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In der Rubrik News haben wir 19140 Angebote für Sie gefunden
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Med-X-Press legt dritten Nachhaltigkeitsbericht vor
17.07.2024Nachhaltigkeit ist nicht nur Chefsache! Der Pharmalogistiker Med-X-Press GmbH und die Schwestergesellschaft MXP Fulfillment GmbH, Goslar, veröffentlichen den dritten freiwillig erstellten Nachhaltigkeitsreport für das Jahr 2023.
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Med-X-Press legt dritten Nachhaltigkeitsbericht vor
18.07.2024Nachhaltigkeit ist nicht nur Chefsache! Der Pharmalogistiker Med-X-Press GmbH und die Schwestergesellschaft MXP Fulfillment GmbH, Goslar, veröffentlichen den dritten freiwillig erstellten Nachhaltigkeitsreport für das Jahr 2023.
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GEA expertise at the Carbon Capture Technology Expo in Hamburg in October
17.07.2024GEA will participate with a booth and a presentation at the Carbon Capture Technology Expo on October 23 and 24, 2024 at the Hamburg Messe. At this world-leading exhibition and conference on Carbon Capture, utilization and storage, GEA will exhibit a Carbon Capture plant "GEA CEBO for 50t /day CO? capture capacity". The aim is to identify and discuss the opportunities for carbon removal technologies as a key solution on the road to net zero emissions and to accelerate their adoption. The GEA stand can be found in hall A4, stand number 4D15.
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GEA expertise at the Carbon Capture Technology Expo in Hamburg in October
18.07.2024GEA will participate with a booth and a presentation at the Carbon Capture Technology Expo on October 23 and 24, 2024 at the Hamburg Messe. At this world-leading exhibition and conference on Carbon Capture, utilization and storage, GEA will exhibit a Carbon Capture plant "GEA CEBO for 50t /day CO? capture capacity". The aim is to identify and discuss the opportunities for carbon removal technologies as a key solution on the road to net zero emissions and to accelerate their adoption. The GEA stand can be found in hall A4, stand number 4D15.
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CatalYm Announces New Financing of $150M to Support Broad Phase 2b Development Program for Visugromab
17.07.2024CatalYm today announced the completion of a $150 million Series D financing. The oversubscribed round was led by new investors, Canaan Partners and Bioqube Ventures, and joined by Forbion’s Growth Opportunities Fund (“Forbion Growth”), Omega Funds and Gilde Healthcare. Existing investors Jeito Capital, Brandon Capital Partners, Novartis Venture Fund and Vesalius Biocapital III also participated in the round. The proceeds will fund the expansion of the company’s broad Phase 2b development of visugromab into randomized Phase 2b studies in select checkpoint naïve frontline and second-line treatment settings. Visugromab has already demonstrated outstanding anti-tumor activity in combination with checkpoint inhibitor treatment.
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CatalYm Announces New Financing of $150M to Support Broad Phase 2b Development Program for Visugromab
18.07.2024CatalYm today announced the completion of a $150 million Series D financing. The oversubscribed round was led by new investors, Canaan Partners and Bioqube Ventures, and joined by Forbion’s Growth Opportunities Fund (“Forbion Growth”), Omega Funds and Gilde Healthcare. Existing investors Jeito Capital, Brandon Capital Partners, Novartis Venture Fund and Vesalius Biocapital III also participated in the round. The proceeds will fund the expansion of the company’s broad Phase 2b development of visugromab into randomized Phase 2b studies in select checkpoint naïve frontline and second-line treatment settings. Visugromab has already demonstrated outstanding anti-tumor activity in combination with checkpoint inhibitor treatment.
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Asceneuron Secures $100 Million Series C Financing to Advance Groundbreaking Therapeutics in Neurodegenerative Diseases
18.07.2024Asceneuron SA, a clinical stage biotech company developing small molecules targeting tau protein aggregation, a root cause of neurodegenerative disease, today announces an $100 million oversubscribed Series C financing to advance the clinical development of its groundbreaking clinical pipeline of OGA inhibitors for the treatment of neurodegenerative diseases. The financing was led by Novo Holdings with new investment from EQT Life Sciences – LSP Dementia Fund, OrbiMed and SR One, alongside participation from existing investors M Ventures, Sofinnova Partners, GSK Equities Investments Limited and Johnson & Johnson Innovation – JJDC, Inc.
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Asceneuron Secures $100 Million Series C Financing to Advance Groundbreaking Therapeutics in Neurodegenerative Diseases
22.07.2024Asceneuron SA, a clinical stage biotech company developing small molecules targeting tau protein aggregation, a root cause of neurodegenerative disease, today announces an $100 million oversubscribed Series C financing to advance the clinical development of its groundbreaking clinical pipeline of OGA inhibitors for the treatment of neurodegenerative diseases. The financing was led by Novo Holdings with new investment from EQT Life Sciences – LSP Dementia Fund, OrbiMed and SR One, alongside participation from existing investors M Ventures, Sofinnova Partners, GSK Equities Investments Limited and Johnson & Johnson Innovation – JJDC, Inc.
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AskBio receives FDA Fast Track and MHRA Innovation Passport designations for AB-1005 investigational GDNF gene therapy for Parkinson’s disease
18.07.2024Bayer AG and Asklepios BioPharmaceutical, Inc. (AskBio), a gene therapy company wholly owned and independently operated as a subsidiary of Bayer AG, today announced that the United States (U.S.) Food and Drug Administration (FDA) has granted Fast Track Designation for AB-1005, which is being developed for moderate Parkinson’s disease. AB-1005 has also been awarded the Innovation Passport, the United Kingdom Medicines and Healthcare products Regulatory Agency (UK MHRA) innovative medicine designation, for the treatment of Parkinson’s disease.
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AskBio receives FDA Fast Track and MHRA Innovation Passport designations for AB-1005 investigational GDNF gene therapy for Parkinson’s disease
22.07.2024Bayer AG and Asklepios BioPharmaceutical, Inc. (AskBio), a gene therapy company wholly owned and independently operated as a subsidiary of Bayer AG, today announced that the United States (U.S.) Food and Drug Administration (FDA) has granted Fast Track Designation for AB-1005, which is being developed for moderate Parkinson’s disease. AB-1005 has also been awarded the Innovation Passport, the United Kingdom Medicines and Healthcare products Regulatory Agency (UK MHRA) innovative medicine designation, for the treatment of Parkinson’s disease.
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