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BioWorld - Wednesday, May 27, 2026
Home » Keywords » Sutro Biopharma Inc.

Items Tagged with 'Sutro Biopharma Inc.'

ARTICLES

Antibody-drug conjugates floating on light purple background
Immuno-oncology

Next-generation dual-payload ADCs advance in oncology pipelines

March 2, 2026
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Researchers from Sutro Biopharma Inc. presented data on dual-payload antibody-drug conjugates (ADCs) engineered to overcome drug resistance, demonstrating enhanced cytotoxicity and potential efficacy in resistant cancer models.
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Antibody-drug conjugates floating on light purple background
Immuno-oncology

Sutro Biopharma outlines ADC pipeline

Nov. 13, 2025
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Sutro Biopharma Inc. has outlined its next-generation antibody-drug conjugate (ADC) pipeline following recent IND clearance and initiation of phase I for its tissue factor-targeting ADC, STRO-004.
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3D illustration demonstrating antibody-drug conjugate.
Cancer

Sutro Biopharma unveils best-in-class anti-tissue factor ADC

May 23, 2025
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Tissue factor (TF), a transmembrane protein overexpressed in tumors such as cervical, head and neck, NSCLC, and pancreatic cancers, initiates the extrinsic coagulation pathway under normal subendothelial expression. TF-targeted vedotin antibody-drug conjugates (ADCs) are in clinical evaluation for solid tumors, but toxicities, including peripheral neuropathy, ocular effects and epistaxis, limit their use.
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3D rendering of an antibody drug conjugate
Immuno-oncology

Sutro prioritizes preclinical ADC programs

March 14, 2025
Sutro Biopharma Inc. has announced plans to prioritize its three wholly owned preclinical programs in its next-generation antibody-drug conjugate (ADC) pipeline, while deprioritizing additional investment into development of luveltamab tazevibulin across all indications.
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3D rendering of drug linked to antibody

Ipsen enters ADC space licensing Sutro’s ROR1 drug STRO-003

April 2, 2024
By Karen Carey
Jumping in for the first time to the hot antibody-drug conjugate (ADC) space, Paris-based Ipsen SA pulled in exclusive global rights to a preclinical ROR1-targeting candidate from Sutro Biopharma Inc. in a deal worth up to $900 million. STRO-003, the first ADC to join Ipsen’s portfolio, contains an anti-ROR1 human IgG1 antibody (SP-11385) conjugated to an exatecan warhead, or payload.
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Immuno-oncology

Sutro Biopharma discovers new antibody-drug conjugates for diagnosis and treatment of cancer

Feb. 13, 2024
Sutro Biopharma Inc. has described antibody-drug conjugates (ADCs) comprising a cytotoxic drug linked to an antibody or polypeptide residue through a linker reported to be useful for the diagnosis and treatment of cancer.
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Cancer

Sutro Biopharma presents new STING agonists for cancer

Jan. 2, 2024
Sutro Biopharma Inc. has divulged stimulator of interferon genes protein (STING; TMEM173) agonists reported to be useful for the treatment of cancer.
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Antibody-drug conjugate illustration
Cancer

STRO-003, novel ROR1-targeted ADC with potent activity in breast and lung cancer models

Nov. 24, 2022
Researchers from Sutro Biopharma Inc. presented the discovery and preclinical characterization of a novel receptor tyrosine kinase-like orphan receptor 1 (ROR1)-targeted antibody-drug conjugate (ADC), STRO-003, being developed for the treatment of cancer.
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Antibody-drug conjugate illustration

Sutro to develop immunostimulatory ADCs for Astellas targets in deal worth $1.3B

June 28, 2022
By Tamra Sami
Astellas Pharma Inc. and Sutro Biopharma Inc. signed an exclusive global licensing deal under which Sutro will develop immunostimulatory antibody-drug conjugates (iADCs) for three biological targets for Astellas.
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Oh say, can you ADC? Dawn’s early light in the past for burgeoning sector

Jan. 4, 2021
By Randy Osborne
Sutro Biopharma Inc.’s stock-perking news in early December with STRO-002, a folate receptor alpha-targeting antibody-drug conjugate (ADC) to treat ovarian cancer, reminded investors of potential in the class, which has been more than realized in recent years and could yield more upside in the near term. As of the Oct. 30 cutoff date, STRO-002 tallied one complete response and nine partial responses in the challenging indication, which works out to an overall response rate of 32% (10 out of 31) in evaluable patients.
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