Therapy-Related Myelodysplastic Syndrome

2

Review clinical trials related to Therapy-Related Myelodysplastic Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Personalized NK Cell Therapy in CBT

This phase II clinical trial studies how well personalized natural killer (NK) cell therapy works after chemotherapy and umbilical cord blood transplant in treating patients with myelodysplastic syndrome, leukemia, lymphoma or multiple myeloma. This clinical trial will test cord blood (CB) selection for human leukocyte antigen (HLA)-C1/x recipients based on HLA-killer-cell immunoglobulin-like receptor (KIR) typing, and adoptive therapy with CB-derived NK cells for HLA-C2/C2 patients. Natural killer cells may kill tumor cells that remain in the body after chemotherapy treatment and lessen the risk of graft versus host disease after cord blood transplant.

Participants needed: 100
Trial details
Phase: Phase 2Age: 15-80Biological sex: AllType: InterventionalSponsor: M.D. Anderson Cancer CenterUpdated: May 22, 2026Locations: 1
Eligibility criteria

Patients must have one of the following hematologic malignancies: acute myelogen... [+18]

Human immunodeficiency virus (HIV) positive; HIV results will be determined by n... [+3]

Status: Recruiting

Venetoclax Basket Trial for High Risk Hematologic Malignancies

This trial is evaluating the safety and tolerability of venetoclax with chemotherapy in pediatric and young adult patients with hematologic malignancies, including myelodysplastic syndrome (MDS), acute myeloid leukemia derived from myelodysplastic syndrome (MDS/AML), and acute lymphoblastic leukemia (ALL)/lymphoblastic lymphoma (LBL). The names of the study drugs involved in this study are below. Please note this is a list for the study as a whole, participants will receive drugs according to disease cohort. * Venetoclax * Azacitidine * Cytarabine * Methotrexate * Hydrocortisone * Leucovorin * Dexamethasone * Vincristine * Doxorubicin * Dexrazoxane * Calaspargase pegol * Hydrocortisone

Participants needed: 30
Trial details
Phase: Phase 1Age: 1-40Biological sex: AllType: InterventionalSponsor: Andrew E. Place, MDUpdated: Mar 12, 2026Locations: 5
Eligibility criteria

MDS with excess blasts (>10%) [+89]

Use of strong or moderate CYP3A inhibitors/inducers within 3 days of study entry [+27]