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TRex Bio Q3 2026 net loss widens to $13.2M

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(High)

Sentiment and the balance of points

Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.

Form Type
8-K

Rhea-AI Filing Summary

TRex Bio, Inc. (TRXB) reported a third-quarter 2026 net loss of $13.239 million, compared with $7.860 million a year earlier. Research and development expenses were $11.429 million, versus $6.969 million, and general and administrative expenses were $2.487 million, versus $1.744 million. Cash, cash equivalents and marketable securities totaled $78.2 million at September 30, 2026, before the October IPO, which generated approximately $119.0 million in net proceeds. Based on its current operating plan, the company expects its resources, including those proceeds, to fund operations and capital expenditures into the second half of 2029.

TRex Bio reported positive Phase 1a results for TRB-061; topline Phase 1b data in atopic dermatitis are expected in mid-2027. The ongoing Phase 1b study assesses safety, pharmacokinetics, blood and skin biomarkers, and exploratory clinical activity. TRB-071 is in IND-enabling studies, with a Phase 1 trial expected in the first half of 2027, subject to regulatory allowance to proceed. Lilly intends to advance partnered TRB-051 into a Phase 2a trial in lupus with cutaneous involvement. TRex Bio also disclosed a material weakness in internal control over financial reporting.

1 point · 0 major

How this balance works

Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.

It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.

Rhea-AI Sentiment measures something else, the tone of the wording.

1 major · 2 points

Hollow bars mark forward-looking points. How the balance works

Positive

  • Moderate point. Forward-looking: it has not happened yet and may not happen.Cash resources plus IPO proceeds are expected to fund operations into the second half of 2029.

Negative

  • Major pointTRex Bio disclosed a material weakness in internal control over financial reporting.
  • Moderate pointThird-quarter net loss rose to $13.239 million from $7.860 million a year earlier.

Filing Explained

The IPO’s ownership mechanics included a 9,539,237-share sale and conversion of 17,742,217 preferred shares into common.

The company reports that its October 2026 IPO was completed with 9,539,237 common shares sold; issuing shares increases the total share count and reduces existing holders’ percentage ownership absent offsetting changes.

Immediately before the IPO closed, all outstanding redeemable convertible preferred stock automatically converted into 17,742,217 common shares.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.
Net loss $13.239 million Three months ended September 30, 2026; $7.860 million in the third quarter of 2025.
Research and development expenses $11.429 million Three months ended September 30, 2026; $6.969 million in the third quarter of 2025.
General and administrative expenses $2.487 million Three months ended September 30, 2026; $1.744 million in the third quarter of 2025.
Cash, cash equivalents and marketable securities $78.2 million As of September 30, 2026; excludes approximately $119.0 million in net proceeds from the October IPO.
IPO gross proceeds Approximately $133.5 million October 2026 initial public offering.
IPO net proceeds Approximately $119.0 million October 2026 initial public offering, after underwriting discounts, commissions and estimated offering expenses.
IPO shares and public offering price 9,539,237 shares at $14.00 per share October 2026 initial public offering.
Expected funding horizon Into the second half of 2029 Based on the current operating plan and cash resources together with IPO net proceeds.
proof of mechanism medical
"supporting proof of mechanism and dose selection"
Evidence from laboratory or early clinical tests that a drug, device, or treatment is interacting with its intended biological target and producing the expected biochemical or cellular effect. Like showing a new key actually turns the lock before testing whether it opens the whole door, proof of mechanism lowers scientific uncertainty by confirming the therapy works the way researchers expect, which helps investors judge early development risk.
pharmacokinetics medical
"assessing safety, pharmacokinetics"
Pharmacokinetics is the study of how a substance, such as a drug or chemical, moves through and is processed by the body over time. It tracks how it is absorbed, distributed, broken down, and eventually eliminated. For investors, understanding pharmacokinetics helps gauge the effectiveness, safety, and potential risks of new medications or treatments, which can influence a company’s success and valuation in the healthcare industry.
pharmacodynamic biomarkers medical
"pharmacodynamic biomarkers in blood and skin"
Pharmacodynamic biomarkers are measurable signs that show whether a drug is affecting the body the way it’s supposed to — for example a change in a blood protein or a scan reading that moves when the drug hits its target. For investors they act like a dashboard gauge, giving early evidence about whether a treatment works, what dose might be right, and how risky or promising a development program is, so they help guide funding and valuation decisions.
IND-enabling studies regulatory
"continues to advance through IND-enabling studies"
Ind-enabling studies are early research efforts that test whether a new drug or treatment is safe and effective enough to move forward in development. They are like preliminary tests to ensure a product works as intended before investing more resources into large-scale trials. For investors, these studies are important because successful results can signal potential progress toward bringing a new product to market, impacting its future value.
immunoregulatory Tregs medical
"activation and expansion of immunoregulatory Tregs"
redeemable convertible preferred stock financial
"conversion of all outstanding redeemable convertible preferred stock"
A redeemable convertible preferred stock is a special class of company shares that combines three features: it pays priority dividends like a safer, higher-ranking share; it can be converted into regular common shares so holders can join in upside; and it can be redeemed, meaning the company can buy it back for cash. For investors this matters because it offers a mix of downside protection and potential upside, but can change ownership stakes (dilution) and cash obligations depending on whether it’s converted or redeemed.
Net loss $13.239 million Compared with $7.860 million in the third quarter of 2025.
Research and development expenses $11.429 million Compared with $6.969 million in the third quarter of 2025.
General and administrative expenses $2.487 million Compared with $1.744 million in the third quarter of 2025.
Guidance

