ATYR PHARMA, INC. (NASDAQ:LIFE) Files An 8-K Regulation FD DisclosureItem 7.01 Regulation FD Disclosure.
aTyr Pharma, Inc. (the “Company”) is participating at the 2018 American Thoracic Society (ATS) Annual Meeting held in San Diego, CA from May 18 – 23, 2018.During the ATS Annual Meeting, the Company is presenting a poster presentation entitled, “Preclinical Characterization of ATYR1923 (iMod.Fc), an Immune-Modulatory Therapeutic With Potentially Broad Application in Interstitial Lung Diseases.” The poster presentation has been posted on the Company’s website and is attached hereto as Exhibit 99.1.
The information under this Item 7.01, including Exhibit 99.1 hereto, is being furnished herewith and shall not be deemed “filed” for the purposes of Section18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall such information be deemed incorporated by reference into any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such filing.
Item 9.01 Exhibits.
aTYR PHARMA INC ExhibitEX-99.1 2 life-ex991_6.htm EX-99.1 life-ex991_6.pptx.htm 0 1 2 3 4 5 Ashcroft index score per field (0–8) * * ‡ ‡ Bleomycin No Bleomycin Veh PO TGFβ Ab Pirf Veh IV iMod Mouse Resolaris ATYR 1923 † ‡ ‡ ‡ ‡ ‡ 0 1 2 3 4 5 Ashcroft index score per field (0–8) Bleomycin No Bleomycin Veh PO Dex Pirf Veh IV Resolaris ATYR 1923 * 0.01 10 0 50 100 0.11 Half-life 4.5 days Ninted,…To view the full exhibit click
About ATYR PHARMA, INC. (NASDAQ:LIFE)
aTyr Pharma, Inc. is a clinical-stage biotherapeutics company. The Company is engaged in the discovery and clinical development of medicines for patients suffering from severe, rare diseases using its Physiocrine biology, a discovered set of physiological modulators. The Company focuses on the development of Physiocrine-based therapeutics for the treatment of rare diseases, including facioscapulohumeral muscular dystrophy (FSHD) and limb-girdle muscular dystrophy (LGMD) 2B. The Company is developing Resolaris, an intravenous protein therapeutic for the treatment of rare myopathies with an immune component (RMICs). The Company is investigating Resolaris in patients with LGMD2B. The Company is conducting approximately three open label trials in patients with early onset FSHD, in adult patients with FSHD or LGMD2B and a long-term extension study in adult patients with FSHD. The Company has not generated any revenues.