This morning, Executive Chairman Dr. Behzad Aghazadeh discussed $IMMU's recent #FDAapproval and virtual launch plans to deliver our critical new therapy to people with #mTNBC during #COVID19 with @AlexisTVNews and @BrianSozzi on @YahooFinance’s “The First Trade’.
#ICYMI because you were appropriately socially distancing, our recent #FDAapproval of #TRODELVY received a shoutout on the Nasdaq building in @TimesSquareNYC! We hope for more wins like this for patients everywhere in the future. Thank you, @Nasdaq!
📸: Copyright Nasdaq 2020
FDA granted approval to sacituzumab govitecan-hziy (Trodelvy) for mTNBC. Great news for the field & need to build on progress. In academics, it is said ‘we stand on shoulder of giants’. The giants in drug approval are pts in the trial. #bcsm#oncoalert https://t.co/dOZ5BKNN3q
Yesterday’s FDA approval underscores our commitment to bringing critical new therapies for hard-to-treat cancers. Learn more: https://t.co/NhNlZo3VNZ #mTNBC#TNBC#BreastCancer
Thank you to our IMMU colleagues whose hard work and commitment led to our first FDA approval! This milestone would not be possible without your efforts and dedication to people with #mTNBC.
We are excited to announce the @US_FDA approval of our critical new therapy in metastatic triple-negative breast cancer (#mTNBC). Learn more: https://t.co/NhNlZo3VNZ #CancerTreatment#metastatic#TNBC
Today, we announced that our Phase 3 confirmatory ASCENT study will be stopped due to compelling evidence of efficacy. Please read our full press release for more information: https://t.co/6thPZkzLbh. $IMMU
Oral breast session at #ASCO18: Sacituzumab govitecan ADC with SN-38 payload in ER-positive Her2-neg pts: 31% ORR and MDR of 7.4 mo. PFS data not yet mature.