Spyre Therapeutics
Spyre Therapeutics is a clinical-stage biotechnology company developing YTE-modified monoclonal antibodies (SPY001, SPY002, SPY003, SPY072) and fixed-dose combinations for inflammatory bowel disease and rheumatic diseases, targeting quarterly or twice-annual dosing versus bi-weekly standards of care.
- Company typePublic
- Founded2023
- HeadquartersSunrise, United States
- Headcount101–250
- GTM typeB2B
- OfferingHardware or Manufacturing
What Spyre Therapeutics does
Spyre Therapeutics is a clinical-stage biotechnology company developing a pipeline of novel half-life extended monoclonal antibodies for inflammatory bowel disease (IBD) and rheumatic diseases. The company was rebranded in late 2023 from Aeglea BioTherapeutics and is publicly traded on NASDAQ under the ticker SYRE, headquartered in Waltham, Massachusetts, with 101–250 employees. Its core scientific platform applies the YTE modification to FcRn-binding regions of antibodies, producing a greater than 3x half-life extension that enables quarterly or twice-annual subcutaneous dosing compared with bi-weekly dosing for approved standards of care such as Takeda's Entyvio.
The pipeline comprises three monotherapy candidates (SPY001 targeting α4β7, SPY002 targeting TL1A, and SPY003 targeting IL-23) plus three fixed-dose combination products (SPY120, SPY130, SPY230) coformulated in single injectors, and a distinct anti-TL1A antibody (SPY072) for rheumatic indications. All candidates are investigational and being evaluated in Phase 2 studies including the SKYLINE-UC and SKYWAY-RD trials. Phase 2 data for SPY001 showed 40% clinical remission at Week 12 versus 27% for Entyvio, with 51% endoscopic improvement versus 41%, while SPY003 demonstrated approximately an 85-day confirmed half-life in interim Phase 1 results.
The business model is pre-revenue biopharmaceutical product sales contingent on regulatory approval; no products are approved or commercialized, and there are no published prices. The company has no commercial distribution infrastructure, but has appointed a Chief Commercial Officer (Kate Tansey Chevlen) in January 2026 to prepare for potential commercialization. As of year-end 2025, Spyre held approximately $757 million in cash, cash equivalents, and marketable securities, expected to fund operations into the second half of 2028, supported by capital raises totaling approximately $866.5 million across April 2026 offerings, $316.2 million in October 2025, and a $180 million private placement in March 2024.
Spyre Therapeutics firmographics
Firmographics- Name
- Spyre Therapeutics
- Legal name
- Spyre Therapeutics, Inc.
- Website
- https://spyre.com
- Company type
- Public
- Founded year
- 2023
- Operating status
- Operating
- Headcount range
- 101–250 employees
- Short description
- Spyre Therapeutics is a clinical-stage biotechnology company developing YTE-modified monoclonal antibodies (SPY001, SPY002, SPY003, SPY072) and fixed-dose combinations for inflammatory bowel disease and rheumatic diseases, targeting quarterly or twice-annual dosing versus bi-weekly standards of care.
- Ownership category
- akta.pro rank
Spyre Therapeutics industry classification
Industry- Product category
- Clinical-Stage Biopharmaceuticals (Immunology / IBD / Rheumatic Disease)
- NAICS
- Biological Product (except Diagnostic) Manufacturing (325414)
- SIC
- Biological Products, (No Disgnostic Substances) (2836)
- akta.pro primary industry
- Gastroenterology Specialty Pharmaceuticals (HLAIACAE)
- akta.pro secondary industry
- Bispecific & Multispecific Antibodies (HLAAAAAF)
Keywords
Where Spyre Therapeutics is headquartered
LocationHeadquarters
- HQ city
- Sunrise
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Spyre Therapeutics business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales, Others
Revenue model
- Biopharmaceutical Product Sales: Pre-revenue clinical-stage biotechnology company. The company is developing a pipeline of novel antibody therapeutics targeting inflammatory bowel disease and rheumatic diseases. Upon successful clinical development and regulatory approval, the company plans to commercialize its pipeline candidates. No products have been approved or commercialized yet.
