A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With Myelofibrosis

Launched by GERON CORPORATION · May 10, 2022

Keywords

ClinConnect Summary

This clinical trial is studying a new combination treatment for myelofibrosis, a serious blood disorder. The researchers want to find out how safe and effective a drug called imetelstat is when used together with another drug called ruxolitinib. The study has two parts: the first part will help determine the best dose of imetelstat to use, while the second part will evaluate how well this combination works for patients with myelofibrosis.

To participate in this trial, you need to have been diagnosed with myelofibrosis and be at a certain risk level according to specific medical criteria. You should also be eligible to receive ruxolitinib treatment, either because you've been on it for a while or you're a new candidate for it. Participants can expect to undergo regular check-ups and tests to monitor their health and the effects of the treatment. It's important to note that this trial does not accept patients who have had certain previous treatments or specific health issues. If you or a loved one are considering this trial, it could be a chance to access a new treatment option for myelofibrosis.

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Eligibility criteria

• Inclusion Criteria:
• • Diagnosis of primary myelofibrosis (PMF) according to the revised World Health Organization (WHO) criteria or post-essential thrombocythemia-MF or post-polycythemia vera according to the International Working Group for Myelofibrosis Research and Treatment (IWG-MRT) criteria.
• • Dynamic International Prognostic Scoring System (DIPSS) intermediate-1, intermediate-2 or high-risk MF.
• * Candidate for ruxolitinib treatment:
• • 1. Part 1 participants: On ruxolitinib treatment for at least 12 weeks with at least 4 consecutive weeks immediately prior to enrollment at a stable dose.
• • 2. Part 2 participants: Candidate for ruxolitinib treatment as assessed by the investigator and has not previously been treated with a JAK inhibitor (Cohort A) OR currently receiving JAK inhibitor treatment per standard of care for at least 12 weeks (maximum 48 weeks) with at least 4 consecutive weeks at a stable dose prior to enrollment (Cohort B).
• * Clinical signs/symptoms of MF demonstrated by one of the following:
• • 1. Measurable splenomegaly demonstrated by either a palpable spleen measuring ≥5 cm below the left costal margin or a spleen volume ≥450 cm\^3 by MRI or CT, AND
• • 2. active symptoms of MF on the MFSAF v4.0.
• • Ineligible for or unwilling to undergo hematopoietic stem cell transplant at time of study entry.
• • Hematology laboratory test values within protocol defined limits.
• • Biochemical laboratory test values within protocol defined limits.
• • Eastern Cooperative Oncology Group Performance Status score of 0, 1, or 2.
• • Participants should follow protocol defined contraceptives procedures.
• • A woman of childbearing potential must have a negative serum or urine pregnancy test at screening.
• Exclusion Criteria:
• • Peripheral blood blast count of ≥10% or bone marrow blast count of ≥10%.
• • Prior treatment with JAK inhibitor (except for participants being dosed optimized on ruxolitinib or other JAK inhibitor treatment prior to screening and enrollment in part 1 or Part 2 Cohort B).
• • Known allergies, hypersensitivity, or intolerance to imetelstat or ruxolitinib or excipients.
• • Prior treatment with imetelstat.
• • Major surgery within 28 days prior to enrollment.
• • Any investigational drug regardless of class or mechanism of action, hydroxyurea, chemotherapy, (except for ruxolitinib or other JAK inhibitor for participants being dose optimized on JAK inhibitor treatment prior to enrollment), immunomodulatory or immunosuppressive therapy, corticosteroids \>30 mg/day prednisone or equivalent ≤14 days prior to enrollment.
• • Prior history of hematopoietic stem cell transplant.
• • Prior history of partial or complete splenectomy.
• * Diagnosis or treatment for malignancy other than MF, except:
• • Malignancy treated with curative intent and with no known active disease present for ≥3 years before enrollment.
• • Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease.
• • Adequately treated cervical carcinoma in situ without evidence of disease.
• • Clinically significant cardiovascular disease.
• • Known history of human immunodeficiency virus (HIV) or any uncontrolled active systemic infection requiring IV antibiotics.
• • Active systemic hepatitis infection requiring treatment or any known acute or chronic liver disease unless related to MF. Carriers of hepatitis virus are permitted to enter the study.