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- Klinische proef NCT07578064
A Randomized, Self-controlled Post-marketing Clinical Study on the Comparison of Shengbai Oral Liquid and Leucogen Tablets in the Treatment of Moderate Neutropenia Caused by Anti-tumor Drugs in Breast Cancer Patients
4 mei 2026 bijgewerkt door: Hongxia Wang
The subjects were randomly assigned to Group A or Group B in a 1:1 ratio, stratified by early/late stage.
Group A: In the first cycle, they took Shengbai Oral Liquid (40 ml, three times a day), and in the second cycle, they took Leucogen Tablets (20 mg, three times a day).
Group B: In the first cycle, they took Leucogen Tablets (20 mg, three times a day), and in the second cycle, they took Shengbai Oral Liquid (40 ml, three times a day).
Studie Overzicht
Toestand
Werving
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
60
Fase
- Fase 4
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Hongxia wang, PhD
- Telefoonnummer: 13524491606 021-64175590
- E-mail: whx365@126.com
Studie Locaties
-
-
Shanghai Municipality
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Shanghai, Shanghai Municipality, China, 200032
- Werving
- Fudan University Shanghai Cancer Center
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Inclusion Criteria:
- Age range: 18 to 80 years old, gender unrestricted;
- Patients with breast cancer confirmed by histopathology.
- ECOG performance status score ≤ 2; expected survival time ≥ 12 weeks;
- During the period of anti-tumor drug treatment before enrollment (including but not limited to chemotherapy drugs: paclitaxel, capecitabine, vinorelbine; CDK4/6 inhibitors: palbociclib, dalpiciclib, ribociclib, abemaciclib; antibody-drug conjugates: trastuzumab emtansine, trastuzumab deruxtecan, sacituzumab govitecan, larotrectinib), grade II-III neutropenia occurred, and it is planned to continue the original treatment plan and dose for at least 2 cycles.
- The subject meets the criteria for continuing anti-tumor drug treatment; normal bone marrow hematopoietic function, no bleeding tendency (INR < 1.5); blood routine meets the following requirements: Hb ≥ 8g/dl, platelet count ≥ 75×109/L; liver and kidney function meets the following requirements: AST and ALT ≤ 3 ULN, total bilirubin ≤ 2 ULN, serum creatinine ≤ 1.5 ULN; no obvious heart and lung function disorders;
- The subject has high compliance and voluntarily signs the informed consent form.
Exclusion Criteria:
- 1. Having participated in other new drug clinical trials within 4 weeks before enrollment; planning to participate in other new drug clinical trials during the study period; planning to add other anti-tumor treatments during the study period; 2. Having received bone marrow radiotherapy involving 25% of the bone marrow; having undergone hematopoietic stem cell transplantation or bone marrow transplantation; 3. Uncontrolled acute or chronic infection; having severe underlying diseases such as heart, lung, liver or kidney diseases; having primary diseases of the hematopoietic system; having diseases such as hypersplenism, hyperthyroidism, adrenal insufficiency, connective tissue diseases, etc. that can cause a decrease in white blood cells; 4. Uncontrolled digestive system symptoms that affect the administration of the study drug; confirmed or suspected allergy to the study drug or its related components; 5. Uncontrolled psychological or mental disorders; judged by the investigator as unsuitable for participation in this study.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Group A: In the first cycle, they took Shengbai Oral Liquid (40 ml, three times a day), and in the s
In the first cycle, they took Shengbai Oral Liquid (40 ml, three times a day), and in the second cycle, they took Leucogen Tablets (20 mg, three times a day).
|
In the first cycle, they took Shengbai Oral Liquid (40 ml, three times a day), and in the second cycle, they took Leucogen Tablets (20 mg, three times a day).
|
|
Experimenteel: Group B: In the first cycle, they took Leucogen Tablets (20 mg, three times a day), and in the secon
In the first cycle, they took Leucogen Tablets (20 mg, three times a day), and in the second cycle, they took Shengbai Oral Liquid (40 ml, three times a day).
|
In the first cycle, they took Leucogen Tablets (20 mg, three times a day), and in the second cycle, they took Shengbai Oral Liquid (40 ml, three times a day).
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Lowest neutrophil count (ANC) in the two stages
Tijdsspanne: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the lowest values of neutrophils (ANC) in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Rate of ANC decline (Grade II/III/IV), duration of ANC decline in the two stages
Tijdsspanne: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the decline rates of grade II /III /IV ANC and the duration of ANC decline in each group during two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
Dosage of G-CSF
Tijdsspanne: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the dosage of G-SCF in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
The incidence of febrile neutropenia
Tijdsspanne: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the incidence of febrile neutropenia in each group during two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
Infection incidence rate
Tijdsspanne: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the incidence of infection in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
Antibiotic utilization rate
Tijdsspanne: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the utilization rate of antibiotics in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
The completion rate of anti-tumor drugs
Tijdsspanne: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the completion rates of anti-tumor drugs in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
6 augustus 2025
Primaire voltooiing (Geschat)
30 september 2026
Studie voltooiing (Geschat)
31 december 2026
Studieregistratiedata
Eerst ingediend
29 juli 2025
Eerst ingediend dat voldeed aan de QC-criteria
4 mei 2026
Eerst geplaatst (Werkelijk)
11 mei 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
11 mei 2026
Laatste update ingediend die voldeed aan QC-criteria
4 mei 2026
Laatst geverifieerd
1 mei 2025
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- BC-NEU-001
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .