A randomized, multiple-dose, multicenter, comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab (Hetero) and reference medicinal product (Rituximab, Roche) in Indian patients of non-hodgkin's lymphoma (HERILY)

Objective: To compare the antitumor efficacy, safety, and pharmacodynamic (PD) characteristics of Hetero-rituximab (test) with reference medicinal product (rituximab, Roche) in non-Hodgkin's lymphoma. Patients and Methods: One hundred and thirty-five patients with diffuse large B-cell lymphoma...

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Main Authors: Suresh Advani, Ghanashyam Biswas, Shubhadeep Sinha, Neetu Naidu Rayala, Sreenivasa Chary, Pankaj Thakur, Anushrita, Santanu Tripathi, Vamsi Krishna Bandi
Format: Article
Language:English
Published: Thieme Medical and Scientific Publishers Pvt. Ltd. 2018-01-01
Series:Indian Journal of Medical and Paediatric Oncology
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Online Access:http://www.ijmpo.org/article.asp?issn=0971-5851;year=2018;volume=39;issue=3;spage=316;epage=320;aulast=Advani
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author Suresh Advani
Ghanashyam Biswas
Shubhadeep Sinha
Neetu Naidu Rayala
Sreenivasa Chary
Pankaj Thakur
Anushrita
Santanu Tripathi
Vamsi Krishna Bandi
author_facet Suresh Advani
Ghanashyam Biswas
Shubhadeep Sinha
Neetu Naidu Rayala
Sreenivasa Chary
Pankaj Thakur
Anushrita
Santanu Tripathi
Vamsi Krishna Bandi
author_sort Suresh Advani
collection DOAJ
description Objective: To compare the antitumor efficacy, safety, and pharmacodynamic (PD) characteristics of Hetero-rituximab (test) with reference medicinal product (rituximab, Roche) in non-Hodgkin's lymphoma. Patients and Methods: One hundred and thirty-five patients with diffuse large B-cell lymphoma (DLBCL) were randomized to receive intravenous infusion of either test or reference product. Efficacy (best overall response [BOR] rate [primary end point]), safety, PD (CD19), and immunological assessments (secondary end points) were done at the end of cycle 3 and cycle 6. Results: At the end of 6 cycles, BOR rate was 73.47% in Hetero-rituximab test arm compared to the 69.09% in reference arm. Anti-rituximab antibodies were found to be negative at cycle 3 and cycle 6 for all patients. Patients treated with Hetero-rituximab show a significant depletion in CD19+ cell which was comparable with reference drug. Safety and immunogenic potential of the test drug was comparable to the reference drug in the patients of DLBCL. Conclusion: BOR rate at cycle 3, cycle 6, and end of the study lies within the prespecified limit for noninferiority which concludes that test product is therapeutically noninferior to reference medicinal product.
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spelling doaj-art-a688fa2a19704e16a6c2f6d7b4bd66ca2025-08-20T03:03:59ZengThieme Medical and Scientific Publishers Pvt. Ltd.Indian Journal of Medical and Paediatric Oncology0971-58512018-01-0139331632010.4103/ijmpo.ijmpo_25_17A randomized, multiple-dose, multicenter, comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab (Hetero) and reference medicinal product (Rituximab, Roche) in Indian patients of non-hodgkin's lymphoma (HERILY)Suresh AdvaniGhanashyam BiswasShubhadeep SinhaNeetu Naidu RayalaSreenivasa CharyPankaj ThakurAnushritaSantanu TripathiVamsi Krishna BandiObjective: To compare the antitumor efficacy, safety, and pharmacodynamic (PD) characteristics of Hetero-rituximab (test) with reference medicinal product (rituximab, Roche) in non-Hodgkin's lymphoma. Patients and Methods: One hundred and thirty-five patients with diffuse large B-cell lymphoma (DLBCL) were randomized to receive intravenous infusion of either test or reference product. Efficacy (best overall response [BOR] rate [primary end point]), safety, PD (CD19), and immunological assessments (secondary end points) were done at the end of cycle 3 and cycle 6. Results: At the end of 6 cycles, BOR rate was 73.47% in Hetero-rituximab test arm compared to the 69.09% in reference arm. Anti-rituximab antibodies were found to be negative at cycle 3 and cycle 6 for all patients. Patients treated with Hetero-rituximab show a significant depletion in CD19+ cell which was comparable with reference drug. Safety and immunogenic potential of the test drug was comparable to the reference drug in the patients of DLBCL. Conclusion: BOR rate at cycle 3, cycle 6, and end of the study lies within the prespecified limit for noninferiority which concludes that test product is therapeutically noninferior to reference medicinal product.http://www.ijmpo.org/article.asp?issn=0971-5851;year=2018;volume=39;issue=3;spage=316;epage=320;aulast=AdvaniDiffuse large B-cell lymphomanon-Hodgkin's lymphomarituximab
spellingShingle Suresh Advani
Ghanashyam Biswas
Shubhadeep Sinha
Neetu Naidu Rayala
Sreenivasa Chary
Pankaj Thakur
Anushrita
Santanu Tripathi
Vamsi Krishna Bandi
A randomized, multiple-dose, multicenter, comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab (Hetero) and reference medicinal product (Rituximab, Roche) in Indian patients of non-hodgkin's lymphoma (HERILY)
Indian Journal of Medical and Paediatric Oncology
Diffuse large B-cell lymphoma
non-Hodgkin's lymphoma
rituximab
title A randomized, multiple-dose, multicenter, comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab (Hetero) and reference medicinal product (Rituximab, Roche) in Indian patients of non-hodgkin's lymphoma (HERILY)
title_full A randomized, multiple-dose, multicenter, comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab (Hetero) and reference medicinal product (Rituximab, Roche) in Indian patients of non-hodgkin's lymphoma (HERILY)
title_fullStr A randomized, multiple-dose, multicenter, comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab (Hetero) and reference medicinal product (Rituximab, Roche) in Indian patients of non-hodgkin's lymphoma (HERILY)
title_full_unstemmed A randomized, multiple-dose, multicenter, comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab (Hetero) and reference medicinal product (Rituximab, Roche) in Indian patients of non-hodgkin's lymphoma (HERILY)
title_short A randomized, multiple-dose, multicenter, comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab (Hetero) and reference medicinal product (Rituximab, Roche) in Indian patients of non-hodgkin's lymphoma (HERILY)
title_sort randomized multiple dose multicenter comparative parallel study to evaluate the safety and efficacy of intravenous infusion of rituximab hetero and reference medicinal product rituximab roche in indian patients of non hodgkin s lymphoma herily
topic Diffuse large B-cell lymphoma
non-Hodgkin's lymphoma
rituximab
url http://www.ijmpo.org/article.asp?issn=0971-5851;year=2018;volume=39;issue=3;spage=316;epage=320;aulast=Advani
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