A Study of Ruxolitinib in Combination With Nilotinib in Patients With Chronic Phase CML

NCT ID: NCT02973711

Last Updated: 2021-02-16

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1/PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-01-31
• Study Completion Date: 2021-08-31

Brief Summary

This study combines two drugs (ruxolitinib and the tyrosine kinase inhibitor, nilotinib) in an attempt to eliminate the CML (Chronic Myeloid Leukemia) stem cell population and thus allow for the deepest and most durable response possible in patients with CML in chronic phase who have achieved a complete hematologic remission (CHR), complete cytogenetic remission (CCyR), and major molecular remission (MMR), but not a complete molecular remission (CMR). The study will look at safety and tolerability of ruxolitinib when combined with nilotinib in a phase I study and will help establish the MTD (Maximum Tolerated Dose) of ruxolitinib when combined with nilotinib. Once the optimal dose of ruxolitinib is established in the phase I setting, a phase II evaluation will seek to establish the efficacy of this combination.

Conditions

Leukemia, Chronic Myeloid

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Nilotinib + Ruxolitinib

The first part of the trial will be Phase I and will enroll 25 participants. Participants will receive nilotinib BID and either 10, 15 or 20 mg of ruxolitinib BID. Maximum tolerated dose (MTD) of ruxolitinib will be determined.

The second part of the trial will be a Phase II and will enroll 25 subjects. Participants will receive nilotinib and the MTD of ruxolitinib.

Group Type: EXPERIMENTAL

Nilotinib

Intervention Type: DRUG

Nilotinib 300 mg BID

Ruxolitinib

Intervention Type: DRUG

Ruxolitinib, 10, 15 or 20mg BID

Interventions

Nilotinib

Nilotinib 300 mg BID

Intervention Type: DRUG

Ruxolitinib

Ruxolitinib, 10, 15 or 20mg BID

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients ≥ 18 years of age
• ECOG (Eastern Cooperative Oncology Group) Performance Status 0, 1, or 2
• Must have a diagnosis of Philadelphia chromosome positive (Ph+) chronic myeloid leukemia (CML) in chronic phase, with no previous evidence of accelerated or blast-phase disease.
• Must be actively receiving treatment for their CML with a tyrosine kinase inhibitor (TKI): imatinib, dasatinib, nilotinib or bosutinib, and must be on stable dose for > 1 year.
• Must have an ongoing complete hematologic response (CHR) on a TKI
• Must have an ongoing complete cytogenetic response (CCyR) on a TKI
• Must be in a major molecular remission (MMR) on a TKI for a minimum of 1 year leading up to enrollment.
• Adequate end organ function
• Adequate electrolytes
• Adequate platelet count
• Adequate neutrophil count
• Written informed consent prior to any screening procedures

Exclusion Criteria

• Patients in complete molecular remission (CMR) on a TKI.
• Patients who have failed nilotinib or not tolerated nilotinib in the past
• Certain cardiovascular disorders
• Currently receiving treatment with strong CYP3A4 inhibitors which cannot be discontinued prior to starting study drug
• Actively receiving herbal medicines that are strong CYP3A4 inhibitors and/or inducers and treatment cannot be discontinued prior to starting study drug
• Currently receiving treatment with any medications that have the potential to prolong the QT interval that cannot be discontinued prior to starting study drug
• Impaired gastrointestinal (GI) function or GI disease that may significantly alter the absorption of the drug
• Acute or chronic pancreatic disease within the last year
• Cytopathologically confirmed Central Nervous System (CNS) infiltration
• Another primary malignancy that requires systemic chemotherapy or radiation
• Acute or chronic liver disease or severe renal disease considered unrelated to the cancer
• History of significant congenital or acquired bleeding disorder unrelated to cancer
• Major surgery within 4 weeks prior to Day 1 of the study or who have not recovered from prior surgery
• Past treatment with ruxolitinib
• Treatment with other investigational agent within 30 days of Day 1
• Inability to grant consent or history of non-compliance to medical regimens
• Women who are breastfeeding
• Women of child-bearing potential, unless they are using highly effective contraception

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Michigan Rogel Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Patrick Burke, M.D.

Role: PRINCIPAL_INVESTIGATOR

University of Michigan Rogel Cancer Center

Locations

The University of Michigan Comprehensive Cancer Center

Ann Arbor, Michigan, United States

Wake Forest University Health Sciences

Winston-Salem, North Carolina, United States

Countries

United States

Other Identifiers

HUM00122063

Identifier Type: OTHER

Identifier Source: secondary_id

UMCC 2015.103

Identifier Type: -

Identifier Source: org_study_id