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Spyre Therapeutics, Inc. (AGLE)·Q1 2024 Earnings Summary

Executive Summary

  • Q1 2024 was execution-focused: Spyre completed GLP tox for SPY001, reaffirmed FIH start in Q2 2024 with interim PK/safety by year-end 2024; SPY002 remains on track for H2 2024 FIH, and combinations targeted for 2025 .
  • Balance sheet strengthened by a March 2024 $180M private placement, lifting liquidity to $485.0M and extending runway well into 2027, de-risking funding needs through multiple readouts .
  • Operating spend grew as pipeline scaled (R&D $34.9M vs $13.8M YoY; G&A $12.8M vs $5.2M YoY), while net loss improved sequentially vs Q4 as Q4’s CVR-driven other expense flipped to Q1 other income (interest) .
  • Estimate comparison: S&P Global consensus was unavailable for AGLE/SYRE in our feed this quarter; no formal beat/miss call can be made. A third-party aggregator noted EPS of -$1.20 vs an estimate of -$1.17 (non-S&P) .

What Went Well and What Went Wrong

  • What Went Well

    • Advanced SPY001: completed 28-day GLP tox with favorable safety; FIH initiation guided for Q2 2024; interim PK/safety by YE 2024; half-life data supports q8–q12 week SC dosing potential .
    • TL1A momentum: SPY002 lead candidates bind TL1A monomers/trimers with subnanomolar potency; NHP PK half-life ~24 days; FIH expected H2 2024 .
    • Capital and runway: Raised $180M in March; total liquidity $485.0M at 3/31/24; runway “well into 2027,” funding multiple clinical readouts .
  • What Went Wrong

    • No revenue; net loss widened YoY on opex scale-up (R&D $34.9M vs $13.8M; G&A $12.8M vs $5.2M), reflecting accelerated development and higher stock comp/pro services .
    • Sequential opex still elevated (R&D +$1.2M vs Q4), though G&A declined vs Q4; CVR-related P&L volatility remains a watch item given prior-quarter swing .
    • Consensus benchmarking limited: S&P Global estimates unavailable for formal comparison this quarter, reducing visibility on perceived “beat/miss” drivers (see Estimates Context) .

Financial Results

Income statement and sequential trends (oldest → newest):

MetricQ3 2023Q4 2023Q1 2024
Revenue ($USD Millions)$0.000 $0.000 $0.000
R&D Expense ($USD Millions)$24.660 $33.682 $34.928
G&A Expense ($USD Millions)$8.584 $14.072 $12.846
Other Income (Expense) ($USD Millions)$(21.767) $(17.266) $3.949
Net Loss ($USD Millions)$(40.107) $(63.180) $(43.857)
Diluted EPS ($)$(9.34) $(4.05) $(1.20)
Weighted Avg Shares (Millions)4.294 15.608 36.513

YoY comparables (Q1 2024 vs Q1 2023):

MetricQ1 2023Q1 2024
Revenue ($USD Millions)$0.198 $0.000
R&D Expense ($USD Millions)$13.776 $34.928
G&A Expense ($USD Millions)$5.228 $12.846
Other Income (Expense) ($USD Millions)$0.348 $3.949
Net Loss ($USD Millions)$(18.422) $(43.857)
Diluted EPS ($)$(4.89) $(1.20)
Weighted Avg Shares (Millions)3.771 36.513

Balance sheet and cash:

MetricDec 31, 2023Mar 31, 2024
Cash & Cash Equivalents ($USD Millions)$188.893 $227.552
Marketable Securities ($USD Millions)$150.384 $257.089
Restricted Cash ($USD Millions)$0.322 $0.319
Total Liquidity (Cash, Mkt Sec, Restricted) ($USD Millions)$339.6 $485.0
Total Liabilities ($USD Millions)$73.288 $81.928
Stockholders’ Equity ($USD Millions)$184.016 $152.269
Net Cash Used in Operating Activities ($USD Millions)$31.0 (Q4’23) $28.5 (Q1’24)

Notes:

  • Q4’s larger net loss was driven in part by CVR liability mark-to-market in “Other (expense),” while Q1 benefited from interest income on higher cash/marketable securities .
  • No segments or revenue-generating products; margin metrics are not meaningful at this stage .

