Welcome to our dedicated page for MAIA Biotechnology news (Ticker: MAIA), a resource for investors and traders seeking the latest updates and insights on MAIA Biotechnology stock.
MAIA Biotechnology, Inc. (NYSE American: MAIA) is a clinical-stage biopharmaceutical company whose news flow is closely tied to the development of ateganosine (THIO), a first-in-class telomere-targeting therapy for advanced non-small cell lung cancer (NSCLC). News about MAIA often centers on clinical milestones, regulatory designations, and financing activities that support its oncology programs.
Investors and observers following MAIA’s news can expect regular updates on its Phase 2 THIO-101 and Phase 3 THIO-104 trials. These items include announcements of first patient dosing, expansion into new countries, enrollment progress, and presentations of trial-in-progress posters at major conferences such as the Society for Immunotherapy of Cancer (SITC), the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, and the European Society for Medical Oncology (ESMO) Congress.
MAIA’s press releases, many of which are furnished via Form 8-K filings, also highlight regulatory developments such as the U.S. FDA Fast Track designation for ateganosine in NSCLC and Orphan Drug Designations in additional tumor types. Another recurring theme in the company’s news is insider activity: open-market share purchases by the CEO and directors, and participation by board members in private placement financings, which the company frames as signals of confidence in the ateganosine platform.
On this news page, readers can review MAIA’s announcements related to clinical data signals, trial design details, international site activations, and capital raises that fund key study steps. For those tracking the progress of telomere-targeting approaches in oncology and the later-line NSCLC treatment landscape, MAIA’s news provides an ongoing record of how its investigational therapy is advancing through mid- to late-stage clinical development.
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MAIA Biotechnology (NYSE American: MAIA) has reported promising updates on disease control data in the Part A safety lead-in of its ongoing THIO-101 phase 2 trial. The trial is evaluating THIO in sequential combination with cemiplimab for patients with advanced Non-Small Cell Lung Cancer (NSCLC) who have previously failed 2 or more prior lines of treatment.
Key findings include:
- 82% disease control rate: 9 out of 11 patients with post-baseline scans met the primary endpoint of disease control
- Disease control is defined as Complete Response, Partial Response, or Stable Disease per RECIST 1.1
- All patients had previously failed immune checkpoint inhibitor (CPI) and platinum-based chemotherapy treatments
- No new safety analysis was conducted at this time
The company's CEO, Vlad Vitoc, expressed encouragement with these preliminary results, noting that they align with pre-clinical data showing THIO's potential to enhance CPI effectiveness in resistant cases.