公司资料

ADC Therapeutics 股价、新闻与催化剂

股票代码:
ADCT
交易所:
NYSE
行业:
Biopharma
所在地:
Switzerland

股票表现

1.08 USD (-11.48%)

收盘价

最后更新: 2026年10月1日

403M USD

市值

股价为何变动

截至 2026年10月1日,ADCT 下跌 11.5%,收于 $1.08。当前新闻监测窗口内未发现新的同公司新闻。

公司概览

Antibody-Drug Conjugate Company

ADC Therapeutics is a commercial-stage oncology company focused on antibody-drug conjugates. Its capabilities span clinical development, manufacturing, medical affairs, and commercialization, with a current strategic focus on the CD19-directed medicine ZYNLONTA.

ZYNLONTA Commercial Franchise

ZYNLONTA, or loncastuximab tesirine, is approved in the United States and conditionally approved in Europe for relapsed or refractory diffuse large B-cell lymphoma after at least two prior lines of systemic therapy. The company markets the product in later-line disease while working toward broader use and full approval.

Earlier-Line DLBCL Development

LOTIS-5 evaluated ZYNLONTA with rituximab, while LOTIS-7 evaluates ZYNLONTA with glofitamab in relapsed or refractory DLBCL. The company is assessing the regulatory and Phase 3 paths for these combinations following FDA feedback and completion of LOTIS-7 enrollment.

Expansion Across B-Cell Malignancies

Investigator-sponsored studies are evaluating ZYNLONTA in follicular lymphoma and marginal zone lymphoma. These programs may support publication, treatment-guideline inclusion, breakthrough designation requests, and development in disease settings beyond DLBCL.

Focused Commercial and Regulatory Organization

ADC Therapeutics has reorganized around ZYNLONTA's commercial opportunity and the regulatory work needed to sustain and expand the franchise. This narrower structure prioritizes clinical evidence, manufacturing, medical affairs, and market access for a single core asset.

未来催化剂

  • Presentation of LOTIS-5, LOTIS-7, and marginal zone lymphoma data at the 2026 ASH Annual Meeting.
  • Update on the regulatory strategy and timing for obtaining full approval of ZYNLONTA following the LOTIS-5 pre-sBLA meeting.
  • Submission of LOTIS-7 and marginal zone lymphoma data for FDA Breakthrough Therapy designation in 2026.
  • Presentation of updated follicular lymphoma data in the second quarter of 2027.

近期新闻

新闻标题由机器翻译,详情为英文原文。

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