Actively Recruiting

Phase 2
Age: 18Years - 75Years
All Genders
NCT05636787

Clinical Trial Investigating the Chemotherapeutic Compound Treosulfan (Trecondi® Ideogen) in Myeloma Patients

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2024-07-08

120

Participants Needed

1

Research Sites

251 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Clinical trial investigating the chemotherapeutic compound treosulfan (Trecondi® Ideogen) in myeloma patients.

CONDITIONS

Official Title

Clinical Trial Investigating the Chemotherapeutic Compound Treosulfan (Trecondi® Ideogen) in Myeloma Patients

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Myeloma patients after standard first-line induction treatment; additional induction allowed for refractory cases
  • Fit for high-dose chemotherapy and autologous stem cell transplantation
  • Age between 18 and 75 years
  • ECOG performance status less than 3
  • Creatinine clearance of 35 ml/min or higher
  • Left ventricular ejection fraction 40% or higher within 3 months before study treatment
  • Voluntary written informed consent given
Not Eligible

You will not qualify if you...

  • Uncontrolled acute infection
  • Transplantation comorbidity index (HCTCI) greater than 6 points
  • Active malignant disease except certain early-stage skin or cervical cancers or early prostate cancer; other cancers must be treated and inactive for at least 6 months
  • Major bleeding disorders or coagulopathy
  • Medical conditions interfering with treatment completion or tolerance
  • Lack of cooperation for study treatment
  • Known pregnancy or breastfeeding; inadequate contraceptive measures during and 12 months after treatment
  • Use of investigational anti-cancer agents within 14 days before trial start
  • Known allergies or contraindications to chemotherapy drugs used in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Departement of Medical Oncology, University Hospital Berne

Bern, Switzerland, 3010

Actively Recruiting

Loading map...

Research Team

T

Thomas Pabst, Prof Dr. med

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here