Sequential Hetrombopag and Recombinant Human Thrombopoietin for Cancer Therapy-Induced Thrombocytopenia
A Multicenter, Exploratory Clinical Study of Sequential Hetrombopag and Recombinant Human Thrombopoietin for Cancer Therapy-Induced Thrombocytopenia
This is a multicenter, randomized, exploratory clinical study. The study plans to enroll 96 participants with cancer therapy-induced thrombocytopenia. participants will be stratified by baseline platelet countand randomized 1:1 to the hetrombopag sequential group (Experimental Group A) or the recombinant human thrombopoietin (rhTPO) group (Experimental Group B).
Studieoversikt
Status
Status
Forhold
Forhold
Intervensjon / Behandling
Intervensjon / Behandling
Studietype
Studietype
Registrering (Antatt)
Registrering
Fase
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
Studiekontakt
- Navn: Zhengzheng Shan
- Telefonnummer: +86-15639934037
- E-post: sally900603@126.com
Deltakelseskriterier
Kvalifikasjonskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Age 18-75 years (inclusive), male or female;
- Patients with histologically or cytologically confirmed malignant tumors, including but not limited to lung cancer, breast cancer, colorectal cancer, gastric cancer, etc.;
- Currently receiving anticancer therapy in 21-day cycles, with grade 3 or higher thrombocytopenia during treatment, and expected to be able to receive the current anticancer regimen for ≥ 1 more cycle;
- ECOG PS score 0-2;
- With permitted use of red blood cells, erythropoietin, and recombinant human granulocyte colony-stimulating factor consistent with routine clinical practice: absolute neutrophil count (ANC) ≥ 1.0×10^9/L and hemoglobin (Hb) ≥ 80 g/L;
- No significant hepatic impairment;
- No significant renal impairment;
- Expected survival ≥ 12 weeks;
- Female participants of childbearing potential must have a negative serum pregnancy test within 7 days before the first dose, must not be lactating, and must agree to use effective contraception during the study and for 7 days after the last dose of study drug; male participants whose partners are women of childbearing potential must be surgically sterilized or must agree to use reliable contraception from the signing of the informed consent form until 7 days after the last dose of study drug;
- Voluntary participation in this study with signed informed consent and good compliance.
Exclusion Criteria:
- Concomitant hematopoietic system diseases, including but not limited to leukemia, primary immune thrombocytopenia, myeloproliferative neoplasms, multiple myeloma, and myelodysplastic syndromes;
- Other diseases causing thrombocytopenia other than cancer therapy-induced thrombocytopenia (CTIT) within 6 months before randomization, including but not limited to chronic liver disease and hypersplenism;
- Uncontrolled active infection;
- Tumor bone marrow invasion or bone marrow metastasis;
- Severe cardiac clinical symptoms or diseases within 6 months before randomization;
- Arterial or venous thrombotic events (stroke, transient ischemic attack, myocardial infarction, deep vein thrombosis, or pulmonary embolism) within 3 months before randomization, or clinical symptoms and history suggestive of thrombophilia;
- Concomitant severe bleeding symptoms or clear clinical manifestations of bleeding tendency, such as gastrointestinal or cerebral hemorrhage;
- Conditions affecting drug absorption (e.g., dysphagia, history of total gastrectomy);
- Receipt of whole-pelvis, whole-spine, or extensive sternal radiotherapy in the previous cycle or expected during the current cycle;
- Treatment with rhIL-11, rhTPO and/or TPO-RA drugs within 7 days before randomization;
- Treatment with romiplostim or romiplostim N01 within 1 month before randomization;
- Platelet transfusion within 3 days before randomization;
- Known or expected allergy or intolerance to the active ingredients or excipients of the study drug;
- Known history of positive human immunodeficiency virus (HIV) test or acquired immunodeficiency syndrome (AIDS);
- Known active viral hepatitis;
- Any other condition that, in the investigator's opinion, poses a significant risk to the subject's health or safety or may affect the efficacy evaluation.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Antall våpen
Våpen og intervensjoner
Deltakergruppe / ArmDeltakergruppe / Arm |
Intervensjon / BehandlingIntervensjon / Behandling |
|---|---|
|
Eksperimentell: Hetrombopag sequential group
|
hetrombopag (orally) + rhTPO (subcutaneous injection) |
|
Eksperimentell: Recombinant human thrombopoietin group
|
rhTPO (subcutaneous injection) |
Hva måler studien?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Response rate
Tidsramme: Up to 6 weeks
|
Proportion of participants achieving treatment response |
Up to 6 weeks
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Uønskede hendelser
Tidsramme: Inntil 8 uker
|
Inntil 8 uker
|
|
the proportion of participants whose platelet count recovers to ≥ 80×10^9/L
Tidsramme: Up to 14 days
|
Up to 14 days
|
|
the proportion of participants whose platelet count recovers to ≥ 100×10^9/L
Tidsramme: Up to 14 days
|
Up to 14 days
|
|
Time to first platelet count ≥ 80×10^9/L
Tidsramme: Up to 3 weeks
|
Up to 3 weeks
|
|
Platelet counts at each visit
Tidsramme: From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
|
Proportion of participants receiving at least one platelet-raising rescue therapy
Tidsramme: From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
|
Bleeding events
Tidsramme: From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
Samarbeidspartnere og etterforskere
Sponsor
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Studiestart
Primær fullføring (Antatt)
Primær fullføring
Studiet fullført (Antatt)
Studiet fullført
Datoer for studieregistrering
Først innsendt
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Først lagt ut
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Sist oppdatering lagt ut
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Cytopeni
- Hematologiske sykdommer
- Blodplateforstyrrelser
- Hemic og lymfatiske sykdommer
- Trombocytopeni
- Peptider
- Aminosyrer, peptider og proteiner
- Proteiner
- Biologiske faktorer
- Karbohydrater
- Intercellulære signalpeptider og proteiner
- Glykoproteiner
- Glykokonjugater
- Kolonistimulerende faktorer
- Hematopoietiske cellevekstfaktorer
- Cytokiner
- hetrombopag
- Trombopoietin
Andre studie-ID-numre
Andre studie-ID-numre
- 2026-KY-1560
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
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