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AnaptysBio Q1 2027 collaboration revenue falls to $30.3M

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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

AnaptysBio reported fiscal first-quarter 2027 collaboration revenue of $30.3 million for the three months ended September 30, 2026, versus $76.3 million a year earlier; the prior-year quarter included $50 million in milestone revenue. Net income from continuing operations was $3.9 million, compared with $56.3 million.

Jemperli global net sales were $365 million in the quarter, up 20% year over year, and $1.0 billion for nine months, up 29%. AnaptysBio receives royalties equal to 12% of annual net sales between $1.0 billion and $1.5 billion. The FDA approved Jemperli in October for adults with stage II and III MSI-H/dMMR locally advanced rectal cancer; Quimilza's FDA target action date for generalized pustular psoriasis is December 12, 2026.

Cash, cash equivalents and investments totaled $153.0 million as of September 30, 2026, versus $164.1 million as of June 30, 2026. AnaptysBio estimates Sagard will have accrued approximately $330 million in royalties and sales milestones through September 30, and anticipates paydown of the remaining approximately $270 million in non-recourse debt monetization in calendar H2 2027.

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.

0 major · 2 points

How the balance works

Positive

  • Moderate pointJemperli global net sales growth: 20% for the quarter and 29% for the first nine months, year over year.

Negative

  • Moderate pointCollaboration revenue was $30.3 million versus $76.3 million; the prior-year quarter included $50 million in milestone revenue.
  • Moderate pointContinuing-operations net income was $3.9 million, compared with $56.3 million in the prior-year quarter.

Filing Explained

The post-trial hearing in AnaptysBio’s litigation with GSK and Tesaro was held October 20, 2026; AnaptysBio seeks reversion of Jemperli rights, but no reversion is reported as completed, with judgment anticipated in calendar Q4 2026 or Q1 2027.

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.
Collaboration revenue $30.3 million Three months ended September 30, 2026; $76.3 million in the prior-year quarter
Income from continuing operations $3.9 million Three months ended September 30, 2026; $56.3 million in the prior-year quarter
Cash, cash equivalents and investments $153.0 million As of September 30, 2026; $164.1 million as of June 30, 2026
Jemperli global net sales $365 million Three months ended September 30, 2026; 20% year-over-year growth
Jemperli global net sales $1.0 billion Nine months ended September 30, 2026; 29% year-over-year growth
Jemperli royalty rate 12% of net sales Applies to net sales between $1.0 billion and $1.5 billion in a calendar year
Annualized Jemperli royalty expectation >$390 million Expected as early as 2029 at GSK peak monotherapy sales guidance of >$2.7 billion
Quimilza FDA target action date December 12, 2026 Generalized pustular psoriasis
MSI-H/dMMR medical
"stage II and III MSI-H/dMMR locally advanced rectal cancer"
PDUFA regulatory
"FDA target action date (PDUFA) of December 12, 2026"
PDUFA is the Prescription Drug User Fee Act, the U.S. law under which drug companies pay fees that fund the FDA's review of new medicines. In company news the term usually appears as the PDUFA date, the target deadline by which the FDA aims to decide on a drug application; that date tells investors when to expect the approval or rejection decision for the product.
non-recourse debt monetization financial
"remaining ~$270 million non-recourse debt monetization"
Non-recourse debt monetization is a financing move where a company converts an asset or future cash flow into immediate cash by selling or securitizing it, while the buyer’s recovery is limited to that specific asset if payments stop. For investors, it matters because it can boost short-term liquidity and change a company’s risk and leverage picture—like selling the title to a car to raise money without the buyer being able to chase you personally if the car’s value falls.
pivotal Phase 3 medical
"AZUR-2 – pivotal Phase 3"
A pivotal Phase 3 is a large, final clinical trial designed to show whether a new treatment actually works and is safe enough for regulatory approval. Think of it as the product’s final exam or full dress rehearsal: positive results are the main evidence regulators use to decide if the drug can be sold, while negative or ambiguous results can halt approval and value. Investors watch these trials closely because their outcomes strongly affect a company’s future sales prospects, regulatory risk, and stock value.
annualized royalties financial
">$390 million in annualized Jemperli royalties"
Collaboration revenue $30.3 million Compared with $76.3 million in the prior-year quarter
Income from continuing operations $3.9 million Compared with $56.3 million in the prior-year quarter
Basic earnings per share from continuing operations $0.13 Compared with $2.02 in the prior-year quarter
Cash, cash equivalents and investments $153.0 million Compared with $164.1 million as of June 30, 2026
Guidance

