Under construction – not a live service
Sign in
Not yet recruitingNo phase

Atorvastatin Combined With NAC Plus Romiplostim for Management of ITP

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Peking University People's Hospital
Trial code
NCT07662525
Record updated
23 June 2026
Original description
This is a prospective, single-arm, open-lable, single-center study and we aimed to determine whether atorvastatin combined with N-acetyl-L-cysteine (NAC) plus romiplostim could induce sustained response off-treatment (SRoT) in adult patients with ITP following CS failure.Read full original descriptionShow less

Atorvastatin Combined With N-Acetyl-L-Cysteine Plus Romiplostim for Management of Steroid-Resistant/Relapsed Immune Thrombocytopenia

This is a prospective, single-arm, open-lable, single-center study and we aimed to determine whether atorvastatin combined with N-acetyl-L-cysteine (NAC) plus romiplostim could induce sustained response off-treatment (SRoT) in adult patients with ITP following CS failure.

Inclusion: Diagnosed with primary ITP; Aged ≥18 years; Patients with treatment failure or relapse after first-line corticosteriod therapy for ITP; Platelet count <30×10⁹/L.

Exclusion: Presence of active malignant tumors; Active HBV, HCV or HIV infection; Active infection requiring systematic treatment; Leukemia, myelodysplastic syndrome, aplastic anemia, myelofibrosis or other hematological disorders that may cause thrombocytopenia; History or presence of myocardial infarction, unstable ischemic heart disease, stroke, or NYHA Class IV heart failure; AST > 2 times the upper limit of normal (ULN), ALT > 2×ULN, or TBIL ≥ 1.5×ULN; eGFR < 50 mL/min/1.73m²; Pregnant or lactating women, and who were possibly pregnant, planning to become pregnant, or who had partners planning to become pregnant; Any other subjects deemed ineligible for enrollment by the investigator.

ClinicalTrials.gov NCT07662525