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Clinical Trials/NCT04671420
NCT04671420
Withdrawn
Phase 3

A Phase 3 Multi-Centre, Randomised, Double-Blind, Parallel-Arm Study to Evaluate the Efficacy and Safety of HLX01 Versus Rituximab (Mabthera®) as First Line Treatment in Patients With Low Tumour Burden Follicular Lymphoma.

Shanghai Henlius Biotech0 sitesOctober 2020

Overview

Phase
Phase 3
Intervention
HLX01
Conditions
CD20-positive Follicular Lymphoma, With Low Tumour Burden
Sponsor
Shanghai Henlius Biotech
Primary Endpoint
Overall Response Rate
Status
Withdrawn
Last Updated
5 years ago

Overview

Brief Summary

The study is a Phase 3 multi-centre, randomised, double-blind, parallel-arm study to evaluate the efficacy and safety of HLX01 versus European Union (EU)-sourced Mabthera® as first line treatment in patients with low tumour burden FL.

The study will consist of a Screening Period (up to 42 days), Treatment Period (Week 1 to Week 44/Month 11), and End of Study (EOS; Month 12 Visit). Approximately 212 patients (106 in each treatment group) will be enrolled.

Utilising a 1-sided 97.5% CI for the risk difference, a reference proportion of 83.2% for Mabthera®, delta for non-inferiority of -17%, and assuming a true difference of 1%, a sample size of 106 patients per arm (212 total) provides approximately 85% power to show non-inferiority of HLX01 to Mabthera® on a primary endpoint of risk difference in ORR up to Week 28. No dropout is included, as all patients will either have data provided for ORR (based on best response), or will be classed as non-responder.

Registry
clinicaltrials.gov
Start Date
October 2020
End Date
October 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shanghai Henlius Biotech
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Voluntary written informed consent before any study-related activities
  • ≥ 18 years of age
  • Histologically-confirmed, stage II to IV NHL (CD20+ FL of grades 1, 2, or 3a) by World Health Organization classification of lymphoid neoplasms (2016 revision) \[11\]
  • Low tumour burden according to the GELF criteria
  • The Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  • Availability of tumour sample within 12 months before start of study drug treatment
  • At least 1 bi-dimensionally measurable nodal lesion \>1.5 cm or extranodal lesion \>1 cm in its longest diameter by CT scan as defined by the Modified Lugano Response Classification 2014
  • Adequate organ function

Exclusion Criteria

  • Prior treatment for FL. Patients previously treated with radiotherapy for stage I FL may be eligible provided they have a measurable lesion located outside the radiation field
  • Transformation to high-grade lymphoma
  • Patients with advanced disease that are considered for treatment with combined chemo immunotherapy
  • Presence or history of central nervous system (CNS) lymphoma involvement
  • Treatment with an investigational agent within 28 days of the first dose of study drug infusion
  • Prior treatment with a chimeric antibody, including HLX01 and Mabthera®
  • History of another malignancy within 2 years of screening, with the exception of curatively treated non-melanoma skin cancer, carcinoma in situ of the uterine cervix, breast or bladder, localised prostate cancer stage T1c or less - and provided that the patient remains relapse free
  • Major surgery within 28 days of the first dose of study drug infusion (excluding lymph node biopsy)
  • Known human immunodeficiency virus (HIV) infection (Serological test for HIV should be performed at screen unless prohibited by local regulations)
  • Active and/or severe infections, including any ongoing infection requiring IV anti microbial treatment

Arms & Interventions

HLX01

Intervention: HLX01

EU-sourced rituximab (Mabthera®)

Intervention: Mabthera®

Outcomes

Primary Outcomes

Overall Response Rate

Time Frame: rom the first dose of study drug through Week 28

Overall Response Rate up to Week 28, defined as the proportion of patients achieving either complete response (CR) or PR as best response from the first dose of study drug through Week 28 as assessed by a blinded independent review committee according to the Modified Lugano Response Classification 2014.

Secondary Outcomes

  • AEs(up to 12 months)
  • Time-to-progression of disease (TTPD)(up to 12 months)
  • SAEs(up to 12 months)
  • Immunogenicity(up to 12 months)
  • PFS(up to 12 months)
  • Cmax(up to 12 months)
  • Ctrough(up to 12 months)

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