Aeglea BioTherapeutics

We are thrilled to announce the appointment of Scott Burrows to the role of Chief Financial Officer and Heidy Abreu King-Jones to the role of Chief Legal Officer and Corporate Secretary of Aeglea Therapeutics. We are excited to work with them to develop treatment for #IBD.

We have completed our acquisition of @spyretx along with an oversubscribed $210M private investment. Together we will advance a robust pipeline of antibody therapeutics with potential to transform the #IBD treatment paradigm. Read more: bit.ly/42VHtIP

Today we honor Cesar Chavez, who worked tirelessly for civil rights. Chavez showed us that with a strong conviction and a willingness to do the hard things, you can make your dreams a reality.

Are you diagnosed with #Homocystinuria but struggling to stick with your treatment? @HCUAmerica has resources to help you "get back on track." Check out all the support they have to offer: hcunetworkamerica.org/back-to-care/

Are you attending ACMG 2023 in Salt Lake City? Dr. Roberto Zori will be presenting 2 year pegzilarginase data in a featured platform presentation tomorrow at 8:45am MST. Come check it out!

The Aeglea team is full of women with different backgrounds, perspectives, beliefs and experiences. It is those differences that allow us to see things in new ways - to redefine what's possible. We are proud to celebrate #InternationalWomensDay with this diverse group.

Thank you to all our employees who work with passion and purpose every day to achieve our vision of redefining the possible and delivering groundbreaking medicines. You are what can make our vision a reality and you are changing the world. #employeeapprceiationday

Today we announced our fourth quarter and full year 2022 financial results and program updates. Learn the latest about what's happening at Aeglea here: ir.aeglea.com/press-releases…

We were so excited to celebrate #RareDiseaseDay2023 by meeting with Danae', Garrett and Alex and hearing their experiences living with #HCU as well as how they fill their lives with photography, music and family. We are honored to have spent the day with you!

Today is #RareDiseaseDay! We are excited to be celebrating by hosting a #Homocystinuria Patient Panel in our office today to continue our neverending journey to learn more about the patient communities we serve.

Registration for #RareDiseaseDay at NIH 2023 is open! Tues. 2/28/23, 9 a.m.–5 p.m. EST @ NIH Main Campus OR Virtually! To see the agenda & to register, visit: ncats.nih.gov/rdd #RDDNIH #RareDisease #policy #advocacy #awareness

New @DiversityRare & @RareDiseases survey aims to uncover gaps & barriers experienced by underrepresented communities. Together, we can identify and combat longstanding barriers experienced by the #RareDisease community! Participate and pass on: rarediseasediversitysurvey.org

📣 Tune in TODAY at 4 pm EST! ➡️ Register here to watch: bit.ly/3JZaIV4 #ClinicalTrials #Homocystinuria #HCU #HopeConnectsUs

It's that time of year again. #RareDiseaseDay is just around the corner and the FDA is hosting an event on February 27 where you can learn about FDA initiatives and provide your perspective. Register here: bit.ly/3wQUaXE #FDARareDiseaseDay

Looking for an opportunity to advocate for those living with #RareDiseases? Registration is open for #RareDiseaseWeek on Capitol Hill! Visit everylifefoundation.org/rare-advocates…. Thanks @EveryLifeOrg for hosting such a great event. #RareDC2023 #RareDisease #policy #advocacy

#RareDiseaseDay is a worldwide movement to raise awareness among policymakers & the public about #RareDiseases & their impact on patients’ lives. To learn more & access resources, visit @RareDiseases' website rarediseases.org/rare-disease-d… #ShowYourStrips #advocacy #awareness #policy

This Thanksgiving we are thankful for all of our amazing employees here at Aeglea and the work they are doing to help patients with #rarediseases! We celebrated with a coming together for a potluck and good conversation. #HappyThanksgiving

Whether you’re making sandwiches, burritos, quesadillas, or tacos, you’ll need a wrap for that! Check out this video from our #MakeitLoPro series for some lower protein options! bit.ly/3UmfLAO

Congratulations to Linda Neuman on her promotion to chief medical officer. We are so proud to have you on our team and helping us to bring important medicines to the rare disease community. bit.ly/3ycdrEK