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ab-101

·Code: AB-101

ab-101: developed by 1 company · 4 clinical trials tracked.

ab-101 evidence translation

What we can confirm

What it means

Source-backed records connect ab-101 to ABUS; that link alone does not prove the drug works.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

How could ab-101 → ABUS affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors
Development Pipeline (1)
Clinical Trials (4)

A Phase 1 Study to Evaluate the Efficacy and Safety of AB-101, an Allogeneic Cord Blood- Derived NK-Cell Therapy in Combination With B-Cell Depleting mAb in Patients Who Failed Treatment for Class III or IV Lupus Nephritis or Other Forms of Refractory Systemic Lupus Erythematosus

NCT06265220·Phase 1·ARTV
Active, not recruiting

Primary endpoint: Incidence of Treatment-Emergent Adverse Events and Serious Adverse Events

Interventionalopen51 targetStarted 2024-04Completion 2027-089 sites · United StatesArtiva Biotherapeutics, Inc.

A Phase 2, Open-Label, Multi-Center Study of Innate Cell Engager AFM13 in Combination With Allogeneic Natural Killer Cells (AB-101) in Subjects With Recurrent or Refractory Hodgkin Lymphoma and CD-30 Positive Peripheral T-Cell Lymphoma

NCT05883449·Phase 2
Terminated

Primary endpoint: Objective Response Rate (ORR) by Independent Radiology Committee

InterventionalRandomizedopen25 targetStarted 2023-10Completion 2025-0615 sites · United StatesAffimed GmbH

A Double-Blind, Randomized, Placebo-Controlled, Single and Multiple Dose Study Evaluating the Safety, Tolerability, PK and PD of AB-101, an Oral PD-L1 Inhibitor, in Healthy Subjects and Subjects With Chronic HBV Infection.

NCT05960240·Phase 1·ABUS
Completed

Primary endpoint: Parts 1 and 2: Incidence of adverse events (AEs), serious AEs (SAEs), immune related AEs (irAEs) and discontinuations due to AEs and irAEs.

InterventionalRandomizedsingle128 enrolledStarted 2023-08Completion 2026-0210 sites · Hong Kong, Italy, Moldova, New Zealand…Arbutus Biopharma Corporation

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.

NCT04673617·Phase 1/Phase 2·ARTV
Completed

Primary endpoint: Phase 1: Safety and tolerability of AB-101 as monotherapy, and in combination with rituximab (including the DLBCL specific cohort) and in combination with bendamustine and rituximab.

Interventionalopen45 enrolledStarted 2021-03Completion 2025-1021 sites · United StatesArtiva Biotherapeutics, Inc.

Frequently asked questions

Who is developing ab-101?

ab-101 is being developed by Arbutus Biopharma Corp.

How many clinical trials involve ab-101?

BioSniper tracks 4 clinical trials involving ab-101.