STOCK TITAN

Septerna swings to $26.6M net loss in Q3 2026

Septerna expects its existing cash runway to fund operations at least into mid-2029.

Available on EDGAR Accepted by SEC EDGAR Learn about SEC filing dates
(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

Septerna, Inc. reported third-quarter 2026 revenue of $18.9 million, compared with $21.5 million a year earlier, and a $26.6 million net loss, versus $8.2 million net income. Research and development expenses were $36.6 million, compared with $24.3 million, and general and administrative expenses were $9.6 million, compared with $7.1 million.

The SEP-479 Phase 1 trial in healthy volunteers is ongoing, with single- and multiple-ascending-dose data expected in the first quarter of 2027. Septerna selected SEP-204 as an oral TSHR negative allosteric modulator development candidate and anticipates a Phase 1 trial in the first quarter of 2027, following successful completion of remaining preclinical work. Preclinical data showed reduced thyroid enlargement and orbital proptosis in Graves’ disease animal models.

Cash, cash equivalents and marketable securities totaled $565.2 million as of September 30, 2026. Under its Novo collaboration, Novo assumed responsibility for a development candidate and initiated IND-enabling toxicology studies; Septerna has achieved $13 million in research milestones to date.

0 points · 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.

0 major · 2 points

How the balance works

Positive

  • None.

Negative

  • Moderate pointRevenue was $18.9 million, versus $21.5 million a year earlier.
  • Moderate pointQuarterly results shifted from $8.2 million net income to a $26.6 million net loss.
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.
Revenue $18.9 million Quarter ended September 30, 2026; $21.5 million in the year-earlier quarter.
Net loss $26.6 million Quarter ended September 30, 2026; compared with $8.2 million net income in the year-earlier quarter.
Cash, cash equivalents and marketable securities $565.2 million As of September 30, 2026.
Research and development expenses $36.6 million Quarter ended September 30, 2026; $24.3 million in the year-earlier quarter.
General and administrative expenses $9.6 million Quarter ended September 30, 2026; $7.1 million in the year-earlier quarter.
Research milestones achieved under collaboration $13 million Total achieved to date under the Novo collaboration.
single-ascending dose (SAD) technical
"single-ascending dose (SAD) and multiple-ascending dose (MAD) clinical trial"
A single-ascending dose (SAD) study is an early-stage clinical trial in which small groups of participants each receive one dose of an experimental drug, with the dose increased stepwise between groups to assess initial safety, tolerability and how the body handles the drug. Investors watch SAD results because they reveal early safety and dosing limits—like checking a vehicle on short test drives at increasing speeds—which help gauge clinical risk, development timelines and the likelihood the program will advance.
multiple-ascending dose (MAD) technical
"single-ascending dose (SAD) and multiple-ascending dose (MAD) clinical trial"
A multiple-ascending dose (MAD) study is a clinical trial stage where a drug is given to different groups of people in repeated doses that increase stepwise, like climbing a staircase of strength levels. It checks safety, side effects and how the body handles the drug when taken repeatedly, helping determine safe and effective dosing for later trials. Investors care because MAD results reveal tolerability, risk and dosing viability—key factors that affect a drug’s development timeline and commercial potential.
negative allosteric modulator (NAM) technical
"oral TSHR negative allosteric modulator (NAM) development candidate"
A negative allosteric modulator (NAM) is a drug that attaches to a different spot on a cell’s receptor than the normal activating molecule and reduces the receptor’s activity — like turning down the volume on a radio without changing the station. For investors, NAMs matter because they can offer more precise control of a drug’s effects, potentially improving safety, dosing and competitive differentiation, which influences development costs, approval prospects and commercial value.
IND-enabling toxicology studies technical
"initiated IND-enabling toxicology studies"
GLP toxicology studies technical
"generally well tolerated in 28-day GLP toxicology studies"
GLP toxicology studies are safety tests conducted under strict Good Laboratory Practice rules to measure whether a drug or chemical causes harm in animals or lab systems before human trials. They matter to investors because passing these standardized tests lowers regulatory and development risk, making a program more likely to advance toward human testing and eventual approval — like passing a series of safety crash tests before a car can be sold.
Revenue $18.9 million Compared with $21.5 million in the year-earlier quarter
Research and development expenses $36.6 million Compared with $24.3 million in the year-earlier quarter
General and administrative expenses $9.6 million Compared with $7.1 million in the year-earlier quarter
Net loss $26.6 million Compared with $8.2 million net income in the year-earlier quarter
Guidance

Septerna expects its existing cash runway to fund operations at least into mid-2029.