Based on its current operating plan, TRex Bio expects its resources, together with IPO net proceeds, to fund operations and capital expenditure requirements into the second half of 2029.

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

How much cash did TRXB have at September 30, 2026, and how long did it expect to fund operations?

Cash, cash equivalents and marketable securities totaled $78.2 million at September 30, 2026, excluding approximately $119.0 million in net IPO proceeds received in October. Based on its current operating plan, TRex Bio expected its resources, including the IPO proceeds, to fund operations and capital expenditures into the second half of 2029.

What was TRXB’s third-quarter 2026 net loss?

TRex Bio reported a $13.239 million net loss for the third quarter of 2026, compared with a $7.860 million net loss for the third quarter of 2025.

What did TRex Bio report from the TRB-061 Phase 1a trial?

TRex Bio reported reproducible activation and expansion of immunoregulatory Tregs, supporting proof of mechanism and dose selection. TRB-061 was generally well tolerated across dose levels, with no treatment-related serious adverse events or dose-limiting toxicities observed.

When does TRXB expect to start a Phase 1 trial of TRB-071?

TRex Bio expects to initiate the Phase 1 trial in the first half of 2027, subject to regulatory allowance to proceed. TRB-071 was advancing through IND-enabling studies.

How many common shares resulted from TRex Bio’s preferred-stock conversion before its IPO?

All outstanding redeemable convertible preferred stock automatically converted into 17,742,217 shares of common stock immediately before the October 2026 IPO closing.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d)

of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): November 13, 2026

 

TRex Bio, Inc.

(Exact name of registrant as specified in its charter)

 

 

Delaware

001-43501

36-4902297

(State or other jurisdiction

of incorporation)

(Commission

File Number)

(IRS Employer

Identification No.)

 

 

269 East Grand Avenue, Suite 300

South San Francisco, CA

94080

(Address of principal executive offices)

(Zip Code)

(Registrant’s telephone number, including area code): (650) 567-5582

Not Applicable

(Former name or former address, if changed since last report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

 

☐

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

 

☐

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

 

☐

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

 

☐

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class

Trading

Symbol(s)

Name of each exchange

on which registered

Common Stock, par value $0.0001 per share

TRXB

The Nasdaq Global Select Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company ☒

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

 


 

Item 2.02 Results of Operations and Financial Condition.

