Aeglea BioTherapeutics to Participate in Multiple Conferences in September 2021

<br /> Aeglea BioTherapeutics to Participate in Multiple Conferences in September 2021<br />

PR Newswire


AUSTIN, Texas

,

Sept. 1, 2021

/PRNewswire/ — Aeglea BioTherapeutics, Inc. (NASDAQ: AGLE), a clinical-stage biotechnology company developing a new generation of human enzyme therapeutics to benefit people with rare metabolic diseases, today announced its participation in the following medical and investor conferences:



Investor Meetings


  • 2021 Wells Fargo Virtual Healthcare Conference

    ,

    September 9

  • H.C. Wainwright 23

    rd

    Annual Global Investment Conference

    ,

    September 13

  • 2021 Cantor Virtual Global Healthcare Conference

    ,

    September 27



Medical Conferences


  • International Parkinson and Movement Disorder Society annual congress (MDS Virtual Congress 2021)

    ,

    September 17 – 22

  • 50

    th

    Child Neurology Society (CNS) Annual Meeting

    ,

    September 29 – October 2

At both the MDS Virtual Congress and the CNS Annual Meeting, a poster presentation will outline a subset analysis from the Company



s previously reported Phase 1/2 and Phase 2 open label extension studies of pegzilarginase in patients with Arginase 1 Deficiency (ARG1-D). In the poster, analysis of gait kinematics and spasticity was completed using video compilations.

To access live and/or archived Investor Conference webcasts, visit the

Events & Presentations

section of the Company



s website. A replay of Company webcasts is archived on the website for 30 days following presentations.


About Aeglea BioTherapeutics

Aeglea BioTherapeutics is a clinical-stage biotechnology company redefining the potential of human enzyme therapeutics to benefit people with rare metabolic diseases with limited treatment options. Aeglea’s lead product candidate, pegzilarginase, is in a pivotal Phase 3 trial for the treatment of Arginase 1 Deficiency and has received both Rare Pediatric Disease and Breakthrough Therapy Designations. The Company began dosing patients in a Phase 1/2 clinical trial of AGLE-177 for the treatment of Homocystinuria in

June 2021

. AGLE-177 has also been granted Rare Pediatric Disease Designation. Aeglea has an active discovery platform focused on engineering small changes in human enzymes to have a big impact on the lives of patients and their families. For more information, please visit

Home



.

Cision
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SOURCE Aeglea BioTherapeutics, Inc.