COMMUNIQUÉS West-GlobeNewswire

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Reunion Neuroscience Announces Positive Topline Results from RECONNECT Phase 2 Clinical Trial of RE104 for the Treatment of Postpartum Depression (PPD)
18/08/2025 -
OneMedNet initiates new Subscription Revenue model in partnership with Circle CVI
18/08/2025 -
Theratechnologies Announces Filing of Special Meeting Materials and Receipt of Interim Order in Relation to its Acquisition by CB Biotechnology, an Affiliate of Future Pak
18/08/2025 -
Theratechnologies annonce le dépôt des documents relatifs à l’assemblée extraordinaire et l’obtention d’une ordonnance provisoire concernant son acquisition par CB Biotechnology, un membre du même groupe que Future Pak
18/08/2025 -
Aptose Reports Early Data Demonstrating Tuspetinib Improves Standard of Care Treatment Across Diverse Populations of Newly Diagnosed AML in Phase 1/2 TUSCANY Trial
18/08/2025 -
BioXcel Therapeutics Announces Positive FDA Pre-sNDA Meeting Comments for sNDA Submission for BXCL501 in Agitation Associated with Bipolar Disorders or Schizophrenia
18/08/2025 -
FibroGen Announces Approval of Sale of FibroGen China to AstraZeneca by the China State Administration for Market Regulation
18/08/2025 -
SRx Health Solutions Signed a Letter of Intent to Acquire the Assets of Royal Uranium
18/08/2025 -
Traws Pharma Receives Approval to Proceed with Phase 2 COVID Studies with Ratutrelvir, Expects Results by Year-End 2025
18/08/2025 -
Virbac:: Paul Martingell's compensation terms
18/08/2025 -
VIRBAC: Informations sur les conditions de rémunération de Paul Martingell
18/08/2025 -
Clarity Health Care is Coming to Malvern
18/08/2025 -
New Novartis ESC data highlights strength of cardiovascular portfolio
18/08/2025 -
Valneva’s Chikungunya Vaccine IXCHIQ® Now Authorized in Canada for Individuals Aged 12 and Older
18/08/2025 -
Le vaccin IXCHIQ® de Valneva contre le chikungunya désormais autorisé au Canada pour les personnes âgées de 12 ans et plus
18/08/2025 -
Ascentage Pharma Announces Global Registrational Phase III Study of Lisaftoclax for First-line Treatment of Patients with Higher-Risk Myelodysplastic Syndrome Cleared by US FDA and EMA
18/08/2025 -
rYojbaba Co., Ltd. Announces Closing of $5 Million Initial Public Offering of Japanese Common Shares
15/08/2025 -
Novo Nordisk A/S: Wegovy® approved in the US for the treatment of MASH
15/08/2025 -
BioSig Technologies, Inc. & Streamex Announce Closing of $15 Million Public Offering
15/08/2025
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