AgilisBio (@AgilisBio) header
AgilisBio (@AgilisBio) profile picture

Engineering DNA Therapeutics for Rare Diseases

Cambridge, MA
Joined January 2014
Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)Photo by AgilisBio (@AgilisBio)
AgilisBio retweeted
Agilis team Working hard to help these families! #CureAADC
1
2
AgilisBio retweeted
Yankees game! Thanks FARA #cureFA #attnyy
1
3
AgilisBio retweeted
$PTCT picking up Agilis Bio for $50M in cash and ~$150M in $PTCT shares up front, up to $745M in milestones; synthetic bio firm focused on DNA-based therapeutics, including collaboration with $XON to develop Friedreich’s ataxia therapy
1
2
2
$PTCT to Acquire Agilis Biotherapeutics for $50M cash + $150M stock Everyone getting into gene therapy...
Nabbing late-stage drug, PTC acquires gene therapy startup Agilis for $200M in cash/stock $PTCT +8% @BrittanyMeiling endpts.com/nabbing-late-stag…
1
5
8
AgilisBio retweeted
Delighted to spend a day talking about AADC Deficiency with Dr Hwu and NIH, at NCATS #NCATS #NIH #genetherapy #cureAADC
2
4
Blessed to have known Charles Krauthammer. He is a brilliant, kind, elegant, funny and perhaps above all, wise, man. An intellectual giant whose voice will be missed beyond measure.
77
353
20
4,036
An abstract regarding @AgilisBio's principal investigator, AGIL-AADC, a #genetherapy, and its clinical trials for AADC deficiency was presented at the American Society of Gene and Cell Therapy (ASGCT) in Chicago. READ: raredr.com/link/3465
1
1
Katherine High @spark_tx gave a great round off to her plenary session, #genetherapy coming of age #ASGCT18
9
1
13
We want to see you show off your muscles in your new Lend Us Some Muscle t-shirts 👚👕  or tattoos in honor of Friedreich's Ataxia Awareness Day [May 19] 💪. Or show us your muscl-y-est pose. Tag and share your pics 📸! Don’t forget to hashtag #LendUsSomMuscle #LUSM2018  #CureFA
1
2
13
NCATS and NIH talk about partnerships with rare disease researchers. Seems like a great resource. Good work to @SangamoTx and @AgilisBio for taking advantage. @ncats_nih_gov #WODCUSA #RareDisease
2
4
Replying to @NIH
@NIH initiatives on gene editing, with great resource #raredisease #clinical #research network and collaboration with @AgilisBio to develop gene therapy for #patients good effort done on coordinating, disseminating and educating! @OrphanConf #WODCUSA @AtaxiaUK – at Fort Washington, MD
2
2
Breaking News! The ASF’s sixth multi-disciplinary Angelman Syndrome Clinic will open on May 7th at NYU Langone Health in New York, NY! Made possible by generous donors, the new NYU AS Clinic was created through a partnership between the ASF and @nyulangone.
1
2
2
11
FA researcher Professor Arnulf Koeppen, MD receives 2018 Dr. L. Clarke Jr. and Elaine F. Stout Award for his work in understanding FA neuropathology". #CureFA @TheUSCAP @AlbanyMed #USCAP2018
1
3
1
4
AgilisBio retweeted
Your FAST board and FIRE team are working hard to find a cure for Angelman syndrome. #angelmansyndrome #myreason — at Texas A&M University facebook.com/cureangelman.or…
4
7
Had lots of fun at the Prestigious DeVere Selsdon Estate today! Yay they’ve nominated us as their chosen Charity to Partner with thanks to Caroline Morrone, Tracey Montgomery and Matt Brierley. Had a chance... facebook.com/AADCResearchTru…
4
3
Today kicks off a virtual event for #RareDiseaseDay from the @US_FDA featuring an announcement regarding a #NORD/FDA collaboration & video interviews including one from NORD's Director of Research Programs, Vanessa Boulanger: bit.ly/2EWKbHO
TOMORROW is #RareDiseaseDay! Retweet to raise awareness! What are you doing for the big day tomorrow?
7
133
18
131
🚨 We’re LIVE!! 🚨 Can’t think of a better way to start the week. The Ataxian is available NOW on iTunes, Amazon, Google Play, Xbox, and Sony Playstation Network. 👏👏👏 📝 Show us some ❤️ with a review! #thankyou #CureFA #raredisease #retweet #mustsee vimeo.com/127990377
1
3
14