A Phase 1/2 Multicenter Open-label Study to Investigate Treatment of Hydroxyurea in Combination With Valproic Acid (VPA), or 6- Mercaptopurine in Combination With VPA in Patients With AML or HR-MDS Unfit for Standard Therapy

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The purpose of this study is to investigate the safety, tolerability, and preliminary efficacy of the combination treatment of hydroxyurea capsules and valproic acid capsules, or the combination treatment of 6-mercaptopurine tablets and valproic acid capsules in male and female patients aged 18 years or older with acute myeloid leukemia or high- risk myelodysplastic syndrome. The population to be studied is newly diagnosed AML patients who are considered unfit for standard induction chemotherapy, HR-MDS unfit/ineligible for standard treatment, and relapsed/refractory AML/HR-MDS patients who are considered unfit for standard therapy ,or are, for some reason, ineligible for another type of therapy. Clinically, hydroxyurea, valproic acid and 6-mercaptopurine are historically very well-known therapeutic agents with low toxicity profiles. The rationale for this study is that the combination of these drugs with low toxicity will be well tolerated in elderly AML patients with comorbidities, or lower performance status. This combination could have a beneficial therapeutic effect on overall survival and contribute to a better quality of life.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

‣ Participants are eligible for the study only if all of the following criteria apply:

‣ o Female or male, age 18 years or older

• Written informed consent

• Patients with Newly diagnosed AML, as defined by ELN 2022 criteria, or relapsed/refractory AML who: - are unfit, defined as HCT-CI ≥ 3, or - in the opinion of the investigator are not candidates for standard therapy or unlikely to tolerate or derive significant clinical benefit from standard therapy, or

‣ the patient has declined standard therapy

‣ Newly diagnosed HR-MDS, or relapsed/refractory HR-MDS who:

• are unfit, defined as HCT-CI ≥ 3, or

• in the opinion of the investigator are not candidates for standard therapy or unlikely to tolerate or derive significant clinical benefit from standard therapy, or

• has declined standard therapy

‣ Secondary AML (MDS-related/ therapy- induced), or

‣ Acute promyelocytic leukemia not eligible for standard therapy and/or specific therapy.

• Adequate renal and hepatic functions unless clearly disease related as indicated by the following laboratory values:

‣ Serum creatinine ≤1.5 x ULN;

⁃ Estimated creatinine clearance ≥ 40 mL/min (Cockcroft-Gault equation);

⁃ Hepatic function;

‣ i. Serum bilirubin ≤ 1.5 x upper limit of normal (ULN); ii. Aspartate aminotransferase (AST)

• ≤2.5 × ULN

• ≤5 × ULN for patients with liver metastases

⁃ iii. Alanine aminotransferase (ALT)

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⁃ ≤2.5 × ULN

• ≤5 × ULN for patients with liver metastases

⁃ iv. Alkaline phosphatase (ALP)

‣ 1\. ≤2.5 × ULN

• European Cooperative Oncology Group (ECOG) performance status 0, 1, 2 or 3

• Female patients of childbearing potential must have a negative serum pregnancy test within 3 days prior to taking their first dose of study medication. Male patients and female patients of reproductive potential must agree to practice highly effective methods of contraception (such as hormonal implants, combined oral contraceptives, injectable contraceptives, intrauterine device with hormone spirals, total sexual abstinence, vasectomy) throughout the study and for \>3 months after the last dose of study medication. Female patients are considered NOT of childbearing potential if they have a history of surgical sterility or evidence of post-menopausal status defined as any of the following:

∙ Natural menopause with last menses \>1 year ago

‣ Radiation induced oophorectomy with last menses \>1 year ago

‣ Chemotherapy induced menopause with last menses \>1 year ago

Locations
Other Locations
Norway
Haukeland University Hospital
RECRUITING
Bergen
Contact Information
Primary
Bjørn Tore Gjertsen, MD, PhD
bjorn.tore.gjertsen@helse-bergen.no
004741566248
Backup
Irini Ktoridou-Valen, MD
irini.ktoridou-valen@helse-bergen.no
004746664928
Time Frame
Start Date: 2024-05-23
Estimated Completion Date: 2029-09-30
Participants
Target number of participants: 48
Treatments
Active_comparator: Hydroxyurea (HU) + Valproic Acid (VPA) part 1
Combination treatment 1 (T1): hydroxyurea + valproic acid, combination treatment 2 (T2): 6-mercaptopurine + valproic acid.~Each patient enrolled will receive at least one cycle with T1: hydroxyurea and valproic acid. The 1st cycle in the study always constitutes of hydroxyurea (1000 mg twice a day) plus valproic acid (300 mg + 600 mg) for 14 days; then 14 days with no medication.~Each cycle duration is 28 days. Patients who do not experience clinical benefit after 1st cycle, or experience unacceptable and unmanageable toxicity after 1st cycle, will not be eligible to continue on this regimen and they will be allocated to treatment combination 2. T2 constitutes of 6-mercaptopurine ( 50 mg once a day) plus valproic acid 300 mg + 600 mg ) for 14 days; followed by 14 days with no medication. Each cycle duration is 28 days.
Active_comparator: Hydroxyurea (HU) + Valproic Acid (VPA) part 2
Part B consists of two cohort expansions where the setup is identical to part A: one for HU + VPA and one for 6-MP + VPA, 16 patients in each, in total 32 new patients.~In part B the same principles will apply for response, withdrawal and allocation from HU+ VPA to 6-MP + VPA. The treatment duration in all arms can last to up 6 cycles in total. Each cycle duration is 28 days.
Sponsors
Leads: Haukeland University Hospital

This content was sourced from clinicaltrials.gov

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