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ANAB Positive Sentiment Score: 75/100

Anaptys Announces Third Quarter 2025 Financial Results and Provides Business Update

Key Takeaway: AnaptysBio reported its third quarter 2025 financial results, highlighting a significant increase in Jemperli sales and the strategic intent to separate its biopharma programs from royalty assets. The company is optimistic about its pipeline, particularly rosnilimab, which has shown promising Phase 2b data. The separation aims to align investment strategies with distinct asset values.
Price reaction · baseline $34.74 (2025-11-04 close) · hit after-hours · 1 other ANAB headline(s) in the window, move may be shared
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Market Sentiment Analysis

POSITIVE FACTORS

  • Jemperli sales grew significantly, indicating strong market performance.
  • Rosnilimab shows promise with positive Phase 2b trial data.
  • The intent to separate biopharma operations could enhance asset value.

CONCERNS & RISKS

  • Forward-looking statements carry risks and uncertainties.
  • Potential challenges in advancing product candidates and obtaining approvals.

Full Press Release Details

SAN DIEGO, Nov. 04, 2025 (GLOBE NEWSWIRE) -- AnaptysBio, Inc. (Nasdaq: ANAB), a clinical-stage biotechnology company focused on delivering innovative immunology therapeutics, today reported financial results for the third quarter ended September 30, 2025, and provided a business update.
“Our intent to separate our wholly owned biopharma programs from our royalty assets provides investors with the opportunity to realize and enhance the potential value of two distinct sets of assets.Jemperlisales grew to $785 million YTD with GSK indicating dMMR endometrial market share is now ~5% greater than Keytruda1, reflectingJemperli’sdifferentiated overall survival data and supporting GSK’s peak sales guidance of far more than $2.7 billion2in monotherapy indications,” said Daniel Faga, president and chief executive officer of Anaptys. “Our biopharma portfolio is strategically positioned with multiple attractive, high-potential assets, including rosnilimab, ANB033 and ANB101. Rosnilimab’s transformational profile was highlighted in a late-breaking presentation of Phase 2b data in RA at ACR Convergence 2025 and we anticipate reporting top-line Phase 2 data through Week 12 in ulcerative colitis in November or December.”INTENT TO SEPARATE BUSINESS

ROYALTY MANAGEMENT CO

GSKJemperliFinancial Collaboration

Vanda Imsidolimab Financial Collaboration

BIOPHARMA CO

Rosnilimab (Pathogenic T Cell Depleter)

ANB033 (CD122 antagonist)

ANB101 (BDCA2 modulator)

