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Rituximab, Eltrombopag and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia

Primary Purpose

Immune Thrombocytopenia

Status
Unknown status
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
Rituximab
Eltrombopag
Dexamethasone
Sponsored by
Hospital Universitario Dr. Jose E. Gonzalez
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Immune Thrombocytopenia

Eligibility Criteria

16 Years - 90 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinically confirmed immune thrombocytopenic (IT) Platelet count less than 30,000/mm3 on two ocasionts with bleeding.
  • Subject ≥ 16 years
  • Subject has signed and dated written informed consent.
  • No sepsis or fever or active infection
  • Not pregnant or nursing

Exclusion Criteria:

  • Previous treatment (only corticosteroids at dose or prednisone equivalent of 300 mg)
  • Performance status above or equal to 2.
  • Pregnancy and lactation
  • Previous splenectomy
  • Connective tissue disease
  • Autoimmune hemolytic anemia
  • Relapse

Sites / Locations

  • Servicio de Hematología, Hospital Universitario "Dr. José Eleuterio González", Universidad Autónoma de Nuevo LeónRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Rituximab, eltrombopag and dexamethasone

Arm Description

Each patient will receive Rituximab 100 mg weekly days 1, 7, 14, 21 Eltrombopag 50 mg PO days 1-28 Dexamethasone 40 mg IV/PO days 1-4

Outcomes

Primary Outcome Measures

Clinical Response
Platelet counts to >30×109/L on two consecutive occasions

Secondary Outcome Measures

Complete Response
Platelet counts to >100×109/L on two consecutive occasions

Full Information

First Posted
July 1, 2016
Last Updated
July 12, 2016
Sponsor
Hospital Universitario Dr. Jose E. Gonzalez
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1. Study Identification

Unique Protocol Identification Number
NCT02834286
Brief Title
Rituximab, Eltrombopag and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia
Official Title
Low-dose Rituximab in Combination With Eltrombopag and High-dose Dexamethasone as Frontline Treatment for Immune Thrombocytopenia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2015 (undefined)
Primary Completion Date
March 2017 (Anticipated)
Study Completion Date
September 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitario Dr. Jose E. Gonzalez

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine the response rate and response duration with the combination of low-dose rituximab, eltrombopag and high-dose dexamethasone.
Detailed Description
Immune thrombocytopenia is an autoimmune disorder characterized by formation of autoantibodies against platelet antigens leading platelet destruction. Corticosteroids increase the platelet count in about 80 percent of patients. However, many patients have a relapse when the dose of corticosteroid is reduced. Debilitating side effects are common in patients who require long-term corticosteroid therapy to maintain the platelet count. Eltrombopag, it is a small molecule agonist of the c-mpl (TpoR) receptor, which is the physiological target of the hormone thrombopoietin, has been shown to be effectively raise the platelet count in adult patients (aged 18 years and over) who have had their spleen removed or where splenectomy is not an option and have received prior treatment with corticosteroids or immunoglobulins, and these medicines did not work (refractory ITP). There are a few case reports where eltrombopag was an option as first line treatment for IT. The purpose of this study is to determine the response rate and response duration with the combination of rituximab (100 mg weekly four weeks), eltrombopag (50mg PO once a day, day 1-28) and high-dose dexamethasone (40mg PO days 1-4) in untreated adult patients with <30*109/L platelet count diagnosed with immune thrombocytopenia. A complete response is defined as an increase in platelet counts to >150×109/L on two consecutive occasions. A clinical response is defined as an increase in the platelet count between >30×109/L on two consecutive measures and no bleeding. Duration of response is considered from the day of the initial administration to the first time of relapse (platelet count <30×109/L) or to time of analysis Patients will be evaluated each week during 4 weeks and then every month for at least 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Immune Thrombocytopenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rituximab, eltrombopag and dexamethasone
Arm Type
Experimental
Arm Description
Each patient will receive Rituximab 100 mg weekly days 1, 7, 14, 21 Eltrombopag 50 mg PO days 1-28 Dexamethasone 40 mg IV/PO days 1-4
Intervention Type
Drug
Intervention Name(s)
Rituximab
Intervention Description
Rituximab 100 mg weekly days 1, 7, 14, 21
Intervention Type
Drug
Intervention Name(s)
Eltrombopag
Intervention Description
Eltrombopag 50 mg PO days 1-28
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Description
Dexamethasone 40 mg IV/PO days 1-4
Primary Outcome Measure Information:
Title
Clinical Response
Description
Platelet counts to >30×109/L on two consecutive occasions
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Complete Response
Description
Platelet counts to >100×109/L on two consecutive occasions
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinically confirmed immune thrombocytopenic (IT) Platelet count less than 30,000/mm3 on two ocasionts with bleeding. Subject ≥ 16 years Subject has signed and dated written informed consent. No sepsis or fever or active infection Not pregnant or nursing Exclusion Criteria: Previous treatment (only corticosteroids at dose or prednisone equivalent of 300 mg) Performance status above or equal to 2. Pregnancy and lactation Previous splenectomy Connective tissue disease Autoimmune hemolytic anemia Relapse
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David Gómez, MD
Phone
+5583486136
Email
dgomezalmaguer@gmail.com
Facility Information:
Facility Name
Servicio de Hematología, Hospital Universitario "Dr. José Eleuterio González", Universidad Autónoma de Nuevo León
City
Monterrey
State/Province
Nuevo León
ZIP/Postal Code
64460
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Perla R Colunga, MD
Phone
+558110761973
Email
colunga.perla@gmail.com
First Name & Middle Initial & Last Name & Degree
David Gómez-Almaguer, MD
First Name & Middle Initial & Last Name & Degree
Perla R. Colunga-Pedraza, MD
First Name & Middle Initial & Last Name & Degree
Olga Cantú-Rodríguez, MD
First Name & Middle Initial & Last Name & Degree
César H. Gutiérrez-Aguirre, MD
First Name & Middle Initial & Last Name & Degree
Mónica Sánchez-Cárdenas, MD
First Name & Middle Initial & Last Name & Degree
José C Jaime-Pérez, MD
First Name & Middle Initial & Last Name & Degree
Luz Tarín-Arzaga

