Oral-ATO for TP53-mutated Myeloid Malignancies

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe University of Hong Kong

About this trial

This is an open-label, phase 2 study of oral arsenic trioxide (Arsenol ®) in combination with ascorbic acid and investigator choice of low-intensity therapy in patients with previously untreated or relapse/refractory TP53-mutated acute myeloid leukemia (AML), myelodysplastic neoplasm (MDS), chronic myelomonocytic leukemia (CMML).

Eligibility criteria

Qualifiers

Willing and able to provide informed consent

Age ≥18 years

Diagnosis of acute myeloid leukemia (AML), myelodysplastic neoplasm (MDS) or chronic myelonocytic leukaemia (CMML) by World Health Organization (WHO) 2022 criteria (1, 3)

Presence of TP53 mutation

Disqualifiers

Willing and able to provide informed consent

Age ≥18 years

Diagnosis of acute myeloid leukemia (AML), myelodysplastic neoplasm (MDS) or chronic myelonocytic leukaemia (CMML) by World Health Organization (WHO) 2022 criteria (1, 3)

Presence of TP53 mutation

Trial design

Treatments tested in this trial

  • Oral arsenic trioxide

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators