Intravenous Administration of RGI-2001 in Patient Undergoing Allogenic Hematopoietic Stem Cell Transplantation (AHSCT)

The clinical trial is a Phase 1/2a, open-label, multi-center, dose-escalation study to evaluate the safety, tolerability and pharmacokinetic profile of RGI-2001 in patients undergoing AHSCT, with radiation or non-radiation myeloablative preparative treatment.

In Part 1 (Phase 1: Dose Escalation Phase), patients will receive a single intravenous administration of RGI-2001 approximately 30 minutes after completion of the transplant (either allogeneic PBSCs or allogenic bone marrow transplantation (unmodified)) with the dosage based upon the assigned treatment cohort. Eligible patients will be enrolled in five to seven centers in the United States. Patients who are undergoing AHSCT will be enrolled in a sequential group dose-escalating fashion to determine the safety, tolerability, pharmacokinetic profile, and the MTD or MFD of RGI-2001. It is anticipated that up to six dose levels will be evaluated in Part 1, with an option for an additional cohort (Cohort 7) if the MTD is not reached and pharmacodynamic markers suggest higher doses are warranted.

In Part 2 (Expansion Phase), one or more doses below the MTD or MFD will be selected based on a potential correlation between GvHD and biological activity to further assess safety and biologic activity. Approximately 30 patients who are undergoing either allogeneic PBSCs or allogenic bone marrow transplantation (unmodified) will be enrolled in Part 2 of the study.

Patients will be monitored for safety for 29 days after the transplant procedure.

All patients will be followed for 100 days following transplant procedure for the incidence of acute GvHD, according to the Modified Keystone Criteria for grading acute GvHD (Przepiorka D, et al)

Inclusion criteria

• Subject has a hematological malignancy or aplastic anemia (AA) and is undergoing a first allogeneic transplant procedure.
• Meet one of the following underlying disease criteria:

a. Acute myelogenous leukemia (AML) i. First or subsequent morphologic remission b. Acute lymphoblastic leukemia (ALL) i. First or subsequent morphologic remission c. Chronic myelogenous leukemia (CML) i. Chronic phase; or ii. Accelerated phase d. Multiple Myeloma (MM) i. Not more than 20% plasma cells in the bone marrow e. Myelodysplastic syndrome (MDS), including chronic myelomonocytic leukemia (CMML), who have received at least one previous induction regimen and have <10% blasts f. Myeloproliferative disorder (MPD), including; i. myeloid metaplasia, and ii. myelofibrosis g. Non-Hodgkin's Lymphoma (NHL) i. High-risk NHL in first remission; or ii. Relapsed or refractory NHL h. Hodgkin's lymphoma (HL) beyond first remission i. Aplastic anemia (AA)

• Male or female, age ≥18 years of age
• Reasonable expectation of survival for at least 3 months, if the transplant procedure is successful
• Eastern Cooperative Oncology Group (ECOG) status of 0-2 or Karnofsky Performance Status (KPS) of > 60
• Transplant Donor

• Part 1 (Phase 1: Dose Escalation Phase):

Unrelated transplant donor with no more than 1 HLA allele or antigen mismatch, defined as loci A, B, C and DR (note: DQ is excluded)

• Part 2 (Phase 2a: Expansion Phase):Related or unrelated transplant donor, with no more than 1 HLA allele or antigen mismatch, defined as loci A, B, C and DR (note: DQ is excluded).
• Source of the allograft

• Part 1 (Phase 1: Dose Escalation Phase):Unmodified (non-manipulated) bone marrow, or mobilized peripheral blood stem cell (PBSC) transplant, using G-CSF as the mobilizing agent.
• Part 2: (Phase 2a: Expansion Phase) Unmodified (non-manipulated) bone marrow, or mobilized peripheral blood stem cell (PBSC) transplant, using G-CSF as the mobilizing agent.
• Anti-graft-versus-host disease (GvHD) prophylaxis:

A calcineurin inhibitor [either tacrolimus (FK506) or cyclosporin A)], in combination with either methotrexate (MTX), mycophenolate mofetil (MMF) or sirolimus (RAPA) all at doses as per the institutional protocols

• Adequate hepatic function, with bilirubin not exceeding the upper limit of normal (except when attributed to Gilbert's Disease), and AST and ALT of less than 1.5 times the upper limit of normal
• No clinically significant cardiac conduction disorder on screening ECG
• Serum creatinine ≤ 2.0 mg/dL
• Female patients of childbearing potential must have a negative serum pregnancy test prior to enrollment and must agree to use dual method of contraception for 30 days after study drug administration. Approved methods of contraception include, an IUD with spermicide, a female condom with spermicide, a diaphragm with spermicide, a cervical cap with spermicide, use of a condom with spermicide by sexual partner or a sterile sexual partner.
• If male, subjects must be sterile or willing to use an approved method of contraception from the time of Informed Consent to 30 days after study drug treatment. Males must be willing to refrain from sperm donation within 30 days after study drug treatment.
• No clinically significant acute or chronic medical condition that in the opinion of the investigator will interfere with study participation
• No clinically significant laboratory abnormalities as determined by the Principal Investigator, in consultation with the Sponsor's Medical Monitor
• No active infection
• Have signed written informed consent before undergoing any study related procedures and is willing to comply with all study procedures

Exclusion criteria

• Female subjects who are pregnant or lactating
• Subjects about to undergo a non-ablative or non-myeloablative transplant
• AML or ALL patient who are in relapse (>5% blasts) or who are defined as primary refractory
• Blast crisis CML
• Radiation, chemotherapy, immunotherapy in the previous 3 weeks, unrelated to the transplant procedure
• Subjects who, in the judgment of the Investigator have not recovered from the effects of previous therapy
• Subject who is about to undergo cord blood transplantation
• Procedures that are intended to deplete regulatory T-cells from donor transplant materials
• Known or suspected HIV infection
• Active hepatitis A, B, or C infection in recipient or donor
• Uncontrolled active infection requiring IV antibiotics in recipient or donor
• Major surgery within 1 month before Day 0
• Participation in an investigational study within 1 month prior to Day 0
• Prior treatment with anti-CD3 antibodies
• Treatment with anti-CD20 antibodies or anti-thymocyte globulin (ATG) within 3 months of the AHSCT procedure (i.e. infusion of transplant material and RGI-2001).
• Vaccination within the preceding 2 weeks prior to the planned dose of RGI-2001
• Planned vaccination within 2 months after study drug administration
• Known history of cardiac dysfunction (e.g. <50% ejection fraction), ischemia, conduction abnormalities, or myocardial infarction in the previous six months
• Cardiac pacemaker or automatic implantable cardioverter-defibrillator
• Marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval >450 ms
• Congenital long QT syndrome or family history of long QT syndrome
• History of additional risk factors for torsades de pointes (TdP) (e.g., heart failure, hypokalemia)
• Bundle branch block
• Connective tissue/rheumatologic disorders
• History of autoimmune disease
• History of solid tumor, excluding non-melanoma skin or cervical carcinoma after curative resection, within the preceding 5 years
• Uncontrolled diabetes
• Prior allogeneic hematopoietic stem cell transplantation
• Any other prior organ transplant
• Psychiatric or addictive disorders that preclude obtaining reliable informed consent
• Any other condition that, in the opinion of the investigator, renders the subject unsuitable for study participation