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Sutro Biopharma Inc's Business Segments
Sutro Biopharma Inc's reported revenue by business segment and by geographic region, quarterly and annual, normalized against the consolidated income statement. Free below: the top 3 rows per table, this quarter and this fiscal year. Subscriber access adds the full segment history and operating income by segment.
Segment Data As of FY
Reportable Segments
4
Largest Segment
Member
Total Revenue
$ 10
Regions Reported
-
Revenue Share by Reportable Segment - FY
- Member0%
- Ongoing Performance Related to Unsatisfied Performance Obligations0%
- Astellas License and Collaboration Agreement Materials Supply14.5%
- Collaboration and License Agreements and Supply Agreements Vaxcyte Inc1.6%
Revenue by Reportable Segment - FY
| Segment | Revenue (Millions) | % of Total |
|---|---|---|
| Member | $ 24 | - |
| Ongoing Performance Related to Unsatisfied Performance Obligations | $ 16 | - |
| Astellas License and Collaboration Agreement Materials Supply | $ 1 | 14.5% |
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Revenue by Product & Service Category - FY
- Ongoing Performance Related to Unsatisfied Performance Obligations82.3%
- Materials Supply7.5%
- Research and Development Services3.8%
Revenue by Product & Service Category - FY
| Category | Revenue (Millions) | % of Total |
|---|---|---|
| Ongoing Performance Related to Unsatisfied Performance Obligations | $ 12 | 82.3% |
| Materials Supply | $ 1 | 7.5% |
| Research and Development Services | $ 1 | 3.8% |
Product and service categories are a supplemental disclosure and are not required to sum to consolidated revenue or to the reportable segments above.
Annual Results
Revenue Share by Reportable Segment - FY
- Member0%
- Ongoing Performance Related to Unsatisfied Performance Obligations0%
- Astellas License and Collaboration Agreement Materials Supply14.5%
- Collaboration and License Agreements and Supply Agreements Vaxcyte Inc1.6%
Revenue by Reportable Segment - FY
| Segment | Revenue (Millions) | % of Total |
|---|---|---|
| Member | $ 24 | - |
| Ongoing Performance Related to Unsatisfied Performance Obligations | $ 16 | - |
| Astellas License and Collaboration Agreement Materials Supply | $ 1 | 14.5% |
1 more segments available
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Description of Sutro Biopharma Inc
Sutro Biopharma Inc is a biotechnology company based in South San Francisco, California. It was founded in 2003 with the aim of using its proprietary XpressCF+ technology platform to develop innovative and next-generation antibody-drug conjugates (ADCs) and bispecific antibodies.
The XpressCF+ platform is a powerful cell-free protein synthesis system that enables the rapid and precise production of complex proteins. This technology allows Sutro Biopharma to engineer precise antibodies and conjugates that can specifically target cancer cells and deliver highly potent cytotoxic agents. The platform offers several advantages over traditional cell-based protein production methods, including high purity, flexibility, and scalability.
Sutro Biopharma has established numerous partnerships and collaborations with leading pharmaceutical and biotechnology companies to develop novel therapeutics. The company's ADC pipeline includes multiple candidates for various types of cancer, such as ovarian, lung, and hematological malignancies. These ADCs are designed to selectively activate their cytotoxic payload where needed while minimizing off-target effects, potentially reducing side effects and improving patient outcomes.
Sutro Biopharma's bispecific antibody program aims to create molecules that can simultaneously target two different antigens, such as tumor cells and immune cells, to enhance the body's immune response against cancer. Their bispecific antibodies exhibit potent anti-tumor activity and have the potential to improve the durability and magnitude of therapeutic response.
Apart from its core ADC and bispecific antibody programs, Sutro Biopharma actively pursues research and development in other therapeutic areas. The company has expanded its technology platform to include other protein therapeutics, including cytokines, growth factors, and other biotherapeutics.
