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sacituzumab govitecan

Generic: sacituzumab·Code: IMMU-132

sacituzumab govitecan: developed by 1 company · 25 clinical trials tracked.

sacituzumab govitecan evidence translation

What we can confirm

25 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 · 6 study sponsors
Development Pipeline (1)
CompanyPhase
IMMUNOMEDICS INC (IMMU)
metastatic triple-negative breast cancer (mTNBC)
Phase 3
Clinical Trials (25)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

NCT07178730·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

NCT07339059·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

NCT07492914·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

NCT06963905·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)

NCT07011654·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

NCT07063212·Phase 2·FATE
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)

NCT06801834·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)

NCT06081244·Phase 3
Recruiting

Primary endpoint: pathological complete remission (pCR)

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

SERIES: SEquencing Sacituzumab Govitecan AfteR T-DXd In ER+/HER2 LOW/ULTRA LOW MetaStatic Breast Cancer

NCT06263543·Phase 2
Recruiting

Primary endpoint: Overall response rate (ORR)

Interventionalopen75 targetStarted 2024-06Completion 2028-123 sites · United StatesReshma L. Mahtani, D.O.

Adaptive RADiation Therapy With Concurrent Sacituzumab Govitecan (SG) for Bladder Preservation in Patients With MIBC (RAD-SG).

NCT05833867·Phase 1
Recruiting

Primary endpoint: Rate of acute-dose limiting toxicities

Interventionalopen20 targetStarted 2024-04Completion 2027-101 site · United StatesShilpa Gupta, MD

Frequently asked questions

Who is developing sacituzumab govitecan?

sacituzumab govitecan is being developed by IMMUNOMEDICS INC.

How many clinical trials involve sacituzumab govitecan?

BioSniper tracks 25 clinical trials involving sacituzumab govitecan.