said Dr. Ralf Kronenwett, director of International Medical Affairs, Myriad Genetics. “In light of mounting clinical recommendations to reduce overtreatment in breast cancer, the results are particularly encouraging. With around a third of all new breast cancer cases occurring in patients aged 54 or younger³, using EndoPredict among premenopausal women provides important insights to inform personalized treatment, including whether there’s a benefit to using chemotherapy or not.”

The study shows that patients with EndoPredict low-risk scores had a 97% distant recurrence free survival (DRFS) versus 76% for high-risk patients. Importantly, 19% of node-positive premenopausal patients had EndoPredict low-risk scores with 100% DRFS and were able to safely avoid chemotherapy and continue onto endocrine therapy alone.

Another key result from an exploratory subgroup analysis within the study found similar DRFS rates in low-risk patients with or without ovarian function suppression (OFS), with less than 5% distant recurrence after 10 years in both groups.

“This important study shows that premenopausal patients with a low-risk EndoPredict score have a good long-term outcome without chemotherapy and may be considered for treatment with endocrine therapy only,” said Dr. Anastasia Constantinidou, Bank of Cyprus Oncology Centre and Cyprus Cancer Research Institute. “These findings are relevant to better inform personalized treatment decisions for a large proportion of premenopausal women with ER+, HER2- early-stage breast cancer.”

About the study
EndoPredict is a prognostic test that predicts patient risk of breast cancer recurrence to help identify who can consider safely forgoing chemotherapy. It analyzes 12 genes to create a molecular score, which is combined with tumor features, such as tumor size and nodal status, to establish a patient risk score (EPclin).

The Clinical Validation of EndoPredict in Premenopausal Women study tested tumor samples from 385 premenopausal women with ER+, HER2- primary breast cancer (pT1-3, pN0-1) who did not receive chemotherapy in addition to endocrine therapy. All samples were retrospectively tested blinded to clinical and outcome data with EndoPredict. Associations of EPclin Risk Scores with 10-year DRFS were evaluated by Cox proportional hazards models and Kaplan-Meier analysis. The primary outcome was 10-year DRFS.

In addition to EPclin, clinical variables of interest included age at diagnosis, tumor size, tumor grade, nodal status, Ki 67 expression, and continuous estrogen receptor (ER) expression and progesterone receptor (PgR) expression.

More information about this study can be found here.

¹ Constantinidou et al. Clin Cancer Res 2022 (https://aacrjournals.org/clincancerres/article/doi/10.1158/1078-0432.CCR-22-0619/708058/Clinical-Validation-of-EndoPredict-in)
² Constantinidou et al 2021 ASCO (https://ascopubs.org/doi/abs/10.1200/JCO.2021.39.15_suppl.537)
³ SEER Cancer Statistics Review, 1975-2016. Bethesda, MD: National Cancer Institute;2019.

About Myriad Genetics
Myriad Genetics is a leading genetic testing and precision medicine company dedicated to advancing health and well-being for all. Myriad develops and offers genetic tests that help assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where genetic insights can significantly improve patient care and lower healthcare costs. Fast Company named Myriad among the World’s Most Innovative Companies for 2022. For more information, visit www.myriad.com.

Myriad, the Myriad logo, BRACAnalysis, BRACAnalysis CDx, Colaris, Colaris AP, MyRisk, Myriad MyRisk, MyRisk Hereditary Cancer, MyChoice CDx, Prequel, Prequel with Amplify, Amplify, Foresight, Precise, FirstGene, Health.Illuminated., RiskScore, Prolaris, GeneSight, and EndoPredict are trademarks or registered trademarks of Myriad Genetics, Inc. © 2022 Myriad Genetics, Inc. All rights reserved.

Safe Harbor Statement
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements relating to using EndoPredict among premenopausal women to provide important insights to inform personalized treatment, including whether there’s a benefit to using chemotherapy or not. These “forward-looking statements” are management’s expectations of future events as of the date hereof and are subject to a number of known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated. Such factors include those risks described in the company’s filings with the U.S. Securities and Exchange Commission, including the company’s Annual Report on Form 10-K filed on February 25, 2022, as well as any updates to those risk factors filed from time to time in the company’s Quarterly Reports on Form 10-Q or Current Reports on Form 8-K.

