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Terminated Phase 2 Interventional Results available

A Study of AL101 Monotherapy in Patients With Notch Activated Triple Negative Breast Cancer

ClinicalTrials.gov ID: NCT04461600

Public ClinicalTrials.gov record NCT04461600. 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 Sep 11, 2026, 4:47 PM EDT

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

Official title

A Phase 2, Multi-center, Open-label, Single Arm Study of AL101 Monotherapy in Patients With Notch Activated Triple Negative Breast Cancer

Brief summary

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

The current study is designed to evaluate the efficacy and safety of AL101 monotherapy in subjects with Notch-activated recurrent or metastatic TNBC; Notch activation will be determined by a Next Generation Sequencing (NGS) test.

Study identification

NCT ID
NCT04461600
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ayala Pharmaceuticals, Inc,
Industry
Enrollment
18 participants

Conditions and interventions

Interventions

Drug

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
Aug 13, 2020
Primary completion
Mar 22, 2022
Completion
Oct 10, 2022
Last update posted
Feb 11, 2024

2020 – 2022

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Banner MD Anderson Cancer Center Gilbert Arizona 85234
Mayo Clinic Phoenix Arizona 85054
University of California at San Francisco San Francisco California 94158
University of Colorado Aurora Colorado 80045
Mayo Clinic Jacksonville Florida 32224
Comprehensive Hematology Oncology St. Petersburg Florida 33709
H. Lee Moffitt Cancer Center Tampa Florida 33612
The University of Chicago Chicago Illinois 60637
Carle Clinic Urbana Illinois 61801
University of Louisville- James Brown Cancer Center Louisville Kentucky 40202
Maryland Oncology Hematology Columbia Maryland 20144
University of Michigan Ann Arbor Michigan 48109
Mayo Clinic Rochester Minnesota 55905
Central Cancer Care Bolivar Missouri 63613
Memorial Sloan Kettering Cancer Center (MSKCC) New York New York 10065
University Health Cleveland Medical Center Cleveland Ohio 44106
Charleston Oncology Charleston South Carolina 29414

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04461600, 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 Feb 11, 2024 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04461600 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →