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Active, not recruiting Phase 2 Interventional Results available

TRADE: Dose Escalation Tolerability of Abemaciclib in HR+ HER2- Early Stage Breast Cancer

ClinicalTrials.gov ID: NCT06001762

Public ClinicalTrials.gov record NCT06001762. 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 Oct 29, 2026, 6:12 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

The TRADE Study: A Phase 2 Trial to Assess the ToleRability of Abemaciclib Dose Escalation in Patients With Early-Stage HR-positive and HER2-negative Breast Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

In this research study, investigators are testing if a dose-increasing strategy for abemaciclib will have less side effects and be better tolerated than the standard dosage of abemaciclib for participants with early-stage high-risk hormone receptor positive breast cancer. The names of the study drugs involved in this study are: * Abemaciclib (CDK4 and CDK6 inhibitor) * Tamoxifen (Selective estrogen receptor modulator) * Anastrozole/Letrozole (Non-steroidal aromatase inhibitors) * Exemestane (steroidal aromatase inhibitor) * LHRH (Gonadotropin-releasing hormone agonist, or Luteinizing hormone-releasing hormone agonist)

Study identification

NCT ID
NCT06001762
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
90 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Oct 5, 2023 (Actual)
Primary completion
Jan 22, 2025 (Actual)
Completion
Jan 1, 2027 (Estimated)
Last update posted
Jul 2, 2026

2023 – 2027

United States locations

U.S. sites
12
U.S. states
4
U.S. cities
10
Facility City State ZIP Site status
Stamford Hospital Stamford Connecticut 06904 —
Eastern Maine Medical Center (Northern Light) Brewer Maine 04412 —
New England Cancer Specialists Scarborough Maine 04074 —
Boston Medical Center Boston Massachusetts 02118 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Dana-Farber Cancer Institute at Steward St. Elizabeth's Brighton Massachusetts 02135 —
Dana-Farber Cancer Institute at Foxborough Foxborough Massachusetts 02035 —
Dana-Farber Cancer Institute at Merrimack Valley Methuen Massachusetts 01844 —
Dana-Farber Cancer Institute at Milford Milford Massachusetts 01757 —
Dana-Farber Cancer Institute at South Shore South Weymouth Massachusetts 02190 —
Dana-Farber Cancer Insitute at Londonderry Hospital Londonderry New Hampshire 03053 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06001762, 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 Jul 2, 2026 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06001762 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →