Eltrombopag Combining Rituximab Versus Eltrombopag in the Management of Primary Immune Thrombocytopenia (ITP) in Adults

Official title

A Multicenter, Randomized, Open-label Study To Compare The Efficacy And Safety Of Eltrombopag Combining Rituximab With Eltrombopag In Adult ITP Patients

Overview

This multicenter randomized, open-label study aimed to compare the efficacy and safety of eltrombopag combining rituximab with eltrombopag in China adult ITP patients .This study was be conducted in adult ITP patients who had not responded to or had relapsed after previous treatment of ITP, including first line therapy and /or splenectomy.

Detailed description

The primary objective of this study was to evaluate the efficacy and safety of eltrombopag combining rituximab treating previously treated ITP patients compared to eltrombopag. The secondary objective was to evaluate the efficacy of eltrombopag combining rituximab in ITP patients with positive autoantibody compared to eltrombopag .In addition, health-related quality of life (HRQoL) measure was assessed in all participants.

224 eligible subjects were randomized to either eltrombopag combining rituximab or eltrombopag treatment in 1:1 ratio. 112 enrolled patients are randomly picked up to take eltrombopag combining with rituximab at the indicated dose. 112 enrolled patients are randomly picked up to take eltrombopag at the indicated dose.

The initial dose of eltrombopag administration was an oral 75 mg once daily in all participants .The dose of eltrombopag was adjusted according to the subject platelet count during the period from week 1 to week 24.

Subjects in eltrombopag combining rituximab treatment group received single dose infusion of rituximab 375 mg/m(2) within 14 days after enrollment.

Interventions

• Drug eltrombopag combining rituximab
  After enrollment,all subjects receive eltrombopag treatment,the initial dose of eltrombopag administration was an oral 75 mg once daily.Complete blood count including platelet count was done once a week.The dose of eltrombopag was adjusted according to the subject platelet count during the period from week 1 to week 24. If the platelet count \>250×10\^9/L, the eltrombopag will stop until the platelet count \<30×10\^9/L. All subjects receive single dose infusion of rituximab 375 mg/m(2) within 1
• Drug eltrombopag
  After enrollment,all subjects receive eltrombopag treatment,the initial dose of eltrombopag administration was an oral 75 mg once daily.Complete blood count including platelet count was done once a week.The dose of eltrombopag was adjusted according to the subject platelet count during the period from week 1 to week 24. If the platelet count \>250×10\^9/L, the eltrombopag will stop until the platelet count \<30×10\^9/L. Efficacy and safety will be evaluated at Week 4, Week 8, and Week 12.

Primary outcome measures

• Treatment response [Time frame: From the start of study treatment (Day 1) up to the end of week 12.]

Secondary outcome measures (9)

• Drug efficacy [Time frame: From the start of study treatment (Day 1) up to the end of week 4, week 8 and week 12.]
• Long-term treatment response [Time frame: From the start of study treatment (Day 1) up to the end of week 16, week 20 and week 24]
• Time to Response [Time frame: From the start of study treatment (Day 1) up to the end of week 24]
• Duration of response [Time frame: From the start of study treatment (Day 1) up to the end of week 24.]
• Evaluation of effectiveness [Time frame: From the start of study treatment (Day 1) up to the end of week 24.]
• Number of participants with clinically significant bleeding as assessed using the world health organization (WHO) bleeding scale. [Time frame: From the start of study treatment (Day 1) up to the end of week 24.]
• Immune Thrombocytopenia Patient Assessment Questionnaire (ITP-PAQ) [Time frame: From the start of study treatment (Day 1) up to the end of week 24.]
• Functional Assessment of Chronic Illness Therapy fatigue subscale (FACIT-F) [Time frame: From the start of study treatment (Day 1) up to the end of week 24.]
• Number of Participants with side effects of the drugs [Time frame: From the start of study treatment (Day 1) up to the end of week 24.]

Eligibility criteria

Inclusion criteria

• Signed written informed consent
• Age from 18 to 60 years old
• Diagnosed with ITP and have a platelet count of <30 ×10\^9/L on Day 1 (or within 48 hours prior to dosing on Day 1).
• Patients who have no response or relapsed after splenectomy(at least more than 6 months). Or patients who have not been splenectomised and have either not responded to one or more prior therapies, or who have relapsed prior therapy.
• Subjects treated with previous therapy(including but not limited to corticosteroid, azathioprine, danazol, cyclosporin A, mycophenolate mofetil) must have been completed prior to randomization, or must not be increasing a dose after enrollment.
• No pre-existing cardiac disease within the last 3 months. No arrhythmia known to increase the risk of thrombolic events (e.g. atrial fibrillation), or patients with a Corrected QT interval (QTc) >450msec or QTc >480 for patients with a Bundle Branch Block.
• No pre-existing infection within the last 1 months(including but not limited to pulmonary infection)
• Laboratory tests for coagulation function showed that prothrombin time (PT/INR) and activated partial thromboplastin time (APTT) no exceed normal by more than 20%. No history of clotting disorder, other than ITP.
• White blood cell count, neutrophil absolute value, hemoglobin, within the reference range, with the following exceptions:

• Hemoglobin: females and males 10.0 g/dl are eligible for inclusion,
• Absolute neutrophil count (ANC) ≥1500/µL (1.5×109/L) is required for inclusion
• The following blood chemistry test result no exceed normal by more than 20%:alanine aminotransferase, aspartate aminotransferase, total bilirubin, creatinine,serum albumin must not be below the lower limit of normal (LLN) by more than 10%.
• Subject is non-childbearing potential of childbearing potential and use acceptable methods of contraception throughout the study.
• Subjects fully understand and are able to comply with the requirements of the research protocol and are willing to complete the study as planned.

Exclusion criteria

• Patients with any prior history of arterial or venous thrombosis, and with following risk factors: cancer, Factor V Leiden, ATIII deficiency, antiphospholipid syndrome.
• Pregnant or lactating women;
• Subjects is currently receiving treatment with another study medication.
• Any laboratory or clinical evidence for HIV infection.
• Any clinical history for hepatitis C infection; chronic hepatitis B infection; or any evidence for active hepatitis at the time of subject screening. Laboratory test shows positive serology for Hepatitis C or Hepatitis B (HB). In addition, if negative for HBsAg but HBcAb positive (regardless of HBsAb status), a HB DNA test will be performed and if positive the subject will be excluded.
• History of platelet aggregation that prevents reliable measurement of platelet counts.
• Any clinically relevant abnormality, other than ITP,which in the opinion of the investigator makes the subject unsuitable for participation in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences a — Tianjin

Identifiers

NCT: NCT04518475 · IIT2020011

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