AnaptysBio expects to achieve >$390 million in annualized Jemperli royalties payable to Anaptys as early as 2029 at GSK's peak monotherapy sales guidance of >$2.7 billion.

FAQ

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

What were ANAB's fiscal first-quarter 2027 revenue and net income?

ANAB reported $30.3 million in collaboration revenue and $3.9 million in net income from continuing operations for the three months ended September 30, 2026. The prior-year quarter had $76.3 million in collaboration revenue and $56.3 million in continuing-operations net income; it included $50 million of milestone revenue.

How much were Jemperli sales, and what royalties does ANAB receive?

GSK reported $365 million in global Jemperli net sales for the three months ended September 30, 2026, and $1.0 billion for the nine months ended that date. AnaptysBio receives royalties equal to 12% of net sales between $1.0 billion and $1.5 billion in a calendar year.

What annual Jemperli royalties does ANAB expect?

AnaptysBio expects to achieve more than $390 million in annualized Jemperli royalties as early as 2029, at GSK's peak monotherapy sales guidance of more than $2.7 billion.

What Jemperli clinical milestones are expected?

Data from the AZUR-2 pivotal Phase 3 trial and the JADE pivotal Phase 3 trial are expected in 2028. AZUR-4's primary completion date is in Q4 2026. Regulatory submissions are expected in Japan in calendar H1 2027 and in Europe and China in calendar H2 2027; a European regulatory decision is expected in calendar H2 2027.

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

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0001370053false00013700532026-11-122026-11-12

 

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 12, 2026

 

 

ANAPTYSBIO, INC.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-37985

20-3828755

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

10770 Wateridge Circle, Suite 210

 

San Diego, California

 

92121

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: 858 362-6295

 

N/A

(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

 

ANAB

 

The Nasdaq Stock Market LLC

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 12, 2026, AnaptysBio, Inc. (“AnaptysBio”) issued a press release announcing its financial results for the three months ended September 30, 2026. A copy of the press release is attached as Exhibit 99.1 to this Current Report on Form 8-K.

The information in this Item 2.02, including Exhibit 99.1 to this Current Report on Form 8-K, shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended. The information contained in this Item 2.02 and in the accompanying Exhibit 99.1 shall not be incorporated by reference into any registration statement or other document filed by AnaptysBio with the Securities and Exchange Commission, whether made before or after the date of this Current Report on Form 8-K, regardless of any general incorporation language in such filing (or any reference to this Current Report on Form 8-K generally), except as shall be expressly set forth by specific reference in such filing.

 

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

Exhibit Number

Exhibit Title or Description

99.1

Press release issued by AnaptysBio, Inc. regarding its financial results for the three months ended September 30, 2026, dated November 12, 2026.

104

Cover Page Interactive Data File (the cover page XBRL tags are 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.

 

 

 

AnaptysBio, Inc.

 

 

 

 

Date:

November 12, 2026

By:

/s/ Christopher M. Murphy

 

 

 

Name: Christopher M. Murphy
Title: Chief Financial Officer

 


 

Exhibit 99.1

 

Anaptys Reports Fiscal First Quarter 2027 Financial Results and
Provides Business Update

•
Jemperli global net sales of $1.0 billion (£753 million) for the nine months ended September 30, 2026, representing 29% year-over-year growth
•
Jemperli approved in the U.S. as the first and only immunotherapy for adults with stage II and III microsatellite instability-high (MSI-H)/ mismatch repair deficient (dMMR) locally advanced rectal cancer
•
Litigation with GSK and Tesaro: post-trial hearing held on October 20, 2026, with a judgment anticipated in calendar Q4 2026 or Q1 2027

SAN DIEGO, November 12, 2026 — AnaptysBio, Inc. (Nasdaq: ANAB), a company focused on managing the financial collaborations for Jemperli with Tesaro, a GSK company, and Quimilza (imsidolimab) with Vanda, today reported financial results for the fiscal first quarter ended September 30, 2026, and provided a business update.