Go-to-market motion1 record
Distribution channels2 records
Marketing channels4 records
Spyre Therapeutics product offering
Product offeringCore offering
Spyre Therapeutics is a clinical-stage biotechnology company developing a pipeline of novel, half-life extended monoclonal antibodies targeting validated mechanisms (α4β7, TL1A, IL-23) for the treatment of inflammatory bowel disease (ulcerative colitis, Crohn's disease) and rheumatic diseases (rheumatoid arthritis, psoriatic arthritis, axial spondyloarthritis). The pipeline includes monotherapy candidates (SPY001, SPY002, SPY003, SPY072) and fixed-dose combination products (SPY120, SPY130, SPY230), all incorporating the YTE modification technology for extended half-life enabling quarterly or twice annual subcutaneous dosing.
Product overview
Spyre Therapeutics is a clinical-stage biotechnology company developing a pipeline of novel half-life extended monoclonal antibodies targeting validated mechanisms for gastrointestinal and rheumatic diseases. The company's portfolio includes monotherapy candidates (SPY001 targeting α4β7, SPY002 targeting TL1A, SPY003 targeting IL-23) and combination products (SPY120, SPY130, SPY230) that pair these antibodies for enhanced efficacy. All antibodies incorporate the YTE modification for extended half-life enabling quarterly or twice annual dosing. The company is also developing SPY072, a distinct anti-TL1A antibody for rheumatic diseases.
Differentiator
Problem solved
Functional benefit
Products and services
- SPY001 Novel, half-life extended monoclonal antibody targeting α4β7 for the potential treatment of inflammatory bowel disease (IBD), with demonstrated similar potency and selectivity as vedolizumab in preclinical studies and a differentiated pharmacokinetic profile supporting quarterly or twice annual maintenance dosing. Currently in Phase 2 clinical development (SKYLINE-UC).
- SPY002 Novel, half-life extended monoclonal antibody targeting TL1A for the potential treatment of inflammatory bowel disease, exhibiting comparable or superior potency to first-generation anti-TL1As in head-to-head preclinical studies. Currently in Phase 2 clinical development (SKYLINE-UC trial; achieved 33% clinical remission and 42% endoscopic improvement at Week 12).
- SPY003 Novel, half-life extended monoclonal antibody targeting IL-23 for the potential treatment of inflammatory bowel disease, exhibiting comparable potency to risankizumab in head-to-head preclinical studies and an approximately 85-day confirmed half-life in interim Phase 1 results. Currently in Phase 2 clinical development.
- SPY120 High-concentration fixed-dose combination of SPY001 (anti-α4β7) and SPY002 (anti-TL1A) for the potential treatment of IBD, with superior efficacy compared to either monotherapy alone in preclinical colitis models, coformulated for delivery in a single injector on a quarterly or twice annual basis.
- SPY130 High-concentration fixed-dose combination of SPY001 (anti-α4β7) and SPY003 (anti-IL-23) for the potential treatment of IBD, demonstrating additive efficacy in preclinical colitis models, coformulated for single-injector delivery on a quarterly or twice annual basis.
- SPY230 High-concentration fixed-dose combination of SPY002 (anti-TL1A) and SPY003 (anti-IL-23) for the potential treatment of IBD, demonstrating additive efficacy in preclinical models, coformulated for single-injector delivery on a quarterly or twice annual basis.
- SPY072 Novel, half-life extended monoclonal antibody targeting TL1A for the potential treatment of rheumatic diseases including rheumatoid arthritis (RA), psoriatic arthritis (PsA), and axial spondyloarthritis (axSpA). Distinct from SPY002 which is being studied in IBD. Currently in Phase 2 clinical development (SKYWAY-RD).
Quantifiable outcome
- SPY001 achieved 40% clinical remission rate at Week 12 vs 27% for Entyvio in ulcerative colitis
- +4 more outcomes
Companies that use Spyre Therapeutics
Customer profileSegments3 records
Ideal customer profiles1 record
Spyre Therapeutics technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
Spyre Therapeutics partnerships and signals
Strategic signalScale indicators14 records
Recent moves6 records
Expansion highlights6 records
Spyre Therapeutics competitors and assessment
Company assessmentBroad incumbents
- AbbVie: Markets Skyrizi (risankizumab, anti-IL-23) and Humira in IBD/rheumatic diseases. Directly competes with SPY003 in IL-23 mechanism and sets the efficacy bar Spyre's programs must clear.
