Safety, Tolerability, Pharmacokinetics & Pharmacodynamics of Toripalimab for Patients With Recurrent Malignant Lymphoma

S

Shanghai JunTop Biosciences

Status and phase

Completed
Phase 1

Conditions

Malignant Lymphoma

Treatments

Biological: Toripalimab

Study type

Interventional

Funder types

Other

Identifiers

NCT03316144
Junshi-JS001-011

Details and patient eligibility

About

The primary objective is to assess the safety and tolerability of JS-001 in subjects with recurrent malignant lymphoma, and to evaluate its preliminary efficacy. The secondary objectives are to: 1) characterize the single-dose and multi-dose pharmacokinetic (PK) profile of JS-001, 2) characterize the immunogenicity of JS-001; 3) assess the dose-efficacy relationship of JS-001 single agent, and 4) preliminarily evaluate biomarkers associated with the efficacy of JS-001.

Enrollment

13 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Willing to sign Informed Consent;
  • Re-entry into the study is allowed with a second informed consent;
  • Willing to provide blood sample for biomarker analysis(mandatory). The tissue sample is optional;
  • A diagnosis of an advanced malignant tumor confirmed by histology or cytology (including typical Hodgkin's lymphoma and B cell source non-hodgkin's lymphoma);
  • No standard of care for the patient;
  • At least 1 measurable lesion;
  • Aged 18-65 years;
  • Anticipated life expectancy of at least 6 months;
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1;
  • At least 4 weeks elapsed since receiving systemic chemotherapy;
  • At least 4 weeks elapsed since receiving definite radiotherapy;
  • At least 2 weeks since the last dose of systemic steroid therapy (>10 mg/day prednisone or equivalent);
  • At least 4 weeks since receiving anti-cancer biotherapy;
  • Recovered from previous treatment related adverse reaction; willing to use an acceptable contraceptive method;
  • A negative pregnancy test for female subjects of childbearing potential;

Exclusion criteria

  • Active central nervous system (CNS) metastases and/or carcinomatous meningitis;
  • Known history of another primary solid tumor, unless the participant has undergone potentially curative therapy with no evidence of that disease for 2 years, or underwent successful definitive resection of basal or squamous cell carcinoma of the skin, or in situ cervical cancer;
  • Active, known or suspected autoimmune disease.Autoimmune diseases caused by lymphoma are not included in this list;
  • Patients who have had car-T cell therapy
  • Prior therapy with anti-PD-1, anti-PD-L1, anti-PD-L2,or anti-cytotoxic T-lymphocyte antigen 4 (CTLA-4) blocking antibodies;
  • Significant medical disease;
  • Active infection;
  • Active tuberculosis or history of tuberculosis with one year;
  • Infection of Human immunodeficiency virus (HIV);
  • A complication requiring immune-suppression;
  • Received a live vaccine within 4 weeks prior to first dose of study drug pleural or abdominal effusion with symptoms;
  • Drug or alcohol abuse (for subjects in the pharmacokinetic cohorts) ; evidence of interstitial lung disease;
  • Active hepatitis B or C, or with significant risk of hepatitis reactivation;
  • Known immediate or delayed hypersensitivity reaction or idiosyncrasy to monoclonal antibodies or drugs chemically related to the study drug. History of serious hypersensitivity reaction or serious hepatotoxicity related to any drug.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

13 participants in 3 patient groups

1 mg/kg Toripalimab
Experimental group
Description:
humanized anti-PD-1 monoclonal antibody is to be injected intravenously 1mg/kg Q2w until disease progresses or unacceptable tolerability occurs
Treatment:
Biological: Toripalimab
3 mg/kg Toripalimab
Experimental group
Description:
humanized anti-PD-1 monoclonal antibody is to be injected intravenously 3mg/kg Q2w until disease progresses or unacceptable tolerability occurs
Treatment:
Biological: Toripalimab
10 mg/kg Toripalimab
Experimental group
Description:
humanized anti-PD-1 monoclonal antibody is to be injected intravenously 10mg/kg Q2w until disease progresses or unacceptable tolerability occurs
Treatment:
Biological: Toripalimab

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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