“Jemperli’s continued commercial growth in endometrial cancer, with global net sales reaching $1 billion through September 30, 2026, and its recent U.S. approval in adults with stage II and III MSI-H/dMMR locally advanced rectal cancer reinforce our confidence in its long-term potential in monotherapy indications,” said Daniel Faga, president and chief executive officer. “We remain focused on protecting and returning the value of our financial collaborations to shareholders as we approach a judgment in our litigation with GSK and Tesaro in calendar Q4 2026 or Q1 2027 and the FDA target action date for Quimilza in December 2026.”

GSK Jemperli Financial Collaboration

•
GSK announced commercial performance for Jemperli
o
$365 million (£273 million) in global net sales for the three months ended September 30, 2026, representing 20% year-over-year growth1
o
$1.0 billion (£753 million) in global net sales for the nine months ended September 30, 2026, representing 29% year-over-year growth1
▪
Anaptys receives royalties equal to 12% of net sales between $1.0 billion and $1.5 billion in a given calendar year
•
Anaptys continues to expect to achieve >$390 million in annualized Jemperli royalties payable to Anaptys as early as 2029 at GSK’s peak monotherapy sales guidance of >$2.7 billion2
•
Anaptys estimates Sagard will have accrued ~$330 million in royalties and sales milestones through September 30, 2026 and anticipates paydown of the remaining ~$270 million non-recourse debt monetization in calendar H2 2027
•
Jemperli development and regulatory updates announced by GSK include:
o
AZUR-1 – dostarlimab monotherapy in adults with stage II and III MSI-H/dMMR locally advanced rectal cancer
▪
In October 2026, GSK received U.S. Food and Drug Administration (FDA) approval
▪
GSK presented first results from the AZUR-1 trial as a late-breaking abstract at ESMO Congress 2026 in Madrid, Spain, on October 25, 2026
▪
Regulatory submission expected in Japan in calendar H1 2027 and in Europe and China in calendar H2 2027

 


 

▪
Regulatory decision expected in Europe in calendar H2 2027
o
AZUR-2 – pivotal Phase 3 – dostarlimab versus standard of care in untreated TN40 or stage III dMMR/ MSI-H resectable colon cancer
▪
Data expected in 2028
o
AZUR-4 – Phase 2 – dostarlimab plus chemotherapy versus standard of care (chemotherapy) in untreated stage III MMRp/MSS resectable colon cancer
▪
Primary completion date in Q4 2026
o
JADE – pivotal Phase 3 – dostarlimab monotherapy versus placebo in locally advanced unresected head and neck squamous cell carcinoma (PD-L1 CPS≥1) post chemoradiation
▪
Data expected in 2028

Vanda Quimilza (imsidolimab) Financial Collaboration

•
FDA target action date (PDUFA) of December 12, 2026, for Quimilza in generalized pustular psoriasis (GPP)

GSK and Tesaro Litigation Update

•
The post-trial hearing was held before the Delaware Chancery Court on October 20, 2026
•
Anaptys is seeking reversion of Jemperli rights as a remedy; the Company anticipates a judgment in calendar Q4 2026 or Q1 2027

