ClinicalTrials.gov record
Recruiting Phase 2 Interventional

Study of Patritumab Deruxtecan Plus Pembrolizumab With Other Anticancer Agents in Participants With High-Risk Early-Stage Triple-Negative or Hormone Receptor-Low Positive/HER-2 Negative Breast Cancer (MK-1022-010, HERTHENA-Breast-03)

ClinicalTrials.gov ID: NCT06797635

Public ClinicalTrials.gov record NCT06797635. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 29, 2026, 8:46 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label Randomized Phase 2 Study to Evaluate Safety and Efficacy of Patritumab Deruxtecan Plus Pembrolizumab Administered Either Before or After Carboplatin/Paclitaxel Plus Pembrolizumab Compared With Pembrolizumab in Combination With Chemotherapy Followed by Surgery and Adjuvant Pembrolizumab for High-Risk Early-Stage Triple-Negative or Hormone Receptor-Low Positive/Human Epidermal Growth Factor Receptor-2 Negative Breast Cancer (HERTHENA-Breast03)

Study identification

NCT ID
NCT06797635
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
372 participants

Conditions and interventions

Interventions

  • Capecitabine Drug
  • Carboplatin Drug
  • Cyclophosphamide Drug
  • Doxorubicin hydrochloride Drug
  • Epirubicin hydrochloride Drug
  • Olaparib Drug
  • Paclitaxel Drug
  • Patritumab deruxtecan Biological
  • Pembrolizumab Biological

Drug · Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 19, 2025
Primary completion
Dec 30, 2029
Completion
Dec 30, 2034
Last update posted
Mar 12, 2026

2025 – 2034

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
UCLA Hematology/Oncology - Parkside ( Site 0021) Santa Monica California 90404 Recruiting
Orchard Healthcare Research Inc. ( Site 0006) Skokie Illinois 60077 Recruiting
Intermountain Health St. Vincent Regional Hospital - Cancer Centers of Montana ( Site 0003) Billings Montana 59102 Recruiting
Northwest Cancer Specialists (Compass Oncology) ( Site 8003) Tigard Oregon 97223 Recruiting
SCRI Oncology Partners ( Site 7000) Nashville Tennessee 37203 Recruiting
Texas Oncology - DFW ( Site 8000) Dallas Texas 75246 Recruiting
Houston Methodist Hospital ( Site 0022) Houston Texas 77030 Recruiting
Virginia Oncology Associates (VOA) ( Site 8001) Norfolk Virginia 23502 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06797635, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 12, 2026 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06797635 live on ClinicalTrials.gov.

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