Sutro Biopharma's portfolio also includes proprietary technology for site-specific conjugation chemistry, which allows precise attachment of payloads to antibodies, thereby enhancing the therapeutic index and reducing off-target toxicities. This technology has the potential to address challenges associated with traditional conjugation methods.
Overall, Sutro Biopharma Inc is a cutting-edge biotechnology company that focuses on developing pioneering therapeutic molecules utilizing its advanced XpressCF+ platform. With a strong pipeline and a commitment to innovation, they aim to revolutionize cancer treatment and improve patient outcomes in the field of biopharmaceuticals.
The XpressCF+ platform is a powerful cell-free protein synthesis system that enables the rapid and precise production of complex proteins. This technology allows Sutro Biopharma to engineer precise antibodies and conjugates that can specifically target cancer cells and deliver highly potent cytotoxic agents. The platform offers several advantages over traditional cell-based protein production methods, including high purity, flexibility, and scalability.
Sutro Biopharma has established numerous partnerships and collaborations with leading pharmaceutical and biotechnology companies to develop novel therapeutics. The company's ADC pipeline includes multiple candidates for various types of cancer, such as ovarian, lung, and hematological malignancies. These ADCs are designed to selectively activate their cytotoxic payload where needed while minimizing off-target effects, potentially reducing side effects and improving patient outcomes.
Sutro Biopharma's bispecific antibody program aims to create molecules that can simultaneously target two different antigens, such as tumor cells and immune cells, to enhance the body's immune response against cancer. Their bispecific antibodies exhibit potent anti-tumor activity and have the potential to improve the durability and magnitude of therapeutic response.
Apart from its core ADC and bispecific antibody programs, Sutro Biopharma actively pursues research and development in other therapeutic areas. The company has expanded its technology platform to include other protein therapeutics, including cytokines, growth factors, and other biotherapeutics.
Sutro Biopharma's portfolio also includes proprietary technology for site-specific conjugation chemistry, which allows precise attachment of payloads to antibodies, thereby enhancing the therapeutic index and reducing off-target toxicities. This technology has the potential to address challenges associated with traditional conjugation methods.
Overall, Sutro Biopharma Inc is a cutting-edge biotechnology company that focuses on developing pioneering therapeutic molecules utilizing its advanced XpressCF+ platform. With a strong pipeline and a commitment to innovation, they aim to revolutionize cancer treatment and improve patient outcomes in the field of biopharmaceuticals.
Sutro Biopharma Inc. operates in the biopharmaceutical sector as a clinical-stage company with a focus on developing innovative therapies, particularly in the domains of oncology and autoimmune diseases. Their approach centers on using cutting-edge techniques to create novel therapeutics that deliver targeted treatment solutions to address significant unmet medical needs. Below is an extensive overview of Sutro Biopharmas segments, products, and services:
1. Segments:
a. Antibody-Drug Conjugates (ADCs):
Sutro Biopharma is prominent in the development of ADCs, a sophisticated class of therapeutics that combine the specificity of monoclonal antibodies with the potency of cytotoxic drugs. This segment is characterized by:
- Mechanism of Action: ADCs are designed to bind specifically to antigens present on the surface of cancer cells, thereby delivering cytotoxic encapsulated drugs directly to tumor locations. This targeted approach minimizes systemic toxicity and enhances efficacy against malignancies.
- Indications: The ADCs developed by Sutro predominantly target hematological malignancies and solid tumors, providing treatment options for cancers such as multiple myeloma, B-cell lymphomas, and various gynecological cancers.
b. Cytokine-Based Therapies:
In addition to ADCs, Sutro innovates in the field of cytokine therapies. These agents employ genetically modified cytokines aimed at modulating the immune response. The salient features include:
- Enhanced Efficacy: By modifying cytokines like IL-2 and IL-12, Sutros therapies aim to amplify immune activation against tumors while potentially reducing adverse effects commonly associated with cytokine treatments.
