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sacituzumab govitecan

Generic: sacituzumab·Code: IMMU-132

sacituzumab govitecan: sourced relationships with 1 company · 29 clinical trials tracked.

sacituzumab govitecan evidence translation

What we can confirm

29 tracked trials

What it means

Source-backed records connect sacituzumab govitecan to IMMU; that link alone does not prove the drug works.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

How could sacituzumab govitecan → IMMU affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 2 study sponsors
Dated Pipeline Records (1)
CompanyDated record stage
IMMUNOMEDICS INC (IMMU)
developer · Reported 2020-02-27 · Current development: unknownSource
metastatic triple-negative breast cancer (mTNBC)
Phase 3
Clinical Trial Registry Records (29)showing 10 most recent

NeoAdjuvant Dynamic Marker - Adjusted Personalized Therapy Comparing Sacituzumab Govitecan+Pembrolizumab vs. SoC Chemotherapy in Clinical Stage II-III, Triple-negative Early Breast Cancer

NCT07178730Registry updated 2026-08-05·Phase 3
Not yet recruiting

Primary endpoint: Cohort I: 3-year event-free survival (EFS)

InterventionalRandomizedopen765 targetStarted 2026-08Completion 2033-0326 sites · GermanyWomen's Cancer Study Group GmbH

Phase II Study of Sacituzumab Govitecan With Atezolizumab/Durvalumab as Maintenance Therapy for Extensive-Stage Small Cell Lung Cancer

NCT07339059Registry updated 2026-04-23·Phase 2
Recruiting

Primary endpoint: Disease Control

Interventionalopen35 targetStarted 2026-06Completion 2029-121 site · United StatesBindu R Potugari

A Single-Arm, Phase II Prospective Study Of Lucanoximab Combined With Tagolimab As Neoadjuvant Therapy For Resectable Head And Neck Squamous Cell Carcinoma

NCT07492914Registry updated 2026-05-13·Phase 2
Recruiting

Primary endpoint: Major Pathological Response Rate (MPR)

Interventionalopen30 targetStarted 2026-05Completion 2031-031 site · ChinaWest China Hospital

Phase Ib Randomized Open-label Trial of Sacituzumab Govitecan Plus Nivolumab or Sacituzumab Govitecan Plus Nivolumab and Relatlimab as Second-line Therapy for Patients With Metastatic Triple Negative Breast Cancer

NCT06963905Registry updated 2026-05-22·Phase 1/Phase 2
Recruiting

Primary endpoint: Incidence and severity of dose limiting toxicities in patients treated with sacituzumab govitecan combinations

InterventionalRandomizedopen60 targetStarted 2025-12Completion 2030-121 site · United StatesYale University

Phase I/II Study of Naxitamab and Sacituzumab Govitecan in Patients With Metastatic Triple-negative Breast Cancer (TNBC)

NCT07011654Registry updated 2026-05-20·Phase 1/Phase 2
Recruiting

Primary endpoint: Safety and Adverse Events (AEs)

Interventionalopen31 targetStarted 2025-09Completion 2030-071 site · United StatesM.D. Anderson Cancer Center

A Phase II Study of Sacituzumab Govitecan in Combination With Cetuximab in Patients With Recurrent Metastatic HNSCC That Has Progressed After First-Line Therapy

NCT07063212Registry updated 2026-02-19·Phase 2
Recruiting

Primary endpoint: Objective Response Rate

Interventionalopen40 targetStarted 2025-07Completion 2028-017 sites · United StatesMemorial Sloan Kettering Cancer Center

A Global, Multicenter, Randomized, Open-label, Phase 3 Study of Sacituzumab Govitecan Versus Standard of Care (SOC) in Participants With Previously Treated Extensive Stage Small Cell Lung Cancer (ES-SCLC)

NCT06801834Registry updated 2026-08-12·Phase 3·GILD
Recruiting

Primary endpoint: Overall Survival (OS)

InterventionalRandomizedopen695 targetStarted 2025-04Completion 2029-1050 sites · Argentina, Australia, Belgium, Brazil…Gilead Sciences

NeoAdjuvant Dynamic Marker - Adjusted Personalized Therapy Comparing Sacituzumab Govitecan Versus Sacituzumab Govitecan+Pembrolizumab in Low-risk, Triple-negative Early Breast Cancer (ADAPT-TN-III)

NCT06081244Registry updated 2026-08-03·Phase 3
Recruiting

Primary endpoint: pathological complete remission (pCR)

InterventionalRandomizedopen348 targetStarted 2024-10Completion 2029-0943 sites · GermanyWomen's Cancer Study Group GmbH

A Multicenter, Open Label, Two Cohort, Single Arm, Phase II Study to Evaluate the Efficacy and Safety of the Anti-TROP2 Antibody-drug Conjugate Sacituzumab Govitecan in Patients With Advanced Differentiated and Anaplastic Thyroid Neoplasms.

NCT06235216Registry updated 2026-09-16·Phase 2
Recruiting

Primary endpoint: Objective response rate (ORR)

Interventionalopen42 targetStarted 2024-09Completion 2027-1211 sites · SpainGrupo Espanol de Tumores Neuroendocrinos

A Phase II Study of Sacituzumab Govitecan for Advanced Esophageal Squamous Cell Carcinoma Patients

NCT06329869Registry updated 2026-09-21·Phase 2
Recruiting

Primary endpoint: Overall objective response rates (ORR)

Interventionalopen35 targetStarted 2024-08Completion 2027-111 site · TaiwanNational Taiwan University Hospital

Frequently asked questions

Which companies have sourced relationships with sacituzumab govitecan?

sacituzumab govitecan has dated SEC/FDA relationship records for IMMUNOMEDICS INC.

How many clinical trials involve sacituzumab govitecan?

BioSniper tracks 29 clinical trials involving sacituzumab govitecan.