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Biweekly Gemcitabine-Oxaliplatin and Dexamethasone for Relapsed/Refractory Malignant Lymphoma

Biweekly Gemcitabine-Oxaliplatin and Dexamethasone for Relapsed/Refractory Malignant Lymphoma

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00561301
Enrollment
43
Registered
2007-11-20
Start date
2006-11-30
Completion date
2009-10-31
Last updated
2007-11-20

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

Conditions

Lymphoma

Brief summary

\- To evaluate the feasibility of combination chemotherapies comprising of gemcitabine-dexamethasone-oxaliplatin for patients with refractory or relapsed malignant non-Hodgkin lymphoma (NHL)

Detailed description

\- The feasibility will be evaluated in terms of objective response rate, efficacy of stem cell collection, disease-free survival, and overall survival.

Interventions

DRUGGemDOx

gemcitabine oxliplatin

Sponsors

Cooperative Study Group A for Hematology
Lead SponsorNETWORK

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients who have refractory to first-line CHOP-like regimen * Patients who have first relapse after * first-line CHOP-like regimen * upfront autologous or allogeneic hematopoietic stem cell transplantation * Age 15 years or more * ECOG performance status ≤ 2 * Adequate bone marrow function * Adequate kidney,liver,cardiac

Exclusion criteria

* Patients who have received GEM or OX

Design outcomes

Primary

MeasureTime frame
objective response rate10/2009

Secondary

MeasureTime frame
toxicities, progression-free survival, overall survival, ASCC efficacy, rate for proceeding to ASCT10/2009

Countries

South Korea

Contacts

Primary ContactYae Eun Jang
redpin75@paran.com82-2-3010-7290

Outcome results

None listed

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