- Applications: These therapies are designed to treat not only cancers but also autoimmune diseases, offering a dual approach in immune modulation.
Products:
a. STRO-001:
This ADC is Sutros lead product candidate, targeting CD74, a protein prominently expressed on several cancer cell types, particularly in multiple myeloma and B-cell lymphomas. Key attributes include:
- Targeted Action: The unique targeting of CD74 allows for selective delivery of cytotoxic agents, designed to induce apoptosis in malignant cells while sparing healthy tissues.
- Clinical Advancement: STRO-001 has progressed through various clinical trial phases, demonstrating promising safety and efficacy profiles.
b. STRO-002:
An emerging product candidate, STRO-002 targets the folate receptor-alpha (FolRα), which shows high expression in numerous gynecological cancers including ovarian and endometrial tumors. Its development features:
- Antigen Specificity: Targeting FolRα enables a focused therapeutic approach aimed at highly affected cancer cells.
- Therapeutic Potential: STRO-002 is anticipated to offer novel treatment options for patients who have limited responses to existing therapies.
c. STRO-003:
This ADC is designed to target DYRK1A, an antigen linked to specific B-cell malignancies. Noteworthy points include:
- Unique Targeting Strategy: By focusing on DYRK1A, STRO-003 aims to address cancer types that may not respond to other treatments effectively.
- Innovative Approach: This candidate represents Sutros commitment to exploring less conventional targets in the fight against cancer.
Services:
a. Preclinical Development:
Sutro Biopharma provides extensive preclinical development services, essential for early-stage drug evaluation. Their offerings encompass:
- Target Identification: Systematically identifying and validating cancer-specific targets for potential therapeutics.
- Formulation Development: Crafting ADCs through sophisticated drug conjugation techniques, which include stability and solubility optimization.
- Preclinical Testing: Conducting in-vitro assays and in-vivo animal studies to ascertain pharmacodynamics and efficacy.
b. Clinical Development:
The company is involved in comprehensive clinical development strategies designed to transition drug candidates from preclinical to clinical settings, which includes:
- Trial Design and Execution: Designing robust clinical trial protocols (Phase 1, 2, and 3) to assess safety, efficacy, and optimal dosing.
- Patient Engagement: Managing recruitment processes to ensure diverse patient representation and collecting data for regulatory submission.
- Regulatory Management: Navigating the complexities of regulatory compliance to secure necessary approvals for investigational therapies.
c. Manufacturing:
Sutro Biopharma leverages its proprietary XpressCF+® platform, which is central to its manufacturing capabilities. Key aspects include:
- Rapid Production Workflow: This platform facilitates quick and adaptable production of protein-based therapeutics, essential for meeting the dynamic demands of clinical trials and eventual commercialization.
- Scalability: The manufacturing solutions provided can be tailored to support both early-stage clinical trials and later-stage commercial production, ensuring consistency and quality throughout the development process.
Conclusion:
Sutro Biopharma Inc. stands at the forefront of the biopharmaceutical industry, focusing on pioneering ADCs and cytokine therapies aimed at transforming treatment paradigms in oncology and autoimmune diseases. With a robust pipeline of product candidates, including STRO-001, STRO-002, and STRO-003, along with comprehensive preclinical, clinical, and manufacturing services, Sutro Biopharma is well-positioned to make significant strides in addressing the unmet needs of patients facing these challenging health conditions.
1. Segments:
a. Antibody-Drug Conjugates (ADCs):
Sutro Biopharma is prominent in the development of ADCs, a sophisticated class of therapeutics that combine the specificity of monoclonal antibodies with the potency of cytotoxic drugs. This segment is characterized by:
- Mechanism of Action: ADCs are designed to bind specifically to antigens present on the surface of cancer cells, thereby delivering cytotoxic encapsulated drugs directly to tumor locations. This targeted approach minimizes systemic toxicity and enhances efficacy against malignancies.
