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Study details
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DESTINY-Endometrial01 Trial

AstraZeneca
NCT IDNCT06989112ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

600

Study length

about 5.9 years

Ages

18+

Sex

Female only

Locations

58 sites in AR, AZ, CA +28

What this study is about

Researchers are testing whether Trastuzumab Deruxtecan plus Rilvegostomig or Pembrolizumab, as a treatment, is more effective than chemotherapy (carboplatin + paclitaxel) plus Pembrolizumab for women with HER2-positive endometrial cancer. The trial will measure how long the treatment keeps the cancer from progressing.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Carboplatin
  • 2.Take Docetaxel
  • 3.Take Paclitaxel
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

carboplatin, docetaxel, paclitaxel (Taxane chemotherapy; stabilizes microtubules), pembrolizumab (Immune checkpoint inhibitor; blocks PD-1 to boost T-cell attack on cancer), trastuzumab deruxtecan

Drug routes

infusion, injection, intravenous

Endpoints

Primary: Progression-free survival (PFS), as assessed by BICR

Secondary: Duration of response (DoR), as assessed by BICR and investigator, Objective response rate (ORR), as assessed by BICR and investigator, Overall Survival (OS), Overall survival (OS) according to HER2 expression to determine the clinical utility of a HER2 diagnostic test, Overall survival (OS) according to MMR status to determine the clinical utility of a MMR diagnostic test, Patient-reported tolerability, Pharmacokinetics of T-DXd, total anti-HER2 antibody, DXd and rilvegostomig, Progression Free Survival (PFS) as assessed by the investigator

Body systems

Oncology