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Study details
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ACE1831 Trial

Acepodia Biotech, Inc.
NCT IDNCT05653271ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

42

Study length

about 4.7 years

Ages

18+

Locations

5 sites in FL, GA, IN +2

About this study

Researchers are testing a new treatment called ACE1831 for people with relapsed or refractory CD20-expressing B-cell malignancies. The trial will evaluate the safety, tolerability, and effectiveness of ACE1831 in adults.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take ACE1831
  • 2.Take Cyclophosphamide
  • 3.Take Fludarabine
  • +1 more
PhasePhase 1
DrugCyclophosphamide
Routeinfusion
Primary goalChange from baseline clinical laboratory tests results

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low11%
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

cyclophosphamide (Alkylating chemotherapy; crosslinks DNA strands), fludarabine, obinutuzumab

Drug routes

infusion, injection, intravenous

Endpoints

Primary: Change from baseline clinical laboratory tests results, Change from baseline in ECOG status, Change from baseline in electrocardiogram (ECG) results, Change from baseline in physical examination results, Change from baseline in urinalysis results, Change from baseline in vital signs results, Incidence of adverse events (AEs), Dose Limiting Toxicities (DLTs), adverse events of special interest (AESIs), and serious adverse events (SAEs), Maximum Tolerated Dose (MTD)

Secondary: Objective Response Rate (ORR)

Body systems

Oncology