FAQ

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

What were SEPN’s third-quarter 2026 revenue and net results?

SEPN reported $18.9 million in revenue and a $26.6 million net loss for the quarter ended September 30, 2026. Revenue was $21.5 million in the year-earlier quarter, which recorded $8.2 million in net income.

What made up SEPN’s third-quarter 2026 collaboration revenue?

Revenue included $2.7 million from amortization of Novo Nordisk’s upfront payment, $5.2 million from research milestones, and $11.0 million for research services associated with the collaboration.

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

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google
false000198408600019840862026-11-092026-11-09

 

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 09, 2026

 

 

Septerna, Inc.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-42382

84-3891440

(State or other jurisdiction
of incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

250 East Grand Avenue

 

South San Francisco, California

 

94080

(Address of principal executive offices)

 

(Zip Code)

 

Registrant’s telephone number, including area code: 650 338-3533

 

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:

☐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 $0.001 per share

 

SEPN

 

The Nasdaq Global 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 09, 2026, Septerna, Inc. (the “Company”) announced its financial results and business highlights for the quarter ended September 30, 2026. A copy of the press release issued in connection with the announcement is being furnished as Exhibit 99.1 to this Current Report on Form 8-K.

The information included under Item 2.02 of this Current Report on Form 8-K, including Exhibit 99.1, 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, and shall not be incorporated by reference in any filing 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

 

99.1

 

Press Release issued by Septerna, Inc. on November 9, 2026, furnished herewith.

 

 

 

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.

 

 

 

Septerna, Inc.

 

 

 

 

Date:

November 9, 2026

By:

/s/ Jeffrey Finer, M.D., Ph.D.

 

 

 

Jeffrey Finer, M.D., Ph.D.
Chief Executive Officer
 

 


 

 

img205902741_0.gif

 

Exhibit 99.1

Septerna Highlights Business Progress and Reports Third Quarter 2026 Financial Results

Phase 1 Clinical Trial for PTH1R Agonist SEP-479 Ongoing; SAD / MAD Data Expected in Q1 2027

 

Plans to Initiate Phase 1 Clinical Trial of Newly Selected Oral TSHR NAM Development Candidate SEP-204 in Q1 2027

 

Cash Position of $565.2 Million Expected to Support Operating Plans at Least into mid-2029


SOUTH SAN FRANCISCO, Calif. – November 09, 2026
– Septerna, Inc. (Nasdaq: SEPN), a clinical-stage biotechnology company pioneering a new era of G protein-coupled receptor (GPCR) drug discovery, today highlighted pipeline progress and anticipated milestones and reported financial results for the third quarter ended September 30, 2026.

 

“We are building momentum across our portfolio, with an upcoming important clinical milestone for SEP-479, our oral PTH1R agonist for hypoparathyroidism, and the selection of SEP-204 as our oral TSHR NAM development candidate for Graves’ disease and thyroid eye disease,” said Jeffrey Finer, M.D., Ph.D., Chief Executive Officer and Co-founder of Septerna. “With Phase 1 data for SEP-479 and the initiation a Phase 1 trial of SEP-204 expected in the first quarter of 2027, we are moving closer to realizing our ambition to translate our GPCR expertise into differentiated oral medicines for patients with significant unmet needs.”

Recent Portfolio Progress and Anticipated Milestones

•
SEP-479 PTH1R Agonist for Hypoparathyroidism:
o
Septerna’s Phase 1 single-ascending dose (SAD) and multiple-ascending dose (MAD) clinical trial of SEP-479, an oral small molecule PTH1R agonist in development for hypoparathyroidism, is ongoing in healthy volunteers, with data expected in the first quarter of 2027.

 

•
SEP-204 TSHR NAM for Graves’ Disease and Thyroid Eye Disease:
o
In conjunction with last week’s American Thyroid Association (ATA) annual meeting, Septerna announced the selection of SEP-204 as its oral TSHR negative allosteric modulator (NAM) development candidate as a potential disease-modifying treatment for Graves’ disease and thyroid eye disease.
o
Preclinical data presented at ATA demonstrated that SEP-204 potently and selectively inhibited TSHR, restored normal thyroid hormone T4 levels and reduced thyroid enlargement and orbital proptosis in Graves’ disease animal models. SEP-204 was generally well tolerated in 28-day GLP toxicology studies and demonstrated a favorable pharmacokinetic profile anticipated to support once-daily oral dosing in humans. Additional details are available in the data release.
o
Following the successful completion of the remaining preclinical development activities, Septerna anticipates initiating a Phase 1 clinical trial for SEP-204 in healthy volunteers in the first quarter of 2027.

