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Romiplostim, Rituximab and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia

Primary Purpose

Immune Thrombocytopenia, Thrombotic Thrombocytopenic Purpura

Status
Unknown status
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
Romiplostim
Rituximab
Dexamethasone
Sponsored by
David Gomez Almaguer
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Immune Thrombocytopenia focused on measuring thrombocytopenia

Eligibility Criteria

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

Inclusion Criteria:

  • Clinically confirmed immune thrombocytopenia (IT) Platelet count less than 30,000/mm3 on two occasions.
  • Subject ≥ 16 years
  • Subject has signed and dated written informed consent.

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
  • Active infection, sepsis or fever
  • Positive for hepatitis B virus or hepatitis C virus or human immunodeficiency virus.

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

Romiplostim, Rituximab, Dexamethasone

Arm Description

Each patient will receive Rituximab 100 mg weekly days 1, 7, 14, 21, Romiplostim 2mcg/Kg subcutaneously weekly days 1, 7, 14, 21 and 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
January 30, 2020
Last Updated
October 8, 2020
Sponsor
David Gomez Almaguer
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1. Study Identification

Unique Protocol Identification Number
NCT04588194
Brief Title
Romiplostim, Rituximab and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia
Official Title
Romiplostim in Combination With Low-dose Rituximab and High-dose Dexamethasone as Frontline Treatment for Immune Thrombocytopenia
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2020 (Anticipated)
Primary Completion Date
November 1, 2021 (Anticipated)
Study Completion Date
November 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
David Gomez Almaguer

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

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, romiplostim 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. Romiplostim, 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 romiplostim 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), romiplostim (2mcg/Kg four weekly) 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, Thrombotic Thrombocytopenic Purpura
Keywords
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
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Romiplostim, Rituximab, Dexamethasone
Arm Type
Experimental
Arm Description
Each patient will receive Rituximab 100 mg weekly days 1, 7, 14, 21, Romiplostim 2mcg/Kg subcutaneously weekly days 1, 7, 14, 21 and Dexamethasone 40 mg IV/PO days 1-4.
Intervention Type
Drug
Intervention Name(s)
Romiplostim
Intervention Description
Romiplostim 2mcg/Kg subcutaneously weekly days 1, 7, 14, 21
Intervention Type
Drug
Intervention Name(s)
Rituximab
Intervention Description
Rituximab 100 mg weekly days 1, 7, 14, 21
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Description
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 thrombocytopenia (IT) Platelet count less than 30,000/mm3 on two occasions. Subject ≥ 16 years Subject has signed and dated written informed consent. 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 Active infection, sepsis or fever Positive for hepatitis B virus or hepatitis C virus or human immunodeficiency virus.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David Gómez, MD
Phone
83486136
Email
dgomezalmaguer@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Mónica Bustillos, MD
Phone
6142255724
Email
moni.bm88@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Gómez, MD
Organizational Affiliation
Hospital Universitario J. Eleuterio González
Official's Role
Principal Investigator
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
Mónica Bustillos, MD
Phone
6142255724
Email
moni.bm88@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
Luz Tarín-Arzaga, MD
First Name & Middle Initial & Last Name & Degree
Mónica Bustillos, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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
PubMed Identifier
23616916
Citation
Cooper N, Terrinoni I, Newland A. The efficacy and safety of romiplostim in adult patients with chronic immune thrombocytopenia. Ther Adv Hematol. 2012 Oct;3(5):291-8. doi: 10.1177/2040620712453596.
Results Reference
result
PubMed Identifier
27307776
Citation
Vishnu P, Aboulafia DM. Long-term safety and efficacy of romiplostim for treatment of immune thrombocytopenia. J Blood Med. 2016 May 25;7:99-106. doi: 10.2147/JBM.S80646. eCollection 2016.
Results Reference
result

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Romiplostim, Rituximab and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia

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