Phase 1b Study of AEVI-007 in Subjects With Relapsed or Refractory Multiple Myeloma

Completed · Phase 1

Conditions studied: Multiple Myeloma

In brief

This is a multicenter, open-label, dose-escalation Phase 1b study of AEVI-007 in subjects with relapsed or refractory Multiple Myeloma. The objectives of the study are to evaluate the safety, pharmacokinetics and pharmacodynamics of AEVI-007.

Key facts

Study ID: NCT04671251
Run by: Avalo Therapeutics, Inc.
People needed: 13
Starts: 2020-12-15
Expected to finish: 2022-03-30
Last updated by the study team: 2024-02-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subject has active R/R multiple myeloma.
Subject has measurable myeloma based on any of the following:
Serum M-protein > 0.5 g/dL
Urine M-protein > 200 mg/24 hours
Serum free light chains > 10 mg/dL
Measurable plasmacytoma or extramedullary disease
Subject has active myeloma despite prior therapy with a proteasome inhibitor, an immunomodulatory agent and an anti-CD38 antibody.
Note: Subject must not be a candidate for regimens known to provide clinical benefit.
Subject has an Eastern Cooperative Oncology Group performance status (ECOG PS) score of 0 or 1.
Subject is > 18 years of age.
Subject has adequate hematopoietic, renal and hepatic function, defined as:
Absolute neutrophil count > 1,000/μL; platelet count > 75,000/μL in patients with < 50% marrow involvement
Absolute neutrophil count > 750/μL; platelet count > 50,000/μL in patients with >50% marrow involvement
Serum creatinine < 2.5 mg/dL or calculated creatinine clearance of > 30 mL/min according to the Cockcroft-Gault equation
Aspartate transaminase/alanine transaminase ≤2.5× the upper limit of normal (ULN) and total bilirubin < 2× the ULN
If applicable, the subject has undergone prior autologous hematopoietic stem cell transplantation more than 100 days prior to the Screening Visit.
Female patients of childbearing potential who are heterosexually active and male patients with female sexual partners of childbearing potential must agree to use an effective method of contraception (eg, oral contraceptives, double-barrier methods such as a condom and a diaphragm, intrauterine device) or abstain from sexual activity during the study and for 220 days (5 half-lives) following the last dose of study medication, or to abstain from sexual intercourse for this duration of study participation. A woman not of childbearing potential is one who has undergone bilateral oophorectomies or who is post-menopausal, defined as the absence of menstrual periods for 12 consecutive months.
Subject has provided written informed consent for this study.

You may not qualify if…

Subject has currently active infection requiring use of systemic antimicrobial therapy.
Subject has received corticosteroids (>10 mg/daily prednisone or equivalent) or chemotherapy within 2 weeks of study drugs (4 weeks for nitrosourea, melphalan or monoclonal antibodies).
Subject has hyperviscosity syndrome.
Subject has central nervous system involvement by myeloma, including leptomeningeal involvement.
Subject is judged to be at risk for impending fracture.
Subject has known amyloidosis or POEMS (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal protein, Skin changes) syndrome.
Subject had another malignancy within 1 year of study entry with high probability of recurrence.
Subject is pregnant or lactating.
Subject has a history of, or tests positive for, hepatitis B, untreated hepatitis C or human immunodeficiency virus (HIV). Subject with hepatitis C who has received a full course of anti-viral therapy or who is currently receiving anti-viral therapy with undetectable levels of hepatitis C RNA is eligible for the trial.
Subject has undergone major surgery or trauma within 4 weeks of study entry.
Subject has been previously treated with an anti IL 18 antibody.
Subject is currently taking immunomodulatory drugs, including pharmacologic doses of systemic glucocorticoids (> 10 mg prednisone daily or equivalent), anti tumor necrosis factor alpha (TNFα) antibodies, anti-IL-17 antibodies, anti IL 12/23 antibodies, phosphodiesterase-4 (PDE-4) inhibitors, janus kinase (JAK) inhibitors, IL-6 inhibitors, rituximab, methotrexate, cyclosporine, mycophenolate.
Subject with known active autoimmune disorders including, but not limited to, rheumatoid arthritis, lupus, systemic sclerosis, Sjogren's syndrome, psoriatic arthritis, ulcerative colitis, Crohn's disease, vasculitis, multiple sclerosis. Subjects with autoimmune endocrinopathies on stable doses of replacement hormone therapy are eligible for the trial.
Subject has had a prior allogeneic transplant.
Subject has New York Heart Association (NYHA) Class III or IV Congestive Heart Failure (CHF), myocardial infarction or acute coronary syndrome within 6 months prior to the Screening Visit, ongoing angina pectoris, severe peripheral vascular disease, or any other concomitant medical disorder that might interfere with the subject's participation in the trial or interpretation of the study data.
Subject has psychiatric, substance abuse or social conditions that would interfere with the subject's participation or cooperation with the requirements of the trial.
Subject has known hypersensitivity to any of the components of AEVI-007.

Where it is running

University of California, Davis Comprehensive Cancer Center — Sacramento, California, United States
James R. Berenson, MD., Inc. — West Hollywood, California, United States
Florida Cancer Specialists — Lake Mary, Florida, United States
Florida Cancer Specialists — Sarasota, Florida, United States
American Oncology Partners of Maryland, PA — Bethesda, Maryland, United States
Levine Cancer Institute — Charlotte, North Carolina, United States
Froedtert Hospital & the Medical College of Wisconsin — Milwaukee, Wisconsin, United States

Full record on ClinicalTrials.gov

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