Instil Bio plans to start a phase 1 trial of AXN-2510 for solid tumors following FDA IND clearance.
Quiver AI Summary
Instil Bio, Inc. announced the clearance of an Investigational New Drug (IND) application for its drug AXN-2510 by the FDA, enabling the company to begin a phase 1 trial before the end of 2025. This trial will assess the safety and efficacy of ‘2510 as a monotherapy for patients with relapsed or refractory solid tumors. The company also expects initial safety and efficacy results from a separate phase 2 trial of ‘2510 in combination with chemotherapy for first-line non-small cell lung cancer (NSCLC) to be shared in the latter half of 2025. The announcement highlights the significance of evaluating ‘2510 in a global setting as a major step in its clinical development.
Potential Positives
- Clearance of the IND application for AXN-2510 by the FDA, allowing progression to clinical trials.
- Initiation of a phase 1 trial of ‘2510 aimed at evaluating safety and efficacy in relapsed/refractory solid tumors, indicating progress in drug development.
- Anticipation of sharing initial safety and efficacy results from the ongoing phase 2 study in first-line NSCLC, potentially showcasing the drug’s effectiveness.
Potential Negatives
- While the press release announces the clearance of the IND for AXN-2510, it also highlights the costly and time-consuming nature of the product development process, emphasizing the uncertainty of clinical success that may negatively impact investor confidence.
- The reliance on collaborations and third parties for manufacturing and clinical trials introduces additional risks and uncertainties, which could hinder the company’s progress and impact its reputation.
- The press release notes multiple external risks, including macroeconomic conditions and political tensions, that could materially affect the company's business operations and overall financial health.
FAQ
What is AXN-2510?
AXN-2510 is a novel PD-L1xVEGF bispecific antibody developed by Instil Bio for treating solid tumors.
When will the phase 1 trial of AXN-2510 start?
The phase 1 trial of AXN-2510 is expected to begin before the end of 2025.
What are the goals of the phase 1 trial?
The trial aims to evaluate the safety, efficacy, pharmacokinetics, and pharmacodynamics of AXN-2510.
When will initial results from the phase 2 trial be shared?
Initial safety and efficacy results from the phase 2 trial will be shared in the second half of 2025.
Who is conducting the phase 2 trial of AXN-2510?
The phase 2 trial of AXN-2510 is being conducted by ImmuneOnco in China.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$TIL Hedge Fund Activity
We have seen 20 institutional investors add shares of $TIL stock to their portfolio, and 18 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- BOXER CAPITAL MANAGEMENT, LLC removed 275,375 shares (-77.5%) from their portfolio in Q1 2025, for an estimated $4,780,510
- BALYASNY ASSET MANAGEMENT L.P. added 255,691 shares (+414.9%) to their portfolio in Q1 2025, for an estimated $4,438,795
- MILLENNIUM MANAGEMENT LLC added 158,991 shares (+298.6%) to their portfolio in Q1 2025, for an estimated $2,760,083
- SUPERSTRING CAPITAL MANAGEMENT LP removed 148,017 shares (-100.0%) from their portfolio in Q1 2025, for an estimated $2,569,575
- UBS GROUP AG removed 73,806 shares (-81.0%) from their portfolio in Q1 2025, for an estimated $1,281,272
- VELAN CAPITAL INVESTMENT MANAGEMENT LP added 69,000 shares (+inf%) to their portfolio in Q1 2025, for an estimated $1,197,840
- 683 CAPITAL MANAGEMENT, LLC removed 34,557 shares (-100.0%) from their portfolio in Q1 2025, for an estimated $599,909
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
$TIL Analyst Ratings
Wall Street analysts have issued reports on $TIL in the last several months. We have seen 1 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
Here are some recent analyst ratings:
- H.C. Wainwright issued a "Buy" rating on 05/23/2025
To track analyst ratings and price targets for $TIL, check out Quiver Quantitative's $TIL forecast page.