 

•
SEP-631 MRGPRX2 NAM for Mast Cell-Driven Diseases:
o
Following positive Phase 1 results reported in March 2026, Septerna continues to evaluate capital-efficient, signal-finding clinical studies of SEP-631 in mast cell-driven diseases with high unmet need.
•
Additional Programs:
o
Under its global collaboration with Novo, initiated in July 2025, Septerna and Novo are advancing oral small molecule programs for obesity, type 2 diabetes and other cardiometabolic diseases. Novo recently assumed responsibility for a development candidate delivered by Septerna’s research team and initiated IND-enabling toxicology studies. To date, Septerna has achieved a total of $13 million in research milestones under the collaboration.
o
Septerna also continues to advance wholly owned discovery-stage programs utilizing its Native Complex Platform® across multiple therapeutic areas, including a PTH1R agonist program for osteoporosis.

 

Corporate Announcements

o
In August 2026, Septerna announced the appointment of Rajiv Patni, M.D., as Chief Medical Officer. Dr. Patni is a physician-scientist and accomplished biopharmaceutical executive with more than 25 years of experience leading research, development, regulatory, and medical affairs organizations.

 

Third Quarter 2026 Financial Results


 

 

img205902741_0.gif

 

•
Cash Position: Cash, cash equivalents, and marketable securities totaled $565.2 million as of September 30, 2026. Septerna expects its existing cash runway to fund operations at least into mid-2029.
•
Revenue: Revenue was $18.9 million for the quarter ended September 30, 2026, compared to $21.5 million for the quarter ended September 30, 2025. Revenue for the quarter ended September 30, 2026 included the amortization of $2.7 million of the $195.0 million upfront payment from Novo Nordisk, and $5.2 million from the achievement of research milestones, in addition to $11.0 million for research services associated with the collaboration.
•
R&D Expenses: Research and development (R&D) expenses were $36.6 million for the quarter ended September 30, 2026, compared to $24.3 million for the quarter ended September 30, 2025.
•
G&A Expenses: General and administrative (G&A) expenses were $9.6 million for the quarter ended September 30, 2026, compared to $7.1 million for the quarter ended September 30, 2025.
•
Net (Loss) Income: Net loss was $26.6 million for the quarter ended September 30, 2026, compared to net income of $8.2 million for the quarter ended September 30, 2025.

About Septerna

Septerna, Inc. is a clinical-stage biotechnology company with a world-class team of GPCR experts and drug developers advancing cutting-edge science to unlock the full potential of GPCR therapies for patients with significant unmet needs. The company’s proprietary Native Complex Platform® is designed to enable new approaches to GPCR drug discovery and has led to the development of a diverse pipeline of novel oral small molecule drug candidates. Septerna is advancing programs in endocrinology, immunology and inflammation, metabolic diseases and additional therapeutic areas, both independently and with partners. For more information, please visit www.septerna.com. Septerna intends to use its Investor Relations website and LinkedIn as means of disclosing material nonpublic information and for complying with its disclosure obligations under Regulation FD. Accordingly, investors should monitor Septerna’s Investor Relations website and follow https://www.linkedin.com/company/septernainc on LinkedIn, in addition to following Septerna’s press releases, SEC filings, public conference calls, presentations, and webcasts.

