Brief: Genmab Gets FDA Breakthrough Therapy Designation For Rinatabart Sesutecan
Aug 26 (Reuters) - Genmab A/S GMAB.CO: GENMAB RECEIVES FDA BREAKTHROUGH THERAPY DESIGNATION FOR RINATABART SESUTECAN (RINA-S®) IN ADVANCED ENDOMETRIAL CANCER (EC) RINA-S CONTINUES TO BE EVALUATED AS A SINGLE-AGENT IN PATIENTS WITH ADVANCED EC IN PHASE 1/2 RAINFOL™-01 TRIAL AND WILL BE FURTHER EVALUATED IN A PLANNED PHASE 3 TRIAL Source text: ID:nGNE4tWzCk Further company coverage: GMAB.CO (Gdansk Newsroom) ((gdansk.newsroom@thomsonreuters.com;))
Recent news on Genmab A/S
See all newsBrief: Genmab Q3 Net Sales Of Darzalex At $4.24 Bln
European shares rise as retreating bond yields and oil prices boost risk appetite
Live Markets: Oil prices can rise even with a new MoU
Live Markets: What the AI capex cycle might mean for European growth
Live Markets: Ignore politics and buy the dip in Spain's Bonos