A Study in Leukemia Patients With Karonudib

Inclusion Criteria:

1. Written informed consent.

2. Age 18-75 years (may be extended to older if deemed fit).

3. The patient has received standard of care treatments and has refractory or relapsedor progressive disease with no suitable standard of care options available. For expansion cohort (Cohort V): Patients can only have received a maximum of 70% ofanthracycline lifetime exposure to date of proposed dosing day. Cohorts I-IV: AML, ALL, DLBCL, Burkitt lymphoma, multiple myeloma or high-risk MDS,according to the WHO 2016 criteria.

4. Expansion cohort (Cohort V): Relapsed, Recurrent or Progressive AML or MDS accordingto the ELN 2017 criteriaWHO 2016 criteria.

5. For expansion cohort (Cohort V): Patients can only have received a maximum of 70% ofanthracycline lifetime exposure to date of proposed dosing day.

6. The patient has received standard of care treatments and has refractory or relapseddisease with only experimental therapies as further treatment options.

7. Life expectancy of at least 8 weeks (as per investigators clinical assessment).

8. ECOG PFS 0-2

9. Patients must have measurable disease by blood or bone marrow or imagingexamination.

10. Have a normal left ventricular ejection fraction (LVEF) based on institutionalranges.

11. Adequate hepatic and renal function defined as:

12. Total bilirubin < 3 x ULN (does not apply to patients with Gilberts Syndrome).

13. AST and ALT ≤ 5 x ULN.

14. The calculated GFR is at least 30 ml/min using Cockcroft-Gault method.

15. Platelet count≥10 x 109/L. (Can be supported by platelet transfusion)

16. Subject must be able to take oral medication.

17. Negative pregnancy test according to CTFG guidance 2014 for females ofchild-producing potential.

Exclusion Criteria:

1. Age less than 18 years.

2. Less than 4 weeks since stopping previous systemic chemotherapy treatment with theexception of stable dose Hydroxyurea, Trophosphamide, oral Cyclophosphamide, ImID orThioguanine which needs to be stopped 10 x t1/2 prior to Karonudib administration.

3. Less than 1 week since stopping palliative radiotherapy.

4. Less than 2 weeks after surgery except access surgical procedures.

5. Less than 6 months since a clinically significant cardiovascular event such asmyocardial infarction, unstable angina, angioplasty, bypass surgery, stroke or TIA.

6. Congestive heart failure NYHA class > II.

7. History of arrhythmias or arrhythmias discovered during the screening period (apartfrom atrial fibrillation without ventricular tachycardia and premature extra beats).

8. Patients requiring anti-arrhythmic drugs except for stable dose beta-blocking orcalcium channel blocking agents.

9. QTc interval >470 ms at baseline (Fridericia correction).

10. Use of Fentanyl (must be stopped at least 1 week prior to initiation of Karonudib).

11. Use of anti-oxidants vitamins and Acetylcysteine (must be stopped within 48 hours ofstarting treatment with Karonudib).

12. Use of antidepressant medications which are substrate for CYP2D6 (must be stopped atleast 3 weeks prior to starting treatment with Karonudib).

13. Any severe acute or chronic medical condition that places the patient at increasedrisk or interferes with the interpretation of study results.

14. Intracerebral engagement (patient with previously known engagement are eligibleprovided that there is no evidence of disease progression for a minimum of 8 weeksprior to inclusion.

15. Known acute or chronic infection with hepatitis B or C except for DNA-negativehepatitis B with stable dose anti-viral agents.

16. Known HIV infection.

17. Pregnant or breast-feeding women.

18. Patients with reproductive potential not implementing accepted and effective meansof contraception.

19. Participation in any other clinical trial with a pharmaceutical product within 5 xt½, or minimum 1 week, since last dosing of the IMP, whichever is the shorter.

20. Acute promyelocytic leukemia (AML M3).

21. Uncontrolled ongoing systemic or localized infection.

22. Unable to comply with study procedures.

23. Peripheral neurological toxicity CTCAE grade 2 or higher.