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Xilio Therapeutics Highlights Upcoming Milestones and Recent Corporate Updates

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Xilio Therapeutics (NASDAQ: XLO) reported $35.8 million in gross proceeds from Series B warrant exercises and estimates $137.5 million in cash and cash equivalents as of December 31, 2025. The company said this funding extends its anticipated cash runway into the second quarter of 2027. Recent program updates include a development milestone for a masked antibody program under the AbbVie collaboration and nomination of a development candidate for a wholly owned masked T cell engager targeting CLDN18.2. Corporate changes include the appointment of Sara Bonstein as chair of the board. Anticipated next milestones include an IND submission for XTX501 in mid-2026 and initial Phase 1 data for XTX501 in H2 2027, subject to FDA clearance.

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Positive

  • Raised $35.8M in gross proceeds from Series B warrant exercises
  • Reported $137.5M in cash and cash equivalents as of Dec 31, 2025
  • Cash runway extended into Q2 2027 under current operating plans
  • Nominated development candidate for masked T cell engager targeting CLDN18.2
  • Achieved a development milestone under the AbbVie collaboration

Negative

  • Initial cash estimate is preliminary unaudited and may change
  • Planned initial Phase 1 data for XTX501 is subject to IND clearance, creating timing uncertainty

News Market Reaction

+2.60%
3 alerts
+2.60% News Effect
-3.8% Trough Tracked
+$1M Valuation Impact
$50M Market Cap
1.4x Rel. Volume

On the day this news was published, XLO gained 2.60%, reflecting a moderate positive market reaction. Argus tracked a trough of -3.8% from its starting point during tracking. Our momentum scanner triggered 3 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $1M to the company's valuation, bringing the market cap to $50M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Series B warrant proceeds: $35.8 million Estimated cash and equivalents: $137.5 million Cash runway: Into Q2 2027 +5 more
8 metrics
Series B warrant proceeds $35.8 million Gross proceeds from Series B warrant exercises announced January 2026
Estimated cash and equivalents $137.5 million Preliminary, unaudited as of December 31, 2025
Cash runway Into Q2 2027 Based on cash as of December 31, 2025 and current plans
XTX501 IND timing Middle of 2026 Planned IND submission for bispecific PD-1/masked IL-2 candidate
XTX501 Phase 1 data timing Second half of 2027 Initial Phase 1 data, subject to FDA IND clearance
STEAP1 candidate nomination First half of 2026 Planned nomination for masked T cell engager with co-stimulation
T cell engager INDs 2027 Submit INDs for at least two masked T cell engager programs
Efarindodekin alfa option package First half of 2027 Deliver Phase 1/2 option data package to Gilead

Market Reality Check

Price: $0.5971 Vol: Volume 380,244 vs 20-day ...
normal vol
$0.5971 Last Close
Volume Volume 380,244 vs 20-day average 420,781 (relative volume 0.9) suggests typical trading interest ahead of the update. normal
Technical Price $0.7052 is trading below the $0.74 200-day moving average and 58.52% below the 52-week high.

Peers on Argus

XLO showed a 1.45% pre-news gain while momentum scanners only flagged JSPR, movi...
1 Down

XLO showed a 1.45% pre-news gain while momentum scanners only flagged JSPR, moving down by 9.76%. Broader peers showed mixed moves, pointing to a stock-specific reaction rather than a coordinated biotech sector move.

Historical Context

5 past events · Latest: Nov 13 (Negative)
Pattern 5 events
Date Event Sentiment Move Catalyst
Nov 13 Earnings and pipeline Negative -9.3% Q3 2025 financials, clinical updates, and going concern disclosure.
Nov 07 Phase 2 data Positive -3.0% Late-breaking vilastobart Phase 2 data in MSS mCRC at SITC.
Nov 07 Portfolio showcase Positive -3.0% SITC presentations on masked immunotherapies and platform data.
Nov 03 Equity compensation Negative -5.7% Inducement stock option grant under 2022 plan to a new employee.
Oct 30 Conference preview Positive -0.8% Planned late-breaking Phase 2 vilastobart data at SITC meeting.
Pattern Detected

Recent news, including positive clinical and portfolio updates, frequently coincided with negative price reactions, indicating a pattern of weak trading responses even to constructive developments.

