← Back to Search

Anti-tumor antibiotic

Chemotherapy for Multiple Myeloma

Phase 2
Waitlist Available
Led By Frits van Rhee, MD, PhD
Research Sponsored by University of Arkansas
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Patients must be either untreated or have not had more than one cycle of systemic MM therapy, excluding bisphosphonates and localized radiation.
Patients must be at least 18 years of age and not older than 75 years of age at the time of registration.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Summary

This trial is testing a new lower-dose, shorter-cycle chemotherapy regimen to see if it can help people with high-risk myeloma achieve longer remissions and improved survival.

Who is the study for?
This trial is for adults aged 18-75 with newly diagnosed active multiple myeloma that requires treatment. Participants should have high-risk disease characteristics, adequate kidney function (serum creatinine level < 3 mg/dL), and good heart and lung function. They must not have received more than one cycle of systemic therapy, excluding certain treatments like bisphosphonates.
What is being tested?
The study tests a combination of chemotherapy drugs (Cyclophosphamide, Velcade, Dexamethasone, Cisplatin, Thalidomide, Etoposide, Melphalan, Adriamycin) given in lower doses but more frequently to prevent myeloma cells from regrowing between cycles. The goal is to achieve longer remissions and improve survival time for those with high-risk myeloma.
What are the potential side effects?
Potential side effects include nausea and vomiting from the chemotherapy drugs; numbness or tingling due to Thalidomide; increased risk of infection; blood clots; fatigue; hair loss; low blood cell counts leading to bleeding or bruising easily.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have had no or just one round of treatment for my multiple myeloma, not counting bone treatments or spot radiation.
Select...
I am between 18 and 75 years old.
Select...
My kidney function is good, with a creatinine level below 3 mg/dL.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Trial Design

1Treatment groups
Experimental Treatment
Group I: MEL--VTD-PACEExperimental Treatment8 Interventions
Melphalan, Velcade, Thalidomide, Dexamethasone, Cisplatin, Adriamycin, Cyclophosphamide and Etoposide
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Bortezomib D-mannitol
FDA approved
Dexamethasone
FDA approved
Cisplatin
FDA approved
Cyclophosphamide
FDA approved
Thalidomide
FDA approved
Etoposide
FDA approved
Melphalan
FDA approved
Doxorubicin
FDA approved

Find a Location

Who is running the clinical trial?

University of ArkansasLead Sponsor
493 Previous Clinical Trials
150,873 Total Patients Enrolled
54 Trials studying Multiple Myeloma
11,890 Patients Enrolled for Multiple Myeloma
Frits van Rhee, MD, PhDPrincipal InvestigatorUAMS
5 Previous Clinical Trials
38 Total Patients Enrolled
5 Trials studying Multiple Myeloma
38 Patients Enrolled for Multiple Myeloma

Media Library

Adriamycin (Anti-tumor antibiotic) Clinical Trial Eligibility Overview. Trial Name: NCT00869232 — Phase 2
Multiple Myeloma Research Study Groups: MEL--VTD-PACE
Multiple Myeloma Clinical Trial 2023: Adriamycin Highlights & Side Effects. Trial Name: NCT00869232 — Phase 2
Adriamycin (Anti-tumor antibiotic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT00869232 — Phase 2
~5 spots leftby Oct 2025