#WhyAgios? Our work matters because patients matter. You can feel the dedication at our company from our patient wall, to employees’ personal reflections on their jobs, to the great science happening in our labs. Agios is #WhereScienceMeetsHeart
We are re-imagining The Other Side of Possible. Over the past 12+ years, our employees have been committed to patients first & following the science. This foundation will remain constant at Agios & accelerate our impact moving forward. #AgiosTomorrow https://t.co/IiuZA4E95z
Today marks a transformational milestone for Agios as we move forward with a singular focus on genetically defined diseases. We are selling our oncology business to @Servier, patient-focused company committed to the cancer community. #AgiosTomorrow https://t.co/3sgiPiiSWo
Whenever we have exciting news for patients, we ring this bell! This is Agios tradition and we did not let the pandemic stop us from carrying it on as we celebrated our recently announced ACTIVATE Phase 3 data for people with pyruvate kinase (PK) deficiency. #AlwaysanAgioi
We announced clinical proof-of-concept has been established for mitapivat, our first-in class PKR activator, in sickle cell disease based on data from a Phase 1 @NIH study. https://t.co/6OnNnCfoQn
Really @omnimtwash, you need a doctor’s note to confirm my autoimmune issue to refund my deposit during a global pandemic?! Not sure you have the right priorities here.
Massachusetts will hold its 2020 Presidential Primary Election on March 3rd.
The voter registration deadline is TODAY.
Register online to vote here: https://t.co/8wwiwydJ1w
RT TO SAVE LIVES.
We’re pleased to announce that the Phase 3 ClarIDHy trial achieved its primary endpoint in previously treated mIDH1 cholangiocarcinoma. Thanks to all the patients & physicians who participated in the study, without whom this would not be possible. https://t.co/GjVGeiraKG
A big thank you to all the patients who volunteer for studies to make milestones possible – like our recent sNDA approval for newly diagnosed AML patients with an IDH1 mutation who are ineligible for intensive chemotherapy.
#BREAKING: The @US_FDA approved the sNDA for our IDH1m inhibitor for newly diagnosed adult AML patients with an IDH1 mutation who are ≥75 years old or who have comorbidities that preclude use of intensive induction chemotherapy https://t.co/icy82tO5e0