Recent Company History

Over the last few months, Xilio focused on advancing its masked immunotherapy platform and managing capital. Clinical data for vilastobart and efarindodekin alfa at SITC in November 2025 showed encouraging response and biomarker signals, yet shares sold off after those events. Corporate actions around stock option repricing and inducement grants in late October–November 2025 reflected efforts to realign employee incentives. Q3 2025 results highlighted rising collaboration revenue and a strengthened cash balance but also noted going concern risks, framing today’s runway and financing update in a broader de-risking narrative.

Market Pulse Summary

This announcement details receipt of $35.8 million from Series B warrant exercises and preliminary y...
Analysis

This announcement details receipt of $35.8 million from Series B warrant exercises and preliminary year-end cash of $137.5 million, supporting a runway into Q2 2027. It also outlines IND and data milestones for XTX501 and masked T cell engager programs, plus a development milestone under the AbbVie collaboration. In light of prior going concern disclosures and heavy dependence on partnerships, investors may watch execution on these timelines and any further business development updates.

Key Terms

investigational new drug (IND), Phase 1, Phase 2, T cell engager, +1 more
5 terms
investigational new drug (IND) regulatory
"Submit an investigational new drug (IND) application for XTX501 in the middle of 2026"
An investigational new drug (IND) is a drug or biologic that is being tested but has not yet been approved for general use; it is the application and formal status that allows a company to begin human clinical trials under regulator oversight. Investors care because an IND marks the transition from lab work to human testing — like getting a permit to run real-world experiments — which creates important milestones, costs, timelines and regulatory risk that drive a development-stage company's value.
Phase 1 medical
"Report initial Phase 1 data for XTX501 in the second half of 2027"
Phase 1 is the first stage of testing a new drug or medical treatment in people, focused primarily on safety, how the body handles the product, and finding a tolerated dose. Think of it as a short, tightly controlled experiment with a small group to check for dangerous side effects before wider testing; for investors it is an early milestone that reduces some uncertainty but still carries high risk and potential for both big value changes and setbacks.
Phase 2 medical
"Deliver the Phase 1/2 option data package to Gilead for the efarindodekin alfa program"
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.
T cell engager medical
"masked T cell engager program targeting the tumor-associated antigen for CLDN18.2"
A T cell engager is an engineered protein drug that physically links a patient’s T cell — the immune system’s attack cell — to a diseased cell so the T cell will recognize and kill it. For investors it matters because clinical trial results, manufacturing success and safety profiles determine whether the therapy becomes a widely adopted, high-value treatment or a costly failure; think of it like a matchmaker that must reliably bring soldiers to the right target without triggering friendly fire.
tumor-associated antigen medical
"targeting the tumor-associated antigen for CLDN18.2, which has broad potential"
Molecules—often proteins—found on the surface or inside cancer cells that the immune system can recognize as abnormal; some are largely unique to tumors while others also appear at low levels on healthy tissue. Investors care because these markers are targets for diagnostics, immunotherapies and vaccines, so showing a reliable, targetable marker is like putting a bull's-eye on a disease: it can speed development, raise the value of a drug program and influence regulatory and commercial prospects.

AI-generated analysis. Not financial advice.

Received $35.8 million in gross proceeds from Series B warrant exercises, including full exercise by Coastlands Capital, Frazier Life Sciences and Gilead Sciences, Inc., and extended anticipated cash runway into second quarter of 2027

Achieved development milestone for masked antibody-based program under AbbVie agreement

Nominated development candidate for wholly-owned masked T cell engager program targeting CLDN18.2

Appoints Sara Bonstein as chair of board of directors

WALTHAM, Mass., Jan. 08, 2026 (GLOBE NEWSWIRE) -- Xilio Therapeutics, Inc. (Nasdaq: XLO), a clinical-stage biotechnology company discovering and developing masked immuno-oncology therapies for people living with cancer, today highlighted upcoming milestones and recent corporate updates.

“2025 was marked by robust execution at Xilio as we delivered on key priorities across our deep portfolio of differentiated I-O therapies, demonstrated additional clinical validation of our masking technology and further strengthened our financial position through strategic partnerships and our recent equity financing,” said René Russo, Pharm.D., president and chief executive officer of Xilio. “In the year ahead, we have a strong foundation to advance our potential best-in-class bispecific PD-1/IL-2 and T cell engager programs toward the clinic and maximize the value of our vilastobart and efarindodekin alfa programs through strategic partnerships.”

