Recent Updates
Recently added Catalysts
ANAB Positive Sentiment Score: 70/100

Anaptys Provides Update on Business Separation and Announces Fourth Quarter and Full Year 2025 Financial Results

Key Takeaway: AnaptysBio, Inc. announced plans to spin-off its biopharma operations into a new public company, First Tracks Biotherapeutics, aiming to enhance investor value. The company reported strong financial results for Q4 and the full year 2025, highlighting the promising potential of its pipeline assets, including ANB033, currently in Phase 1b trials. However, the separation process carries inherent risks and uncertainties.
Price reaction · baseline $52.83 (2026-03-03 close) · hit pre-market · clean, no other ANAB news in the window
day 0 close · peak
+14.6%
day 1
+8.4%
day 3
+13%

Market Sentiment Analysis

POSITIVE FACTORS

  • AnaptysBio plans to spin-off its biopharma operations, potentially unlocking value.
  • The company reported strong financial results with a significant annualized run rate.
  • Multiple high-potential assets are advancing in clinical trials.

CONCERNS & RISKS

  • The separation of companies involves risks and uncertainties.
  • Future results depend on successful clinical trials and regulatory approvals.

Full Press Release Details

SAN DIEGO, March 03, 2026 (GLOBE NEWSWIRE) -- AnaptysBio, Inc. (Nasdaq: ANAB), a clinical-stage biotechnology company focused on delivering innovative immunology therapeutics, today provided an update on the potential spin-off of its biopharma operations and reported financial results for the fourth quarter and year ended Dec. 31, 2025.
“We are approaching a defining inflection point for Anaptys, as we plan to spin-off in Q2 2026 our wholly owned biopharma portfolio into a public company, to be called First Tracks Biotherapeutics, to unlock and amplify value for investors across two distinct sets of assets,” said Daniel Faga, president and chief executive officer of Anaptys. “In our royalty portfolio,Jemperliexited Q4 2025 on a ~$1.4 billion annualized run rate, reinforcing GSK’s peak sales guidance of far more than $2.7 billion2in monotherapy indications. At the same time, our biopharma portfolio is advancing multiple attractive, high-potential assets, including ANB033, which has pipeline-in-a-product potential, initially in a Phase 1b trial for both celiac disease and eosinophilic esophagitis.”

INTENT TO SEPARATE BUSINESS

AnaptysBio (formerly referred to as “Royalty Management Co”)

GSKJemperliFinancial Collaboration

Vanda Imsidolimab Financial Collaboration

First Tracks Biotherapeutics (formerly referred to as “Biopharma Co”)ANB033 (CD122 antagonist)

Rosnilimab (Pathogenic T Cell Depleter)

ANB101 (BDCA2 modulator)

FINANCIAL UPDATES

Cash Position and Stock Repurchase Program

Fourth Quarter and Full Year 2025 Financial Results

About Anaptys

Anaptys is a clinical-stage biotechnology company focused on delivering innovative immunology therapeutics for autoimmune and inflammatory diseases. The company’s pipeline includes rosnilimab, a pathogenic T cell depleter, which has completed a Phase 2b trial for rheumatoid arthritis; ANB033, a CD122 antagonist, in a Phase 1b trial for celiac disease and eosinophilic esophagitis; and ANB101, a BDCA2 modulator, in a Phase 1a trial. Anaptys has also discovered and out-licensed in financial collaborations multiple therapeutic antibodies, including a PD-1 antagonist (Jemperli(dostarlimab-gxly)) to GSK and an IL-36R antagonist (imsidolimab) to Vanda Pharmaceuticals. To learn more, visitwww.AnaptysBio.comor follow us onLinkedIn.
Anaptys recently announced the intent to separate its biopharma operations from its substantial royalty assets by year-end 2026, enabling investors to align their investment philosophies and portfolio allocation with the strategic opportunities and financial objectives of each company. Learn morehere.

