Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 1Phase 2 Interventional

AB-101 as Monotherapy and With Immunotherapy in Patients With Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT04673617

Public ClinicalTrials.gov record NCT04673617. 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 May 5, 2026, 6:33 AM 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 Multi-Center, Open-Label, Phase 1/2 Clinical Trial to Evaluate the Safety and Anti-Tumor Activity of AB-101 Monotherapy and AB-101 With Immunotherapy in Patients With Relapsed/Refractory Non-Hodgkin Lymphoma of B-Cell Origin.

Study identification

NCT ID
NCT04673617
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Artiva Biotherapeutics, Inc.
Industry
Enrollment
45 participants

Conditions and interventions

Interventions

  • AB-101 Drug
  • Bendamustine Drug
  • Cyclophosphamide Drug
  • Fludarabine Drug
  • Interleukin-2 Drug
  • Rituximab Drug

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
Mar 28, 2021
Primary completion
Oct 5, 2025
Completion
Oct 5, 2025
Last update posted
Apr 2, 2026

2021 – 2025

United States locations

U.S. sites
21
U.S. states
18
U.S. cities
20
Facility City State ZIP Site status
Artiva Clinical Trial Site Birmingham Alabama 35249
Artiva Clinical Trial Site Tucson Arizona 85719
Artiva Clinical Trial Site Orange California 92868
Artiva Clinical Trial Site San Diego California 92093
Artiva Clinical Trial Site Gainesville Florida 32608
Artiva Clinical Trial Site Atlanta Georgia 30342
Artiva Clinical Trial Site Chicago Illinois 60612
Artiva Clinical Trial Site Iowa City Iowa 52242
Artiva Clinical Trial Site Wichita Kansas 67214
Artiva Clinical Trial Site Louisville Kentucky 40241
Artiva Clinical Trial Site Detroit Michigan 48201
Artiva Clinical Trial Site Lake Success New York 11042
Artiva Clinical Trial Site New York New York 11021
Artiva Clinical Trial Site Columbus Ohio 43214
Artiva Clinical Trial Site Portland Oregon 97239
Artiva Clinical Trial Site Philadelphia Pennsylvania 19107
Artiva Clinical Trial Site Philadelphia Pennsylvania 19111
Artiva Clinical Trial Site Providence Rhode Island 02903
Artiva Clinical Trial Site Dallas Texas 75246
Artiva Clinical Trial Site Salt Lake City Utah 84112
Artiva Clinical Trial Site Richmond Virginia 23298

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04673617, 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 Apr 2, 2026 · Synced May 5, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04673617 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →