- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07662525
Atorvastatin Combined With NAC Plus Romiplostim for Management of ITP
19 juni 2026 uppdaterad av: Fu Haixia, Peking University People's Hospital
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.
Studieöversikt
Status
Har inte rekryterat ännu
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This is a prospective, single-arm trial designed to investigate whether atorvastatin combined with N-acetyl-L-cysteine (NAC) plus romiplostim can induce a sustained response off-treatment (SRoT) in adult patients with immune thrombocytopenia (ITP) who experienced failure of first-line corticosteroid therapy.
In this study, SRoT is defined as an off-treatment period during which the platelet count remains above 30×10⁹/L in the absence of bleeding events or rescue therapy.
The primary endpoint was the proportion of patients who achieved SRoT by Week 24 after the discontinuation of romiplostim.
From Week 1 to Week 24, atorvastatin and NAC was administrated as the dose of 20mg qd and 400mg tid,respectively, and were discontinued at the end of Week 24.
During the initial 24 weeks, romiplostim was initiated at a starting dose of 3 μg/kg per week.
The weekly dose was adjusted based on platelet counts, with a maximum dose of 10 μg/kg per week, to maintain platelet levels within the range of 100-200×10⁹/L.
From Week 25 to Week 35, romiplostim was gradually tapered and discontinued, with the goal of maintaining a platelet count ≥30×10⁹/L and no less than twice the baseline level.
After all medications (including atorvastatin, NAC, and romiplostim) were discontinued (no later than Week 36), patients were followed up for an additional 24 weeks to evaluate the sustained response rate at 24 weeks post-treatment cessation.
Studietyp
Interventionell
Inskrivning (Beräknad)
50
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Fu Haixia, Dr.
- Telefonnummer: +861088326002
- E-post: fuhaixia_210@163.com
Studera Kontakt Backup
- Namn: Xiaohui Zhang, Dr.
- Telefonnummer: 861088326001
- E-post: zhangxh@bjmu.edu.cn
Studieorter
-
-
-
Beijing, Kina
- Peking University People's Hospital
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Nej
Beskrivning
Inclusion Criteria:
- 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 Criteria:
- Pregnant or lactating women, and who were possibly pregnant, planning to become pregnant, or who had partners planning to become pregnant;
- 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;
- Any other subjects deemed ineligible for enrollment by the investigator.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: combined therapy
atorvastatin 20mg qd , N-acetyl-L-cysteine (NAC) 400mg tid, and romiplostim
|
From Week 1 to Week 24, atorvastatin and NAC was administrated as the dose of 20mg qd and 400mg tid,respectively, and were discontinued at the end of Week 24.
For romiplostim, the initial dose was 3 μg/kg per week.
The weekly dose was adjusted based on platelet counts, with a maximum dose of 10 μg/kg per week, to maintain platelet levels within the range of 100-200×10⁹/L during the initial 24-week period.
From Week 25 to Week 35, romiplostim was gradually tapered and discontinued with the goal of maintaining a platelet count ≥30×10⁹/L and no less than twice the baseline level.
After all medications (including atorvastatin, NAC, and romiplostim) were discontinued (no later than Week 36), patients were followed up for an additional 24 weeks to evaluate the sustained response rate at 24 weeks post-treatment cessation.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
24-week SRoT rate
Tidsram: 24 weeks post-treatment cessation
|
Sustained response off-treatment (SRoT) rate is defined as the proportion of patients who maintain a platelet count ≥30×10^9/L and at least a two-fold increase from the baseline count without active bleeding following treatment discontinuation.
|
24 weeks post-treatment cessation
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
24-week SCRoT rate
Tidsram: 24 weeks after treatment discontinuation
|
Sustained complete response off-treatment (SCRoT) rate was defined as the proportion of patients who maintain a platelet count of ≥100×10⁹/L without active bleeding after treatment discontinuation.
|
24 weeks after treatment discontinuation
|
|
ORR
Tidsram: Up to the end of week 24
|
Overall response rate (ORR) is defined as the proportion of patients who achieve platelet count ≥30×10^9/L and more than twice the baseline level, with no signs of active bleeding.
|
Up to the end of week 24
|
|
CR rate
Tidsram: Up to the end of week 24
|
Complete response (CR) rate is defined as the proportion of patients who achieve a platelet count ≥100×10⁹/L with no signs of active bleeding.
|
Up to the end of week 24
|
|
TTR
Tidsram: Up to the end of week 24
|
Time to response (TTR) is defined as the days from treatment initiation to first platete count reaching ≥30×10^9/L
|
Up to the end of week 24
|
|
Sustained response
Tidsram: Up to the end of week 24
|
Platelet count ≥30×10⁹/L and at least doubled from baseline on at least three of four scheduled visits during the final 8 weeks of the initial 24-week treatment phase without active bleeding.
|
Up to the end of week 24
|
|
Bleeding events
Tidsram: Up to the end of week 24; Week 25 to 24 weeks post-treatment cessation
|
Bleeding incidence and severity per WHO bleeding score
|
Up to the end of week 24; Week 25 to 24 weeks post-treatment cessation
|
|
Adverse Events
Tidsram: Up to the end of week 24; Week 25 to 24 weeks post-treatment cessation
|
The proportion of patients with adverse events
|
Up to the end of week 24; Week 25 to 24 weeks post-treatment cessation
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Beräknad)
1 juni 2026
Primärt slutförande (Beräknad)
30 december 2027
Avslutad studie (Beräknad)
30 december 2028
Studieregistreringsdatum
Först inskickad
16 maj 2026
Först inskickad som uppfyllde QC-kriterierna
19 juni 2026
Första postat (Faktisk)
23 juni 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
23 juni 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
19 juni 2026
Senast verifierad
1 juni 2026
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
- Cytopeni
- Patologiska processer
- Autoimmuna sjukdomar
- Immunsystemets sjukdomar
- Blödning
- Hudmanifestationer
- Hematologiska sjukdomar
- Blodkoagulationsstörningar
- Hemorragiska störningar
- Blodplättssjukdomar
- Trombotiska mikroangiopatier
- Purpura, trombocytopenisk
- Purpura
- Trombocytopeni
- Patologiska tillstånd, tecken och symtom
- Tecken och symtom
- Hemiska och lymfsjukdomar
- Purpura, Trombocytopenisk, Idiopatisk
- Heterocykliska föreningar, 1-ring
- Heterocykliska föreningar
- Fettsyror
- Lipider
- Azoler
- Pyrrol
- Heptansyror
- Atorvastatin
- romiplostim
Andra studie-ID-nummer
- 2025PHD049-001
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .