A Phase 2 Study of Tipifarnib in Subjects With Chronic Myelomonocytic Leukemia, Other Myelodysplastic /Myeloproliferative Neoplasias, and Acute Myeloid Leukemia
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Kura Oncology, Inc.
- Enrollment
- 44
- Locations
- 8
- Primary Endpoint
- Objective Response Rate (ORR)
Study Overview
Brief Summary
A Phase 2 study to investigate the antitumor activity in terms of overall response rate (ORR) of tipifarnib in approximately 36 eligible subjects with Myelodysplastic/Myeloproliferative Neoplasias (MDS/MPN), including Chronic Myelomonocytic Leukemia (CMML), and 36 eligible subjects with Acute Myeloid Leukemia (AML). Subjects received tipifarnib 1200 mg to be taken orally with food, twice daily, for 7 days in alternating weeks (Days 1 to 7 and Days 15 to 21) in 28-day cycles. Following amendment 3 subjects (Cohorts 1-4) will receive tipifarnib administered at a dose of 400 mg, orally with food, twice a day (bid) for 21 days in 28-day cycles.
Detailed Description
This Phase 2 study will investigate the antitumor activity in terms of ORR of tipifarnib in subjects with Myelodysplastic/Myeloproliferative Neoplasias (MDS/MPN cohorts) and Acute Myeloid Leukemia (AML cohorts). For MDS/MPN cohorts, this study will assess the antitumor activity of tipifarnib, in terms of ORR, in subjects with MDS/MPN, including CMML, who have a high ratio of expression of CXCR4 to CXCR2 (CXCR4/2 ratio) in their bone marrow and in those with a low CXCR4/2 ratio. For AML cohorts, this study will assess the antitumor activity of tipifarnib, in terms of ORR, in subjects with AML who have a high ratio of expression of CXCR4 to CXCR2 (CXCR4/2 ratio) in their bone marrow and in those with low CXCR4/2 ratio. Subjects enrolled in the study will consist of patients with KRAS, NRAS wild type status.
- Subjects with MDS/MPN with high CXCR4/2 ratio
- Subjects with MDS/MPN with low CXCR4/2 ratio
- Subjects with AML with high CXCR4/2 ratio
- Subjects with AML with low CXCR4/2 ratio
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Subject is at least 18 years of age.
- •For subjects to be enrolled in the CMML or MDS/MPN cohorts:
- •a. Diagnosis of CMML or MDS/MPN as defined by the World Health Organization (WHO) criteria (2008).
- •For subjects enrolled in the AML cohort:
- •Documented pathological evidence of AML, as defined by WHO criteria (2008)
- •Refractory to previous induction chemotherapy, relapsed disease, or age ≥ 60 and not appropriate for standard cytotoxic therapy due to age, performance status, and/or adverse risk factors according to the treating physician
- •Eastern Cooperative Oncology Group (ECOG) performance status 0 -
- •Subject is willing and able to comply with scheduled visits, treatment plans, laboratory tests and other procedures (including bone marrow assessments).
- •At least 1 week since the last systemic therapy regimen prior to Cycle 1 Day
- •Subjects on a stable dose of hydroxyurea for at least 2 weeks prior to Cycle 1 Day 1 may continue on hydroxyurea until Cycle 1 Day
- •Subjects must have recovered to NCI CTCAE v. 4.03 < Grade 2 from all acute toxicities (excluding Grade 2 toxicities that are not considered a safety risk by the Sponsor and Investigator) or toxicity must be deemed irreversible by the Investigator.
- •Acceptable liver function:
- •Total bilirubin ≤ upper limit of normal (ULN).
- •AST (SGOT) and ALT (SGPT) ≤ 1.5 x ULN.
- •Acceptable renal function with serum creatinine ≤ 1.5 x ULN or a calculated creatinine clearance ≥ 60 mL/min using the Cockcroft-Gault or Modification of Diet in Renal Disease formulas.
- •Female subjects must be:
- •Of non-child-bearing potential (surgically sterilized or at least 2 years post-menopausal); or
- •If of child-bearing potential, subject must use a highly effective method of contraception, such as combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation, progestogen-only hormonal contraception associated with inhibition of ovulation, intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion, vasectomised partner or sexual abstinence. Both females and male subjects with female partners of child-bearing potential must agree to use a highly effective method of contraception for 2 weeks prior to screening, during, and at least 28 days after last dose of trial medication for females and 90 days for males. Female subjects must have a negative serum or urine pregnancy test within 72 hours prior to start of trial medication.
- •And, not breast feeding at any time during the study.
- •Written and voluntary informed consent understood, signed and dated.
Exclusion Criteria
- •Neoplasia harbours RAS mutation (NRAS mutant, KRAS mutant or double mutant)
- •Acute promyelocytic leukemia or Bcr-Abl positive leukemia (chronic myelogenous leukemia in blast crisis)
- •Clinically active CNS leukemia
- •CMML with t(5;12) that have not yet received imatinib.
- •Participation in any interventional study within 1 week of randomization or 5 half-lives of the prior treatment agent (whichever is longer).
- •Ongoing treatment with an anticancer agent for CMML, MDS/MPN or AML not contemplated in this protocol. Subjects on a stable dose of hydroxyurea for at least 2 weeks prior to Cycle 1 Day 1 may continue on hydroxyurea until Cycle 1 Day
- •Hematopoietic stem cell transplantation (HSCT) performed within 3 months prior to Cycle 1 Day
- •Concurrent use of granulocyte macrophage colony-stimulating factor (GM-CSF).
- •Prior treatment (at least 1 full treatment cycle) with a farnesyltransferase inhibitor.
- •Active coronary artery disease requiring treatment, myocardial infarction within the prior year, New York Heart Association grade III or greater congestive heart failure, cerebro-vascular attack within the prior year, or current serious cardiac arrhythmia requiring medication except atrial fibrillation.
- •Major surgery, other than diagnostic surgery, within 2 weeks prior to Cycle 1 Day 1, without complete recovery.
- •Active, concurrent malignancy requiring radiation, chemotherapy, or immunotherapy (excluding non-melanoma skin cancer, adjuvant hormonal therapy for breast cancer and hormonal treatment for castration sensitive prostate cancer).
- •Active and uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy. Known infection with human immunodeficiency virus (HIV), or an active infection with hepatitis B or hepatitis C.
- •Concomitant disease or condition that could interfere with the conduct of the study, or that would, in the opinion of the investigator, pose an unacceptable risk to the subject in this study.
- •The subject has legal incapacity or limited legal capacity.
- •Significantly altered mental status that would limit the understanding or rendering of informed consent and compliance with the requirements of this protocol. Unwillingness or inability to comply with the study protocol for any reason.
Arms & Interventions
Tipifarnib, Oral
Single arm
Intervention: Tipifarnib (Drug)
Outcomes
Primary Outcomes
Objective Response Rate (ORR)
Time Frame: Up to 12 months
The ORR was estimated based on the number of participants who achieved an objective response (OR) (complete response \[CR\], complete cytogenetic remission \[CCR\], partial remission \[PR\], marrow response \[MR\], or clinical benefit \[CB\] performed by Principal Investigator according to the MDS/MPN International Working Group \[IWG\] criteria).
Secondary Outcomes
- Progression Free Survival (PFS)(1 year)
- Duration of Response (DoR)(Up to approximately 15 months)
- Overall Survival (OS)(Up to approximately 15 months)
- Number of Participants Who Experienced Treatment-emergent Adverse Events (TEAEs)(Up to approximately 3 years)