Spyre Therapeutics(SYRE)
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Spyre Therapeutics(SYRE) - 2022 Q4 - Annual Report
2023-03-02 20:13
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, DC 20549 FORM 10-K ☒ ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 2022 ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission file number 001-37722 AEGLEA BIOTHERAPEUTICS, INC. (Exact name of Registrant as specified in its charter) (State or Other Jurisdiction of Incorporation or Organizati ...
Spyre Therapeutics(SYRE) - 2022 Q3 - Quarterly Report
2022-11-03 19:05
UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, DC 20549 FORM 10-Q (Mark One) ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended September 30, 2022 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission File Number: 001-37722 AEGLEA BIOTHERAPEUTICS, INC. (Exact Name of Registrant as Specified in its Charter) Delaware 46-4312787 (State or other ...
Spyre Therapeutics(SYRE) - 2022 Q2 - Quarterly Report
2022-08-04 18:04
UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, DC 20549 FORM 10-Q (Mark One) ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended June 30, 2022 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission File Number: 001-37722 AEGLEA BIOTHERAPEUTICS, INC. (Exact Name of Registrant as Specified in its Charter) Delaware 46-4312787 (State or other juri ...
Spyre Therapeutics(SYRE) - 2022 Q1 - Quarterly Report
2022-05-05 18:40
UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, DC 20549 FORM 10-Q (Mark One) ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended March 31, 2022 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission File Number: 001-37722 AEGLEA BIOTHERAPEUTICS, INC. (Exact Name of Registrant as Specified in its Charter) Delaware 46-4312787 (State or other jur ...
Spyre Therapeutics(SYRE) - 2021 Q4 - Annual Report
2022-03-08 20:09
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, DC 20549 FORM 10-K ☒ ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 2021 ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission file number 001-37722 AEGLEA BIOTHERAPEUTICS, INC. (Exact name of Registrant as specified in its charter) (State or Other Jurisdiction of Incorporation or Organizati ...
Aeglea BioTherapeutics (AGLE) Investor Presentation - Slideshow
2022-01-11 04:40
业绩总结 - 2021年第三季度收入为140万美元,前九个月收入为1510万美元,其中包括1200万美元的许可收入和310万美元的开发费用收入[116] - 2021年第三季度研发费用为1490万美元,前九个月研发费用为4030万美元[116] - 2021年第三季度一般管理费用为680万美元,前九个月一般管理费用为2000万美元[116] - 2021年第三季度净亏损为2030万美元,前九个月净亏损为4540万美元[116] - 截至2021年9月30日,公司现金、现金等价物和可市场化证券总额为1.143亿美元,无债务[116] - 预计资金使用可持续至2023年[116] 用户数据 - Pegzilarginase在Phase 3临床试验中将精氨酸水平降低了80%,在90.5%的患者中实现了精氨酸水平正常化[21] - Pegzilarginase的全球可寻址市场超过2500名患者,其中1150名患者在监管和上市计划中[20] - 预计在美国有超过250名患者,全球范围内有超过2500名患者存在显著未满足的医疗需求[56] 新产品和新技术研发 - Pegzilarginase获得了美国罕见儿科疾病(PRV资格)、突破性疗法、美国孤儿药和欧盟孤儿药的监管认证[20] - Aeglea的AGLE-177(同型半胱氨酸尿症)和AGLE-325(胱氨酸尿症)正在进行临床试验,预计将为超过30000名和10000名患者提供治疗[13] - AGLE-177在CBS -/-小鼠模型中以每周低至2 mg/kg的剂量显示出显著的生存益处[84] - AGLE-177在毒理学研究中显示出显著降低同型半胱氨酸水平的药理效应[89] - 预计AGLE-177的临床试验在2022年获得数据[92] 市场扩张和并购 - 2021年,Aeglea与Immedica Pharma AB签署了针对欧洲及部分中东国家的许可和供应协议[11] - 计划在2022年上半年提交美国生物制品许可申请(BLA)和欧盟市场授权申请(MAA)[11] - 公司正在与医疗保健专业人士(HCP)和患者社区合作,以加速诊断和提高对ARG1-D的认识[60] 未来展望 - 预计2022年上半年提交生物制剂许可申请(BLA),并计划请求优先审查[49] - Aeglea在2021年宣布的积极顶线数据为未来的市场推广奠定了基础[21] 负面信息 - Pegzilarginase治疗组患者中,85.7%出现任何治疗相关不良事件(TEAE),而安慰剂组为100%[27] - Pegzilarginase治疗组中,19.0%患者出现严重不良事件(SAE),安慰剂组为36.4%[27] - 在12周和24周的GMFM-E评分中,Pegzilarginase组的平均变化未达到统计显著性(p=0.0568和p=0.1087)[40]
Spyre Therapeutics(SYRE) - 2021 Q3 - Quarterly Report
2021-11-04 19:04
UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, DC 20549 FORM 10-Q (Mark One) ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended September 30, 2021 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission File Number: 001-37722 AEGLEA BIOTHERAPEUTICS, INC. (Exact Name of Registrant as Specified in its Charter) Delaware 46-4312787 (State or other ...
