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CompletedNCT02206308Updated Aug 1, 2014

Safety, Pharmacokinetics and Pharmacodynamics of Recombinant Chimeric Anti-CD20 Monoclonal Antibody in Patients With B-cell Non-Hodgkin's Lymphoma.

A Phase 1 interventional study of Chimeric anti-CD20 monoclonal antibody in B-cell Non Hodgkin's Lymphoma, sponsored by Sinocelltech Ltd.. Completed. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2014-08-01.

Sponsored by Sinocelltech Ltd. · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
15
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

The purpose of this study is to determine whether SCT400 is safe and effective in the treatment of B-cell Non Hodgkin's lymphoma

02

Conditions studied

  • B-cell Non Hodgkin's Lymphoma

Keywords

  • Chimeric anti-CD20 monoclonal antibody(SCT400)
  • escalating doses
  • safety
  • pharmacokinetics and pharmacodynamics
03

In context

Lymphoma

5,578 studies on the registry are indexed under Lymphoma; 825 are open to participants now.

This study's enrollment of 15 is below the median of 40 across 4,508 interventional studies indexed under Lymphoma.

Browse Lymphoma studies →

Lead sponsor

Sinocelltech Ltd. is the lead sponsor of 78 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • aged from 18 to 75 years
  • having histologically confirmed NHL expressing CD20 antigen
  • having relapsed non-Hodgkin's lymphoma(NHL) after at least one prior course of standard therapy
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 according to WHO scale, and 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

Exclusion Criteria:

  • single measurable lesion ≥7 cm in diameter
  • with serious hematologic dysfunction (white blood cell count of \<3.0×103/μL; absolute neutrophil count of \<1.5×103/ μL; platelet count of \< 75×103/μL; hemoglobin level of \< 8.0 g/dL; serum immunoglobulin G(IgG) level of \<600 mg/dL);, hepatic dysfunction (total bilirubin level of > 1.5×upper limit of normal(ULN); aspartate amino transferase (AST) and alanine amino transferase (ALT) levels of >2.5 × ULN (≥5 × ULN for patients with liver metastases)); and renal dysfunction (serum creatinine level of > 1.5×ULN )
  • having to be at least 4 weeks beyond prior anticancer therapy including corticosteroid, or participating in other clinical trial or have not recovered from significant toxicities of prior therapy
  • had received rituximab or other anti-CD20(+) monoclonal antibody treatment within 1 year before enrollment
  • had received hematopoietic cytokines, e.g CSF、EPO within 1 week prior to study entry
  • with other malignancies ; or central nervous system (CNS) lymphoma, AIDS- related lymphoma; or active opportunistic infection, a serious nonmalignant disease
  • having hepatitis B virus surface antigen and /or antibodies to hepatitis C virus or human immunodeficiency virus
  • with pleural effusions or ascites secondary to lymphoma; or high risk of tumor lysis syndrome; or recent major surgery (within 28 days )
  • 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
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
15 participants (actual)

Study arms

  • Experimental
    single arm

    Three escalating single-dose groups of chimeric anti-CD20 monoclonal antibody(SCT400) : 250 mg/m2 , 375 mg/m2,500 mg/m2, once a week for 4 doses;

    Biological: Chimeric anti-CD20 monoclonal antibody

Interventions

  • BiologicalChimeric anti-CD20 monoclonal antibody

    Also known as: SCT400

06

What researchers measure

Primary outcomes

  1. Number of participants with infusion-related reaction and with drug-related adverse events.

    Time frame: up to 27 weeks

Secondary outcomes

  1. Area Under the plasma concentration versus time curve (AUC) of SCT400

    Time frame: prior to the initial dose on day 1 and 0,2,4,8,24,48,72,96,120 hours post-dose

Other outcomes

  1. Time to disease progression

    Time frame: up to 27 weeks

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02206308
Lead sponsor
Sinocelltech Ltd.
Responsible party
Sponsor
First posted
Aug 1, 2014
Start date
May 2012
Primary completion
Jul 2013
Completion
Jul 2013
Last update
Aug 1, 2014

Study contacts

Yuan kai Shi, PhD
principal investigator · Cancer Institute and Hospital, Chinese Academy of Medical Sciences; Beijing, China

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2013. You cannot join it, but the record below documents what was studied.

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