- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02456207
A Pharmacokinetic Study Comparing SCT400 And Rituximab in Patients With B-cell Non-Hodgkin's Lymphoma
A Phase II, Multi-center, Randomized and Open Study to Evaluate and Compare the PK, PD and Safety of SCT400 With Rituximab in Patients With CD20+ B-cell Non-Hodgkin's Lymphoma
The primary objective of the study is to assess the pharmacokinetic (PK) similarity of SCT400 versus rituximab (MabThera®) in patients with CD20+ B-cell Non-Hodgkin's Lymphoma.
The secondary objective of the study is to evaluate the pharmacodynamics (PD) and safety of SCT400 versus rituximab (MabThera®), as well as the presence of human anti-chimeric antibodies (HACA).
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Forventet)
Fase
- Fase 2
Kontakter og plasseringer
Studiesteder
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-
Beijing
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Beijing, Beijing, Kina, 100076
- Rekruttering
- Cancer Hospital Chinese Academy of Medical Sciences
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Ta kontakt med:
- Shuting Li
- Telefonnummer: 010-87788495
- E-post: cancergcp@163.com
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- aged from 18 to 75 years;
- having histologically confirmed NHL expressing CD20 antigen;
- having obtained CR (complete remission) or CRu (uncertain complete remisson) after the prior therapy;
- ECOG performance status of 0 to 1
- expected survival of at least ≥ 3 months;
- signed an informed consent form which was approved by the institutional review board of the respective medical center .
Exclusion Criteria:
- had received rituximab or other anti-CD20(+) monoclonal antibody treatment within 1 year before enrollment;
- having to be at least 4 weeks beyond prior anticancer therapy including corticosteroid, or have not recovered from significant toxicities of prior therapy;
- participating in other clinical trial within 30 days before enrolment;
- with serious hematologic dysfunction (white blood cell count of <3.0×103/uL; absolute neutrophil count of <1.5×103/ uL; platelet count of < 75×103/uL; hemoglobin level of < 8.0 g/dL); hepatic dysfunction (total bilirubin level of > 1.5×ULN; aspartate amino transferase (AST) and alanine amino transferase (ALT) levels of >2.5 × ULN; renal dysfunction (serum creatinine level of > 1.5×ULN ); and International normalized ratio (INR) and partial thromboplastin time or activated partial thromboplastin time (aPTT) > 1.5 × ULN (unless on therapeutic coagulation);
- had received live vaccine within 4 weeks prior to study entry;
- with other malignancies ; or central nervous system (CNS) lymphoma, AIDS-related lymphoma; or active opportunistic infection, a serious nonmalignant disease;
- seropositive for HCV antibody, or HIV antibody, or hepatitis B virus surface antigen (HBsAg). HBc antibody seropositive, but HBV DNA and HBsAg negative patients may participle following consultation with a hepatitis expert regarding monitoring and use of HBV antiviral therapy, and provided they agree to receive treatment as indicated,
- recent major surgery (within 28 days prior to study entry );
- with a history of allergic reaction or protein product allergy including murine proteins;
- pregnant or lactating or not accepted birth control methods including male patients.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Experimental
SCT400:375 mg/m2, iv, one infusion
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|
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Aktiv komparator: Active Comparator
Rituximab: 375 mg/m2, iv, one infusion
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Area under the curve (AUC) for SCT400 and rituximab concentrations
Tidsramme: 85 days
|
85 days
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Sammenligning av AE mellom de to studiearmene
Tidsramme: 85 dager
|
85 dager
|
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AUC for SCT400 and rituximab concentrations
Tidsramme: 1 week ,2 weeks, 4 weeks, 8 weeks and 12 weeks
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1 week ,2 weeks, 4 weeks, 8 weeks and 12 weeks
|
|
Maximum observed concentration of the SCT400 and rituximab
Tidsramme: 85 days
|
85 days
|
|
Change from baseline of CD19+ , CD20+ B-cells
Tidsramme: 85 days
|
85 days
|
|
Comparison of HACA between the two study arms
Tidsramme: 85 days
|
85 days
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i immunsystemet
- Neoplasmer etter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Lymfesykdommer
- Immunproliferative lidelser
- Lymfom
- Lymfom, B-celle
- Lymfom, Non-Hodgkin
- Fysiologiske effekter av legemidler
- Antirevmatiske midler
- Antineoplastiske midler
- Immunologiske faktorer
- Antineoplastiske midler, immunologiske
- Rituximab
Andre studie-ID-numre
- SCT400NHL2
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