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A Phase I Study of Venetoclax Combined With Vyxeos (CPX-351) for Children, Adolescents and Young Adults With Relapsed or Refractory Acute Leukemia

Who is this study for? Children, adolescents and young adults with relapsed or refractory acute leukemia
What treatments are being studied? Vyxeos+Venetoclax
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This study evaluates the safety and tolerability of combining venetoclax with Vyxeos (CPX-351) in pediatric and young adult patients with acute leukemia that has come back or not responded to treatment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Maximum Age: 39
Healthy Volunteers: f
View:

• Ages 1 Year to 39 Years

• Diagnosis of one of the following:

‣ Acute myeloid leukemia (AML), any subtype except

• Patients with acute promyelocytic leukemia (APML) are NOT eligible

∙ Patients with ML-DS are NOT eligible

⁃ Myeloid sarcoma

⁃ Acute leukemia of ambiguous lineage (ALAL)

• Acute undifferentiated leukemia (AUL)

∙ T/myeloid mixed phenotype acute leukemia (MPAL)

∙ B/myeloid MPAL

∙ MPAL with KMT2A-rearrangement MPAL with t (9;22) are NOT eligible

⁃ T-cell acute lymphoblastic leukemia (T ALL)

⁃ Early thymocyte precursor (ETP) ALL

⁃ KMT2A-rearranged ALL

• Disease Status

‣ Relapsed/Refractory AML, MPA, and AUL

⁃ Untreated therapy related AML

⁃ Relapsed/Refractory KMT2A-rearranged ALL, T-cell ALL, ETEP ALL

• Karnofsky/Lanksy performance level score of greater than or equal to 50 percent.

• Prior therapy requirements

‣ Fully recovered from acute toxicities of Hematopoietic Stem Cell Transplant (HSCT) or Anthracycline Exposure

⁃ 14 days must have elapsed since the completion of systemic cytotoxic therapy other than hydroxyurea, decitabine or azacitidine

⁃ 2 weeks must have elapsed for local palliative radiotherapy (RT); 6 months must have elapsed if prior craniospinal RT or if 50% radiation of pelvis, and at least 6 weeks must have elapsed if other substantial bone marrow radiation

• Adequate renal, liver, cardiac, and central nervous system (CNS) function

Locations
United States
Ohio
Cincinnati Children's Hospital Medical Center
RECRUITING
Cincinnati
Contact Information
Primary
Site Pulblic Contact
cancer@cchmc.org
513-636-2799
Time Frame
Start Date: 2018-12-27
Estimated Completion Date: 2028-01
Participants
Target number of participants: 21
Treatments
Experimental: Venetoclax and Vyxeos combination
Venetoclax will be given orally on Days per the assigned dose level. A single course consisting of 3 doses of Vyxeos and 7-21 doses of venetoclax depending on the assigned dose level will be administered to participants in this study. Vyxeos will be administered by central venous catheter over 90 minutes on Day 1, 3, and 5.~Venetoclax is given daily by mouth per assigned dose level.
Authors
Michael Absalon, Laura Agresta
Related Therapeutic Areas
Sponsors
Leads: Children's Hospital Medical Center, Cincinnati

This content was sourced from clinicaltrials.gov