Clinical trials

2

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Condition / disease
Location
Status: Recruiting

NeoAdj. Therapy Comparing Sacituzumab Govitecan (SG) vs. SG+Pembrolizumab in Low-risk, Triple-neg. EBC (ADAPT-TN-III)

TNBC is known for poor prognosis, aggressive patterns of disease, and significant molecular heterogeneity. (Neo)adjuvant chemotherapy (NACT) is standard of care in all node-positive and in node-negative patients with a tumour size \>5 mm according to current National Comprehensive Cancer Network (NCCN) guidelines. However, TNBC patients with lower stage disease do clearly have a better prognosis compared to more advanced stages. Patients with stage I-II node-negative disease have 3-5 year iDFS rates of 80-90% (with majority of relapses within the first three years) as shown in several trials.Although survival results appear much better in the lower vs. higher stages, there is a high clinical need in this most common group of TNBC patients in Western Europe and USA.

Participants needed: 348
Trial details
Phase: Phase 3Age: 18+Biological sex: FemaleType: InterventionalSponsor: West German Study GroupUpdated: Aug 3, 2026Locations: 43
Eligibility criteria

ER + PR negative or low positive (≤10% positive cells in IHC), and HER2 negative... [+25]

Known hypersensitivity reaction to the compounds or incorporated substances of t... [+18]

Status: Recruiting

NeoAdjuvant Therapy With Trastuzumab-deruxtecan Versus Chemotherapy+Trastuzumab+Pertuzumab in HER2+ Early Breast Cancer

ADAPT-HER2-IV will address question of optimal neoadjuvant therapy in patients with less advanced -HER2+ EBC. ADAPT-HER2-IV is planned as a superiority trial to demonstrate higher pCR rates in both clinically relevant subgroups of low-intermediate risk HER2+ EBC. Moreover, it aims to demonstrate excellent survival in patients treated by T-DXd (with the use of standard chemotherapy at investigator´s decision restricted only to patients with substantial residual tumour burden after T-DXd-treatment).

Participants needed: 702
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: West German Study GroupUpdated: Jun 9, 2026Locations: 44
Eligibility criteria

absolute neutrophil count ≥ 1.5 × 109/L, [+11]

1. Non-operable breast cancer including inflammatory breast cancer [+25]