Skip to content
Study details
Enrolling now

A Phase 2 Study of PCS6422 With Capecitabine in Patients With Advanced or Metastatic Breast Cancer

Processa Pharmaceuticals
NCT IDNCT06568692ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

90

Study length

about 2.1 years

Ages

18+

Locations

13 sites in AZ, CA, FL +7

About this study

This trial is testing a treatment called PCS6422 with capecitabine (Cap) compared to standard dose of Cap alone for people with advanced or metastatic breast cancer. The goal is to see if PCS6422 + Cap is an effective and safe treatment option for those who can't have anthracycline- or taxane-containing therapies, or other available therapies like PD-1 or PARP inhibitors.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Capecitabine
  • 2.Take PCS6422 and capecitabine
PhasePhase 2
Drugcapecitabine
Routeoral
Primary goalEvaluation of Objective Response Rate (ORR)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low14%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

capecitabine

Drug routes

oral (Oral Tablet)

Endpoints

Primary: Evaluation of Objective Response Rate (ORR), Number of patients with adverse events (AEs)

Secondary: Evaluation of Disease Control Rate (DCR), Evaluation of Duration of Response (DOR), Evaluation of Progression Free Survival (PFS)

Body systems

Oncology