On November 13, 2026, TRex Bio, Inc. (the “Company”) issued a press release announcing the Company’s financial results for the quarter ended September 30, 2026. A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.

The information in this Form 8-K, including Exhibit 99.1 attached hereto, is being furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any filing by the Company under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such filing.

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

 

Exhibit
No.

Description

 

 

99.1

Press Release issued by TRex Bio, Inc. on November 13, 2026

 

 

104

 

Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

 


 

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

TRex Bio, Inc.

 

 

By:

/s/ M. Johnston Erwin, Jr.

 

Name: M. Johnston Erwin, Jr.

 

Title: Chief Executive Officer

Date: November 13, 2026

 


img57721924_0.jpg

Exhibit 99.1

TRexBio Reports Third Quarter 2026 Financial Results and Recent Business Highlights

•
Positive Phase 1a results for TRB-061 support proof of mechanism, with topline Phase 1b data in atopic dermatitis expected in mid-2027
•
TRB-071 advancing through IND-enabling studies, with Phase 1 trial initiation expected in the first half of 2027
•
Completed a $133.5 million initial public offering in October 2026, extending expected cash runway into the second half of 2029

SOUTH SAN FRANCISCO, Calif., November 13, 2026 -- TRex Bio, Inc. (“TRexBio”) (Nasdaq: TRXB), a clinical-stage biotechnology company focused on tissue Treg biology for the discovery and development of immunoregulatory medicines, today reported financial results for the third quarter ended September 30, 2026, and provided recent business highlights and anticipated development milestones.

“Our approach begins with understanding how regulatory T cells function in human tissues and using those insights to develop medicines intended to address the underlying immune dysfunction in disease,” said Johnston Erwin, Chief Executive Officer of TRexBio. “The positive Phase 1a results for TRB-061 demonstrated selective activation and expansion of immunoregulatory Tregs in humans, providing clinical evidence that we believe supports this approach. We are now focused on understanding whether these effects can translate into meaningful and durable disease control for patients with atopic dermatitis. With the completion of our IPO, we have the resources to advance TRB-061 toward its planned mid-2027 clinical readout and expect to bring TRB-071, which targets a distinct Treg pathway, into the clinic in the first half of 2027.”

Recent Business and Corporate Highlights

TRB-061: TNFR2 Agonist in Phase 1 Clinical Development for Atopic Dermatitis

•
Reported positive Phase 1a topline results supporting proof of mechanism: In August 2026, TRexBio announced positive topline results from the Phase 1a portion of its ongoing Phase 1a/b clinical trial of TRB-061 in healthy volunteers. TRB-061 was generally well tolerated across all dose levels, with no treatment-related serious adverse events or dose-limiting toxicities observed. Results demonstrated consistent pharmacokinetics and reproducible activation and expansion of immunoregulatory Tregs, supporting proof of mechanism and dose selection for the ongoing Phase 1b trial.
•
Advancing Phase 1b clinical trial in atopic dermatitis: TRexBio continues to evaluate TRB-061 in patients with moderate-to-severe atopic dermatitis. The Phase 1b portion of the trial is assessing safety, pharmacokinetics, pharmacodynamic biomarkers in blood and skin, and exploratory measures of clinical activity. Topline data are expected in mid-2027.

TRB-071: CD30 Agonist in IND-Enabling Development

•
Progressing toward clinical development: TRB-071, an investigational CD30 agonist antibody designed to augment tissue Tregs and block inflammatory signaling pathways, continues to advance through IND-enabling studies. Subject to regulatory allowance to proceed, TRexBio expects to initiate a Phase 1 clinical trial in the first half of 2027.