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
26709028
Citation
Gonzalez-Lopez TJ, Alvarez-Roman MT, Pascual C, Sanchez-Gonzalez B, Fernandez-Fuentes F, Jarque I, Perez-Rus G, Perez-Crespo S, Bernat S, Hernandez-Rivas JA, Andrade MM, Cortes M, Gomez-Nunez M, Olivera P, Martinez-Robles V, Fernandez-Rodriguez A, Fuertes-Palacio MA, Fernandez-Minano C, de Cabo E, Fisac R, Aguilar C, Barez A, Penarrubia MJ, Garcia-Frade LJ, Gonzalez-Porras JR. Eltrombopag safety and efficacy for primary chronic immune thrombocytopenia in clinical practice. Eur J Haematol. 2016 Sep;97(3):297-302. doi: 10.1111/ejh.12725. Epub 2016 Jan 27.
Results Reference
result
PubMed Identifier
25830126
Citation
Kim YK, Lee SS, Jeong SH, Ahn JS, Yang DH, Lee JJ, Kim HJ. Efficacy and safety of eltrombopag in adult refractory immune thrombocytopenia. Blood Res. 2015 Mar;50(1):19-25. doi: 10.5045/br.2015.50.1.19. Epub 2015 Mar 24.
Results Reference
result
PubMed Identifier
24802773
Citation
Gomez-Almaguer D, Herrera-Rojas MA, Jaime-Perez JC, Gomez-De Leon A, Cantu-Rodriguez OG, Gutierrez-Aguirre CH, Tarin-Arzaga L, Hernandez-Reyes J, Ruiz-Arguelles GJ. Eltrombopag and high-dose dexamethasone as frontline treatment of newly diagnosed immune thrombocytopenia in adults. Blood. 2014 Jun 19;123(25):3906-8. doi: 10.1182/blood-2014-01-549360. Epub 2014 May 6.
Results Reference
result
PubMed Identifier
23470153
Citation
Gomez-Almaguer D, Tarin-Arzaga L, Moreno-Jaime B, Jaime-Perez JC, Ceballos-Lopez AA, Ruiz-Arguelles GJ, Ruiz-Delgado GJ, Cantu-Rodriguez OG, Gutierrez-Aguirre CH, Sanchez-Cardenas M. High response rate to low-dose rituximab plus high-dose dexamethasone as frontline therapy in adult patients with primary immune thrombocytopenia. Eur J Haematol. 2013 Jun;90(6):494-500. doi: 10.1111/ejh.12102. Epub 2013 Apr 2.
Results Reference
result

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Rituximab, Eltrombopag and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia

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