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Gritstone bio, Inc. (GRTS)·Q2 2024 Earnings Summary
Executive Summary
- Q2 2024 delivered mixed results: EPS of $0.16 loss beat third‑party consensus, while revenue of $0.92M missed materially; operating expenses fell sharply year over year, reflecting cost actions .
- Clinical narrative strengthened: preliminary randomized Phase 2 data for GRANITE in front‑line metastatic MSS‑CRC show an encouraging PFS trend, with mature PFS data expected in Q3 2024—a key upcoming catalyst .
- Cash increased sequentially to $61.7M (cash, marketable securities, and restricted cash) as of June 30, 2024, supported by an April financing of $32.5M; R&D spend declined $10.2M YoY in Q2 .
- Infectious disease portfolio progressing, with continued efforts to initiate CORAL Phase 2b per BARDA contract and 12‑month durability data from samRNA Phase 1 presented at ESCMID, reinforcing platform potential .
What Went Well and What Went Wrong
What Went Well
- GRANITE Phase 2 signal in MSS‑CRC: “The emerging progression‑free survival (PFS) benefit we reported in April is highly encouraging… we look forward to sharing the updated dataset next month” — Andrew Allen, MD, PhD (CEO) . Preliminary hazard ratios favored GRANITE (overall HR 0.82; high‑risk subgroup HR 0.52), aligning with ctDNA trends .
- Technology validation: EDGE neoantigen prediction presented at AACR; HLA Class I presentation predicted with >80% accuracy, underpinning oncology programs .
- Cost discipline: Q2 R&D expenses fell to $20.8M vs $31.0M YoY; total operating expenses down to $28.5M vs $37.7M YoY, aiding loss reduction and improving operating leverage .
What Went Wrong
- Revenue headwind: Q2 total revenue of $0.92M, primarily grants, declined from $1.96M YoY, and missed third‑party consensus materially (by ~66.7%) .
- Higher G&A: Q2 G&A rose to $7.7M from $6.7M YoY, driven by personnel and stock‑based comp, partially offsetting R&D savings .
- External execution risk persists: Continued delay and preparation for the CORAL Phase 2b BARDA study, with timing contingent on GMP‑grade materials and operational readiness .
Financial Results
Income Statement Comparison
Notes:
- Other income of $4.81M in Q2 2024 contributed to narrower net loss; third‑party summary attributes this to warrant revaluation following April financing .
Revenue Composition
Balance Sheet KPIs
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “This is an exciting time for Gritstone… If we continue to see evidence of a clinical benefit with GRANITE, as measured by PFS, we believe new hope can be brought to patients who have not been helped by immune checkpoint blockade.” — Andrew Allen, MD, PhD (CEO) .
- “Our recent AACR presentation highlights the unique power of EDGE… Our recent presentation at ESCMID showcases the ability of our self‑amplifying mRNA vector (samRNA) to induce long‑lasting immune responses.” — Andrew Allen .
Q&A Highlights
- A Q2 2024 earnings call transcript was not available via our document tools; no Q&A highlights could be retrieved. We searched for earnings‑call transcripts in the Q2 window and found none; a Special Call transcript existed (Aug 2, 2024) but could not be opened due to a database inconsistency [29] (list) and read error.
Estimates Context
- S&P Global consensus estimates were unavailable due to a CIQ mapping issue (GetEstimates error). We anchored to third‑party reported consensus where possible and explicitly note S&P unavailability.
- Q2 2024 comparison (actual vs third‑party consensus):
Note: S&P Global consensus unavailable; third‑party references used for context.
Key Takeaways for Investors
- The Q3 readout of mature PFS from the GRANITE Phase 2 randomized study is the central near‑term catalyst; preliminary HRs and ctDNA trends suggest potential clinical benefit in MSS‑CRC .
- Q2 operating discipline is evident—R&D down $10.2M YoY and total OpEx down ~$9.2M YoY, driving a narrower net loss despite lower revenue .
- Revenue remains grant‑driven and volatile; absent partner revenue, expect continued dependence on grant timing and milestones—Q2 grant revenue was $0.86M, with CEPI the source .
- Liquidity improved sequentially to $61.7M including marketables and restricted cash, bolstered by the April $32.5M raise; continued spend control is critical ahead of clinical and BARDA milestones .
- EPS outperformed third‑party consensus, but revenue under‑delivered significantly—sell‑side models may need to adjust revenue cadence to reflect grant timing and program phasing .
- Platform validation across EDGE (AACR) and samRNA durability (ESCMID) strengthens medium‑term thesis on differentiated vaccine tech across oncology/infectious disease .
- Trading setup: anticipate heightened volatility around Q3 PFS disclosure; positive confirmation could re‑rate oncology optionality, while ambiguous data may refocus attention on liquidity and BARDA execution risk .
Sources
- Q2 2024 8‑K 2.02 press release and financials .
- Q1 2024 8‑K press release and financials .
- Q4 2023 8‑K press release and financials .
- Third‑party consensus and summary context: Nasdaq/Zacks ; Quartr summary .