Tipifarnib in Subjects With Chronic Myelomonocytic Leukemia, Other MDS/MPN, and Acute Myeloid Leukemia

Leukemia, Myelomonocytic, Chronic Clinical Trial

— CMML/AML  

Official title:

A Phase 2 Study of Tipifarnib in Subjects With Chronic Myelomonocytic Leukemia, Other Myelodysplastic /Myeloproliferative Neoplasias, and Acute Myeloid Leukemia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02807272
• Other study ID #: KO-TIP-004
• Status: Completed
• Phase: Phase 2
• Start date: October 2016
• Est. completion date: December 14, 2020

Study information

• Verified date: May 2021
• Source: Kura Oncology, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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 (amendment 3 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.

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. 1. Subjects with MDS/MPN with high CXCR4/2 ratio 2. Subjects with MDS/MPN with low CXCR4/2 ratio 3. Subjects with AML with high CXCR4/2 ratio 4. Subjects with AML with low CXCR4/2 ratio

Recruitment information / eligibility

• Status: Completed
• Enrollment: 45
• Est. completion date: December 14, 2020
• Est. primary completion date: December 14, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subject is at least 18 years of age.

2. 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).

3. For subjects enrolled in the AML cohort:

1. Documented pathological evidence of AML, as defined by WHO criteria (2008)

2. 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

4. Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2.

5. Subject is willing and able to comply with scheduled visits, treatment plans, laboratory tests and other procedures (including bone marrow assessments).

6. At least 1 week since the last systemic therapy regimen prior to Cycle 1 Day 1. 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 14. 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.

7. Acceptable liver function:

1. Total bilirubin upper limit of normal (ULN).

2. AST (SGOT) and ALT (SGPT) 1.5 x ULN.

8. 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.

9. Female subjects must be:

1. Of non-child-bearing potential (surgically sterilized or at least 2 years post-menopausal); or

2. 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.

3. And, not breast feeding at any time during the study.

10. Written and voluntary informed consent understood, signed and dated.

Exclusion Criteria:

1. Neoplasia harbours RAS mutation (NRAS mutant, KRAS mutant or double mutant)

2. Acute promyelocytic leukemia or Bcr-Abl positive leukemia (chronic myelogenous leukemia in blast crisis)

3. Clinically active CNS leukemia

4. CMML with t(5;12) that have not yet received imatinib.

5. Participation in any interventional study within 1 week of randomization or 5 half-lives of the prior treatment agent (whichever is longer).

6. 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 14.

7. Hematopoietic stem cell transplantation (HSCT) performed within 3 months prior to Cycle 1 Day 1.

8. Concurrent use of granulocyte macrophage colony-stimulating factor (GM-CSF).

9. Prior treatment (at least 1 full treatment cycle) with a farnesyltransferase inhibitor.

10. 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.

11. Major surgery, other than diagnostic surgery, within 2 weeks prior to Cycle 1 Day 1, without complete recovery.

12. 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).

13. 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.

14. 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.

15. The subject has legal incapacity or limited legal capacity.

16. 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.

Related Conditions & MeSH terms

• Leukemia
• Leukemia, Myeloid, Acute
• Leukemia, Myelomonocytic, Chronic
• Leukemia, Myelomonocytic, Juvenile

Intervention

Drug:
• Tipifarnib
Oral tablet

Locations

Country	Name	City	State
United States	Johns Hopkins University	Baltimore	Maryland
United States	Cleveland Clinic	Cleveland	Ohio
United States	Mayo Clinic Florida	Jacksonville	Florida
United States	Weill Cornell Medicine	New York	New York
United States	University of Pennsylvania Hospital	Philadelphia	Pennsylvania
United States	Mayo Clinic Rochester	Rochester	Minnesota
United States	Mayo Clinic Arizona	Scottsdale	Arizona
United States	H. Lee Moffitt Cancer Center & Research Institute, Inc.	Tampa	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Kura Oncology, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To assess the antitumor activity of tipifarnib in CMML subjects	To assess the antitumor activity of tipifarnib, in terms of Objective Response Rate (ORR), in subjects with CMML and in subjects with CMML whose disease is KRAS/NRAS wild type.	1 year
Primary	To assess the antitumor activity of tipifarnib in MDS/MPN subjects	To 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 low CXCR4/2 ratio.	1 year
Primary	To assess the antitumor activity of tipifarnib in AML subjects	To 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.	1 year
Secondary	Rate of complete response (CR)	To assess the effect of tipifarnib on rate of complete response, complete cytogenetic remission, partial remission, marrow response, and clinical benefit	1 year
Secondary	Duration of Response	To assess the effect of tipifarnib on duration of response.	1 year
Secondary	Rate of progression free survival (PFS) at 1 year	To assess the effect of tipifarnib on rate of progressive free survival at 1 year.	1 year
Secondary	Rate of survival at 1 year	To assess the effect of tipifarnib on rate of survival at 1 year.	1 year
Secondary	Adverse event (AE) profile	To assess the effect of tipifarnib on adverse event (AE) profile according to National Cancer Institute Common Terminology Criteria for Adverse Events version 4.03 (NCI CTCAE v 4.03).	Until 30 days following end of study