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Clinical Trials in the EU / 2024-519444-33-00
Completed Phase III

A Phase 3, Multicenter, Randomized, Open-label Trial of Trastuzumab Deruxtecan Versus Standard of Care Chemotherapy With or Without Radiotherapy as Adjuvant Treatment for HER2-Expressing (IHC 3+/2+) Endometrial Cancer (DESTINY-Endometrial02/ GOG-3122/ ENGOT-en30/GINECO)

2024-519444-33-00 · tracked via the Priya Life Science EU tracker
Sponsor
Daiichi Sankyo Inc.
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
11/12/2025
Enrollment target
200
Sites
Germany, Poland, France, Greece, Spain, Portugal, Italy

Condition studied

HER2-expressing endometrial cancer (IHC 3+/2+)

Investigational medicinal product(s)

Cisplatin Hikma 1 mg/ml Konzentrat zur Herstellung einer InfusionslösungCarboplatin Hikma 10 mg/ml Konzentrat zur Herstellung einer InfusionslösungPaclitaxel Ribosepharm 6 mg/ml Konzentrat zur Herstellung einer InfusionslösungDocetaxel AqVida 20 mg/ml Konzentrat zur Herstellung einer InfusionslösungDS-8201a

Eligibility

Age group
65+ years, 18-64 years
Sex
Female

Primary endpoint

DFS is defined as time interval from the date of randomization to the first documented local-regional recurrence, distant metastasis, or death due to any cause, whichever occurs first. DFS will be assessed radiographically by BICR or by histopathologic confirmation of disease recurrence per local assessment.

Endpoint detail

OS is defined as the time interval from the date of randomization to the date of death due to any cause., DFS is defined as the time from randomization to the first documented local-regional recurrence, distant metastasis or death due to any cause, whichever occurs first. DFS will be assessed radiographically by investigator or by histopathologic confirmation of disease recurrence per local assessment., Distant metastatic recurrence is defined as recurrence outside of vagina, pelvis, or pelvic lymph nodes., Local recurrence is defined as recurrence in the vagina as assessed radiologically by BICR or by histopathologic confirmation of disease recurrence per local assessment, Regional recurrence is defined as recurrence in the pelvis or pelvic lymph nodes as assessed radiologically by BICR or by histopathologic confirmation of disease recurrence per local assessment, Incidence of TEAEs, SAEs, TEAEs associated with dose modifications, AESIs, TEAEs with death outcome, and changes from baseline in vital signs, clinical laboratory results, ECGs, ECHO/MUGA, and ophthalmologic assessments, Change from baseline and time to deterioration for the following PRO questionnaire: EORTC QLQ-C30 GHS/overall QoL, physical, Change from baseline and time to deterioration for the following PRO questionnaires: EORTC QLQ-EN24: Back and pelvic pain (ENBP), tingling/numbness (ENTN), muscular pain (ENM), Serum concentrations of T-DXd, total anti-HER2 antibody and DXd., ADA incidence: The proportion of participants having treatment-emergent ADA. Titer and nAb may be determined when ADA is positive.

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2024-519444-33-00 on CTIS ↗ ← All trials in the EU