Skip to content
Study details
Enrolling now

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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take ACE1831
  • 2.Take Cyclophosphamide
  • 3.Take Fludarabine
  • +1 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

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.

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