Fiscal First Quarter Financial Results

•
The separation of AnaptysBio and First Tracks Biotherapeutics was completed on April 20, 2026. Beginning in the second quarter of 2026, AnaptysBio reclassified historical First Tracks Biotherapeutics, Inc. related assets, liabilities and expenses as discontinued operations.
•
Cash, cash equivalents and investments totaled $153.0 million as of September 30, 2026, compared to $164.1 million as of June 30, 2026, for a decrease of $11.1 million due primarily to $15.5 million used for operating activities offset by $4.4 million received from stock option exercises.
•
Collaboration revenue was $30.3 million for the three months ended September 30, 2026, compared to $76.3 million for the three months ended September 30, 2025. The decrease is primarily due to $50 million in milestone revenue recognized in Q3 2025 offset by Jemperli royalties increasing 11% quarter over quarter for the three months ended September 30, 2026.
•
General and administrative expenses from continuing operations were $11.6 million for the three months ended September 30, 2026, compared to $1.1 million for the three months ended September 30, 2025. The increase was due primarily to legal costs for the GSK and Tesaro lawsuit, audit and tax costs to support the June 30, 2026 transition year financials, and the allocation of G&A costs between AnaptysBio and First Tracks Biotherapeutics, Inc. for the three months ended September 30, 2025.
o
The expenses recognized for the three months ended September 30, 2026, include $4.8 million in legal costs for the GSK and Tesaro litigation and $2.2 million in recurring expenses, including contractor support, legal services unrelated to the GSK and Tesaro litigation, and other public company expenses.
o
The G&A non-cash, stock-based compensation expense was $3.2 million for the three months ended September 30, 2026, as compared to $0.5 million in the same period in 2025.
•
Research and development expenses from continuing operations were a negative $1.3 million for the three months ended September 30, 2026, compared to a negative $2.0 million for the three months ended September 30, 2025.

 


 

The decrease for the three months ended September 30, 2026 was primarily due to adjustments related to the closeout of clinical contracts reducing expenses incurred prior to the separation.
•
Net income from continuing operations was $3.9 million for the three months ended September 30, 2026, or a net income per share of $0.13, compared to a net income from continuing operations of $56.3 million for the three months ended September 30, 2025, or a net income per share of $2.02.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995, including, but not limited to future clinical, commercial and regulatory developments for Jemperli and Quimilza, future royalty amounts, the Company’s expected paydown of its obligations to Sagard, and the timing or outcome of the Company’s ongoing litigation with GSK. Statements including words such as “plan,” “continue,” “expect,” or “ongoing” and statements in the future tense are forward-looking statements. These forward-looking statements involve risks and uncertainties, as well as assumptions, which, if they do not fully materialize or prove incorrect, could cause its results to differ materially from those expressed or implied by such forward-looking statements. Forward-looking statements are subject to risks and uncertainties that may cause the company’s actual activities or results to differ significantly from those expressed in any forward-looking statement, including risks and uncertainties related to commercial success of the Company’s licensed products, the company’s ability to protect its financial collaborations and return value to its shareholders, the company’s ability to operate efficiently with a limited staff, and other risks and uncertainties described under the heading “Risk Factors” in documents the company files from time to time with the Securities and Exchange Commission. These forward-looking statements speak only as of the date of this press release, and the company undertakes no obligation to revise or update any forward-looking statements to reflect events or circumstances after the date hereof.

About Anaptys

Anaptys manages the financial collaborations for Jemperli with GSK and Quimilza with Vanda, with a focus on protecting and returning the value of its royalties to shareholders. To learn more, visit www.AnaptysBio.com or follow us on LinkedIn.
 

Contact:

Chris Murphy

Chief Financial Officer
investors@anaptysbio.com

 

_______________________________________

 

1. GSK Q3 2026 earnings call, 10/28/2026

2. CEO Emma Walmsley, 2025 JP Morgan CEO Series fireside chat, 9/11/2025, “there's no change to our peak year sales overall ambition for Jemperli, that's for sure, which is far more than £2 billion.”; Converted from GBP to USD using Q3 2025 average exchange rate (1.35x)

 


 

AnaptysBio, Inc.

Balance Sheets

(in thousands, except par value data)

(unaudited)

 

 

 

September 30, 2026

 

 

June 30, 2026

 

ASSETS

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

Cash and cash equivalents

 

$

135,394

 

 

$

133,826

 

Receivables from collaborative partners

 

 

30,494

 

 

 

25,634

 

Short-term investments

 

 

17,599

 

 

 

30,317

 

Prepaid expenses and other current assets

 

 

4,886

 

 

 

8,650

 

Total current assets

 

 

188,373

 

 

 

198,427

 

Property and equipment, net

 

 

97

 

 

 

102

 

Deferred tax asset

 

 

