Financials
Cash Data
- Monthly Burn
- Burn Trend
- Dilution Risk
- SEC Filing
Key Stats
Upcoming Catalysts
FDA decisions, readouts and PDUFA dates · scored by probability of approval
| Catalyst | Drug / Treatment | Stage | Prob. of Approval | Description | Drug Type | Therapeutic Area | Source |
|---|---|---|---|---|---|---|---|
PDUFA 2026 | Example Drug Treatment for example condition requiring FDA review | Phase 3 | Small Molecule | Oncology | - |
ANAB Catalyst Timeline
Dated clinical, regulatory and corporate events for AnaptysBio, Inc.
Catalyst Timeline
Dated clinical, regulatory & corporate events for AnaptysBio, Inc.
Upcoming catalysts 2
Event history 50
Past FDA Catalysts and PDUFA Decisions
How ANAB actually traded into and out of each decision
| Date | Drug | Catalyst | Stage | Reaction | Event Move % | Best Trade % |
|---|---|---|---|---|---|---|
| 2025-10-29 | Rosnilimab | Phase 2b data presentation | Phase 2b |
Drug Pipeline Intelligence
| Drug | Indication | Phase | PTRS | rNPV | Status | Enroll | Velocity | Design | Est. Completion | ML Signal | Last Change |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Rosnilimab Monoclonal antibodyNCT06041269 | Rheumatoid Arthritis | Phase 2 | ACTIVE NOT_RECRUITING | 420 | May 30, 2025 | ||||||
| Rosnilimab Monoclonal antibodyNCT06127043 | Ulcerative Colitis | Phase 2 | ACTIVE NOT_RECRUITING | 132 | May 1, 2026 |
Clinical Trial Results
Readouts, endpoints and source filings for every ANAB program
| Drug Name | Indication | Phase | Date | Trial Results Summary | Title | Source |
|---|---|---|---|---|---|---|
| rosnilimab | moderate-to-severe ulcerative colitis | Phase 2 | 2025-11-10 | clinical remission 400mg Q4W: 7%; clinical remission 800mg Q2W: 7%; endoscopic remission 400mg Q4W: 5%; endoscopic remission 800mg Q2W: 4%; baseline mean m MS score: 6.7; adverse events: >5%Read More | Anaptys Announces Phase 2 Trial of Rosnilimab Did Not Meet Primary or Secondary Endpoints at Week 12 in Moderate-to-Severe Ulcerative ColitisRead More |
Inside Trades
| Insider | Side | Shares | Price | Value | Date |
|---|---|---|---|---|---|
| RENTON HOLLINGSDirector | Option | 5,000 15,995 held | $18.03 | 10/01/2026 |
Hedge Fund 13F Activity
Hedge Funds invested in ANAB
| Fund | % of Portfolio | Current MV | Shares Owned | Activity |
|---|---|---|---|---|
| EcoR1 Capital, LLC | 25.9 % (40 %) | 531.91 M | 7.88 M |
ANAB Institutional Ownership Trends
ANAB Short Interest
Shares sold short, counted twice a month.
Options Data
Option Volume
Option Chain Statistics
| Expiry | Call Vol | Put Vol | Vol P/C | Call OI | Put OI | OI P/C | IV Call | IV Call OI-Wtd | IV Call Vol-Wtd | IV Put | IV Put OI-Wtd | IV Put Vol-Wtd |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2026-11-20 | ||||||||||||
Real-Time Option Chain
| Calls | Strike | Puts | ||||
|---|---|---|---|---|---|---|
| Last | Vol | OI | Last | Vol | OI | |
| No data available | ||||||
Calls vs Puts by Expiry
Competitive positioning
How ANAB ranks across every disease it competes in
ANAB News
Jemperli (dostarlimab) Approved in the U.S. as First and Only Immunotherapy for Adults with MSI-H/dMMR Locally Advanced Rectal Cancer
AnaptysBio's Jemperli (dostarlimab) has received FDA approval as the first immunotherapy for adults with locally advanced rectal cancer characterized by microsatellite instability-high (MSI-H) and mismatch repair deficiency (dMMR). The approval is based on promising data from the AZUR-1 trial, showing a significant percentage of patients achieving sustained clinical responses. This treatment option may help patients avoid traditional therapies like chemotherapy and surgery, with ongoing safety monitoring.
Read more →Anaptys Announces Second Quarter and Transitional Fiscal Year 2026 Financial Results and Provides Business Update
AnaptysBio reported strong financial results for Q2 2026, with Jemperli achieving $644 million in global net sales, reflecting a 34% year-over-year growth. Positive interim results from the AZUR-1 trial for locally advanced rectal cancer were announced, with an FDA action date set for February 2027. The company is also involved in litigation with GSK and Tesaro, with a judgment expected in late 2026 or early 2027.
Read more →Anaptys Announces Participation at the H.C. Wainwright 28th Annual Global Investment Conference
AnaptysBio, Inc. announced its participation in the H.C. Wainwright 28th Annual Global Investment Conference, scheduled for September 15, 2026. CFO Chris Murphy will present at 3:30 PM ET, and a live webcast will be available on the company's investor website. A replay of the presentation will be accessible for 30 days post-event.
Read more →Anaptys Announces First Quarter 2026 Financial Results and Provides Business Update
AnaptysBio reported its financial results for Q1 2026, highlighting a successful spin-off of First Tracks Biotherapeutics and strong sales growth for Jemperli. The company appointed Chris Murphy as CFO and added two experienced members to its Board of Directors. Despite a net loss increase, the company aims to protect its royalty streams and deliver value to shareholders.
