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NCT01842308 · ClinicalTrials.gov registry record · Phase 1

Carfilzomib and Melphalan Before Stem Cell Transplant in Treating Patients With Multiple Myeloma

A Phase 1 study of Refractory Plasma Cell Myeloma and DS Stage I Plasma Cell Myeloma, sponsored by Mayo Clinic.

Completed
Registry status
Phase 1
Development phase
50
Enrollment target
2
Study locations

NCT01842308: Completed Phase 1 study of Refractory Plasma Cell Myeloma and DS Stage I Plasma Cell Myeloma, sponsored by Mayo Clinic.

NCT01842308 is a Phase 1 study of Refractory Plasma Cell Myeloma and DS Stage I Plasma Cell Myeloma that has completed, run by Mayo Clinic. The registered enrollment target is 50 participants, above the 45-participant average among 25 other Refractory Plasma Cell Myeloma trials with a reported enrollment target (11% higher). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01842308, a Phase 1 study of Refractory Plasma Cell Myeloma and DS Stage I Plasma Cell Myeloma, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
Phase 1
Development phase
50 participants
Enrollment target
2
Study locations

Study Summary

This phase I/II trial studies the side effects and best dose of carfilzomib when given together with melphalan and to see how well they work in treating patients with multiple myeloma before stem cell transplant. Carfilzomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as melphalan, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving carfilzomib together with melphalan may kill more cancer cells.

Primary Outcome

Will be defined as the dose level below the lowest dose that induces dose-limiting toxicity(DLT) in at least one-third of patients. For this study, a DLT is any of the following during the first 2 cycles of treatment; Absolute neutrophil count engraftment\* delayed beyond day 21 or Platelet engraftment\* delayed beyond day 30, grade 3+ related sensory or motor neuropathy, or grade 4+ related non-neurologic or non-hematologic adverse event(excluding nausea, vomiting, and diarrhea. Reported below

Interventions

  • DRUG Melphalan
  • OTHER Laboratory Biomarker Analysis
  • DRUG Carfilzomib
  • PROCEDURE Autologous Hematopoietic Stem Cell Transplantation
  • PROCEDURE Autologous Bone Marrow Transplantation

Study Locations (2)

Florida

  • Mayo Clinic in Florida - Jacksonville

Minnesota

  • Mayo Clinic - Rochester

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2013-06-04
Est. Completion 2019-10-28
Phase Phase 1
Mayo Clinic

2,844 total trials

What the finished NCT01842308 record still lists

NCT01842308 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, above the 45-participant average among 25 other Refractory Plasma Cell Myeloma trials with a reported enrollment target (11% higher).

The record links to 4 conditions, with Refractory Plasma Cell Myeloma appearing as the primary indexed condition, and to 5 interventions - of which Melphalan is the first listed.

NCT01842308 reports a single indexed study location in Florida, Minnesota.

Frequently Asked Questions

What is clinical trial NCT01842308 about?

NCT01842308 is a clinical study titled "Carfilzomib and Melphalan Before Stem Cell Transplant in Treating Patients With Multiple Myeloma". This phase I/II trial studies the side effects and best dose of carfilzomib when given together with melphalan and to see how well they work in treating patients with multiple myeloma before stem cell transplant. Carfilzomib may stop the growth of cancer cells by blocking some of the enzymes needed ...

What is the current status of trial NCT01842308?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2013-06-04. Estimated completion is 2019-10-28.

What conditions does trial NCT01842308 study?

This clinical trial studies the following conditions: Refractory Plasma Cell Myeloma, DS Stage I Plasma Cell Myeloma, DS Stage II Plasma Cell Myeloma, DS Stage III Plasma Cell Myeloma.

What interventions are being tested in trial NCT01842308?

The interventions under investigation include: Melphalan (DRUG), Laboratory Biomarker Analysis (OTHER), Carfilzomib (DRUG), Autologous Hematopoietic Stem Cell Transplantation (PROCEDURE), Autologous Bone Marrow Transplantation (PROCEDURE).

Who is sponsoring clinical trial NCT01842308?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01842308 being conducted?

This trial has 2 study locations across Florida, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Refractory Plasma Cell Myeloma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01842308's enrollment target sits among peer trials

50 7th of 25 higher than 18 of 25 other Refractory Plasma Cell Myeloma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Refractory Plasma Cell Myeloma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01842308, the US trial registry maintained by the National Library of Medicine. NCT01842308 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.