Media Contact: Megan Manzari (385) 318-3718 Megan.Manzari@myriad.com

Investor Contact: Foster Harris (385) 350-8015 Foster.Harris@myriad.com

• O teste EndoPredict, da Myriad Genetics, identificou com precisão mulheres na pré-menopausa com câncer de mama ER+, HER2- que poderiam evitar, com segurança, a quimioterapia adjuvante

SALT LAKE CITY, Aug. 31, 2022 (GLOBE NEWSWIRE) — A Myriad Genetics, Inc.  (NASDAQ: MYGN), líder em testes genéticos e medicina de precisão, anunciou hoje que o Clinical Cancer Research Journal¹ publicou um estudo que mostra que o teste de prognóstico para câncer de mama EndoPredict^® previu significativamente a recorrência tardia em mulheres com câncer de mama em estágio inicial, na pré-menopausa, com ER+, HER2-. Este estudo, recém-publicado, representa a primeira validação clínica do EndoPredict em uma população, exclusivamente, na pré-menopausa.

O estudo – apresentado pela primeira vez como um resumo na Reunião Anual da ASCO 2021 por Anastasia Constantinidou et al² – examinou amostras de tumor de 385 mulheres na pré-menopausa, com câncer de mama primário, ER+ e HER2- que não receberam quimioterapia. Os resultados mostram que o EndoPredict identificou com precisão mulheres na pré-menopausa com e sem linfonodos comprometidos que poderiam evitar com segurança a quimioterapia adjuvante, como parte de seu plano de tratamento, devido a um risco de recorrência muito baixo.

“Esta importante publicação, sobre os novos dados do EndoPredict, demonstra nosso compromisso contínuo com o avanço da medicina de precisão para pacientes com câncer de mama”, disse o Dr. Ralf Kronenwett, diretor de Assuntos Médicos Internacionais da Myriad Genetics. “À luz das recomendações clínicas crescentes para reduzir o tratamento excessivo no câncer de mama, os resultados são particularmente encorajadores. Com cerca de um terço de todos os novos casos de câncer de mama ocorrendo em pacientes com 54 anos ou menos³ , o uso do EndoPredict entre mulheres na pré-menopausa fornece informações importantes para orientar o tratamento personalizado, incluindo se há benefícios em usar quimioterapia ou não.”

O estudo mostra que as pacientes com escores de baixo risco do EndoPredict tiveram uma sobrevida livre de recorrência (DRFS) de 97% versus 76% para pacientes de alto risco. É importante ressaltar que 19% das pacientes pré-menopáusicas com linfonodo positivo tiveram escores de baixo risco EndoPredict com DRFS de 100% e que poderiam evitar a quimioterapia com segurança e continuar apenas com a terapia endócrina.

Outro resultado importante de uma análise exploratória de subgrupo, dentro do estudo, encontrou taxas semelhantes de DRFS em pacientes de baixo risco com ou sem supressão da função ovariana (OFS), com menos de 5% de recorrência à distância após 10 anos, em ambos os grupos.

“Este importante estudo mostra que as pacientes na pré-menopausa com uma pontuação EPclin de baixo risco têm um bom resultado a longo prazo, sem quimioterapia, e podem ser consideradas para tratamento apenas com terapia endócrina”, disse a Dra. Anastasia Constantinidou, do “Bank of Cyprus Oncology Centre” e do “Cyprus Cancer Research Institute”. “Essas descobertas são relevantes para orientar melhor as decisões de tratamento personalizado para uma grande proporção de mulheres na pré-menopausa com câncer de mama ER+, HER2- em estágio inicial.”

Sobre o estudo
O EndoPredict é um teste prognóstico que prevê o risco de recorrência do câncer de mama para ajudar a identificar quem pode considerar abandonar a quimioterapia com segurança. Ele analisa 12 genes para criar uma pontuação molecular, que é combinada com características do tumor, como tamanho do tumor e status nodal, para estabelecer uma pontuação de risco da paciente (EPclin).

O estudo “Clinical Validation of EndoPredict in Pre-Menopausal Women” testou amostras de tumores de 385 mulheres na pré-menopausa com câncer de mama primário ER+, HER2- (pT1-3, pN0-1) que não receberam quimioterapia além da terapia endócrina. Todas as amostras foram testadas retrospectivamente, cegas para dados clínicos e de resultados com EndoPredict. Associações de escores de risco EPclin com sobrevida livre de recorrência em 10 anos (DRFS) foram avaliadas por modelos de riscos proporcionais de Cox e análise de Kaplan-Meier. O desfecho primário foi DRFS em 10 anos.

Além de EPclin, as variáveis clínicas de interesse incluíram idade ao diagnóstico, tamanho do tumor, grau do tumor, estado nodal, expressão de Ki 67, expressão contínua de receptor de estrogênio (ER) e expressão de receptor de progesterona (PgR).

Mais informações sobre este estudo podem ser encontradas aqui.

