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XLONasdaq

Xilio Therapeutics, Inc.

Pharmaceutical preparations·Phase 1·Waltham, MA, United States·CEO: Dr. Rene Russo BCPS, Pharm.D.
Oncology

XLO evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

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Prepared research question

What matters most for XLO—catalysts, financial risk and supporting evidence?

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BioSniper AI · XLO

Xilio Therapeutics is a clinical-stage biotechnology company developing tumor-selective immunotherapies using its proprietary masking technology, with a focus on advancing its lead candidates efarindodekin alfa and XTX501 through early-stage clinical trials.

Key risk: No approved products

6.0/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$59.2M

Cash Runway

22.4 mo

Next Catalyst

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates · 4 clinical trials for Xilio Therapeutics, Inc..

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AI OverviewAI overview is shown in English only.

Xilio Therapeutics is a clinical-stage biotechnology company developing tumor-selective immunotherapies using its proprietary masking technology, with a focus on advancing its lead candidates efarindodekin alfa and XTX501 through early-stage clinical trials.

  • Xilio's proprietary masking technology aims to enable tumor-selective activity of immunotherapies, potentially reducing systemic toxicity [sec_mda · as of 2026-05-12].
  • The company has established strategic partnerships with AbbVie and Gilead, including a $6.0 million development milestone achieved under the AbbVie collaboration in Q2 2026 [sec_mda · as of 2026-08-12].
  • As of June 30, 2026, Xilio had cash and cash equivalents of $136.0 million, with an accumulated deficit of $434.7 million [sec_mda · as of 2026-08-12].
  • The company reported a net loss of $35.0 million for the year ended December 31, 2025, and expects to continue incurring significant operating losses [sec_mda · as of 2026-08-12].
  • Xilio's cash runway is projected to fund operations into the first quarter of 2028, excluding potential additional proceeds from warrant exercises or milestone payments [sec_mda · as of 2026-08-12].

What works

  • Proprietary masking technology is clinically validated and has enabled partnerships with major pharma companies like AbbVie and Gilead [sec_mda · as of 2026-05-12].
  • Cash position of $136.0 million as of June 30, 2026, together with a $6.0 million milestone, is expected to fund operations into Q1 2028 [sec_mda · as of 2026-08-12].
  • Collaboration with AbbVie generated a $6.0 million development milestone in Q2 2026, demonstrating partnership progress [sec_mda · as of 2026-08-12].

What to weigh

  • Xilio has not yet commercialized any product candidates and does not expect to generate product revenue for several years, if at all [sec_mda · as of 2026-08-12].
  • The company has an accumulated deficit of $434.7 million as of June 30, 2026, and expects to continue incurring significant operating losses [sec_mda · as of 2026-08-12].
  • All product candidates are in preclinical or early clinical development, with no approved therapies, making the company highly dependent on clinical trial success [sec_mda · as of 2026-08-12].

From the filings

Quoted directly from source documents.

  • Xilio's masking technology is clinically validated and supports partnerships with AbbVie and Gilead.

    masked multi-specifics, and our clinically-validated masking technology has enabled us to establish top-tier strategic partnerships, including with AbbVie Group Holdings Limited, or AbbVie, and Gilead Sciences, Inc., or Gilead.

    SEC MD&A · May 12, 2026

  • Cash and cash equivalents as of June 30, 2026, were $136.0 million.

    As of June 30, 2026, we had cash and cash equivalents of $136.0 million.

    SEC MD&A · August 12, 2026

  • Accumulated deficit as of June 30, 2026, was $434.7 million.

    As of June 30, 2026, we had an accumulated deficit of $434.7 million.

    SEC MD&A · August 12, 2026

  • Xilio has not commercialized any product candidates and does not expect product revenue for several years.

    We have not yet commercialized any of our product candidates, which are in preclinical or early clinical development, and we do not expect to generate revenue from sales of any products for several years, if at all.

    SEC MD&A · August 12, 2026

Risks & what to watch (4)

Key risks

  • No approved productsAll product candidates are in preclinical or early clinical stages; no commercial revenue expected for years [sec_mda · as of 2026-08-12].
  • Significant accumulated deficitAccumulated deficit of $434.7 million as of June 30, 2026, with ongoing operating losses [sec_mda · as of 2026-08-12].
  • Dependence on partnershipsFuture funding relies on milestones and options from AbbVie and Gilead, which may not materialize [sec_mda · as of 2026-08-12].
  • Clinical trial uncertaintySuccess of efarindodekin alfa and XTX501 trials is uncertain; failure could impact viability [sec_mda · as of 2026-08-12].

What to watch

  • Progress of clinical trials for efarindodekin alfa and XTX501, as these are key value drivers [sec_mda · as of 2026-08-12].
  • Achievement of additional milestones under the AbbVie and Gilead collaborations, which could extend cash runway [sec_mda · as of 2026-08-12].
  • Exercise of Series C warrants, which could provide up to $36.2 million in additional gross proceeds [sec_mda · as of 2026-08-12].
  • Updates on cash burn rate and any changes to the projected runway into Q1 2028 [sec_mda · as of 2026-08-12].

Sources: SEC MD&A · Generated August 27, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway6.2

22.4 months

Financial Health6.6

D/E 1.13

Pipeline Maturity6.0

Lead: Phase 1/Phase 2

Pipeline Breadth4.6

2 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal6.5

1 buy · 0 sells (180d)

Runway

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

18

Total value held

$5.6M

Showing top 10 of 18 institutional holders of Xilio Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 30, 2026
% of float
3.8%
Days to cover
3.8
Shares short
174,319
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

XLO short interest

Governance

Frequently asked questions

What is the AI investment thesis for Xilio Therapeutics, Inc.?

Xilio Therapeutics is a clinical-stage biotechnology company developing tumor-selective immunotherapies using its proprietary masking technology, with a focus on advancing its lead candidates efarindodekin alfa and XTX501 through early-stage clinical trials.

What is Xilio Therapeutics, Inc.'s lead drug candidate?

Xilio Therapeutics, Inc.'s most advanced tracked candidate is vilastobart (Phase 1/Phase 2) for Advanced Solid Tumor.

Who is the CEO of Xilio Therapeutics, Inc.?

Dr. Rene Russo BCPS, Pharm.D. is the chief executive officer of Xilio Therapeutics, Inc. (XLO).

Where is Xilio Therapeutics, Inc. headquartered?

Xilio Therapeutics, Inc. (XLO) is headquartered in Waltham, MA, United States.

What therapeutic areas does Xilio Therapeutics, Inc. focus on?

Xilio Therapeutics, Inc. develops therapies across Oncology.

925 companies232,681 SEC filings21,417 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.