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DS-3201b in Participants With Lymphomas

Active, not recruiting · Phase 1 · NCT02732275

Conditions: Lymphoma, Malignant, Non-hodgkin Lymphoma

At a glance

Research payments reported, 2025
$275,418
U.S. investigators named
8
Sites paid
9
Planned or actual enrollment
100

About the trial

Sponsor
Daiichi Sankyo Co., Ltd. (with Daiichi Sankyo)
Tested
DS-3201b (drug), DS-3201b (drug)
Dates
Started 2016-03-31; completion 2027-12-31
Results posted
Not yet

DS-3201b is an experimental drug that is being investigated in clinical research. Adults with non-Hodgkin lymphoma (NHL) may be able to join this study if their disease has come back after remission or is not responding to current treatment This study has three parts. The Dose Escalation part is designed is to find the safe dose of DS-3201b that adults with advanced NHL can tolerate. The Dose Expansion phase will determine how effective DS-3201b is for rare types of NH and collect additional safety data. Last, the Drug-Drug Interaction (DDI) Cohort (US Only) will evaluate the effect of DS-3201b on the pharmacokinetics (PK) of midazolam and digoxin when co-administered to patients with NHL

From ClinicalTrials.gov, last updated 2026-04-28. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Daiichi Sankyo Inc. reported $275,418 in research payments for this study in 2025 (54 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.