¹ Constantinidou et al. Clin Cancer Res 2022; published online ahead of print
² Constantinidou et al 2021 ASCO (https://ascopubs.org/doi/abs/10.1200/JCO.2021.39.15_suppl.537)
³ SEER Cancer Statistics Review, 1975-2016. Bethesda, MD: Instituto Nacional do Câncer; 2019.

Sobre a Myriad Genetics
A Myriad Genetics é uma empresa líder em testes genéticos e medicina de precisão, dedicada a promover a saúde e o bem-estar de todos. A Myriad desenvolve e oferece testes genéticos que ajudam a avaliar o risco de desenvolver doenças ou progressão da doença e orientar as decisões de tratamento em todas as especialidades médicas, onde as informações genéticas podem melhorar significativamente o atendimento ao paciente e reduzir os custos de saúde. A Fast Company nomeou a Myriad entre as empresas mais inovadoras do mundo para 2022. Para obter mais informações, visite www.myriad.com.

Myriad, o logotipo da Myriad, BRACAnalysis, BRACAnalysis CDx, Colaris, Colaris AP, MyRisk, Myriad MyRisk, MyRisk Hereditary Cancer, MyChoice CDx, Prequel, Prequel with Amplify, Amplify, Foresight, Precise, FirstGene, Health.Illuminated., RiskScore, Prolaris , GeneSight e EndoPredict são marcas comerciais ou marcas registradas da Myriad Genetics, Inc. © 2022 Myriad Genetics, Inc. Todos os direitos reservados.

Safe Harbor Statement
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements relating to using EndoPredict among premenopausal women to provide important insights to inform personalized treatment, including whether there’s a benefit to using chemotherapy or not. These “forward-looking statements” are management’s expectations of future events as of the date hereof and are subject to a number of known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated. Such factors include those risks described in the company’s filings with the U.S. Securities and Exchange Commission, including the company’s Annual Report on Form 10-K filed on February 25, 2022, as well as any updates to those risk factors filed from time to time in the company’s Quarterly Reports on Form 10-Q or Current Reports on Form 8-K.

Media Contact: Megan Manzari (385) 318-3718 Megan.Manzari@myriad.com

Investor Contact: Foster Harris (385) 350-8015 Foster.Harris@myriad.com

• Le test EndoPredict de Myriad Genetics identifie avec précision les femmes préménopausées atteintes d’un cancer du sein RE+, HER2- qui pourraient éviter une chimiothérapie adjuvante sans perte de chance

SALT LAKE CITY, 31 août 2022 (GLOBE NEWSWIRE) — Myriad Genetics, Inc. (NASDAQ : MYGN), leader dans le domaine des tests génétiques et de la médecine de précision, a annoncé aujourd’hui que le Clinical Cancer Research Journal¹ avait publié une étude démontrant que le test pronostique du cancer du sein EndoPredict^® prédit de façon significative la récidive à distance chez les femmes préménopausées atteintes d’un cancer du sein RE+, HER2-, à un stade précoce. Cette étude récemment publiée représente la première validation clinique d’EndoPredict au sein d’un groupe constitué uniquement de femmes préménopausées.

L’étude — d’abord présentée sous forme de poster par Anastasia Constantinidou et al² lors de la réunion annuelle de l’ASCO 2021 — a examiné les échantillons tumoraux de 385 femmes préménopausées atteintes d’un cancer du sein primitif RE+, HER2- qui n’ont pas reçu de chimiothérapie. Les résultats montrent qu’EndoPredict a identifié avec précision les femmes préménopausées avec et sans envahissement ganglionnaire qui pourraient éviter une chimiothérapie adjuvante en toute sécurité dans le cadre de leur prise en charge, et ce en raison d’un risque de récidive très faible.

« Cette publication importante sur les nouvelles données d’EndoPredict démontre notre engagement permanent à faire progresser la médecine de précision pour les patientes atteintes d’un cancer du sein », indique le Dr Ralf Kronenwett, Directeur des Affaires Médicales Internationales chez Myriad Genetics. « Compte tenu des recommandations cliniques actuelles visant à réduire le surtraitement du cancer du sein, les résultats sont particulièrement encourageants. Avec environ un tiers de l’ensemble des nouveaux cas de cancer du sein survenant chez des patientes âgées de 54 ans ou moins,³ l’utilisation d’EndoPredict chez des femmes préménopausées fournit des informations importantes permettant d’orienter la prise en charge personnalisée, et notamment de savoir si une chimiothérapie présente un avantage ou non. »

L’étude montre que les patientes avec des scores de risque EndoPredict faible avaient une survie sans récidive à distance de 97 % contre 76 % pour les patientes à risque élevé. Il convient de noter que 19 % des patientes préménopausées avec envahissement ganglionnaire avaient des scores de risque EndoPredict faible avec une survie sans récidive à distance de 100 %. Elles ont pu éviter une chimiothérapie sans perte de chance et poursuivre une hormonothérapie seule.