107,247

 

 

 

106,639

 

Operating lease right-of-use assets

 

 

11,070

 

 

 

11,560

 

Other long-term assets

 

 

256

 

 

 

256

 

Total assets

 

$

307,043

 

 

$

316,984

 

LIABILITIES AND STOCKHOLDERS’ EQUITY

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

Accounts payable

 

$

879

 

 

$

4,394

 

Accrued expenses

 

 

19,339

 

 

 

28,798

 

Current portion of operating lease liability

 

 

2,203

 

 

 

2,161

 

Total current liabilities

 

 

22,421

 

 

 

35,353

 

Liability related to sale of future royalties

 

 

249,819

 

 

 

256,493

 

Long-term taxes payable

 

 

3,619

 

 

 

3,619

 

Operating lease liability, net of current portion

 

 

10,364

 

 

 

10,934

 

Stockholders’ equity:

 

 

 

 

 

 

Preferred stock, $0.001 par value, 10,000 shares authorized and no shares issued or outstanding at September 30, 2026 and June 30, 2026, respectively

 

 

—

 

 

 

—

 

Common stock, $0.001 par value, 500,000 shares authorized, 29,941 shares and 29,728 shares issued and outstanding at September 30, 2026 and June 30, 2026, respectively

 

 

30

 

 

 

30

 

Additional paid in capital

 

 

658,658

 

 

 

652,269

 

Accumulated other comprehensive loss

 

 

(181

)

 

 

(151

)

Accumulated deficit

 

 

(637,687

)

 

 

(641,563

)

Total stockholders’ equity

 

 

20,820

 

 

 

10,585

 

Total liabilities and stockholders’ equity

 

$

307,043

 

 

$

316,984

 

 

 

 

 

 

 


 

AnaptysBio, Inc.

Statements of Operations and Comprehensive Income

(in thousands, except per share data)

(unaudited)

 

 

 

Three Months Ended
September 30,

 

 

2026

 

 

2025

 

Collaboration revenue

 

$

30,274

 

 

$

76,320

 

Operating expenses:

 

 

 

 

 

 

Research and development

 

 

(1,267

)

 

 

(2,035

)

General and administrative

 

 

11,636

 

 

 

1,083

 

Total operating expenses

 

 

10,369

 

 

 

(952

)

Income from operations

 

 

19,905

 

 

 

77,272

 

Other income (expense), net:

 

 

 

 

 

 

Interest income

 

 

1,438

 

 

 

1,861

 

Sublease income

 

 

667

 

 

 

—

 

Non-cash interest expense for the sale of future royalties

 

 

(18,742

)

 

 

(22,515

)

Total other expense, net

 

 

(16,637

)

 

 

(20,654

)

Income before income taxes

 

 

3,268

 

 

 

56,618

 

Benefit (provision) for income taxes

 

 

608

 

 

 

(269

)

Income from continuing operations

 

 

3,876

 

 

 

56,349

 

Loss from discontinued operations, net of tax

 

 

—

 

 

 

(41,236

)

Net income

 

 

3,876

 

 

 

15,113

 

Other comprehensive income:

 

 

 

 

 

 

Unrealized (loss) gain on available for sale securities

 

 

(30

)

 

 

53

 

Total comprehensive income

 

$

3,846

 

 

$

15,166

 

Net income (loss) per common share:

 

 

 

 

 

 

Income from continuing operations - basic

 

$

0.13

 

 

$

2.02

 

Loss from discontinued operations - basic

 

 

—

 

 

 

(1.48

)

Net income per common share - basic

 

$

0.13

 

 

$

0.54

 

Income from continuing operations - diluted

 

$

0.11

 

 

$

1.94

 

Loss from discontinued operations - diluted

 

 

—

 

 

 

(1.42

)

Net income per common share - diluted

 

$

0.11

 

 

$

0.52

 

Weighted-average number of shares outstanding:

 

 

 

 

 

 

Basic

 

 

29,847

 

 

 

27,833

 

Diluted

 

 

35,072

 

 

 

29,018

 

 


 

 

 

 

 


Filing Exhibits & Attachments

2 documents

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