FINANCIAL UPDATES

Stock Repurchase Program and Cash Runway

Third Quarter 2025 Financial Results

About AnaptysAnaptys is a clinical-stage biotechnology company focused on delivering innovative immunology therapeutics for autoimmune and inflammatory diseases. Its lead program, rosnilimab, a pathogenic T cell depleter, completed a Phase 2b trial for the treatment of rheumatoid arthritis and is in a Phase 2 trial for the treatment of ulcerative colitis. The company’s pipeline also includes ANB033, a CD122 antagonist, in a Phase 1b trial for celiac disease with plans to expand development into an additional indication. Additionally, ANB101, a BDCA2 modulator, is in a Phase 1a trial. Anaptys also has 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 StatementsThis 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 rosnilimab’s top-line Phase 2 clinical trial data in ulcerative colitis and ANB033’s phase 1b cohort in celiac disease; whether positive clinical trial results in rosnilimab’s Phase 2b clinical trial in rheumatoid arthritis increases the likelihood of getting positive results from rosnilimab’s Phase 2 clinical trial in ulcerative colitis; expectations regarding the structure, infrastructure, timing and taxation of the proposed separation of companies; timing of paydown of financial obligations to Sagard; timing of initiation of Phase 1b clinical trial in second indication with ANB033; the potential to receive any royalties or milestone payments from the Vanda Pharmaceuticals license agreement; the potential to receive any additional milestones and royalties from the GSK collaboration and the timing therefor; and the projected cash runway for Biopharma Co. 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 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_______________________________________
AnaptysBio, Inc.Consolidated Balance Sheets(in thousands, except par value data)(unaudited)
September 30, 2025 December 31, 2024
ASSETS
Current assets:
Cash and cash equivalents $ 109,833 $ 123,080
Receivables from collaborative partners 75,685 40,765
Short-term investments 139,123 262,293
Prepaid expenses and other current assets 6,009 5,738
Total current assets 330,650 431,876
Property and equipment, net 1,500 1,849
Operating lease right-of-use assets 12,994 14,383
Long-term investments 7,698 35,470
Other long-term assets 256 256
Total assets $ 353,098 $ 483,834
LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)
Current liabilities:
Accounts payable $ 2,893 $ 4,002
Accrued expenses 33,171 39,501
Current portion of operating lease liability 2,040 1,925
Total current liabilities 38,104 45,428
Liability related to sale of future royalties 331,844 353,426
Operating lease liability, net of current portion 12,566 14,112
Stockholders’ (deficit) equity:
Preferred stock, $0.001 par value, 10,000 shares authorized and no shares, issued or outstanding at September 30, 2025 and December 31, 2024, respectively
Common stock, $0.001 par value, 500,000 shares authorized, 27,575 shares and 30,473 shares issued and outstanding at September 30, 2025 and December 31, 2024, respectively 28 30
Additional paid in capital 792,682 829,860
Accumulated other comprehensive gain 47 305
Accumulated deficit (822,173 ) (759,327 )
Total stockholders’ (deficit) equity (29,416 ) 70,868
Total liabilities and stockholders’ (deficit) equity $ 353,098 $ 483,834
AnaptysBio, Inc.Consolidated Statements of Operations and Comprehensive Income (Loss)(in thousands, except per share data)(unaudited)
Three Months EndedSeptember 30, Nine Months EndedSeptember 30,
2025 2024 2025 2024
Collaboration revenue $ 76,320 $ 30,017 $ 126,354 $ 48,167
Operating expenses:
Research and development 31,407 42,212 110,411 121,251
General and administrative 10,209 10,562 34,948 32,195
Total operating expenses 41,616 52,774 145,359 153,446
Income (loss) from operations 34,704 (22,757 ) (19,005 ) (105,279 )
Other income (expense), net:
Interest income 2,924 5,324 10,991 14,531
Non-cash interest expense for the sale of future royalties (22,515 ) (15,413 ) (60,182 ) (32,683 )
Other (expense) income, net (5 ) 5,433 (7 )
Total other expense, net (19,591 ) (10,094 ) (43,758 ) (18,159 )
Income (loss) before income taxes 15,113 (32,851 ) (62,763 ) (123,438 )
Provision for income taxes (83 ) (9 )
Net income (loss) 15,113 (32,851 ) (62,846 ) (123,447 )
Unrealized gain (loss) on available for sale securities 53 1,174 (258 ) 1,556
Comprehensive income (loss) $ 15,166 $ (31,677 ) $ (63,104 ) $ (121,891 )
Net income (loss) per common share:
Basic $ 0.54 $ (1.14 ) $ (2.16 ) $ (4.46 )
Diluted $ 0.52 $ (1.14 ) $ (2.16 ) $ (4.46 )
Weighted-average number of shares outstanding:
Basic 27,833 28,893 29,085 27,688
Diluted 29,018 28,893 29,085 27,688

Frequently Asked Questions

What were AnaptysBio's Q3 2025 financial results?

AnaptysBio reported significant growth in Jemperli sales, reaching $785 million year-to-date.

What is the intent behind AnaptysBio's business separation?

The separation aims to enhance the value of its biopharma programs and royalty assets.

What is the status of rosnilimab's clinical trials?

Rosnilimab has completed a Phase 2b trial for rheumatoid arthritis and is in a Phase 2 trial for ulcerative colitis.

What are the main products in AnaptysBio's pipeline?

Key products include rosnilimab, ANB033, and ANB101, targeting various autoimmune conditions.

What risks are associated with AnaptysBio's forward-looking statements?

Risks include uncertainties in advancing product candidates and obtaining regulatory approvals.

Last updated: Nov 4, 2025