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CPT-11, Carbopplatin, Dexamethasone commbination chemotherapy for refractory aggressive lymphoma

CPT-11, Carbopplatin, Dexamethasone commbination chemotherapy for refractory aggressive lymphoma - CPT, CBDCA, Dex for aggresive lymphoma

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000004501
Enrollment
35
Registered
2010-11-03
Start date
2010-11-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

refactory aggressive lymphoma

Interventions

None listed

Sponsors

Gunma Hematological Study Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. refractory for first line chemotherapy 2. age between 18 and 70 3. PS 0-2 4. expected to be alive for 3 months 5. normal of hematopoiesis and liver and renal function tests

Exclusion criteria

Exclusion criteria: 1. anaphylasis foo\r carboplatin 2. diarrhea 3. ileus 4. peptic ulcer 5. interstitial pneumonitis

Design outcomes

Primary

MeasureTime frame
response rate

Secondary

MeasureTime frame
adverse event

Countries

Japan

Contacts

Public ContactNorifumi Tsukamoto

Gunma University graduate school Medicine and Clinicla Science

027-220-8166

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026