Full Release
US phase 1 trial of ‘2510 is expected to be initiated before the end of 2025
Anticipate ImmuneOnco sharing initial safety and efficacy results from phase 2 trial of ‘2510 + chemo in 1L NSCLC in the second half of 2025
DALLAS, July 02, 2025 (GLOBE NEWSWIRE) -- Instil Bio, Inc. (“Instil”) (NASDAQ: TIL), a clinical-stage biopharmaceutical company focused on developing a pipeline of novel therapies, today announced the clearance of an Investigational New Drug (IND) application for AXN-2510 (“’2510”) by the U.S. Food and Drug Administration.
Instil expects to initiate a phase 1 trial of ‘2510 as monotherapy for patients with relapsed/refractory solid tumors before the end of 2025. The trial is designed to evaluate the safety, efficacy, pharmacokinetics and pharmacodynamics of ‘2510 in patients with solid tumors. Additionally, Instil continues to anticipate that initial safety and efficacy results from the ongoing phase 2 study of ‘2510 in combination with chemotherapy in first-line NSCLC in China will be shared in the second half of 2025 by ImmuneOnco.
“We are pleased to announce the clearance of the ‘2510 IND by the FDA,” said Jamie Freedman, M.D., Ph.D., Chief Medical Officer of Instil. “Evaluating ‘2510 in a global population will be a critical milestone in the clinical development of ‘2510.”
About Instil Bio
Instil Bio is a clinical-stage biopharmaceutical company focused on developing a pipeline of novel therapies. Instil's lead asset, AXN-2510, is a novel and differentiated PD-L1xVEGF bispecific antibody in development for the treatment of multiple solid tumors. For more information, visit www.instilbio.com .
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words (and variations of words) such as "anticipates," "believes," "could,” expects," "exploring," "future," "intends," "may," "plans," "potential," "projects," "will," “target,” and similar expressions are intended to identify forward-looking statements. Forward-looking statements include express or implied statements regarding Instil's expectations with respect to the therapeutic potential of AXN-2510, the clinical development of AXN-2510, patient enrollment and clinical trials and the timing, scope and design thereof, and the availability and timing of data from clinical trials. Forward-looking statements are based on Instil management's current expectations and are subject to various risks and uncertainties that could cause actual results to differ materially and adversely from those expressed or implied by such forward-looking statements, including risks and uncertainties associated with in-licensing product candidates and clinical trial collaborations; the costly and time-consuming product development process and the uncertainty of clinical success; the risks inherent in relying on collaborators and other third parties, including for manufacturing and clinical trial operation; the risks and uncertainties related to successfully initiating, enrolling, completing and reporting data from clinical studies, as well as the risks that results obtained in clinical trials to date may not be indicative of results obtained in ongoing or future trials and that Instil's product candidates may otherwise not be effective treatments in their planned indications; risks related to macroeconomic conditions, including as a result of international conflicts, U.S.-China trade and political tensions, interest rates, inflation, and other factors, which could materially and adversely affect Instil's business and operations; the risks and uncertainties associated with the time-consuming and uncertain regulatory approval process for product candidates across multiple indications and multiple regulatory authorities; the impact of product candidates that may compete with those developed by Instil; the sufficiency of Instil's cash resources; and other risks and uncertainties affecting Instil and its plans and development programs, including those discussed in the section titled "Risk Factors" in Instil's Quarterly Report on Form 10-Q for the quarter ended March 31, 2025 filed with the SEC, as well as Instil's other filings with the SEC. Additional information will be made available in other filings that Instil makes from time to time with the SEC. Accordingly, these forward-looking statements do not constitute guarantees of future performance, and you are cautioned not to place undue reliance on these forward-looking statements. These forward-looking statements speak only as the date hereof, and Instil disclaims any obligation to update these statements except as may be required by law.
Contacts:
Investor Relations:
1-972-499-3350
[email protected]
www.instilbio.com