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Study details
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A Study of BTX-A51 in People With Advanced Solid Tumor and Breast Cancer

Edgewood Oncology Inc.
NCT IDNCT04872166ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

112

Study length

about 6 years

Ages

18+

Locations

6 sites in FL, OH, TN +1

What this study is about

Researchers are testing a treatment called BTX-A51 to see if it's safe, how well it works, and what the best dose might be. The trial will involve people with advanced solid tumors or breast cancer. It will happen in three phases: Phase 1a to find the right dose, Phase 1b to see if it works alone, and Phase 1c to test it when combined with another medication.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take BTX-A51

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

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

Endpoints

Primary: Defining the maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D) of BTX-A51alone and in combination with fulvestrant, Incidence of adverse events after BTX-A51 administration alone and in combination with fulvestrant

Secondary: Duration of response (DoR), Half-life of BTX-A51, Objective response rate (ORR), Overall survival (OS), Progression free survival (PFS)

Body systems

Oncology