Earnings summaries and quarterly performance for SUTRO BIOPHARMA.
Executive leadership at SUTRO BIOPHARMA.
Jane Chung
Chief Executive Officer
Barbara Leyman
Chief Business Development Officer
David Pauling
General Counsel and Chief Administrative Officer
Greg Chow
Chief Financial Officer
Hans-Peter Gerber
Chief Scientific Officer
Venkatesh Srinivasan
Chief Technical Operations Officer
Board of directors at SUTRO BIOPHARMA.
Research analysts who have asked questions during SUTRO BIOPHARMA earnings calls.
Edward Tenthoff
Piper Sandler Companies
2 questions for STRO
Jay Olson
Oppenheimer & Co. Inc.
2 questions for STRO
Reni Benjamin
Citizens JMP Securities
2 questions for STRO
Jiale Song
Jefferies Financial Group Inc.
1 question for STRO
Roger Song
Jefferies
1 question for STRO
Recent press releases and 8-K filings for STRO.
- Sutro Biopharma, Inc. entered into an underwriting agreement on February 9, 2026, to sell 7,868,383 shares of its common stock at an offering price of $13.98 per share.
- The offering is expected to generate approximately $110.0 million in gross proceeds, with estimated net proceeds of $103,399,994.68 after underwriting discounts and commissions of 6.00%.
- Combined with existing cash, cash equivalents, and marketable securities as of January 1, 2026, the company's capital resources are estimated to be approximately $251.4 million, extending its cash runway into the second quarter of 2028.
- The company intends to use the net proceeds primarily for general corporate purposes, including funding research, clinical and process development, manufacturing of product candidates, and potential acquisitions.
- Sutro Biopharma announced the pricing of an underwritten offering of 7,868,383 shares of its common stock at $13.98 per share.
- The offering is expected to generate approximately $110.0 million in gross proceeds.
- The offering is anticipated to close on or about February 11, 2026.
- The net proceeds will be used primarily for general corporate purposes, including funding research, clinical development, and potential acquisitions.
- Sutro Biopharma has undergone a strategic pivot to become a clinical oncology company, accelerating its pipeline and extending its cash runway to mid-2027.
- The company's lead program, STRO-004 (Tissue Factor ADC), is currently in a Phase 1 trial, with initial top-line data anticipated by mid-2026.
- Sutro plans to advance STRO-006 (Integrin beta-6 targeting ADC) to an IND later in 2026 and its first dual payload ADC (targeting PTK7) into the clinic by late 2026 or early 2027.
- A collaboration iADC program with Astellas Pharma is also entering the clinic early 2026, further validating Sutro's differentiated dual payload ADC technology.
- Under CEO Jane Chung (since March 2025), Sutro Biopharma has completed a strategic pivot to become a clinical oncology company, accelerating its pipeline and right-sizing its operations.
- The company's lead program, STRO-004 (Tissue Factor ADC), is in Phase I with initial top-line data anticipated by mid-2026. STRO-006 is on track for an IND later this year (2026), and the first dual payload ADC (PTK7 target) is expected to enter the clinic later this year (2026) or early 2027. A partnered iADC program with Astellas Pharma is also entering the clinic early this year (2026).
- Sutro has extended its cash runway to mid-2027, excluding collaboration milestones. The company emphasizes its differentiated ADC technology, enabling the development of dual payload ADCs with improved safety and efficacy profiles.
- Sutro Biopharma has undergone a strategic transformation since March 2025, redefining its strategy, right-sizing its team, and focusing on becoming a clinical oncology company with a differentiated Antibody-Drug Conjugate (ADC) technology.
- The company has extended its cash runway to mid-2027, which does not include potential collaboration milestones that could further extend it. This runway supports advancing multiple programs into the clinic.
- Sutro's pipeline includes STRO-004 (Tissue Factor ADC), which entered Phase 1 clinical trials in November 2025 and is expected to deliver initial top-line data by mid-2026.
- The company is also advancing STRO-006 (Integrin beta-6 targeting ADC), on track for an Investigational New Drug (IND) application later in 2026, and a first dual payload ADC targeting PTK7, with IND entry moved up to later 2026 or early 2027.
- Sutro's dual payload ADC approach is designed to overcome resistance and improve clinical responses, with preclinical data showing these programs are well-tolerated at doses comparable to single-payload ADCs.
- Sutro Biopharma projects its cash runway to extend into at least mid-2027, including certain expected near-term milestone payments.
- The company anticipates initial Phase 1 data for STRO-004 in mid-2026.
- IND submissions are expected for STRO-006 in 2026 and STRO-227 in 2026-2027.
- The first program from the iADC partnership with Astellas is slated to enter the clinic in early 2026.
- Sutro Biopharma, Inc. (STRO) announced on December 17, 2025, that it has regained compliance with the Nasdaq Stock Market's continued listing standard for minimum share price.
- The company received confirmation from Nasdaq that its common stock maintained an average closing share price of at least $1.00 as of December 16, 2025.
- This compliance was achieved following a 1:10 reverse stock split that became effective on December 3, 2025.
- Sutro announced that the first patient cohort has been dosed in the Phase 1 study for its tissue factor ADC, STRO-004, with top-line data anticipated by mid-2026.
- The company plans to file an Investigational New Drug (IND) application for its integrin beta-6 ADC (STRO-006) in 2026 and is developing a dual payload ADC (STRO-227) targeting PTK7, designed to overcome resistance to single payload ADCs.
- Sutro's cash runway has been extended into the middle of 2027, reflecting strategic efforts to reduce burn and externalize manufacturing.
- In collaboration with Astellas, Sutro is advancing an immunostimulatory ADC program, with the first program expected to enter the clinic in early 2026.
- Sutro Biopharma's XpressCF platform enables the development of next-generation antibodies, including ADCs with 2-3 fold higher drug exposure and site-specific conjugation.
- The company has dosed the first cohort of patients in its Phase 1 study for STRO-004, a tissue factor ADC, and anticipates top-line data by the middle of next year (mid-2026). STRO-004 is designed for improved safety and efficacy, with a high non-severely toxic dose (HNSTD) of 50 mg/kg.
- Sutro plans to file an IND for its integrin beta-6 ADC (STRO-006) next year (2026) and is developing dual payload ADCs to overcome resistance to single payload ADCs.
- The company's partnership with Astellas is developing immunostimulatory ADCs, with Astellas' first program expected to enter the clinic early next year (2026).
- Sutro has extended its cash runway into the middle of 2027, not including potential milestones from partnerships.
- Sutro's XpressCF platform enables next-generation ADCs with enhanced drug exposure, site-specific conjugation, and dual payloads, aiming to overcome resistance to single payload ADCs.
- The company has dosed the first cohort of patients in the Phase 1 study for its tissue factor ADC, STRO-004, with IND clearance in late October and top-line data anticipated by mid-2025.
- Sutro plans to file an IND for an integrin beta-6 ADC next year and is developing a dual payload ADC (STRO-227) targeting PTK7, designed for improved efficacy and safety.
- Sutro has extended its cash runway into mid-2027 by reducing burn and externalizing manufacturing, following a strategic pivot in March.
Quarterly earnings call transcripts for SUTRO BIOPHARMA.
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