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A Phase I/IIa, Open-label, Multicenter Study of the Safety and Efficacy of CHO-H01 As a Single Agent/Combined with Lenalidomide to Subjects with Refractory or Relapsed Non-Hodgkin's Lymphoma

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Trial Profile

A Phase I/IIa, Open-label, Multicenter Study of the Safety and Efficacy of CHO-H01 As a Single Agent/Combined with Lenalidomide to Subjects with Refractory or Relapsed Non-Hodgkin's Lymphoma

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 21 Mar 2025

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At a glance

  • Drugs CHO H01 (Primary) ; Lenalidomide (Primary)
  • Indications Chronic lymphocytic leukaemia; Diffuse large B cell lymphoma; Follicular lymphoma; Mantle-cell lymphoma; Marginal zone B-cell lymphoma; Non-Hodgkin's lymphoma
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors CHO Pharma

Most Recent Events

  • 18 Mar 2025 Planned End Date changed from 1 Jun 2026 to 23 Dec 2026.
  • 18 Mar 2025 Planned primary completion date changed from 1 Dec 2025 to 23 Dec 2026.
  • 24 Jul 2024 Planned number of patients changed from 11 to 37.

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