 


 

Partnered Programs

•
Eli Lilly collaboration: TRB-051, a program developed through TRexBio’s research collaboration with Eli Lilly and Company, is in clinical development. Lilly intends to advance TRB-051 into a Phase 2a clinical trial in lupus with cutaneous involvement.

Corporate Highlights

•
Completed initial public offering: In October 2026, TRexBio completed its IPO of 9,539,237 shares of common stock at a public offering price of $14.00 per share, including 1,205,903 shares sold upon the underwriters’ partial exercise of their option to purchase additional shares. Gross proceeds were approximately $133.5 million, and net proceeds were approximately $119.0 million, after deducting underwriting discounts and commissions and estimated offering expenses. TRexBio’s common stock trades on the Nasdaq Global Select Market under the ticker symbol “TRXB.”

Third Quarter 2026 Financial Results

•
Cash Position and Cash Runway: Cash, cash equivalents and marketable securities totaled $78.2 million as of September 30, 2026, excluding approximately $119.0 million in net proceeds from the IPO completed in October 2026. Based on its current operating plan, TRexBio expects these resources, together with the IPO net proceeds, to fund operations and capital expenditure requirements into the second half of 2029.
•
Research and Development (R&D) Expenses: R&D expenses were $11.4 million for the third quarter of 2026, compared to $7.0 million for the third quarter of 2025. The increase was primarily driven by higher clinical trial costs associated with TRB-061, increased preclinical development and manufacturing activities for TRB-071 and other product candidates, and higher personnel and facility-related costs.
•
General and Administrative (G&A) Expenses: G&A expenses were $2.5 million for the third quarter of 2026, compared to $1.7 million for the third quarter of 2025. The increase was primarily attributable to higher personnel-related expenses and professional fees, including accounting and audit costs associated with preparations to operate as a public company.
•
Net Loss: Net loss was $13.2 million for the third quarter of 2026, compared to $7.9 million for the third quarter of 2025.

About TRexBio

TRexBio is a clinical-stage biotechnology company focused on tissue Treg biology for the discovery and development of immunoregulatory medicines designed to restore immune balance and promote tissue repair to address unmet needs of patients with autoimmune and inflammatory diseases. TRexBio’s Deep Biology Platform decodes Treg functionality in human tissue, mapping key drivers of immune dysregulation and uncovering novel targets and insights that inform drug discovery and translational efforts. This platform has generated multiple therapeutic development candidates across TRexBio’s wholly owned pipeline and through collaborations with leading pharmaceutical partners. TRexBio is led by an experienced management team and headquartered in South San Francisco, California. For more information, visit www.trex.bio.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of applicable federal securities laws, including statements regarding TRexBio’s business strategy, clinical and preclinical development programs, anticipated milestones and financial outlook. These statements include, without limitation, expectations regarding the development, potential therapeutic benefits and clinical

 


 

advancement of TRB-061, TRB-071 and partnered programs; the timing and availability of clinical trial results, including topline data from the Phase 1b trial of TRB-061 in mid-2027; the anticipated initiation of a Phase 1 clinical trial of TRB-071 in the first half of 2027; and the sufficiency of TRexBio’s cash, cash equivalents, marketable securities and IPO proceeds to fund its operations and capital expenditure requirements into the second half of 2029.

