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GlobeNewswire All Public CompaniesQwen · 实盘不做把握 9/10不做原因:不是事件
北京时间·🕒 发布 21:01:00·⟳ 抓取 21:02:30·⚡ 决策 08-27 21:05:42 +3m12s·61.4 天前

GRI Bio发布付费IR推广视频网络研讨会,无新增临床数据或监管进展

该公告仅为付费投资者关系公司制作的推广视频上线通知,不含任何新增临床数据、监管进展、订单、财务信息或实质性业务更新。ERS会议展示为已公布旧闻。无方向、无催化剂、无可交易edge。

📄 原文GlobeNewswire All Public Companies↗ 原文
GRI Bio Featured in "Why Now" On-Demand Video Webcast
Video webcast now available here LA JOLLA, CA, Aug. 27, 2026 (GLOBE NEWSWIRE) -- GRI Bio, Inc. (NASDAQ: GRI) (“GRI Bio”…
不做 GRI Bio(GRI.US)
事件为付费IR推广视频上线通知,无新增临床数据、无监管里程碑、无财务更新、无实质催化剂。JTC Team和Virtual Investor Co.为付费顾问,内容仅重复已知信息。不构成可交易事件。
展开详情(成交明细 / 研究档案 / 原文全文 / 决策记录链)

研究档案

结论摘要

GRI Bio通过GlobeNewswire发布付费IR推广视频(JTC Team/Virtual Investor Co.制作),内容仅重复已知的GRI-0621机制描述和已公布的ERS会议展示计划。无新数据、无新里程碑、无财务更新,属于微市值公司常规IR推广活动,不构成可交易催化。

🔎 新鲜度:最早出现 2026-08-27 · 扩散 low · price-in 风险 low ↗

主要风险

  • 公司自身披露存在Nasdaq维持上市风险,属于微市值临床阶段biotech
工具执行结果 · 成功 1 · 降级 0 · 失败 1 · 取消 0
  1. fetch_decision_experience 失败 stock_tools HTTP · 585 ms
    RuntimeError: RuntimeError: stock_tools MCP session failed: ExceptionGroup('unhandled errors in a TaskGroup', [ConnectError('All connection attempts failed')])
  2. search_processed_events 成功 stock_tools HTTP · 40,622 ms
    {"result": "search_processed_events:agent query=`gri bio video webcast | gri bio why now | gri-0621 ipf`;结构化索引覆盖完整 72 小时;旧记录兼容扫描近 71.9/72 小时、11456 条本臂决策(完整),返回 0 条候选。未命中只表示这些 agent query 表达式没有召回候选,不能据此证明消息首发或不是重复;按当前事件继续正常研判。"}

