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

Launched by INSEL GRUPPE AG, UNIVERSITY HOSPITAL BERN · Nov 23, 2022

Keywords

ClinConnect Summary

This clinical trial is studying a chemotherapy drug called treosulfan (also known as Trecondi® Ideogen) to see how well it works for patients with multiple myeloma, a type of blood cancer. The trial is currently recruiting participants aged 18 to 75 who have completed their first round of standard treatment for myeloma and are considered healthy enough for further treatment, which may include a procedure known as autologous stem cell transplantation. To be eligible, patients must meet certain health criteria, such as having a specific level of kidney function and heart health.

Participants in this trial will receive treatment with treosulfan and will be monitored closely for their response and any side effects. It’s important to note that patients with active infections, severe other health issues, or certain conditions that might interfere with the treatment cannot participate. Additionally, women who are pregnant or breastfeeding cannot join the study. If you or a loved one has multiple myeloma and is interested in this trial, it could be a valuable opportunity to access a new treatment while contributing to medical research.

Gender

ALL

Eligibility criteria

• Inclusion criteria:
• • 1. Eligible are myeloma patients after standard first-line induction treatment. Additional induction regimens in refractory myeloma patients are allowed.
• • 2. Patients must be considered fit for subsequent consolidation with high-dose chemotherapy with autologous stem cell transplantation.
• • 3. Patients must be aged 18-75 years.
• • 4. Patients must have an ECOG \<3.
• • 5. Patients must have a creatinine clearance ≥35 ml/min.
• • 6. Patients must have an LVEF ≥40% within three months prior to start of study HDCT.
• • 7. Patients must have given voluntary written informed consent.
• Exclusion criteria:
• • 1. Patients with an uncontrolled acute infection.
• • 2. Patients with a transplantation comorbidity index (HCTCI) \> 6 points.
• • 3. Patients with concurrent active malignant disease with the exception of basalioma/spinalioma of the skin or early-stage cervix carcinoma, or early-stage prostate cancer. Previous treatment for other malignancies (not listed above) must have been terminated at least 6 months before registration and no evidence of active disease may be documented since then.
• • 4. Patients with major coagulopathy or bleeding disorder.
• • 5. Patients with other medical conditions that could potentially interfere with the completion of treatment according to this protocol or that would impair tolerance to therapy or prolong hematological recovery.
• • 6. Lack of patient cooperation to allow study treatment as outlined in this protocol.
• • 7. Known pregnancy or lactating female patients. The pregnancy test could be omitted from the screening visit and postponed to the study treatment if indicated (a pregnancy test in female patients of child-bearing potential is not mandatory since patients are already under induction chemotherapy or mobilization chemotherapy, and pregnancy was excluded before starting induction chemotherapy; if, however, a pregnancy test is clinically indicated, it can be done either during screening or before the start of study treatment).
• • Patient not willing to implement adequate contraceptive measures (hormonal treatment p.o. or i.m., intra-uterine surgical devices, or latex condoms) to avoid pregnancy during study treatment and for 12 additional months.
• • 8. Use of any anti-cancer investigational agents within 14 days prior to the expected start of trial treatment.
• • 9. Contraindications and hypersensitivity to any of the active chemotherapy compounds.

Trial Officials