A Phase I/II Study of Betalutin for Treatment of Relapsed Non-Hodgkin Lymphoma (LYMRIT-37-01)

  • End date
    Sep 11, 2026
  • participants needed
  • sponsor
    Nordic Nanovector
Updated on 24 January 2022
platelet count
hodgkin's disease
measurable disease
gilbert's syndrome
follicular lymphoma
alkylating agent
refractory follicular lymphoma
indolent non-hodgkin lymphoma


This study is a phase I/II open-label study in patients with relapsed indolent NHL (Part A) or relapsed/refractory FL (Part B). Part A of the study assessed the safety and preliminary efficacy. This seamless design study now has four parts: 1) Part A, Ph I - dose escalation, 2) Part A, Ph II - dose expansion, 3) Part B, Ph II randomized - refinement of dose, and 4) Part B, Phase II, single-arm. As of August 7, 2020, patients are enrolling in the fourth part of the study.

Condition Non-Hodgkin Lymphoma, Follicular Lymphoma
Treatment Betalutin
Clinical Study IdentifierNCT01796171
SponsorNordic Nanovector
Last Modified on24 January 2022


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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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