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SYRE

Spyre Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 2·Waltham, MA, United States·CEO: Dr. Cameron Turtle DPHIL, Ph.D.
ImmunologyDermatologyMusculoskeletal

SYRE evidence brief

What we can confirm

BioSniper Score:
4.9 / 10
Market Cap:
$7.88B

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

BioSniper Score: 4.9 / 10 · Market Cap: $7.88B
BioSniper AIPage evidence connected

Prepared research question

What matters most for SYRE—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · SYRE

Spyre Therapeutics, Inc. (SYRE) is a clinical-stage biotechnology company developing next-generation antibody monotherapies and combinations for inflammatory bowel disease and other immune-mediated diseases, with a focus on extended half-life antibodies targeting α4β7, TL1A, and IL-23 [sec_mda · as of 2026-08-04].

Key risk: Operating losses expected to increase

4.9/10

BioSniper Score

Based on 2 of 6 signals

Limited data coverage

Market Cap

$7.88B

Cash Runway

—

Lead Asset

—

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 8 clinical trials for Spyre Therapeutics, Inc..

AI OverviewAI overview is shown in English only.

Spyre Therapeutics, Inc. (SYRE) is a clinical-stage biotechnology company developing next-generation antibody monotherapies and combinations for inflammatory bowel disease and other immune-mediated diseases, with a focus on extended half-life antibodies targeting α4β7, TL1A, and IL-23 [sec_mda · as of 2026-08-04].

  • Cash & equivalents of $162.0M as of 2026-06-30 [sec].
  • Net income of -$36.2M for the quarter ended June 30, 2026 [sec].
  • Shareholders' equity of $1,101.1M as of 2026-06-30 [sec].
  • Phase 2 SKYLINE platform trial in ulcerative colitis is ongoing, with SPY003 topline induction data expected in September 2026 [sec · filed 2026-08-25].
  • Raised approximately $435.2M in net proceeds from a public underwritten offering in April 2026 [sec_mda · as of 2026-08-04].

What works

  • Spyre has a broad clinical pipeline including extended half-life antibodies against validated targets (α4β7, TL1A, IL-23) and is evaluating paradigm-changing fixed-dose combinations in a Phase 2 platform trial [sec_mda · as of 2026-08-04].
  • The company has a strong cash position, with $162.0M in cash and equivalents as of 2026-06-30, supplemented by a $435.2M public offering in April 2026 [sec] [sec_mda · as of 2026-08-04].
  • Multiple near-term clinical catalysts are expected, including SPY003 topline data in September 2026 and other readouts over the next 12-18 months [sec · filed 2026-08-25].

What to weigh

  • Spyre has incurred significant operating losses since inception and anticipates losses to increase in absolute dollar terms as it advances clinical development and prepares for potential commercialization [sec_mda · as of 2026-08-04].
  • The company will need to secure additional financing in the future to fund further R&D and before any commercial product can be marketed, as current resources are sufficient for at least one year but not beyond [sec_mda · as of 2026-05-05].
  • The company's forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from expectations [sec · filed 2026-04-13].

From the filings

Quoted directly from source documents.

  • SPY003 topline induction data expected in September 2026

    “SPY003 topline induction data expected in September 2026”

    SEC MD&A · August 25, 2026

Catalyst timeline

  • 2024-06-06 · Phase 1 start for SPY001-001 — A Phase 1, randomized, double-blind, placebo-controlled, single and multiple ascending dose study of SPY001-001 in healthy participants.
  • 2024-11-18 · Phase 1 start for SPY002-072 — A Phase 1, randomized, double-blind, placebo-controlled, single ascending dose study of SPY002-072 in healthy participants.
  • 2024-11-26 · Phase 1 start for SPY002-091 — A Phase 1, randomized, double-blind, placebo-controlled, single ascending dose study of SPY002-091 in healthy participants.
  • 2025-03-10 · Phase 1 start for SPY003 — A Phase 1, randomized, double-blind, placebo-controlled, single dose study of SPY003 in healthy participants.
Risks & what to watch (3)›

Key risks

  • Operating losses expected to increase — The company has incurred significant operating losses and anticipates losses to increase in absolute dollar terms as it continues clinical development [sec_mda · as of 2026-08-04].
  • Need for future financing — Current resources fund operations for at least one year; additional financing will be needed to support further R&D and commercialization [sec_mda · as of 2026-05-05].
  • Forward-looking statement risks — Forward-looking statements involve risks and uncertainties that may cause actual results to differ from expectations [sec · filed 2026-04-13].

What to watch

  • SPY003 topline induction data from SKYLINE Part A expected in September 2026 [sec · filed 2026-08-25].
  • Additional topline readouts from the SKYLINE and SKYWAY trials over the next 12-18 months [sec · filed 2026-08-25].
  • Company's ability to secure additional financing beyond current cash runway [sec_mda · as of 2026-05-05].

Sources: Catalysts · News · SEC filings · SEC MD&A · Generated October 9, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 2 of 6 signals · derived from public data

Pipeline inputs are unavailable for this score. It uses only the available signals shown below.

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.8

D/E 0.07

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal0.0

0 buys · 47 sells (180d)

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

198

Total value held

$4.09B

HolderSharesValue
fmr llc11,781,024$594.2M
blackrock, inc.5,521,221$278.5M
rtw investments, lp4,171,996$210.4M
fairmount funds management llc4,018,101$202.7M
perceptive advisors llc3,783,225$190.8M
venrock adviser, llc3,685,448$185.9M
vanguard capital management llc3,057,401$154.2M
driehaus capital management llc2,790,785$140.8M
state street corp2,607,031$131.5M
paradigm biocapital advisors lp1,957,266$98.7M

Showing top 10 of 198 institutional holders of Spyre Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 19, 2026
% of float
14.3%
Days to cover
12.6
Shares short
10,435,737
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

SYRE short interest

Governance

Frequently asked questions

What is the AI investment thesis for Spyre Therapeutics, Inc.?

Spyre Therapeutics, Inc. (SYRE) is a clinical-stage biotechnology company developing next-generation antibody monotherapies and combinations for inflammatory bowel disease and other immune-mediated diseases, with a focus on extended half-life antibodies targeting α4β7, TL1A, and IL-23 [sec_mda · as of 2026-08-04].

Who is the CEO of Spyre Therapeutics, Inc.?

Dr. Cameron Turtle DPHIL, Ph.D. is the chief executive officer of Spyre Therapeutics, Inc. (SYRE).

Where is Spyre Therapeutics, Inc. headquartered?

Spyre Therapeutics, Inc. (SYRE) is headquartered in Waltham, MA, United States.

What therapeutic areas does Spyre Therapeutics, Inc. focus on?

Spyre Therapeutics, Inc. develops therapies across Immunology, Dermatology, Musculoskeletal.

923 companies304,846 SEC filings22,720 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.