Study of Tinostamustine, First-in-Class Alkylating HDACi Fusion Molecule, in Relapsed/Refractory Hematologic Malignancies

Inclusion Criteria:

1. Patient willing and able to sign an informed consent.

2. Patients age ≥18 years at signing the informed consent.

3. Life expectancy > 3 months.

4. Diagnosis of relapsed or refractory lymphoid malignancy for which there are noavailable therapies.

5. Eastern Cooperative Oncology Group (ECOG) performance status ≤2

6. Absolute Neutrophil Count >1,000 µL

7. Platelets ≥100,000 µL

8. Aspartate aminotransferase/alanine aminotransferase (AST/ALT) ≤2.5 upper limit ofnormal (ULN).

9. Total bilirubin <2.0 mg/dL unless elevated due to known Gilbert's syndrome.

10. Creatinine ≤1.5 x ULN.

11. Serum potassium and magnesium at least at the lowest limit of normal (LLN) atbaseline(before every IMP administration; if it is below LNN, (supplementation ispermissible).

12. Males and females of child-bearing potential, and their partners, must be willing touse at least two effective forms of birth control during the study drugadministration and for at least 90 days after the administration of the study drugto be eligible to participate. Vasectomized partners and patients must be willing touse a secondary method of effective birth control. Sexual abstinence is considered ahighly effective method only if defined as refraining from heterosexual intercourseduring the entire period of risk associated with the study treatment. Thereliability of sexual abstinence needs to be evaluated in relation to the durationof the clinical trial and the preferred and usual lifestyle of the patient.

Specific Eligibility Criteria for Each Patient Cohort in Stage 2 Phase of the Study

Cohort 1: relapsed/refractory multiple myeloma (Recruitment to this cohort stopped Dec 2021) 1. At least one line of prior systemic therapy and no other standard therapy available with proven clinical benefit.

Cohort 2: relapsed/refractory Hodgkin's lymphoma

1. At least two lines of prior therapy and no other standard therapy available withproven clinical benefit.

Cohort 3: PTCL (recruitment to this cohort stopped March 2021)

1. Only PTCL patients with histologically or cytologically confirmed Peripheral T-CellLymphoma - Not Otherwise Specified (PTCL-NOS), angioimmunoblastic T-cell lymphoma (AITL), or Anaplastic Large Cell Lymphoma (ALCL).

2. At least one line of prior combination therapy and no other standard therapyavailable with proven clinical benefit

Cohort 4: relapsed/refractory cutaneous T-cell lymphoma (CTCL), subtypes mycosis fungoides (MF) and Sézary syndrome (SS)

1. Only CTCL patients with histologically or cytologically confirmed MF or SS withstage IIb to IVb disease based on modified ISCL/EORTC staging.

2. At least one line and a maximum of four prior standard systemic therapies and noother standard therapy available with proven clinical benefit.

Cohort 5: PTCL (Recruitment to this cohort stopped March 2021)

Eligibility criteria for sub study:

Diagnosis of relapsed or refractory lymphoma, including Diffuse large B cell lymphoma who failed at least 2 lines of prior systemic therapy, Hodgkin lymphoma who failed at least 3 lines of prior systemic therapy, follicular lymphoma grade 1-3a, marginal zone lymphoma and mantle cell lymphoma who failed at least 2 lines of prior systemic lines of prior therapy, T cell lymphoma (including PTCL, CTCL) who failed at least 2 lines of prior systemic therapy for which there are no available therapies. Patients with bulky disease and Multiple Myeloma patients are excluded from this sub study.

Exclusion Criteria:

1. Patients with any central nervous system involvement.

2. Patient who had a hematologic malignancy that has transformed.

3. Any patient who has relapsed within 100 days of stem cell infusion following anallogenic or an autologous bone marrow transplant.

4. Patients with corrected QT (QTc) interval (Fridericia's formula) > 450 msec.

5. Patients who are on treatment with drugs known to prolong the QT/QTc interval.

6. Any serious medical condition that interferes with adherence to study procedures.

7. Patients with a history of another malignancy diagnosed within three years of studyenrollment excluding basal cell carcinoma of the skin, squamous cell carcinoma ofthe skin, or in situ cervical cancer that has undergone potentially curativetherapy.

8. Pregnant or breast feeding females.

9. New York Heart Association (NYHA) stage III/IV congestive heart failure. Thefollowing arrhythmias not adequately controlled, active: atrial fibrillation/flutterwith poor rate control, documented sustained ventricular tachycardia (defined as >30seconds or requiring cardioversion before 30 seconds have elapsed) or TdP.

10. Active infections, or other significant co-morbidities [(e.g., active centralnervous system metastases and/or carcinomatous meningitis, active infectionrequiring systemic therapy, history of human immunodeficiency virus (HIV) infection,or active Hepatitis B or Hepatitis C.

11. Previous cancer therapies within three (3) weeks of dosing as long as the patienthas recovered to eligibility levels prior to treatment in this study.

12. Use of other investigational agents within 30 days or 5 half-lives prior to thefirst dose of study drug unless patient has recovered from any related toxicities ≥Grade 1.

13. Steroid treatment within seven (7) days prior to study treatment. Patients thatrequire intermittent use of bronchodilators, topical steroids or local steroidinjections will not be excluded from the study. Patients who have been stabilized to 10 mg PO QD or less seven (7) days prior to study drug administration are allowed.

14. Patients on Valproic Acid for any indication (epilepsy, mood disorder) must beexcluded from the trial .