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Synergistic effect of low-dose cyclosporine A on eltrombopag in the management of multiline failed immune thrombocytopenia patients: a single-center, self-control study

Synergistic effect of low-dose cyclosporine A on eltrombopag in the management of multiline failed immune thrombocytopenia patients: a single-center, self-control study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062120
Enrollment
Unknown
Registered
2022-07-23
Start date
2022-08-10
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

immune thrombocytopenia

Interventions

Experimental group:low-dose cyclosporine A combined with EPAG

Sponsors

Zhejiang Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients eligible for inclusion were: compliance with Consensus of Chinese Experts on Diagnosis and Treatment of Adult Primary ITP(version 2020) 2.18 years or older; 3.Platelet count<20×10^9/L with varying degrees of bleeding symptoms before admission; 4.Failed from multiple lines of therapy: patients are ineffective or dependent on first-line glucocorticoid therapy, no response to previous rhTPO (at least 15000U qd for 14 days), and failed from prior EPAG ongoing treatment (at least 75mg qd for 30 days).

Exclusion criteria

Exclusion criteria: 1.Key exclusion criteria were severe cardiopulmonary dysfunction, hepatic and renal insufficiency, immunodeficiency; 2.pregnant or lactating women; 3. with a history of thrombosis or autoimmune diseases. 4.Bone marrow aspiration and biopsy were performed before the administration of EPAG, the secondary thrombocytopenia including myelodysplastic syndrome (MDS), aplastic anemia (AA), thrombocytopenia (TTP), etc. were excluded based on comprehensive differentiation diagnosis.

Design outcomes

Primary

MeasureTime frame
blood routine;efficacy;response duration;concomitant medication;bleeding symptoms;safety;

Countries

China

Contacts

Public ContactWu Dijiong

the First Affiliated Hospital of Zhejiang Chinese Medical University Youdian Road NO.54 Department of Hematology Hangzhou, Zhejiang

wdj850@163.com+86 571 86620325

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026