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Safety and Efficacy Evaluation of Decitabine With R-GDP

Safety and Efficacy Evaluation of Decitabine With R-GDP on Refractory or Relapsed NHL Patients

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03535753
Enrollment
50
Registered
2018-05-24
Start date
2017-09-01
Completion date
2020-11-01
Last updated
2018-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

NHL

Brief summary

Assessment of the Safety and efficacy of Administering decitabin plus R-GDP to NHL patients

Detailed description

RR NHL patients will be treated with decitabin plus R-GDP , safety and efficacy will be assessed.

Interventions

DRUGDecitabine and R-GDP

Decitabine and R-GDP

Sponsors

Beijing Immunochina Medical Science & Technology Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Relapsed or refractory Non-Hodgkin's lymphoma(NHL) patiens. 2. Eastern Cooperative Oncology Group(ECOG) score 0-2 3. Expected survival \>3 months 4. Measurable disease.

Exclusion criteria

1. Patients who needs treatment with immunosuppressive agents 2. Hematosepsis or Uncontrolled active infection 3. History of epilepsy or other CNS disease. 4. Active hepatitis B , hepatitis C or HIV infection or any other uncontrolled active infection. 5. Pregnancy or breast-feeding women. 6. Any uncontrolled medical disorders that the researchers considered are not suitable to participate the clinical trial. 7. Any situation that would increase dangerousness of subjects or disturb the outcome of the clinical study according to the researcher's evaluatio

Design outcomes

Primary

MeasureTime frameDescription
OS2 yearsOverall survival

Countries

China

Contacts

Primary Contactxian lu, Dr
luxinan@immunochina.com86

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026