- Indications: The ADCs developed by Sutro predominantly target hematological malignancies and solid tumors, providing treatment options for cancers such as multiple myeloma, B-cell lymphomas, and various gynecological cancers.
b. Cytokine-Based Therapies:
In addition to ADCs, Sutro innovates in the field of cytokine therapies. These agents employ genetically modified cytokines aimed at modulating the immune response. The salient features include:
- Enhanced Efficacy: By modifying cytokines like IL-2 and IL-12, Sutros therapies aim to amplify immune activation against tumors while potentially reducing adverse effects commonly associated with cytokine treatments.
- Applications: These therapies are designed to treat not only cancers but also autoimmune diseases, offering a dual approach in immune modulation.
Products:
a. STRO-001:
This ADC is Sutros lead product candidate, targeting CD74, a protein prominently expressed on several cancer cell types, particularly in multiple myeloma and B-cell lymphomas. Key attributes include:
- Targeted Action: The unique targeting of CD74 allows for selective delivery of cytotoxic agents, designed to induce apoptosis in malignant cells while sparing healthy tissues.
- Clinical Advancement: STRO-001 has progressed through various clinical trial phases, demonstrating promising safety and efficacy profiles.
b. STRO-002:
An emerging product candidate, STRO-002 targets the folate receptor-alpha (FolRα), which shows high expression in numerous gynecological cancers including ovarian and endometrial tumors. Its development features:
- Antigen Specificity: Targeting FolRα enables a focused therapeutic approach aimed at highly affected cancer cells.
- Therapeutic Potential: STRO-002 is anticipated to offer novel treatment options for patients who have limited responses to existing therapies.
c. STRO-003:
This ADC is designed to target DYRK1A, an antigen linked to specific B-cell malignancies. Noteworthy points include:
- Unique Targeting Strategy: By focusing on DYRK1A, STRO-003 aims to address cancer types that may not respond to other treatments effectively.
- Innovative Approach: This candidate represents Sutros commitment to exploring less conventional targets in the fight against cancer.
Services:
a. Preclinical Development:
Sutro Biopharma provides extensive preclinical development services, essential for early-stage drug evaluation. Their offerings encompass:
- Target Identification: Systematically identifying and validating cancer-specific targets for potential therapeutics.
- Formulation Development: Crafting ADCs through sophisticated drug conjugation techniques, which include stability and solubility optimization.
- Preclinical Testing: Conducting in-vitro assays and in-vivo animal studies to ascertain pharmacodynamics and efficacy.
b. Clinical Development:
The company is involved in comprehensive clinical development strategies designed to transition drug candidates from preclinical to clinical settings, which includes:
- Trial Design and Execution: Designing robust clinical trial protocols (Phase 1, 2, and 3) to assess safety, efficacy, and optimal dosing.
- Patient Engagement: Managing recruitment processes to ensure diverse patient representation and collecting data for regulatory submission.
- Regulatory Management: Navigating the complexities of regulatory compliance to secure necessary approvals for investigational therapies.
c. Manufacturing:
Sutro Biopharma leverages its proprietary XpressCF+® platform, which is central to its manufacturing capabilities. Key aspects include:
- Rapid Production Workflow: This platform facilitates quick and adaptable production of protein-based therapeutics, essential for meeting the dynamic demands of clinical trials and eventual commercialization.
- Scalability: The manufacturing solutions provided can be tailored to support both early-stage clinical trials and later-stage commercial production, ensuring consistency and quality throughout the development process.
Conclusion:
Sutro Biopharma Inc. stands at the forefront of the biopharmaceutical industry, focusing on pioneering ADCs and cytokine therapies aimed at transforming treatment paradigms in oncology and autoimmune diseases. With a robust pipeline of product candidates, including STRO-001, STRO-002, and STRO-003, along with comprehensive preclinical, clinical, and manufacturing services, Sutro Biopharma is well-positioned to make significant strides in addressing the unmet needs of patients facing these challenging health conditions.