Guidance Changes

MetricPeriodPrevious GuidanceCurrent GuidanceChange
Cash RunwayMulti-yearInto H2 2026 Well into 2027 Raised (extended)
SPY001 – First-in-Human start20241H 2024 Q2 2024 (on track) Maintained (narrowed window)
SPY001 – Interim PK/safety2024YE 2024 YE 2024 Maintained
SPY002 – First-in-Human start20242H 2024 2H 2024 Maintained
Rational combinations (Phase 2)20252025 2025 Maintained
SPY003 – Candidate nomination2024Mid-2024; IND-enabling 2H 2024 Mid-2024; IND-enabling 2H 2024 Maintained

Why it changed/held: Runway improved with the March $180M PIPE; clinical timelines reiterated as CMC, tox and discovery milestones were achieved .

Earnings Call Themes & Trends

(No Q1’24 earnings call transcript located in our document set; themes below reflect disclosures across the last three earnings press releases.)

TopicPrevious Mentions (Q3’23 and Q4’23)Current Period (Q1’24)Trend
R&D execution & timelinesSPY001/002 targeting IND/FIH in 2024; SPY003 advancing; combos in 2025 SPY001 GLP tox complete; FIH Q2’24; SPY002 FIH H2’24; combos in 2025 On track; specificity increased
Half-life/PK advantagesSPY001 NHP half-life 22 days; target human >35 days Reinforced and linked to potential q8–q12 week dosing Reinforced
TL1A differentiationSubnanomolar binding to monomer/trimer; longer NHP half-life FIH timing reaffirmed; NHP half-life ~24 days emphasized Reinforced
Capital & runwayCash ~$205M (Q3) and $340M (Q4) $180M raise; $485M liquidity; runway into 2027 Strengthened
Leadership & governanceCFO/Legal hires (Q3) Added Mark C. McKenna to Board (Feb 2024) Upgraded board expertise

Management Commentary

  • “With a clean safety profile in SPY001's 28-day GLP toxicity study, we remain on track towards initiating a first-in-human study later this quarter… We expect to report interim PK and safety data from our Phase 1 trial of SPY001 by the end of this year, setting up the first of what we expect to be a string of important catalysts from year-end 2024 through 2025 across our lead programs.” — Cameron Turtle, CEO .
  • “SPY002… lead candidates bind both TL1A monomers and trimers and have in vitro subnanomolar potency and pharmacokinetic half-lives that potentially exceed all clinical-stage TL1A antibodies… The Company expects to begin FIH studies… in the second half of 2024 with healthy volunteer interim data expected in the first half of 2025.” .

Q&A Highlights

  • Not available. We did not locate a Q1 2024 earnings call transcript in our document set; the company issued an earnings press release with detailed updates .

Estimates Context

  • S&P Global consensus data were unavailable for AGLE/SYRE in our feed for Q1 2024; as a result, we cannot provide an S&P-anchored beat/miss assessment this quarter. We will update if S&P data become available.
  • For non-S&P context only, one third-party automated post cited EPS of -$1.20 vs an estimate of -$1.17 (source not S&P; treat cautiously) .

Key Takeaways for Investors

  • Funding overhang reduced: $485M in liquidity and runway into 2027 provide line-of-sight through multiple catalysts across SPY001/002/003 and initial combo work, lowering near-term financing risk .
  • Near-term catalysts: SPY001 FIH in Q2 2024 with interim PK/safety by YE 2024; SPY002 FIH H2 2024; expect heightened newsflow through 2025—key trading drivers around PK, safety, target engagement and dosing intervals .
  • Mechanistic edge: Half-life extension and TL1A monomer/trimer binding differentiation are central to the “best-in-class” thesis; watch for data validating q8–q12 week dosing and potency vs first-gen TL1As .
  • P&L dynamics: Elevated R&D spend reflects pipeline acceleration; sequential net loss improvement vs Q4 owed partly to CVR-related swings and higher interest income—expect ongoing “other income/expense” volatility tied to CVR .
  • Governance/strategy: Addition of industry veteran Mark McKenna supports clinical, BD, and commercialization strategy in IBD—a positive medium-term signal for execution and partnering optionality .
  • Estimate visibility: With limited consensus coverage in S&P feed this quarter, stock may trade more on program updates and financing signals than headline “beats/misses”; prepare for event-driven volatility into data readouts .