COMMUNIQUÉS West-GlobeNewswire
-
Update on Regulatory Review of Lecanemab for Early Alzheimer’s Disease in the European Union
26/07/2024 - 13:20 -
Johnson & Johnson Receives Positive CHMP Opinion for Yuvanci® (Single Tablet Combination Therapy [STCT] of Macitentan and Tadalafil) for Treatment of Patients with Pulmonary Arterial Hypertension (PAH)
26/07/2024 - 13:05 -
Chemomab Therapeutics Regains Compliance With Nasdaq Minimum Bid Price Requirement
26/07/2024 - 13:00 -
Legend Biotech Announces Preliminary Results for the Six-Months Ended June 30, 2024
26/07/2024 - 13:00 -
Ipsen receives CHMP positive opinions for Iqirvo® (elafibranor) in Primary Biliary Cholangitis and Kayfanda® (odevixibat) in Alagille Syndrome, two rare cholestatic liver diseases
26/07/2024 - 12:46 -
Ipsen reçoit des avis positifs du CHMP pour Iqirvo® (elafibranor) dans la cholangite biliaire primitive et Kayfanda® (odévixibat) dans le syndrome d'Alagille, deux maladies rares du foie cholestatiques
26/07/2024 - 12:46 -
Bavarian Nordic Receives Positive CHMP Opinion for Including Mpox Real-world Effectiveness Data in European Marketing Authorization for Smallpox and Mpox Vaccine
26/07/2024 - 08:00 -
Kaerus Bioscience annonce le lancement de l’essai clinique de phase I ciblé sur son nouveau modulateur de canal BK KER-0193 en cours de développement pour le syndrome de l’X fragile
26/07/2024 - 06:29 -
California Institute for Regenerative Medicine Awards Funding for CAR-T NXC-201 U.S. AL Amyloidosis Clinical Trial (NEXICART-2)
26/07/2024 - 03:36 -
California Institute for Regenerative Medicine Awards Funding for CAR-T NXC-201 U.S. AL Amyloidosis Clinical Trial (NEXICART-2)
26/07/2024 - 03:31 -
OnKure Announces the Appointment of Dylan Hartley as Chief Scientific Officer
26/07/2024 - 00:43 -
BioAtla Highlighted Clinical Program and Pipeline Updates at Virtual R&D Day
25/07/2024 - 23:39 -
23andMe to Report Q1 FY2025 Financial Results
25/07/2024 - 22:45 -
La FDA accorde le statut de médicament orphelin et médicament pour une maladie pédiatrique rare (Rare Pediatric Disease Designation-RPDD) au produit candidat de Cellectis UCART22 pour le traitement de la leucémie lymphoblastique aiguë (LLA)
25/07/2024 - 22:30 -
Travere Therapeutics to Report Second Quarter 2024 Financial Results
25/07/2024 - 22:30 -
FDA Grants Orphan Drug and Rare Pediatric Disease Designation Status to Cellectis’ UCART22 product candidate for Acute Lymphoblastic Leukemia (ALL) Treatment
25/07/2024 - 22:30 -
Zymeworks Appoints Leone Patterson as Chief Business and Financial Officer
25/07/2024 - 22:30 -
Cronos Group Inc. to Hold 2024 Second Quarter Earnings Conference Call on August 8, 2024
25/07/2024 - 22:15 -
The Ensign Group Reports Second Quarter 2024 Results; Raises Annual Earnings and Revenue Guidance
25/07/2024 - 22:10
Pages