- Johnson & Johnson: Markets Tremfya (anti-IL-23) and Stelara in IBD and rheumatic indications. Major incumbent across Spyre's two therapeutic areas with established commercial infrastructure.
- Eli Lilly: Markets mirikizumab (Omvoh) in ulcerative colitis and acquired Morphic for its integrin pipeline. Direct competitor in IBD and a likely strategic acquirer of immunology-focused biotechs.
- Takeda Pharmaceutical: Markets Entyvio (vedolizumab, anti-α4β7), the direct competitor to SPY001 in ulcerative colitis and Crohn's. Entyvio's commercial performance is the primary benchmark for Spyre's α4β7 program.
- Merck & Co. Acquired Prometheus Biosciences for $10.8B to access its TL1A program. Now competing with Spyre's SPY002/SPY072 in TL1A for IBD and rheumatic indications with substantially larger commercial resources.
- Roche: Develops immunology biologics including TL1A programs (acquired Telavant) and established IBD/rheumatic franchises. Competes with Spyre across multiple targeted mechanisms in overlapping indications.
Direct peers
- Apogee Therapeutics: Clinical-stage immunology biotech developing antibody therapies for inflammatory diseases, with overlapping TL1A and IL-23 programs in IBD. Board member Michael Henderson is CEO of Apogee, creating direct portfolio overlap with Spyre.
- Prometheus Biosciences: Was a clinical-stage IBD-focused biotech developing TL1A antibody therapy (PRA023) before being acquired by Merck for $10.8B. Directly comparable pipeline focus and the source of multiple Spyre team members.
- Morphic Holding: Clinical-stage biotech developing oral integrin therapies for IBD, acquired by Eli Lilly for ~$3.2B. Directly comparable as an IBD-focused immunology platform targeting validated mechanisms with differentiated delivery.
Emerging players
- Mirador Therapeutics: Recently formed immunology biotech led by Mark McKenna (Spyre board member). Pursues precision immunology approaches in inflammation and immunology with overlapping scientific leadership.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat3 records
Key risks6 records
Key highlights7 records
Customer concentration
Spyre Therapeutics social profiles
Digital presenceSpyre Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
Spyre Therapeutics leadership team
Management profileNumber of profiles
Profiles13 records
Spyre Therapeutics funding detail
Funding detailFunding overview
Funding rounds5 records
Investors20 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Spyre Therapeutics M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Spyre Therapeutics
What does Spyre Therapeutics do?
Spyre Therapeutics is a clinical-stage biotechnology company developing a pipeline of novel, half-life extended monoclonal antibodies targeting validated mechanisms (α4β7, TL1A, IL-23) for the treatment of inflammatory bowel disease (ulcerative colitis, Crohn's disease) and rheumatic diseases (rheumatoid arthritis, psoriatic arthritis, axial spondyloarthritis). The pipeline includes monotherapy candidates (SPY001, SPY002, SPY003, SPY072) and fixed-dose combination products (SPY120, SPY130, SPY230), all incorporating the YTE modification technology for extended half-life enabling quarterly or twice annual subcutaneous dosing.
Is Spyre Therapeutics a public or private company?
Spyre Therapeutics is a public company. It is classified as public and is currently operating.
When was Spyre Therapeutics founded?
Spyre Therapeutics was founded in 2023. It employs 101 to 250 people.
Where is Spyre Therapeutics based?
Spyre Therapeutics is headquartered in Sunrise, United States, in the North America region.
How does Spyre Therapeutics make money?
One revenue line is on record: biopharmaceutical Product Sales.
Who are Spyre Therapeutics's main competitors?
Broad incumbents on record are AbbVie, Johnson & Johnson, Eli Lilly, Takeda Pharmaceutical, Merck & Co. and Roche. Direct peers are Apogee Therapeutics, Prometheus Biosciences and Morphic Holding. Mirador Therapeutics is listed as an emerging player.
Does Spyre Therapeutics have an API?
No public API is recorded for Spyre Therapeutics.
What industry is Spyre Therapeutics in?
Spyre Therapeutics's product category is Clinical-Stage Biopharmaceuticals (Immunology / IBD / Rheumatic Disease). Its primary akta.pro industry code is HLAIACAE, Gastroenterology Specialty Pharmaceuticals, with a secondary code of HLAAAAAF, Bispecific & Multispecific Antibodies. Its NAICS code is 325414 and its SIC code is 2836.