Study of KB004 in Subjects With Hematologic Malignancies (Myelodysplastic Syndrome, MDS, Myelofibrosis, MF)

• Status: Suspended
• Trial end date: 2016-12-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a global, multicenter, open-label, repeat-dose, Phase 1/2 study consisting of a Dose Escalation Phase (Phase 1) and a Cohort Expansion Phase (Phase 2). In both phases, KB004 will be administered by IV infusion once weekly as part of a 21-day dosing cycle.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Humanigen, Inc.; KaloBios Pharmaceuticals
• Treatments: Antibodies; Antibodies, Monoclonal; Immunoglobulins

Criteria

Key Inclusion Criteria (Phase 1):

• Confirmed hematologic malignancy, including Acute Myeloid Leukemia (AML), Chronic Lymphocytic Leukemia (CLL), Chronic Myelogenous Leukemia (CML), Acute Lymphocytic Leukemia (ALL), Myelodysplastic Syndrome (MDS), Multiple Myeloma (MM), Myelofibrosis (MF), Myeloproliferative Neoplasms (MPN) or MDS/MPN overlap diseases. (Once Phase 2 has started subjects with AML will be eligible for inclusion in the Phase 1 portion of the study only if their malignancy has been shown to have c-Cbl mutation, trisomy 3, trisomy 11, inv(16), or elevated FLT3. [Other AML and subjects with MDS will no longer be eligible for inclusion in the Phase 1 portion of the study]).

Key Inclusion Criteria (Phase 2):

• Part A: AML or MDS patients with an acceptable level of EphA3 expression

• Part B: MF patients with an acceptable level of EphA3 expression

Key Inclusion Criteria (Both Phases):

• Confirmed hematologic malignancy refractory to or progressed following standard treatments, or subjects not considered medically suitable to receive standard of care treatment or who refuse standard of care treatment

• Acceptable level of EphA3 expression

• Eastern Cooperative Oncology Group (ECOG) ≤1

• Acceptable laboratory results

Key Exclusion Criteria (Both Phases):

• For subjects with AML, more than 2 prior therapies for AML (induction and consolidation with or without a hypomethylating agent given in a maintenance setting are considered 1 therapy)

• History of or current central nervous system (CNS) involvement that may increase risk of bleeding

• Recent major surgery

• Ongoing surgical or wound healing complications

• Active clinically significant bleeding

• Uncontrolled hypertension

• Significant intercurrent illness

• Known history of prolonged bleeding times or platelet dysfunction

• Active infection requiring IV antibiotics, IV antifungals, or IV antivirals within 2 weeks prior to Cycle 1, Day 1