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Single-center clinical study on the efficacy and safety of romiplostim N01 in promoting platelet engraftment after hematopoietic stem cell transplantation

Single-center clinical study on the efficacy and safety of romiplostim N01 in promoting platelet engraftment after hematopoietic stem cell transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116939
Enrollment
Unknown
Registered
2026-01-16
Start date
2026-01-19
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Acute myeloid leukemia

Interventions

Experimental group
:Subcutaneous injection of ropivastine N01 (5 µg/kg) was administered on the 3rd and 10th days post-transplantation, with a total of 2 doses.

Sponsors

The First Affiliated Hospital of Guilin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1: Malignant hematologic disease patients aged 18-65 years who have undergone allogeneic hematopoietic stem cell transplantation (allo-HSCT) 2: Sign the informed consent form

Exclusion criteria

Exclusion criteria: 1: Active infection (CRP> 50 mg/L or PCT> 0.5 ng/mL) 2: Severe hepatic and renal dysfunction (ALT> 3 times the upper limit of normal, Cr> 2 times the upper limit of normal) 3: History of thrombosis or hereditary thrombotic predisposition

Design outcomes

Primary

MeasureTime frame
platelet implantation time;

Secondary

MeasureTime frame
platelet recovery rate within 100 days post-transplantation;proportion of Treg cells and CD4+ T cells;proportion of NKG2D on NK cell surface;

Countries

China

Contacts

Public Contactxiaotao wang

The First Affiliated Hospital of Guilin Medical University

wxttjl@126.com+86 189 7732 2362

Outcome results

None listed

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