Read more →Anaptys Appoints Chris Murphy as Chief Financial Officer and Owen Hughes to Board of Directors
AnaptysBio has appointed Christopher Murphy as Chief Financial Officer and Owen Hughes to its Board of Directors. These appointments aim to enhance the company's leadership team with expertise in finance, business development, and royalty management. The CEO expressed confidence that these additions will help protect and enhance shareholder value.
Read more →Anaptys to Participate at the H.C. Wainwright 2nd Annual Royalty Company Virtual Conference
AnaptysBio, Inc. will have its CEO, Daniel Faga, participate in a fireside chat at the H.C. Wainwright 2nd Annual Royalty Company Virtual Conference on May 6, 2026. The discussion aims to highlight the company's financial collaborations, particularly with GSK and Vanda. This event is an opportunity for investors to gain insights into AnaptysBio's strategies and future directions.
Read more →Delaware Chancery Court Rules in Favor of Anaptys by Dismissing Tesaro’s Anticipatory Breach Claim
The Delaware Chancery Court has dismissed Tesaro's anticipatory breach claim against AnaptysBio, affirming Anaptys' position on the Collaboration Agreement. This ruling preserves the current royalty rates and sets a trial date for July 2026 to address Anaptys' contract claims against Tesaro and GSK. Anaptys is confident in its legal stance and aims to protect its interests in the Jemperli royalty stream.
Read more →Anaptys Completes Separation of First Tracks Biotherapeutics and Now Exclusively Manages GSK and Vanda Financial Collaborations
AnaptysBio has completed the spin-off of First Tracks Biotherapeutics, transitioning to a focus on managing royalties from Jemperli and imsidolimab. The company will operate under a virtual model with minimal expenses and aims for a high EBIT margin. This strategic shift is designed to enhance shareholder value while navigating inherent risks associated with financial collaborations.
Read more →First Tracks Biotherapeutics, the Planned Spin-Off of Anaptys, Secures Commitments of $145 Million in Private Placement
AnaptysBio announced a $145 million private placement for its spin-off, First Tracks Biotherapeutics. The placement involves the sale of nearly 5.8 million shares at $13.81 each, expected to close upon the completion of the spin-off on April 20, 2026. Proceeds will be used for general corporate purposes, including clinical development of ANB033.
Read more →Anaptys Board of Directors Approves Spin-Off of First Tracks Biotherapeutics
AnaptysBio, Inc. has approved the spin-off of First Tracks Biotherapeutics, which will begin trading on Nasdaq under the ticker TRAX on April 20, 2026. First Tracks Bio aims to develop next-generation antibody therapeutics for autoimmune diseases, with three lead candidates in various clinical trial phases. This strategic separation is intended to enhance focus and value for both companies.
Read more →Anaptys Announces $100 Million Stock Repurchase Plan and Provides a Business Update
AnaptysBio, Inc. has announced a $100 million stock repurchase plan authorized by its Board of Directors. This decision follows the upcoming spin-off of First Tracks Biotherapeutics, which is set for April 20, 2026. The company aims to manage financial collaborations effectively while minimizing operating expenses. Additionally, Susannah Gray has been appointed to the Board, bringing valuable expertise to the company.
Read more →Anaptys Provides Update on Business Separation and Announces Fourth Quarter and Full Year 2025 Financial Results
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.
Read more →Anaptys Announces $100 Million Stock Repurchase Plan
AnaptysBio, Inc. has announced a $100 million stock repurchase plan, expanding its existing program. The company expects to end 2025 with around $300 million in cash, bolstered by a potential $75 million milestone from GSK. The repurchase plan will run until March 31, 2026, but may be adjusted based on market conditions.
Read more →Anaptys Initiates Litigation Against Tesaro, a GSK Subsidiary
AnaptysBio has filed a Verified Complaint against Tesaro, alleging breach of their Collaboration Agreement and tortious interference by GSK. The lawsuit seeks a court declaration affirming Anaptys' rights under the agreement. This follows a history of disputes between the companies, including a previous settlement. The trial is expected in July 2026.
Read more →Anaptys Announces Phase 2 Trial of Rosnilimab Did Not Meet Primary or Secondary Endpoints at Week 12 in Moderate-to-Severe Ulcerative Colitis
AnaptysBio announced that its Phase 2 trial for rosnilimab in ulcerative colitis failed to meet primary and secondary endpoints at Week 12. The company will discontinue the trial, which saves at least $10 million. Rosnilimab showed expected pharmacology but lacked adequate efficacy compared to placebo. Anaptys plans to update progress on rosnilimab for rheumatoid arthritis in the first half of 2026.
Read more →Anaptys Announces Third Quarter 2025 Financial Results and Provides Business Update
AnaptysBio announced plans to split its biopharma operations from royalty assets by the end of 2026. The company expects to record a one-time $75 million milestone payment from GSK in the fourth quarter. This payment triggers after Jemperli reaches $1 billion in global net sales. GSK reported third-quarter Jemperli sales of $303 million, bringing year-to-date revenue to $785 million.
Read more →Anaptys Announces Participation in November Investor Conferences
AnaptysBio, Inc. has announced its participation in several upcoming investor conferences, including the TD Cowen Immunology & Inflammation Summit and the Guggenheim Healthcare Innovation Conference. CEO Daniel Faga and other executives will represent the company at these events. Webcasts of the presentations will be available for 30 days post-conference, promoting transparency and investor engagement.
Read more →