Drugs / ARC-02
last change Jun 2026 re-read 9 days ago

ARC-02

Developed for
B-cell non-Hodgkin lymphoma
Investigated by
Taiho Oncology, Inc.

Trials 1

202720282029
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07691606 Jun 2026 → Jan 2029 expected B-cell non-Hodgkin lymphoma Taiho Oncology, Inc. Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2026-04-28 Taiho Oncology, Inc. Regulatory Taiho Oncology, Taiho Pharmaceutical and Araris Biotech AG Advance ADC ARC-02 into Phase 1 Clinical Development taiho.co.jp ↗
the U.S. Food and Drug Administration (FDA) has completed its Investigational New Drug (IND) review period for ARC-02
2026-04-27 Taiho Oncology, Inc. Regulatory Taiho Oncology, Taiho Pharmaceutical and Araris Biotech AG Advance ADC ARC-02 into Phase 1 Clinical Development taihooncology.com ↗
Taiho Oncology, Inc., Taiho Pharmaceutical Co., Ltd., and Araris Biotech AG (“Araris”) today announced that the U.S. Food and Drug Administration (FDA) has completed its Investigational New Drug (IND) review period for ARC-02, an antibody-drug conjugate (ADC) being developed for the treatment of non-Hodgkin lymphoma, enabling Taiho Oncology to initiate a Phase 1 dose-escalation clinical trial of ARC-02.

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as ARC-02 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07691606 ↗
Route Intravenous “Intravenous (IV) infusion.” NCT07691606 ↗