Ainos Inc Stock Price, News & Analysis

Ainos (NASDAQ:AIMD), a healthcare company specializing in AI-driven point-of-care testing and low-dose interferon therapeutics, has announced its participation in the Webull Corporate Connect Service (CCS). This strategic move aims to enhance investor engagement and transparency through real-time communication with shareholders.

Through the CCS platform, Ainos will showcase corporate milestones, strategic initiatives, and financial results to the investment community. The company's Chairman and CEO, Chun-Hsien Tsai, emphasized that this integration aligns with their commitment to transparent investor communication and will help drive long-term shareholder value.

Ainos (NASDAQ:AIMD) has formed a strategic partnership with Taiwan Tanabe Seiyaku, a Mitsubishi Tanabe Pharma subsidiary, for manufacturing and marketing VELDONA® in Taiwan. The partnership focuses on advancing VELDONA®, a therapeutic candidate for primary Sjögren's syndrome.

The collaboration leverages Taiwan Tanabe Seiyaku's PIC/S GMP-certified facility and expertise in drug manufacturing and market promotion. A clinical study of VELDONA® has received Institutional Review Board approval from Shuang Ho Hospital, with site initiation planned for April 2025 and completion expected in December 2026. Previous U.S. Phase 3 studies showed VELDONA® benefits in improving oral dryness and salivary function for Sjögren's syndrome, an autoimmune disease affecting 0.1-1.0% of the global population.

Ainos (NASDAQ: AIMD) has signed a strategic Memorandum of Understanding (MOU) with Taiwan Tanabe Seiyaku, a subsidiary of Mitsubishi Tanabe Pharma , to advance the manufacturing and Taiwan market promotion of VELDONA®, their Sjögren's syndrome treatment drug. The partnership leverages Taiwan Tanabe Seiyaku's pharmaceutical development and manufacturing expertise. VELDONA®, a low-dose oral interferon-alpha, has shown promising results in clinical trials, demonstrating significant symptom alleviation and disease progression control. The collaboration aims to accelerate VELDONA®'s global market introduction, targeting the growing Sjögren's syndrome market projected to reach billions in the next five years.

Water Tower Research has published a report highlighting Ainos (NASDAQ:AIMD) receiving IRB approval from Shuang Ho Hospital for its VELDONA clinical study in primary Sjogren's syndrome. The trial is expected to begin around April 2025 after TFDA approval, with completion targeted for December 2026. The study will enroll 24 patients over 24-48 weeks to evaluate VELDONA's efficacy in improving salivary flow. Previous U.S. Phase 3 studies showed positive results. The company recently secured exclusive licenses to 28 patent assets for AI Nose VOC sensing, POCT, and other technologies. Ainos maintains sufficient cash to support operations through 2H25.

Ainos (NASDAQ:AIMD) has received IRB approval from Shuang Ho Hospital for its clinical trial of VELDONA® in treating Sjögren's syndrome. The company plans to commence a site initiation visit around April 2025, pending regulatory approvals. The study will recruit 24 patients for a 24- to 48-week treatment period. Previous U.S. clinical trials, including three Phase 3 studies, demonstrated VELDONA® significantly increases unstimulated whole salivary flow. The trial's primary endpoint is to evaluate VELDONA®'s efficacy in improving salivary flow and alleviating dryness symptoms. Patient recruitment will begin in May 2025, with study completion expected by December 2026.

Ainos (NASDAQ: AIMD) has filed complaints with NASDAQ MarketWatch and the SEC regarding suspicious trading activities in its common stock, particularly concerning large-volume sell orders. The healthcare company, which specializes in AI-powered point-of-care testing and interferon therapeutics, suspects potential regulatory violations and has requested thorough investigation to protect stockholder interests. While regulatory bodies won't confirm any investigation details, Ainos maintains its commitment to market transparency and investor protection.

Ainos (NASDAQ:AIMD) reported Q3 2024 financial results with zero revenue compared to $24,489 in Q3 2023. The company reported a net loss of $3.7M, up from $3.0M in Q3 2023. Operating expenses increased to $3.0M from $2.6M, primarily due to higher R&D investments. Cash position strengthened to $5.2M as of September 30, 2024.

Key developments include securing multi-regional patent assets for AI Nose technology, expanding VELDONA® patent portfolio for coronavirus treatments, and progressing clinical trials for Sjögren's syndrome and HIV-related oral warts. The AI Nose platform achieved 79% accuracy in detecting VOCs in semiconductor factories.

Ainos (NASDAQ:AIMD) has secured exclusive licensing rights for 28 multi-regional patent assets from strategic shareholder Taiwan Carbon Nano Technology (TCNT). The patents cover AI Nose gas sensing technology and a breakthrough nitrogen-oxygen separation technology for medical applications. The new separation technology achieves over 99% purity while using one-third of the energy compared to conventional methods, offering significant cost reduction and environmental benefits.

The patent portfolio spans multiple regions including China, Japan, Korea, Taiwan, Germany, the EU, and the US. The agreement grants Ainos exclusive sales rights for the medical-grade nitrogen-oxygen separation technology, positioning the company for expansion in the advanced medical equipment market.

Ainos (NASDAQ:AIMD) showcased VELDONA®'s clinical progress and market potential in a Water Tower Research podcast. VELDONA®, an oral low-dose interferon-α therapeutic, has undergone 68 clinical studies across 16 indications with 6,000 participants, demonstrating strong safety. The company is focusing on two human studies in Taiwan: oral warts in HIV+ patients and Sjogren's syndrome. Previous trials showed over 75% reduction in wart-affected areas. In animal health, Ainos is exploring VELDONA®'s potential for feline chronic gingivostomatitis. Key milestones include completing the FCGS study by March 2025, filing FDA IND in 2025, completing Taiwan human studies in early 2026, and exploring global licensing opportunities.