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, implied and express statements about Septerna’s beliefs and expectations regarding: the translating of SEP-479, SEP-204, SEP-631 and any future preclinical data into similar clinical findings; the availability of SEP-479 Phase 1 clinical data; SEP-479’s potential as a differentiated once-daily oral therapy for patients with hypoparathyroidism; advancing SEP-204 into a Phase 1 clinical trial and timing thereof; SEP-204’s potential as a disease-modifying treatment for Graves’ disease and thyroid eye disease; continuing to advance programs under the Novo collaboration and achieving milestones thereunder; the potential of its proprietary Native Complex Platform®; the continued advancement of SEP-631, including plans to evaluate development strategies for capital-efficient, signal-finding clinical trials; the role of MRGPRX2 in mast cell-driven diseases; SEP-631’s potential to provide a convenient oral treatment option for patients with mast cell-driven diseases; the advancement of its discovery-stage programs across multiple therapeutic areas; the size and growth potential of the markets for its current and future product candidates; its strategic plans for its business, product candidates, and technology; its uses of capital, expenses and financial results, including its expected cash runway at least into mid-2029; and the scope of protection it is able to establish and maintain for intellectual property rights covering its Native Complex Platform® and its product candidates; among others. The words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “might,” “objective,” “ongoing,” “plan,” “predict,” “project,” “potential,” “should,” or “would,” or the negative of these terms, or other comparable terminology 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 risks, uncertainties and important 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 associated with: Septerna’s product candidates successfully entering and advancing through clinical trials (including those for SEP-479, SEP-204 and SEP-631) including uncertainties related to opening investigational new drug applications (INDs) and obtaining other regulatory approvals; risks related to clinical development outcomes including unexpected safety or efficacy findings; the results of preclinical studies including the long-term toxicology studies for SEP-479, SEP-204, and SEP-631, or preclinical studies or clinical trials not being predictive of future clinical outcomes; risks related to the timing of initiating clinical studies and future availability of clinical data; the scope of protection Septerna is able to establish and maintain for intellectual property rights covering its Native Complex Platform® and its product candidates; and Septerna’s ability to identify and enter into future license agreements and collaborations; and general economic, industry and market conditions; among others. These and other risks and uncertainties are described in greater detail in the section entitled “Risk Factors” in Septerna’s Quarterly Report on Form 10-Q for the three months ended September 30, 2026, as well as any subsequent filings with the Securities and Exchange Commission. In addition, any forward-looking statements represent Septerna’s views only as of today and should not be relied upon as representing its views as of any subsequent date. Septerna explicitly disclaims any obligation to update any forward-looking statements subject to any obligations under applicable law. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.


 

 

img205902741_0.gif

 

Investor Contact:

Renee Leck, THRUST

renee@thrustsc.com

Media Contact:

Carly Scaduto, THRUST

carly@thrustsc.com


 

 

img205902741_0.gif

 

SEPTERNA, INC.

Condensed Statements of Operations

(In thousands, except for share and per share data)

(Unaudited)

 

 

 

Three Months Ended September 30,

 

 

Nine Months Ended
September 30,

 

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

Revenue

 

$

18,881

 

 

$

21,495

 

 

$

72,150

 

 

$

21,833

 

Operating expenses (income):

 

 

 

 

 

 

 

 

 

 

 

 

Research and development

 

 

36,556

 

 

 

24,264

 

 

 

101,223

 

 

 

65,723

 

General and administrative

 

 

9,554

 

 

 

7,117

 

 

 

28,292

 

 

 

20,884

 

Gain on sale of non-financial asset

 

 

—

 

 

 

(12,500

)

 

 

—

 

 

 

(12,500

)

Total operating expenses

 

 

46,110

 

 

 

18,881

 

 

 

129,515

 

 

 

74,107

 

(Loss) income from operations

 

 

(27,229

)

 

 

2,614

 

 

 

(57,365

)

 

 

(52,274

)

Interest income and other expense, net

 

 

5,260

 

 

 

5,559

 

 

 

15,035

 

 

 

14,133

 

Provision for income taxes

 

 

(4,621

)

 

 

—

 

 

 

(5,931

)

 

 

—

 

Net (loss) income

 

$

(26,590

)

 

$

8,173

 

 

$

(48,261

)

 

$

(38,141

)

Net (loss) income per share, basic

 

$

(0.57

)

 

$

0.18

 

 

$

(1.06

)

 

$

(0.86

)

Net (loss) income per share, diluted

 

$

(0.57

)

 

$

0.18

 

 

$

(1.06

)

 

$

(0.86

)

Weighted-average shares outstanding, basic

 

 

46,914,946

 

 

 

44,343,085

 

 

 

45,579,174

 

 

 

44,150,041

 

Weighted-average shares outstanding, diluted

 

 

46,914,946

 

 

 

45,602,099

 

 

 

45,579,174

 

 

 

44,150,041

 

 

SEPTERNA, INC.

Condensed Balance Sheets

(In thousands)

(Unaudited)

 

 

 

September 30,
2026

 

 

December 31,
2025

 

Cash, cash equivalents and marketable securities

 

$

565,188

 

 

$

548,658

 

Working capital (1)

 

 

402,486

 

 

 

324,033

 

Total assets

 

 

619,404

 

 

 

596,187

 

Total liabilities

 

 

191,475

 

 

 

214,261

 

Additional paid-in capital

 

 

645,441

 

 

 

548,517

 

Accumulated deficit

 

 

(215,514

)

 

 

(167,253

)

Total stockholders’ equity

 

$

427,929

 

 

$

381,926

 

 

1.
Working capital is defined as total current assets less total current liabilities. See our financial statements and the related notes thereto included in our Quarterly Report on Form 10-Q for the quarter ended September 30, 2026 for further details regarding our current assets and current liabilities.

 


Filing Exhibits & Attachments

2 documents

Keep reading