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: the timing of the release of data from the Company’s clinical trials, including initial data from ANB033's Phase 1b clinical trial in celiac disease and initial data from ANB033's Phase 1b clinical trial in eosinophilic esophagitis; expectations regarding the structure, infrastructure, timing and taxation of the proposed separation of companies; timing of paydown of financial obligations to Sagard; whether any partnership with rosnilimab will take place; the potential to receive any royalties or milestone payments from the Vanda Pharmaceuticals license agreement; the potential to receive any additional milestones or royalties from the GSK collaboration and timing therefor; and the projected cash runway for First Tracks Biotherapeutics. 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 the company’s ability to advance its product candidates, obtain regulatory approval of and ultimately commercialize its product candidates, the timing and results of preclinical and clinical trials, the company’s ability to fund development activities and achieve development goals, the company’s ability to protect intellectual property, the ability to effect the separation of companies as described herein 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.Contact:Nick MontemaranoExecutive Director, Investor Relations858.732.0178investors@anaptysbio.com
___________________________________
1. GSK Q4 2025 earnings call, 2/4/2026
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)
3. ~$250 million accrued to Sagard accruals by YE 2025 and assumes a ~10% quarter-over-quarter growth rate forJemperlifrom Q4’25 through Q2’27 and milestone payments associated with filing ($5mm) and approval ($10mm) of dMMR rectal approval in the EU
AnaptysBio, Inc.Consolidated Balance Sheets(in thousands, except par value data)
December 31, 2025 December 31, 2024
ASSETS
Current assets:
Cash and cash equivalents $ 238,196 $ 123,080
Receivables from collaborative partners 33,850 40,765
Short-term investments 73,442 262,293
Prepaid expenses and other current assets 4,762 5,738
Total current assets 350,250 431,876
Property and equipment, net 1,370 1,849
Operating lease right-of-use assets 12,519 14,383
Long-term investments 35,470
Other long-term assets 256 256
Total assets $ 364,395 $ 483,834
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:
Accounts payable $ 3,871 $ 4,002
Accrued expenses 32,674 39,501
Current portion of operating lease liability 2,080 1,925
Total current liabilities 38,625 45,428
Liability related to sale of future royalties 276,528 353,426
Operating lease liability, net of current portion 12,032 14,112
Stockholders’ equity:
Preferred stock, $0.001 par value, 10,000 shares authorized and no shares, issued or outstanding at December 31, 2025 and December 31, 2024, respectively
Common stock, $0.001 par value, 500,000 shares authorized, 28,019 shares and 30,473 shares issued and outstanding at December 31, 2025 and December 31, 2024, respectively 28 30
Additional paid in capital 809,765 829,860
Accumulated other comprehensive (loss) gain (24 ) 305
Accumulated deficit (772,559 ) (759,327 )
Total stockholders’ equity 37,210 70,868
Total liabilities and stockholders’ equity $ 364,395 $ 483,834
AnaptysBio, Inc.Consolidated Statements of Operations and Comprehensive Income (Loss)(in thousands, except per share data)
Three Months EndedDecember 31, Year EndedDecember 31,
2025 2024 2025 2024
Collaboration revenue $ 108,249 $ 43,113 $ 234,603 $ 91,280
Operating expenses:
Research and development 25,559 42,589 135,970 163,840
General and administrative 15,789 10,194 50,737 42,389
Total operating expenses 41,348 52,783 186,707 206,229
Income (loss) from operations 66,901 (9,670 ) 47,896 (114,949 )
Other (expense) income, net:
Interest income 2,508 5,263 13,499 19,794
Non-cash interest expense for the sale of future royalties (19,711 ) (17,404 ) (79,893 ) (50,087 )
Other (expense) income, net (3 ) 21 5,430 14
Total other (expense) income, net (17,206 ) (12,120 ) (60,964 ) (30,279 )
Gain (loss) before income taxes 49,695 (21,790 ) (13,068 ) (145,228 )
(Provision) benefit for income taxes (81 ) 6 (164 ) (3 )
Net income (loss) 49,614 (21,784 ) (13,232 ) (145,231 )
Other comprehensive income (loss):
Unrealized (loss) gain on available for sale securities (71 ) (454 ) (329 ) 1,102
Comprehensive income (loss) $ 49,543 $ (22,238 ) $ (13,561 ) $ (144,129 )
Net income (loss) per common share:
Basic $ 1.79 $ (0.72 ) $ (0.46 ) $ (5.12 )
Diluted $ 1.58 $ (0.72 ) $ (0.46 ) $ (5.12 )
Weighted-average number of shares outstanding:
Basic 27,789 30,448 28,758 28,382
Diluted 31,343 30,448 28,758 28,382

Frequently Asked Questions

What is AnaptysBio's recent business update?

AnaptysBio plans to spin-off its biopharma operations into a new company called First Tracks Biotherapeutics.

What are the financial results for AnaptysBio?

AnaptysBio reported a strong annualized run rate of approximately $1.4 billion for Q4 2025.

What assets are included in AnaptysBio's pipeline?

The pipeline includes ANB033 for celiac disease and eosinophilic esophagitis, and rosnilimab for rheumatoid arthritis.

When is the spin-off of AnaptysBio scheduled?

The spin-off is planned for Q2 2026.

What are the risks associated with the spin-off?

The separation involves uncertainties regarding regulatory approvals and the advancement of product candidates.

Last updated: Mar 4, 2026