Spyre Therapeutics, Inc.
NASDAQ•SYRE
CEO: Dr. Cameron Turtle DPHIL, Ph.D.
Sector: Healthcare
Industry: Biotechnology
Listing Date: 2016-04-07
Spyre Therapeutics, Inc., a preclinical stage biotechnology company, focuses on developing therapeutics for patients living with inflammatory bowel disease (IBD). It develops SPY001, a human monoclonal immunoglobulin G1 antibody designed to bind selectively to the a4ß7 integrin being developed for the treatment of IBD (ulcerative colitis and Crohn's disease). The company is also developing SPY002, a human monoclonal antibody (mAb)candidates designed to bind to tumor necrosis factor-like ligand 1A; and SPY120, a combination of SPY001 (anti-a4ß7) and SPY002 (anti-TL1A) antibodies, which are in preclinical studies. In addition, its other early-stage programs include SPY003, an anti-IL-23 mAb; SPY004, a novel mechanism of action (MOA) mAb; SPY130, a combination of anti-a4ß7 and anti-IL-23 mAbs; and SPY230, a combination of anti-TL1A and anti-IL-23 mAbs. The company was formerly known as Aeglea BioTherapeutics, Inc. and changed its name to Spyre Therapeutics, Inc. in November 2023. Spyre Therapeutics, Inc. was incorporated in 2013 and is based in Waltham, Massachusetts.
Contact Information
221 Crescent Street, Building 23 Suite 105, Waltham, MA, 02453, United States
617-651-5940
Market Cap
$2.41B
P/E (TTM)
-88.9
17.9
Dividend Yield
--
52W High
$45.76
52W Low
$10.91
52W Range
Rank58Top 85.6%
2.3
F-Score
Modified Piotroski Analysis
Based on 10-year fundamentals
Weak • 2.3 / 9 points
Scoring Range (0-9)
8-9: Excellent Value
6-7: Strong Fundamentals
4-5: Average Quality
0-3: Weak Performance
Data Period: 2016-2025
Financial Dashboard
Q4 2025 Data
Revenue
$90.49M+0.00%
4-Quarter Trend
EPS
-$0.69+0.00%
4-Quarter Trend
FCF
-$44.58M+0.00%
4-Quarter Trend
2025 Annual Earnings Highlights
Key Highlights
Net Loss Significantly Narrows Net loss reduced to $155.2M in 2025, improving $52.8M compared to prior year loss of $208.0M.
R&D Spending Increases Research and development expenses grew 5% to $171.7M, primarily due to increased clinical development activities.
Pipeline Trials Initiated Launched SKYLINE Phase 2 platform trial for UC in May 2025 and SKYWAY Phase 2 basket trial for RD.
Risk Factors
Future Capital Needs Critical Must raise additional capital to fund operations; inability to do so risks continuation as a going concern.
Clinical Development Uncertainties Programs may fail or suffer delays; limited clinical data on long-term safety/efficacy of extended half-life tech.
Regulatory Approval Timelines Approval processes are lengthy and unpredictable; agency disagreement on trial design could cause material delays.
Outlook
Key Data Readouts Expected Topline proof-of-concept data for SPY072 in rheumatic diseases anticipated in Q4 2026.
SKYLINE Phase 2 Progress Induction data from SKYLINE Part A expected Q2 2026; randomized Part B assessment data expected in 2027.
Preparing Commercialization Path Hired first Chief Commercial Officer in January 2026, focusing on future U.S. market commercialization strategy.
Peer Comparison
Revenue (TTM)
$407.32M
$172.35M
$105.97M
Gross Margin (Latest Quarter)
102.3%
100.0%
100.0%
Key Metrics
Symbol | Market Cap | P/E (TTM) | ROE (TTM) | Debt to Assets |
|---|---|---|---|---|
| WVE | $2.45B | -11.5 | -85.0% | 2.8% |
| SYRE | $2.41B | -88.9 | -29.4% | 0.0% |
| SNDX | $2.07B | -7.1 | -206.6% | 65.4% |
Long-Term Trends
Last 4 Quarters
Revenue
Net Income
Operating Cash Flow
4Q Revenue CAGR
N/M
Revenue Volatile
4Q Net Income CAGR
N/M
Profitability Shift
Cash Flow Stability
0%
Cash Flow Needs Attention
Deep Research
Next earnings:May 6, 2026
EPS:-
|Revenue:-
Financials
Earnings Calls
Reports
News
Income Statement
Balance Sheet
Cash Flow Statement
Ratios
% Chg.
Income Statement | LTM |
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No Data