Un autre résultat clé d’une analyse de sous-groupe exploratoire au sein de l’étude a montré des taux de survie sans récidive à distance similaires chez des patientes à risque faible de récidive, avec ou sans suppression de la fonction ovarienne (SFO), avec moins de 5 % de récidives à distance après 10 ans dans les deux groupes.

« Cette étude importante montre que les patientes préménopausées ayant un score de risque EPclin faible ont de bons résultats à long terme sans chimiothérapie et qu’un traitement par hormonothérapie seule peut être envisagé chez ces dernières, » explique le Dr Anastasia Constantinidou, Bank of Cyprus Oncology Centre et Cyprus Cancer Research Institute. « Ces résultats sont pertinents et permettent de mieux orienter les décisions thérapeutiques personnalisées chez une grande partie des femmes préménopausées atteintes d’un cancer du sein RE+, HER2-, à un stade précoce. »

À propos de l’étude
EndoPredict est un test pronostique qui prédit le risque de récidive de cancer du sein afin d’identifier les patientes qui peuvent envisager de renoncer à une chimiothérapie en toute sécurité. Il analyse 12 gènes pour créer un score moléculaire combiné aux caractéristiques de la tumeur, telles que la taille de la tumeur et le statut ganglionnaire, afin d’établir un score de risque (EPclin) personnalisé.

L’étude de validation clinique d’EndoPredict chez des femmes préménopausées a analysé des échantillons tumoraux chez 385 femmes préménopausées atteintes d’un cancer du sein primitif, RE+, HER2- (pT1-3, pN0-1) qui n’ont pas reçu de chimiothérapie en plus d’une hormonothérapie. Tous les échantillons ont été analysés rétrospectivement avec EndoPredict, indépendamment des données cliniques et des résultats. L’association des scores de risque EPclin à la survie sans récidive à distance à 10 ans a été évaluée par les modèles à risques proportionnels de Cox et une analyse de Kaplan-Meier. Le résultat principal était la survie sans récidive à distance à 10 ans.

Outre EPclin, les variables cliniques d’intérêt incluaient l’âge lors du diagnostic, la taille de la tumeur, le grade, le statut ganglionnaire, l’expression du Ki 67 et l’expression continue des récepteurs des œstrogènes (RE) et des récepteurs de la progestérone (PgR).

Pour plus d’informations sur cette étude, veuillez cliquer ici

¹ Constantinidou et al. Clin Cancer Res 2022; published online ahead of print
² Constantinidou et al 2021 ASCO (https://ascopubs.org/doi/abs/10.1200/JCO.2021.39.15_suppl.537)
³ SEER Cancer Statistics Review, 1975-2016. Bethesda, MD: National Cancer Institute;2019.

À propos de Myriad Genetics
Myriad Genetics est une société leader dans le domaine des tests génétiques et de la médecine de précision qui se consacre à faire progresser la santé et le bien-être de tous. Myriad développe et offre des tests génétiques qui aident à évaluer le risque de développer une maladie ou le risque de progression de la maladie et orientent les décisions thérapeutiques dans les spécialités médicales où les données génétiques peuvent améliorer de manière significative les soins aux patients et réduire les coûts de santé. Fast Company a nommé Myriad parmi les Entreprises les plus innovantes du monde en 2022. Pour plus d’informations, veuillez consulter www.myriad.com.

Myriad, le logo Myriad, BRACAnalysis, BRACAnalysis CDx, Colaris, Colaris AP, MyRisk, Myriad MyRisk, MyRisk Hereditary Cancer, MyChoice CDx, Prequel, Prequel with Amplify, Amplify, Foresight, Precise, FirstGene, Health.Illuminated., RiskScore, Prolaris, GeneSight et EndoPredict sont des marques commerciales ou des marques déposées de Myriad Genetics, Inc. © 2022 Myriad Genetics, Inc. Tous droits réservés.

Safe Harbor Statement
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements that the company’s new facilities will reflect the latest advancements in scalable modular design, including automated liquid handling, reduced waste volume, and lower use of plastics. These “forward-looking statements” are management’s present expectations of future events and are subject to a number of risks, uncertainties, assumptions, and other factors that could cause actual results to differ materially and adversely from those described in the forward-looking statements. Such factors include those risks described in the company’s filings with the U.S. Securities and Exchange Commission, including the company’s Annual Report on Form 10-K filed on February 25, 2022, as well as any updates to those risk factors filed from time to time in the company’s Quarterly Reports on Form 10-Q or Current Reports on Form 8-K.