Xilio also announced the appointment of Sara Bonstein as chair of the board of directors, following the retirement of Paul Clancy. Dr. Russo continued, “Sara has been an invaluable member of our board since 2021 and brings more than two decades of executive leadership in finance, corporate strategy and business operations in the biotechnology industry, as well as extensive experience advancing novel therapies from discovery through commercialization. I look forward to continuing to partner with Sara as we advance our pipeline of masked immuno-oncology therapies through development. On behalf of the entire board, I’d also like to express my gratitude to Paul for his leadership and contributions as chair, which have been instrumental in helping shape Xilio over the past five years.”

Ms. Bonstein added, “During my tenure, Xilio has made significant progress demonstrating validation for its novel masking technology through strategic partnerships with Gilead and AbbVie as well as promising clinical data for its most advanced programs. I am excited to chair the board and look forward to working closely with the management team to advance the company’s deep portfolio of differentiated I-O therapies.”

Corporate Updates

In January 2026, Xilio announced the receipt of $35.8 million in gross proceeds from the exercise of Series B warrants, before deducting underwriting discounts and commissions and any offering expenses, including the full exercise of Series B warrants held by Coastlands Capital, Frazier Life Sciences and Gilead Sciences, Inc. The Series B warrants were issued in connection with a follow-on public offering in June 2025.

Xilio today announced:

  • The achievement of a development milestone related to the masked antibody-based immunotherapy program under the company’s collaboration, license and option agreement with AbbVie.
  • The nomination of a development candidate for its masked T cell engager program targeting the tumor-associated antigen for CLDN18.2, which has broad potential as a target for gastric, pancreatic, esophageal and lung cancers.
  • The appointment of Sara M. Bonstein as chair of the board of directors of Xilio. Ms. Bonstein has served as a member of Xilio’s board of directors since August 2021 and succeeds Paul Clancy, who retired from the board of directors on January 6, 2026. Ms. Bonstein has more than 10 years of experience as a chief financial officer for public biotechnology companies, and she currently serves as chief financial officer of Insmed, Inc. where she oversees key financial functions including capital raising, investor relations, accounting, treasury, financial planning and analysis and procurement. Earlier in her career, Ms. Bonstein held finance roles of increasing responsibility at Eli Lilly & Company and Johnson & Johnson. Ms. Bonstein holds a B.S. in finance from The College of New Jersey and an M.B.A. from Rider University.

Anticipated Milestones

Xilio’s anticipated upcoming milestones include:

  • Submit an investigational new drug (IND) application for XTX501 in the middle of 2026
  • Report initial Phase 1 data for XTX501 in the second half of 2027, subject to clearance of the IND by the U.S. Food and Drug Administration
  • Nominate a development candidate for the STEAP1 program (masked T cell engager with co-stimulation) in the first half of 2026
  • Advance at least two masked T cell engager programs into IND-enabling studies and submit IND applications for those programs in 2027
  • Deliver the Phase 1/2 option data package to Gilead for the efarindodekin alfa program in the first half of 2027

Financial Guidance

As of December 31, 2025, Xilio estimates that it had cash and cash equivalents of $137.5 million, including $35.8 million in gross proceeds received in the fourth quarter of 2025 from the exercise of Series B warrants.

Based on its current operating plans, Xilio anticipates that its cash and cash equivalents as of December 31, 2025 will be sufficient to enable it to fund its operating expenses and capital expenditure requirements into the second quarter of 2027.

The cash and cash equivalents information provided above is based on preliminary unaudited information and management estimates for the year ended December 31, 2025, is not a comprehensive statement of the company’s financial results as of and for the fiscal year ended December 31, 2025 and may change. Xilio’s independent registered public accounting firm has not conducted an audit or review of, and does not express an opinion or any other form of assurance with respect to, this preliminary estimate.