原文全文

展开原文 · 6,966 字
Video webcast now available
here
LA JOLLA, CA, Aug. 27, 2026 (GLOBE NEWSWIRE) --
GRI Bio, Inc.
(NASDAQ: GRI) (“GRI Bio” or the “Company”), a biotechnology company developing innovative therapies for inflammatory, fibrotic and autoimmune diseases, today announced that it is featured in a
"Why Now" video webcast
.
During the webcast, Marc Hertz, Ph.D., Chief Executive Officer of GRI Bio, discusses the Company's differentiated approach to treating idiopathic pulmonary fibrosis (IPF) through GRI-0621, a once-daily oral, RARβ/γ-selective agonist designed to modulate the biological pathways associated with inflammation, fibrosis and tissue repair. The discussion also highlights GRI-0621's differentiated mechanism of action and the significant unmet need that remains for patients living with IPF. As previously announced, GRI has been selected for presentation at the 2026 European Respiratory Society (ERS) Congress, being held September 5-9 in Barcelona, Spain, where it will present on data that it believes is supportive of GRI-0621’s differentiated mechanism and its potential to address the underlying biology of IPF.
The video webcast is now accessible for on-demand viewing
here
.
JTC Team and Virtual Investor Co. are paid consultants to GRI Bio, Inc. JTC Team and Virtual Investor Co. are investor relations and corporate communications firms. Any content included in this release shall not be construed as an offer to purchase securities of GRI Bio, Inc. Interested parties are responsible for conducting their own due diligence and are encouraged to review the Company's website and the SEC website for the latest information and filings on the Company.
About GRI Bio, Inc.
GRI Bio is a clinical-stage biopharmaceutical company focused on developing innovative therapies for inflammatory, fibrotic and autoimmune diseases. The Company’s lead program, GRI-0621, is an oral RARβ/γ-selective agonist being developed for the treatment of idiopathic pulmonary fibrosis (IPF), a progressive and life-threatening fibrotic lung disease with significant unmet need. GRI-0621 is designed to modulate pathways associated with inflammation, fibrosis and tissue repair and is being evaluated as a potential novel oral therapeutic for patients with IPF.
In addition to GRI-0621, the Company is also developing a pipeline of novel type 2 diverse NKT (“dNKT”) agonists for the treatment of systemic lupus erythematosus. Additionally, with a library of over 500 proprietary compounds, GRI Bio has the ability to fuel a growing pipeline.
Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “target,” “aim,” “should,” “will,” “would,” or the negative of these words or other similar expressions. These forward-looking statements are based on the Company’s current beliefs and expectations. Forward-looking statements include, but are not limited to, statements regarding: the Company’s expectations with respect to development and commercialization of the Company’s product candidates, the timing of initiation or completion of clinical trials and availability of resulting data, the potential benefits and impact of the Company’s clinical trials and product candidates and any implication that the data or results observed in preclinical trials or earlier studies, topline or interim data or trials will be indicative of results of later studies or clinical trials or final data, the Company’s beliefs and expectations regarding potential shareholder value and future financial performance, the Company’s beliefs about the timing and outcome of regulatory approvals and potential regulatory approval pathways, the Company’s expected future milestones, shareholder value and the length of time the Company’s current resources will fund its planned operations (which current estimate assumes only initial preparatory activities for GRI-0621 as substantial additional capital or resources will be required to fund future clinical trials of GRI-0621). Actual results may differ from the forward-looking statements expressed by the Company in this press release and consequently, you should not rely on these forward-looking statements as predictions of future events. These forward-looking statements are subject to inherent uncertainties, risks and assumptions that are difficult to predict, including, without limitation risks related to: (1) the Company’s inability to maintain the listing of the Company’s common stock on The Nasdaq Capital Market and to comply with applicable listing requirements; (2) changes in applicable laws or regulations; (3) the inability of the Company to raise financing in the future; (4) the success, cost and timing of the Company’s product development activities; (5) the inability of the Company to obtain and maintain regulatory clearance or approval for its respective products, and any related restrictions and limitations of any cleared or approved product; (6) the inability of the Company to identify, in-license or acquire additional technology; (7) the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently developing; (8) the accuracy of the estimated size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; (9) that later data or clinical trials may be inconsistent with or contrary to data and observations to date, including that later data may not indicate a patient benefit, modulate toxicities or validate a mechanism of action; (10) inaccuracy in the Company’s estimates regarding expenses, future revenue, capital requirements and needs for and the ability to obtain additional financing; (11) the Company’s ability to protect and enforce its intellectual property portfolio, including any newly issued patents and its ability to obtain any expected patent term extensions, adjustments, exclusivities or disclaimers; and (12) other risks and uncertainties indicated from time to time in the Company’s filings with the U.S. Securities and Exchange Commission (the “SEC”), including the risks and uncertainties described in the “Risk Factors” section of the Company’s most recent Annual Report on Form 10-K filed with the SEC on January 30, 2026 and subsequently filed reports. Forward-looking statements contained in this announcement are made as of this date, and the Company undertakes no duty to update such information except as required under applicable law.
Investor Contact:
JTC Team, LLC
Jenene Thomas
(908) 824-0775
GRI@jtcir.com

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