公司資料

Moleculin Biotech, Inc. 股價、新聞與催化劑

股票代碼:
MBRX
交易所:
NASDAQ
產業:
Biopharma
所在地:
United States

股票表現

0.61 USD (-0.85%)

收盤價

最後更新: 2026年8月17日

13.1M USD

市值

股價為何變動

Following the latest company update, “Moleculin Biotech Reports Second Quarter 2026 Financial Results and Highlights Continued Advancement of Pivotal MIRACLE Trial”, MBRX closed up 7.16% at $0.6122 on Aug 14, 2026. The move occurred in the trading session associated with this clinical readout update.

公司概覽

Late-Stage Oncology Pipeline

Moleculin Biotech is a clinical-stage company developing treatments for difficult-to-treat cancers and viral diseases. Its portfolio centers on Annamycin in acute myeloid leukemia, supported by earlier-stage programs targeting oncogenic transcription and tumor metabolism.

Annamycin

Annamycin is a next-generation anthracycline designed to avoid multidrug-resistance mechanisms and reduce the cardiotoxicity associated with conventional anthracyclines. The candidate is being developed in relapsed or refractory AML and has also been studied in soft-tissue sarcoma metastatic to the lungs.

MIRACLE Program

MIRACLE is an adaptive pivotal Phase 2/3 study evaluating Annamycin with cytarabine, a regimen referred to as AnnAraC, in second-line relapsed or refractory AML. Part A is designed to enroll approximately 90 patients and identify the dose and regimen to carry into the confirmatory portion of the study.

Additional Development Programs

The pipeline also includes WP1066, a modulator of p-STAT3 and other oncogenic transcription factors under evaluation in brain and pancreatic cancers, and WP1122, a metabolic antitumor and antiviral platform. These programs provide development opportunities beyond Annamycin and hematologic malignancies.

未來催化劑

  • Completion of enrollment in Part A of the MIRACLE trial in September 2026.
  • Initiation of an Atlantic Health investigator-sponsored Annamycin study in pancreatic cancer in the second half of 2026.
  • Unblinding and efficacy readout from MIRACLE Part A between December 2026 and February 2027.
  • Initiation of MIRACLE Part B in the first half of 2027.
  • Planned start of a rolling NDA submission for Annamycin under an accelerated-approval pathway in 2028.

近期新聞

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