- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07933146
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).
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
Contacts et emplacements
Coordonnées de l'étude
- Nom: Zhengzheng Shan
- Numéro de téléphone: +86-15639934037
- E-mail: sally900603@126.com
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Hetrombopag sequential group
|
hetrombopag (orally) + rhTPO (subcutaneous injection) |
|
Expérimental: Recombinant human thrombopoietin group
|
rhTPO (subcutaneous injection) |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Response rate
Délai: Up to 6 weeks
|
Proportion of participants achieving treatment response |
Up to 6 weeks
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Événements indésirables
Délai: Jusqu'à 8 semaines
|
Jusqu'à 8 semaines
|
|
the proportion of participants whose platelet count recovers to ≥ 80×10^9/L
Délai: Up to 14 days
|
Up to 14 days
|
|
the proportion of participants whose platelet count recovers to ≥ 100×10^9/L
Délai: Up to 14 days
|
Up to 14 days
|
|
Time to first platelet count ≥ 80×10^9/L
Délai: Up to 3 weeks
|
Up to 3 weeks
|
|
Platelet counts at each visit
Délai: 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
Délai: 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
Délai: 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)
|
Collaborateurs et enquêteurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Cytopénie
- Maladies hématologiques
- Troubles des plaquettes sanguines
- Maladies hémiques et lymphatiques
- Thrombocytopénie
- Peptides
- Acides aminés, peptides et protéines
- Protéines
- Facteurs biologiques
- Glucides
- Peptides de signalisation intercellulaire et protéines
- Glycoprotéines
- Glycoconjuguis
- Facteurs de stimulation des colonies
- Facteurs de croissance des cellules hématopoïétiques
- Cytokines
- hétrombopag
- Thrombopoïétine
Autres numéros d'identification d'étude
- 2026-KY-1560
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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