Clinical trials

2

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Condition / disease
Location
Status: Not yet recruiting

TROPION Breast Respond in 1L TNBC

There are no real-world data available on the effectiveness and safety of Dato-DXd in adult patients with unresectable or metastatic triple-negative breast cancer who are not candidates for PD-1/PD-L1 inhibitor therapy. This NIS will investigate the effectiveness of Dato-DXd, the demographic and clinical characteristics of the patients, and treatment patterns.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo CompanyUpdated: Oct 9, 2026
Eligibility criteria

Age ≥18 years at the time of screening [+7]

Pregnancy or breastfeeding [+1]

Status: Recruiting

DESTINY Breast Respond HER2-(Ultra)Low Europe

Trastuzumab deruxtecan (T-DXd) as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic HER2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy. Based on the extended therapeutic indication of Trastuzumab deruxtecan (Enhertu®), a new patient population will be enrolled, comprising adult patients with unresectable or metastatic HR-positive, HER2-low, or HER2-(ultra)low breast cancer who have received at least one endocrine therapy in the metastatic setting and are not considered suitable for endocrine therapy as the next line of treatment.

Participants needed: 2,295
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo CompanyUpdated: Aug 19, 2026Locations: 216
Eligibility criteria

Adult patient (age ≥ 18 years) with histological or cytological confirmed diagno... [+9]

Pregnancy or breastfeeding [+1]