TROP2 ADC · ADC
sacituzumab govitecan
8 active trials across 4 of our biomarkers, targeting TROP2. Not approved for any biomarker on marked.bio yet.
Also known as IMMU-132, Trodelvy.
Counts only trials that select patients by one of the biomarkers on marked.bio, not every trial of this drug.
Biomarkers
| Biomarker | Active trials | All trials | Furthest active phase |
|---|---|---|---|
| HER2-low / ultralow (IHC 1+ or 2+/ISH-) | 5 | 6 | Phase 3 |
| BRCA1/2 mutation | 3 | 5 | Phase 2 |
| HER2 (ERBB2) activating mutation | 1 | 1 | Phase 2 |
| MSI-H / dMMR | 0 | 1 | – |
Sponsors
Industry sponsors leading active biomarker-selected trials of sacituzumab govitecan.
- Gilead Sciences 2
Trials
8 of 12 trials shown
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Study of Sacituzumab Govitecan Versus Treatment of Physician's Choice in Patients With Hormone Receptor-positive/Human Epidermal Growth Factor Receptor 2 Negative (HR+/HER2-) Metastatic Breast Cancer Who Have Received Endocrine Therapy
sacituzumab govitecanpaclitaxelnab-paclitaxelcapecitabine
…or-Positive (HR+)/Human Epidermal Growth Factor Receptor 2 Negative (HER2-) (HER2 IHC0 or HER2-low [IHC 1+, IHC 2+/ISH-]) Inoperable, Locally Advanced, or Metastatic Breast Cancer and Have…
HER2-low / ultralow (IHC 1+ or 2+/ISH-)Locally Advanced or Unresectable Metastatic Breast Cancer, Stage IV Breast Cancer
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Sacituzumab Govitecan With Bevacizumab Compared to Usual Chemotherapy (Carboplatin, Pegylated Liposomal Doxorubicin and Bevacizumab) for Treating Recurrent Platinum-Sensitive Ovarian Cancer After PARP Inhibitor Maintenance Therapy
Anti-VEGF Monoclonal Antibodybevacizumab FDA EUcarboplatingemcitabinepegylated liposomal doxorubicindoxorubicinsacituzumab govitecan
Disease must be germline or somatic BRCA1 or BRCA2 mutated or homologous recombination deficiency test positive
BRCA1/2 mutationRecurrent Platinum-Sensitive Fallopian Tube Endometrioid Adenocarcinoma, Recurrent Platinum-Sensitive Fallopian Tube High Grade Serous Adenocarcinoma, Recurrent Platinum-Sensitive Ovarian High Grade Endometrioid Adenocarcinoma, Recurrent Platinum-Sensitive Ovarian High Grade Serous Adenocarcinoma
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Testing Two Different Drugs (Sacituzumab-govitecan and Trastuzumab-deruxtecan) Combinations Prescribed in an Alterning Pattern to Patients With Metastatic or Locally Advanced Triple-negative Breast Cancer
sacituzumab govitecantrastuzumab deruxtecan FDA EU
HER2-low breast cancer, defined as either immunohistochemistry (IHC) 2+ / in situ hybridization (I…
HER2-low / ultralow (IHC 1+ or 2+/ISH-)Triple Negative Breast Neoplasms, Neoplasm Metastasis, HER 2 Low-expressing Breast Cancer
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Sequencing SG vs. T-DXd in HER2-Low/TROP2-High Metastatic Breast Cancer
sacituzumab govitecantrastuzumab deruxtecan FDA EU
…etastatic breast cancer that is:HER2 IHC 1+ triple-negative breast cancer, or HR-positive/HER2-ultralow or HER2 IHC 1+ breast cancer.
HER2-low / ultralow (IHC 1+ or 2+/ISH-)Metastatic Breast Cancer
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Genomic and Transcriptomic Predictors of Sequential SG Sensitivity After T-DXd in ER+/HER2-Low Metastatic Breast Cancer
Genomic and Transcriptomic Predictors of Sequential SG Sensitivity After T-DXd in ER+/HER2-Low Metastatic Breast Cancer
HER2-low / ultralow (IHC 1+ or 2+/ISH-)Breast Cancer
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Sequencing Antibody Drug Conjugates in ER+/HER2 LOW/ULTRA LOW MBC
Histologically confirmed metastatic or advanced and unresectable breast cancer that is HER2 LOW/ULTRA LOW by local testing on either the primary or any metastatic site.
HER2-low / ultralow (IHC 1+ or 2+/ISH-)Breast Cancer, Metastatic Breast Cancer, Advanced Breast Cancer, Hormone-receptor-positive Breast Cancer
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Genomics Guided Targeted Post-neoadjuvant Therapy in Patients With Early Breast Cancer (COGNITION-GUIDE)
atezolizumabinavolisibipatasertibolaparibsacituzumab govitecantrastuzumabpertuzumab
Arm 6 (Trastuzumab / Pertuzumab, ERBBB): HER2 exon-20 insertion, Activating HER2-mutation
HER2 (ERBB2) activating mutationBRCA1/2 mutationEarly-stage Breast Cancer
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Study of Sacituzumab Govitecan in Chinese Patients With Metastatic Triple-negative Breast Cancer Who Received at Least Two Prior Treatments
For individuals with a documented germ-line BRCA1/BRCA2 mutation who received an approved PARP inhibitor, the PARP inhibitor can be used to meet the crite…
BRCA1/2 mutationMetastatic Triple-negative Breast Cancer
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Study Evaluating Treatment of Sacituzumab-govitecan for Patients With Metastatic Esophagogastric Adenocarcinoma
NOTE: patients with advanced MSI-h/dMMR tumors who have not previously been treated with pembrolizumab, nivolumab or any oth…
MSI-H / dMMREsophagogastric Adenocarcinoma
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A Phase I/II Study of Sacituzumab Govitecan Plus Berzosertib in Small Cell Lung Cancer, Extra-Pulmonary Small Cell Neuroendocrine Cancer and Homologous Recombination-Deficient Cancers Resistant to PARP Inhibitors
berzosertibsacituzumab govitecan
Presence of pathogenic or likely pathogenic germline mutation/variant in BRCA1, BRCA2, ATM, BRIP1, BARD1, CDK12, CHEK1, CHEK2, FANCL, PALB2, PPP2R2A, RAD51B, RAD51C, R…
BRCA1/2 mutationHRD Cancer, SCLC, Advanced Solid Tumors
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A Study to Evaluate Rucaparib in Combination With Other Anticancer Agents in Participants With a Solid Tumor (SEASTAR)
rucaparib FDALucitanibsacituzumab govitecan
…cancer OR urothelial carcinoma OR ovarian cancer OR have a solid tumor with a deleterious mutation in BRCA1, BRCA2, PALB2, RAD51C or RAD51D
BRCA1/2 mutationOvarian Cancer, Triple-negative Breast Cancer, Urothelial Carcinoma, Solid Tumor
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Study of DF1001 in Patients With Advanced Solid Tumors
DF1001nivolumabnab-paclitaxelsacituzumab govitecan
Breast Cancer (HER2 Low) Expansion Cohort
HER2-low / ultralow (IHC 1+ or 2+/ISH-)Solid Tumor, Adult
No trials match these filters.