Aeglea BioTherapeutics (AGLE) Investor Presentation - Slideshow
2021-09-11 02:05
财务状况 - 截至2021年6月30日,公司现金、现金等价物和可交易证券总额为1.3041亿美元,且无债务[10] - 预计资金可持续到2023年[10] - 2021年第二季度公司收入为1370万美元,其中包括1200万美元的许可收入和170万美元的开发费用收入[98] - 2021年第二季度研发费用为1360万美元,六个月累计研发费用为2540万美元[98] - 2021年第二季度公司净亏损为680万美元,六个月累计净亏损为2500万美元[98] 产品研发与临床试验 - Pegzilarginase针对的市场地址患者超过2500人[13] - AGLE-177针对的市场地址患者超过30000人[13] - Cystinuria的研究患者地址市场超过10000人[13] - Pegzilarginase在Phase 1/2试验中显示出良好的安全性,约1,850剂次已被施用[25] - 56周分析中,85%(11/13)的患者为临床应答者[47] - 主要终点为血浆精氨酸减少,次要终点包括临床结果、安全性和药代动力学[46] - 32名患者参与了随机2:1(pegzilarginase:安慰剂)的试验,给药周期为24周[46] - AGLE-177的临床试验正在进行中,预计招募16-20名患者[76] - AGLE-177的预临床研究显示,降低血浆同型半胱氨酸水平可改善与疾病相关的异常[94] 临床结果与市场需求 - 在20周分析中,Pegzilarginase治疗后中位数血浆精氨酸水平为112µM,减少了277µM[21] - 在56周分析中,10/13名患者的血浆精氨酸水平达到了正常范围(40-115µM)[21] - 13/13名患者的血浆精氨酸水平达到了目标范围(<200µM)[21] - 预计全球有超过2,500名患者,且患者识别速度超过相关基准[36] - 目前没有有效的治疗方案可用,市场需求显著[47] 风险与不确定性 - 公司在快速变化的竞争环境中运营,面临多种已知和未知的风险和不确定性[4] - 主要不良事件为过敏反应和高氨血症,均为可预期和可管理[25] 未来展望 - 公司在ARG1-D的Phase 3关键试验中已完成入组,预计在2021年第四季度发布顶线数据[16] - 预计在2021年第四季度发布顶线结果[46] - AGLE-177的治疗目标是将血浆同型半胱氨酸浓度降低到安全水平,同时保持正常营养[63]
Spyre Therapeutics(SYRE) - 2021 Q2 - Quarterly Report
2021-08-05 20:33
UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, DC 20549 FORM 10-Q (Mark One) ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended June 30, 2021 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission File Number: 001-37722 AEGLEA BIOTHERAPEUTICS, INC. | Title of each class | Trading Symbol(s) | Name of each exchange on which registered | | --- | ...
Spyre Therapeutics(SYRE) - 2021 Q1 - Quarterly Report
2021-05-10 20:33
UNITED STATES SECURITIES AND EXCHANGE COMMISSION (Mark One) ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended March 31, 2021 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission File Number: 001-37722 AEGLEA BIOTHERAPEUTICS, INC. WASHINGTON, DC 20549 FORM 10-Q (Exact Name of Registrant as Specified in its Charter) Delaware 46-4312787 (State or other jur ...