Contact pour la presse : Megan Manzari (385) 318-3718 Megan.Manzari@myriad.com

Contact pour les investisseurs : Foster Harris (385) 350-8015 Foster.Harris@myriad.com

COPENHAGEN, Denmark, Aug. 31, 2022 (GLOBE NEWSWIRE) — Copenhagen Infrastructure Partners (CIP) has reached final close on its new fund, CI Energy Transition Fund I (CI ETF I). The fund was oversubscribed and closed at the hard cap of EUR 3 billion. This makes CI ETF I the largest dedicated clean hydrogen fund globally.

CI ETF I achieved commitments from investors across the Nordics (~25% of commitments), Europe (~45%), Asia-Pacific (~20%) and North America (~10%) with approximately a 50/50 split between existing investors in CIP funds and new investors. The fund’s investor base comprises approximately 65 institutional investors, primarily pension funds, life insurance companies, sovereign wealth funds, asset managers, and family offices.

“We are very pleased to welcome a prominent group of existing and new institutional investors to CI ETF I and are delighted that investors share our confidence in and appetite for clean energy infrastructure projects and invest alongside CIP in the next phase of the energy transition. Solutions such as Power-to-X will be key for countries and industries to take the next big leap within reaching the commitments of the Paris agreement and achieving energy independence. As an industry pioneer and one of the global market leaders in greenfield renewable infrastructure investments, CIP is uniquely positioned to invest in this segment,” says Jakob Baruël Poulsen, Managing Partner in CIP.

CI ETF I will invest in next generation renewable energy infrastructure including industrial scale Power-to-X (PtX) projects and enables institutional investors to participate in the decarbonization of the so-called hard to abate industries and support the further integration of renewable power generation in the energy mix through grid balancing. The fund will primarily focus on greenfield projects in the OECD and aims to contribute to the decarbonization of industries such as agriculture, aviation, shipping, chemical manufacturing, and steel production through the use of green fuels and feedstock and CO2-free fertilizers.

CI ETF I make up an integral part of CIP’s distinct fund strategies that tap into the main renewable energy transition trends. The fund will apply the same and proven value creation and de-risking approach as CIP’s existing funds, though with a focus for CI ETF on PtX. CI ETF I will apply CIP’s industrial skills to optimize and de-risk its projects through among others project design, partner selection, and contracting. Once de-risked the projects are expected to have core infrastructure characteristics including long term offtake contracts.

CI ETF I is off to a strong start with FID taken on one investment and ownership on several attractive industrial scale development stage PtX projects with diverse exposure to production technologies and offtake markets. The projects which among others are in Western Europe (Denmark, Norway, Spain, Portugal), South America (Chile), and Australia are expected to produce green hydrogen, green ammonia, and sustainable aviation fuel based on GW scale renewable energy production and electrolysis capacity.

CI ETF I’s current portfolio once operational is estimated to reduce more than 7.5 million tonnes of CO2 annually (or the equivalent to removing ~1.6 million cars from the roads permanently) and deliver more than 4 million tonnes of green fuels each year.

For the marketing of CI ETF I, law firms Plesner and Clifford Chance acted as legal counsel, KPMG Acor Tax as tax advisor, and Selinus Capital Advisors, Compagnie Financière Jacques Coeur (CFJC) and Allen Partners as placement agents.

About Copenhagen Infrastructure Partners
Founded in 2012, Copenhagen Infrastructure Partners P/S (CIP) today is the world’s largest dedicated fund manager within greenfield renewable energy investments and a global leader in offshore wind. The funds managed by CIP focuses on investments in offshore and onshore wind, solar PV, biomass and energy-from-waste, transmission and distribution, reserve capacity, storage, advanced bioenergy, and Power-to-X.

CIP manages ten funds and has to date raised approximately EUR 19 billion for investments in energy and associated infrastructure from more than 135 international institutional investors. CIP will accelerate its role in the global energy transition and aim to have EUR 100 billion under management in green energy investments in 2030. CIP has approximately 340 employees and offices in Copenhagen, London, Hamburg, Utrecht, New York, Tokyo, Singapore, Seoul, and Melbourne. For more information, visit www.cip.dk

For further information, please contact:

Simon Augustesen, – VP, Chief Communication and Marketing Officer, Phone: +45 30526721, Email: siau@cip.dk

Thomas Kønig, Partner – Investor Relations, Phone: +45 7070 5151, Email: tkon@cip.dk