Romiplostim, Rituximab and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia

David Gomez Almaguer

Status and phase: Unknown; Phase 2

Conditions: Immune Thrombocytopenia; Thrombotic Thrombocytopenic Purpura

Treatments: Drug: Rituximab; Drug: Dexamethasone; Drug: Romiplostim

Study type: Interventional

Funder types: Other

Identifiers

NCT04588194

Hospital Universitario

Details and patient eligibility

About

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.

Full 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.

Enrollment: 12 estimated patients

Sex: All

Ages: 16 to 90 years old

Volunteers: No 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.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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12 participants in 1 patient group

Romiplostim, Rituximab, Dexamethasone

Experimental group

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.

Treatment:

Drug: Romiplostim

Drug: Dexamethasone

Drug: Rituximab