Forward-looking statements are based on current expectations, estimates and assumptions and are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied. These risks include, but are not limited to: TRexBio’s limited operating history, lack of products approved for commercial sale, incurrence of substantial losses since its inception and anticipation of incurring substantial and increasing losses for the foreseeable future; TRexBio’s need for substantial additional financing to achieve its goals; the uncertainty of clinical development, which is lengthy and expensive, and the risk that results of earlier studies and trials may not be predictive of future trial results or results in other indications; risks related to additional costs or delays in completing, or failing to complete, the development, approval and commercialization of TRexBio’s current or future product candidates in the United States or any other jurisdiction, and the risk that any such approval may be for a more narrow indication than TRexBio seeks; delays or difficulties in the enrollment and dosing of patients in clinical trials; the impact of any significant adverse events or undesirable side effects caused by TRexBio’s product candidates; potential competition, including from large and specialty pharmaceutical and biotechnology companies, many of which already have approved therapies in TRexBio’s current indications; risks related to the material weakness identified in TRexBio’s internal control over financial reporting; TRexBio’s ability to realize the benefits of its current or future collaborations or licensing arrangements and ability to successfully consummate future partnerships; TRexBio’s dependence on the services of its senior management and other clinical and scientific personnel, and its ability to retain these individuals or recruit additional management or clinical and scientific personnel; TRexBio’s ability to grow its organization and manage its growth and expansion of its operations; risks related to the manufacturing of TRexBio’s product candidates, which is complex; TRexBio’s ability to obtain and maintain sufficient intellectual property protection for its product candidates or any future product candidates; TRexBio’s reliance on third parties to conduct its preclinical studies and clinical trials; risks related to the operations of TRexBio’s suppliers, many of which are located outside of the United States; and other risks and uncertainties described in TRexBio’s filings with the U.S. Securities and Exchange Commission, including the section titled “Risk Factors” in its final prospectus for its initial public offering, filed with the SEC on October 9, 2026, as well as the other information TRexBio files with the SEC. TRexBio cautions investors not to place considerable reliance on the forward-looking statements contained in this press release. Forward-looking statements speak only as of the date of this press release. TRexBio undertakes no obligation to update these statements except as required by law. Investors, potential investors, and others should give careful consideration to these risks and uncertainties.

Contacts

Investor Relations: IR@trex.bio

Media Relations: jessica@litldog.com

 

 

 


 

TRex Bio, Inc.

Condensed Statements of Operations

(In thousands)

(Unaudited)

 

 

 

Three Months Ended September 30,

 

 

Nine Months Ended September 30,

 

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

Research and development

 

$

11,429

 

 

$

6,969

 

 

$

37,459

 

 

$

21,935

 

General and administrative

 

 

2,487

 

 

 

1,744

 

 

 

7,475

 

 

 

6,002

 

Total operating expenses

 

 

13,916

 

 

 

8,713

 

 

 

44,934

 

 

 

27,937

 

Loss from operations

 

 

(13,916

)

 

 

(8,713

)

 

 

(44,934

)

 

 

(27,937

)

Interest income

 

 

768

 

 

 

853

 

 

 

2,523

 

 

 

2,421

 

Other expense, net

 

 

(3

)

 

 

—

 

 

 

(6

)

 

 

(66

)

Total other income, net

 

 

765

 

 

 

853

 

 

 

2,517

 

 

 

2,355

 

Loss before provision for income taxes

 

 

(13,151

)

 

 

(7,860

)

 

 

(42,417

)

 

 

(25,582

)

Provision for income taxes

 

 

88

 

 

 

—

 

 

 

130

 

 

 

—

 

Net loss

 

$

(13,239

)

 

$

(7,860

)

 

$

(42,547

)

 

$

(25,582

)

 

TRex Bio, Inc.

Selected Balance Sheet Data

(In thousands)

(Unaudited)

 

 

 

September 30, 2026(1)

 

 

December 31, 2025

 

Cash, cash equivalents and marketable securities

 

$

78,150

 

 

$

67,725

 

Total assets

 

 

88,755

 

 

 

73,133

 

Total liabilities

 

 

14,027

 

 

 

6,237

 

Redeemable convertible preferred stock

 

 

208,838

 

 

 

159,015

 

Total stockholders’ deficit

 

 

(134,110

)

 

 

(92,119

)

 

(1) The balance sheet data as of September 30, 2026 do not reflect the IPO completed in October 2026, which resulted in net proceeds of approximately $119.0 million, or the automatic conversion of all outstanding redeemable convertible preferred stock into 17,742,217 shares of common stock immediately prior to the closing of the IPO.

 


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