Pilot Study Using Propranolol to Decrease Gene Expression of Stress-Mediated Beta-Adrenergic Pathways in Hematopoietic Stem Cell Transplant Recipients

Overview

This is a randomized controlled pilot study designed to evaluate whether the beta-adrenergic antagonist propranolol is effective in decreasing gene expression of stress-mediated beta-adrenergic pathways among a cohort of individuals receiving an autologous hematopoietic stem cell transplant (HCT) for multiple myeloma.

SparkCures ID 731
Trial Phase Phase 2
Enrollment 40 Patients
Treatments
Trial Sponsors
  • Medical College of Wisconsin
NCT Identifier

NCT02420223

Am I Eligible?

The following criteria is a partial list of reasons why patients may or may not be eligible to participate in this clinical trial. Further evaluation with a medical professional will be required to determine full eligibility.

The following criteria is provided for health care professionals.

Inclusion Criteria:

Patients with multiple myeloma receiving an autologous HCT are eligible when the following criteria are met:

  1. 18-70 years of age (70 years is the MCW institutional limit to prescribe high dose melphalan as a conditioning regimen)
  2. ≤ 1 year since initiation of systemic anti-myeloma therapy
  3. Patient is scheduled for autologous hematopoietic stem cell transplant as the upfront therapy for their multiple myeloma
  4. Stable disease, partial response or very good partial response at time of study entry
  5. Karnofsky Performance Status of ≥90 %; patients eligible for HCT are eligible for the study

Exclusion Criteria:

  1. Prior autologous HCT
  2. Non secretory multiple myeloma
  3. Concurrent beta-blocker therapy at or within 3 weeks of study entry.
  4. Previous intolerance to beta-blocker therapy
  5. Any medical contraindications to beta-blocker therapy including, but not limited to, symptomatic hypotension; drug hypersensitivity; sinus bradycardia, sick sinus syndrome, or 2nd or 3rd degree atrioventricular block without a pacemaker; uncompensated heart failure; or uncontrolled asthma
  6. Active, untreated depression screened for by the HCT physician (Patients who screen positive will be offered a referral to the MCW Psycho-Oncology program for further evaluation and treatment)
  7. Concurrent use of medications as specified in the protocol throughout the study or within one week of study entry.

US Trial Locations

Please visit the ClinicalTrials.gov page for historical site information.

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