$VBIO

Valion Bio, Inc.

Tivic is a late-stage biopharmaceutical company developing Entolimod, a recombinant TLR5 agonist, primarily for acute radiation syndrome and also for oncology-related conditions including neutropenia, thrombocytopenia and mucositis. Its pipeline includes Entolasta, a next-generation TLR5 agonist, which is in preclinical development. Tivic holds worldwide exclusive license rights to Entolimod and rights to Entolasta. Tivic’s wholly owned subsidiary, Velocity Bioworks, operates a CGMP-compatible biomanufacturing facility in San Antonio and is a contract development and manufacturing organization serving Tivic and select third-party customers. The company’s activities center on developing its drug candidates and manufacturing services. Tivic is headquartered in San Antonio, Texas.

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Valion Bio, Inc. (VBIO): Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers

Valion Bio, Inc. (VBIO) filed an SEC Form 8-K — Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers. Exhibit 99.1 Valion Bio Advancing Entolimod into U.S. Government-Funded Therapeutic Efficacy Study Following Positive Safety Results NIAID-RNCP elects to evaluate the efficacy of Entolimod on gastrointestinal acute radiation syndrome (“GI-ARS”), after the announcement of positive

Valion Bio Reports Positive Entolimod Safety Results, Plans Fully Funded Efficacy Study

Valion Bio reported positive safety results for Entolimod in a preclinical study, with no treatment-related toxicity or significant body-weight differences in mice. AFRRI plans a fully funded efficacy study to assess survival and gastrointestinal recovery post-radiation. According to the company, the study will be fully funded.

Valion Bio Announces Positive Safety Results from U.S. Government-Funded Entolimod Study, Paving Way for Therapeutic Efficacy Evaluation

Valion Bio, Inc. (VBIO) filed an SEC Form 8-K — Other Events. Exhibit 99.1 Valion Bio Announces Positive Safety Results from U.S. Government-Funded Entolimod Study, Paving Way for Therapeutic Efficacy Evaluation AFRRI study found no evidence of treatment-related toxicity following a single dose of Entolimod, supporting advancement toward a

VBIO sentiment & insider activity

Over the past 7 days, AlphAI's AI scored 7 news stories mentioning VBIO (Valion Bio, Inc.). Coverage has skewed bullish: 6 bullish, 1 neutral, and 0 bearish.

Recent VBIO coverage spans financial news, corporate actions and mergers & acquisitions.

What's driving VBIO

AlphAI scores every news story that mentions VBIO with an AI model for sentiment and relevance, and aggregates insider trades from Valion Bio, Inc.'s SEC EDGAR Form 4 filings. Figures refresh continuously.

News on $VBIO

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Valion Bio, Inc. (VBIO): Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers

Valion Bio, Inc. (VBIO) filed an SEC Form 8-K — Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers. Exhibit 99.1 Valion Bio Advancing Entolimod into U.S. Government-Funded Therapeutic Efficacy Study Following Positive Safety Results NIAID-RNCP elects to evaluate the efficacy of Entolimod on gastrointestinal acute radiation syndrome (“GI-ARS”), after the announcement of positive

$VBIOMedAI 8/10

Valion Bio Announces Positive Safety Results from U.S. Government-Funded Entolimod Study, Paving Way for Therapeutic Efficacy Evaluation

Valion Bio, Inc. (VBIO) filed an SEC Form 8-K — Other Events. Exhibit 99.1 Valion Bio Announces Positive Safety Results from U.S. Government-Funded Entolimod Study, Paving Way for Therapeutic Efficacy Evaluation AFRRI study found no evidence of treatment-related toxicity following a single dose of Entolimod, supporting advancement toward a

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Valion Bio, Inc. (VBIO): Entry into a Material Definitive Agreement

Valion Bio, Inc. (VBIO) filed an SEC Form 8-K — Entry into a Material Definitive Agreement. Item 1.01 Entry into a Material Definitive Agreement. Series B Closing Valion Bio, Inc., a Delaware corporation (the “Company”), and 3i, LP (“3i”) are party to that certain Securities Purchase Agreement, dated as of April 29, 2025 (as assigned and amended as of December 9, 2025,

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Valion Bio’s New Leadership Unveils 30-Day Agenda to Accelerate Clinical Pipeline and Unlock Shareholder Value

Valion Bio, Inc. (VBIO) filed an SEC Form 8-K — Other Events. Exhibit 99.1 Valion Bio ’ s New Leadership Unveils 30-Day Agenda to Accelerate Clinical Pipeline and Unlock Shareholder Value Interim CEO Dean Zikria ’ s initial review prioritizes Entolimod and pipeline advancement, commercialization of Velocity Bioworks, and strategic opportuni

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Valion Bio interim CEO outlines strategic priorities

Valion Bio Inc. (VBIO) interim CEO Dean Zikria outlined strategic priorities, focusing on advancing Entolimod and other pipeline assets, pursuing revenue opportunities for Velocity Bioworks, and evaluating strategic partnerships. Entolimod, the lead drug candidate, has received $35.6 million in non-dilutive funding and holds FDA designations. The company is also developing Entolasta and an oral mucosal formulation. Velocity Bioworks is being evaluated for potential partnerships or a sale.

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