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Adriamycin, Vinblastine, DTIC and Revlimid in Elderly Hodgkin Lymphoma Patients

Phase I Trial of AVD Plus Lenalidomide (Revlimid) in Elderly Intermediate or Advanced Stage Hodgkin Lymphoma Patients

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01056679
Acronym
AVD-Rev
Enrollment
30
Registered
2010-01-26
Start date
2010-04-30
Completion date
2016-02-29
Last updated
2018-03-22

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

Conditions

Hodgkin Lymphoma

Brief summary

The purpose of this study is to determine within the scope of the trial what the maximum tolerated dose (MTD) of lenalidomide in combination with AVD should be.

Interventions

50mg/m2 day 1 + 15

DRUGDTIC

375mg/m2 day 1 + 15

DRUGLenalidomide

day 1 - 21

DRUGVinblastine

6mg/m2 day 1 + 15

Sponsors

University of Cologne
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Hodgkin Lymphoma, intermediate or advanced stage * Age \>60 and \<75 years * ECOG 2 or better * No major organ dysfunction * Ability to take aspirin or LMW Heparin

Exclusion criteria

* HL as composite lymphoma * Prior use of lenalidomide * Prior use of chemo- or radiotherapy

Design outcomes

Primary

MeasureTime frame
Dose limiting toxicities (DLT)

Secondary

MeasureTime frame
Overall response rate (ORR)
Progression free survival (PFS)2 years

Countries

Germany

Outcome results

None listed

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