10-Q · May 14, 2026
Sutro Biopharma reported Q1 2026 revenue of $14.5 million, a 17% decrease from $17.4 million in Q1 2025, and a loss from operations of $29.7 million, significantly improved from the previous year's loss of $68.5…
Earnings analysis · 10-Q
Filed August 12, 2026 · Our reading of the company's report
The latest report
Sutro reported Q2 2026 revenue of $9.839 million and diluted EPS of negative $2.33. Revenue declined 34.4% sequentially and 84.6% year over year, while EPS improved sequentially but worsened year over year; results also…
Sutro reported Q2 2026 revenue of $9.839 million and diluted EPS of negative $2.33. Revenue declined 34.4% sequentially and 84.6% year over year, while EPS improved sequentially but worsened year over year; results also included an $18.422 million restructuring charge. Liquidity increased to $164.3 million from $141.4 million at year-end, but the company remains loss-making, has an accumulated deficit of $1,055.0 million and expects to require additional funding. Pipeline milestones for STRO-006 and the Astellas program are constructive, but novel-platform, clinical, manufacturing and financing risks dominate the outlook.
How much of each revenue dollar the business keeps.
One point per quarterly or annual filing. Both margins are shares of that report's revenue.
Our analysis across the last few reports.
Our model's reading of each filing, not the share price or the market's reaction. Annual and quarterly reports each occupy one position.
Revenue was $9.839 million, down 34.4% from $15.0 million in Q1 2026 and down 84.6% from $64.0 million in Q2 2025, reflecting the volatility of collaboration-driven revenue.
Diluted EPS was negative $2.33, an improvement of $0.61 from negative $2.94 in Q1 2026, but a deterioration of $0.93 from negative $1.40 in Q2 2025.
Cash, cash equivalents and marketable securities increased to $164.3 million at June 30, 2026 from $141.4 million at December 31, 2025, an increase of $22.9 million or 16.2%.
The quarter included an $18.422 million restructuring charge, while management reported that operating expenses declined year over year.
Management expects STRO-006 to enter Phase 1 in Q3 2026 and the second Astellas program to enter the clinic by year-end 2026, providing defined pipeline milestones despite the absence of commercial products.
Management concluded that disclosure controls and procedures were effective at a reasonable assurance level as of June 30, 2026, and reported no changes that materially affected, or were reasonably likely to materially affect, internal control over financial reporting during the quarter.
The company had $164.3 million in cash, cash equivalents and marketable securities as of June 30, 2026, but reported a net loss of $77.0 million for the six months ended June 30, 2026 and states that it will require additional funding. Financing may cause dilution or require the company to relinquish product or technology rights.
Sutro had an accumulated deficit of $1,055.0 million as of June 30, 2026 and has no products approved for commercial sale. The filing states that commercial product revenue is not expected for the foreseeable future and that net losses may increase substantially as development progresses.
The filing emphasizes heightened development and manufacturing uncertainty for novel dual-payload ADCs and cell-free platforms, including STRO-004, STRO-006 and STRO-227. It states that no product developed on a cell-free manufacturing platform has received FDA approval, increasing regulatory, scale-up and supply-chain risk.
The risk-factor discussion expands cybersecurity exposure to AI-enabled attacks, including deepfake-enabled fraud, credential theft and ransomware. The company also states that it has experienced and may experience delays in deploying remedial measures, creating potential risks to clinical, manufacturing and confidential-data operations.
The company relies on third-party contract manufacturers following its March 2025 and September 2025 restructurings and notes that certain raw and intermediate materials are sourced from a sole supplier. Tariffs, trade restrictions and the ongoing conflict in Iran could disrupt supply or increase costs.
The filing identifies an issued third-party patent relating to strained alkyne reagents that is expected to expire in 2031 and could be relevant to certain linker-payloads. Failure to obtain a license could delay commercialization of STRO-004, STRO-006 or STRO-227.
No quantitative revenue or EPS guidance was provided. Management indicated that $164.3 million of cash, cash equivalents and marketable securities is expected to fund operations through at least Q2 2028; STRO-006 is expected to enter Phase 1 in Q3 2026 and a second Astellas program is expected to enter the clinic by year-end 2026.
Sutro Biopharma reported Q1 2026 revenue of $14.5 million, a 17% decrease from $17.4 million in Q1 2025, and a loss from operations of $29.7 million, significantly improved from the previous year's loss of $68.5…
Sutro Biopharma is a clinical-stage oncology company advancing homogeneous and next-generation ADCs enabled by its XpressCF®/XpressCF+® cell-free platforms. The company filed and received IND clearance for STRO-004 in…
Sutro reported Q3 2025 revenue of $9.693M (three months ended Sept. 30, 2025), up from $8.520M year-over-year, while GAAP net loss widened to $56.857M (loss per share $0.67). Operating expenses fell (R&D down to…
Sutro reported revenue of $17,399 (thousands) in Q1 2025, up from $13,008 (thousands) in Q1 2024, and posted a net loss of $75,968 (thousands) or $(0.91) per share. Management completed a March 13, 2025 restructuring…
This is our reading of a public filing, not the filing itself. Analysis can contain errors; check the source document for full context.