About Xilio Therapeutics

Xilio Therapeutics is a clinical-stage biotechnology company discovering and developing masked immuno-oncology (I-O) therapies with the goal of significantly improving outcomes for people living with cancer without the systemic side effects of current I-O treatments. The company is leveraging its proprietary masking technology to advance a pipeline of novel, masked I-O molecules that are designed to optimize the therapeutic index by localizing anti-tumor activity within the tumor microenvironment. Learn more by visiting www.xiliotx.com and follow us on LinkedIn (Xilio Therapeutics, Inc.).

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, statements regarding plans, expectations, development timelines and anticipated milestones for Xilio’s programs; the timing of data releases or program updates; the potential of Xilio’s programs or platform; the timing and receipt of future contingent payments under Xilio’s collaboration agreements with AbbVie or Gilead; Xilio’s estimated cash and cash equivalents and the sufficiency of, and period in which, Xilio expects to be able to fund its operations and capital expenditure requirements; and Xilio’s strategy, goals and anticipated financial performance, milestones, business plans and focus. The words “aim,” “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “seek,” “target” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Any forward-looking statements in this press release are based on management’s current expectations and beliefs and are subject to a number of important risks, uncertainties and other factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, risks related to general market conditions and geopolitical uncertainties; risks and uncertainties related to ongoing and planned research and development activities, including initiating, conducting or completing preclinical studies and clinical trials and the timing and results of such preclinical studies or clinical trials; the delay of any current or planned preclinical studies or clinical trials or the development of Xilio’s current or future product candidates; Xilio’s ability to obtain and maintain sufficient preclinical and clinical supply of current or future product candidates; Xilio’s ability to advance multiple early stage masked T cell engager programs; initial, preliminary, interim or retrospective preclinical or clinical data or results may not be replicated in or predictive of future preclinical or clinical data or results; Xilio’s ability to successfully demonstrate the safety and efficacy of its product candidates and gain approval of its product candidates on a timely basis, if at all; results from preclinical studies or clinical trials for Xilio’s product candidates may not support further development of such product candidates; actions of regulatory agencies may affect the initiation, timing and progress of current or future clinical trials; Xilio’s ability to obtain, maintain and enforce patent and other intellectual property protection for current or future product candidates; Xilio’s need to obtain additional cash resources to advance its pipeline of tumor-activated I-O molecules; the impact of international trade policies on Xilio’s business, including U.S. and China trade policies; and Xilio’s ability to maintain its collaboration or partnership agreements with AbbVie, Gilead and Roche. These and other risks and uncertainties are described in greater detail in the sections entitled “Risk Factor Summary” and “Risk Factors” in Xilio’s filings with the U.S. Securities and Exchange Commission (SEC), including Xilio’s most recent Quarterly Report on Form 10-Q and any other filings that Xilio has made or may make with the SEC in the future. Any forward-looking statements contained in this press release represent Xilio’s views only as of the date hereof and should not be relied upon as representing its views as of any subsequent date. Except as required by law, Xilio explicitly disclaims any obligation to update any forward-looking statements.

This press release contains hyperlinks to information that is not deemed to be incorporated by reference in this press release.

Investor Contact  
Alex Lobo, Precision AQ
alex.lobo@precisionaq.com

Media Contact  
Josie Butler, 1AB
josie@1abmedia.com


FAQ

How much cash did Xilio Therapeutics (XLO) report as of December 31, 2025?

Xilio reported $137.5 million in cash and cash equivalents as of December 31, 2025.

What did the Series B warrant exercises mean for XLO in Q4 2025?

The exercise of Series B warrants generated $35.8 million in gross proceeds in Q4 2025.

When does XLO plan to submit the IND for XTX501?

Xilio anticipates submitting an IND for XTX501 in mid-2026.

What is Xilio's expected cash runway after the Series B proceeds?

Based on current operating plans, cash is expected to fund operations into the second quarter of 2027.

What clinical milestone did XLO achieve with AbbVie?

Xilio reported the achievement of a development milestone for a masked antibody-based program under its collaboration with AbbVie.

What candidate nomination did Xilio announce for CLDN18.2?

Xilio nominated a development candidate for a wholly owned masked T cell engager targeting CLDN18.2.

Who is the new chair of Xilio's board and when did the change occur?

Sara Bonstein was appointed chair of the board following Paul Clancy's retirement effective January 6, 2026.
Xilio Therapeutics, Inc.

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