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AzTrials

Chronic Myeloid LeukemiaPhase 3RE-NICENCT01400074

Efficacy of Nilotinib Versus Imatinib in Ph+ CML in Early CP Who Have a Suboptimal Molecular Response to Imatinib

A Phase 3 study testing Nilotinib, Imatinib in people with Chronic Myeloid Leukemia, run by Seoul St. Mary's Hospital at 1 site in South Korea.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

In this study, the efficacy of nilotinib at 400 mg BID will be compared with imatinib at 400 mg BID in suboptimal molecular response patients. To determine study eligibility, suboptimal molecular response will be defined as patients who have achieved a complete cytogenetic response (CCyR) but have not achieved a MMR… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Chronic Myeloid Leukemia
What is being tested?
Nilotinib, Imatinib
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteSouth Korea
Study dates
Jan 2009to Jun 2014
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Male or female patients ≥ 18 years of age
  • ECOG 0, 1, or 2
  • Diagnosis of Ph+ CML in CP
  • Patients with suboptimal molecular response defined as:
  • Patients must achieve a CCyR at 12 months and must maintain CCyR until study entry (0% Ph+ chromosomes). Cytogenetic confirmation of Ph+ (9;22 translocation) is required on a minimum of 20 metaphases. FISH analysis will not be accepted.
  • at least 18 months and up to 24 months (≥18 to ≤24 months) of treatment with imatinib as first line therapy, at a dose of 400 mg daily, without achieving a MMR (<0.1% IS of Bcr-Abl transcript by RQ- PCR).
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  • The following laboratory results must be present:
  • Total bilirubin <1.5 x ULN
  • SGOT and SGPT <2.5 x ULN
  • Creatinine <1.5 x ULN
  • Serum amylase and lipase ≤ 1.5 x ULN
  • Alkaline phosphatase ≤ 2.5 x ULN unless considered tumor related.
  • Serum potassium, magnesium and calcium ≥ LLN or correctable with supplements to within normal limits prior to the first dose of study medication.
  • Ability to provide written informed consent prior to any study related screening procedures being performed.

Who cannot join

  • Late CP who started imatinib more than 6 months after diagnosis
  • Prior accelerated phase or blast phase CML
  • Rare hereditary problems of galactose intolerance, severe lactase deficiency or glucose galactose malabsorption
  • Hypersensitivity to nilotinib or any of the excipients.
  • Previously documented T315I mutations.
  • Intolerance to imatinib 400 mg daily defined as the inability to maintain at least 400 mg daily for the previous 3 months.
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  • Patients treated with imatinib more than 400mg daily
  • Achieved prior MMR or CCyR on imatinib and lost response to entering the study.
  • Previous treatment with interferon or any other tyrosine kinase inhibitor except imatinib (however, allow hydroxyurea or anagrelide before initial imatinib start)
  • Impaired cardiac function
  • Treatment with inhibitors of CYP3A4 or medications well documented to prolong the QT interval are contraindicated
  • Impaired gastrointestinal (GI) function or GI disease
  • History of acute pancreatitis within 1 year of study entry or past medical history of chronic pancreatitis.
  • Known cytopathologically confirmed CNS infiltration (in absence of suspicion of CNS involvement, lumbar puncture not required).
  • Any other malignancy that is clinically significant or requires active intervention.
  • Severe or uncontrolled medical conditions (i.e. uncontrolled diabetes, acute or chronic liver disease, pancreatic, or severe renal disease unrelated to tumor, active or uncontrolled infection).
  • History of significant congenital or acquired bleeding disorder unrelated to cancer.
  • Previous radiotherapy to ≥ 25% of the bone marrow.
  • Major surgery within 4 weeks prior to Day 1 of study or who have not recovered from prior surgery.
  • Use of therapeutic coumarin derivatives (i.e. warfarin, acenocoumarol, phenprocoumon).
  • Treatment with other investigational agents within 30 days of Day 1.
  • History of non-compliance to medical regimens or inability to grant consent.
  • Women who are pregnant, breast feeding, or of childbearing potential without a negative serum or urine pregnancy test at baseline.

Trial locations and contacts

1 site in 1 country.

South Korea1 site, 1 recruiting
  • Seoul St. Mary's Hospital

    Seoul, 137-701

    Recruiting

Other trials in South Korea

About this study

Official title: A Phase III Multi-center, Open-label, Randomized Study of the Efficacy of Nilotinib Versus Imatinib in Adult Patients With Ph+ CML in Early CP Who Have a Suboptimal Molecular Response to Imatinib

In this study, the efficacy of nilotinib at 400 mg BID will be compared with imatinib at 400 mg BID in suboptimal molecular response patients. To determine study eligibility, suboptimal molecular response will be defined as patients who have achieved a complete cytogenetic response (CCyR) but have not achieved a MMR, after at least 18 months of treatment on first line imatinib therapy at a minimum dose of 400mg daily (Baccarani 2006).

Read the detailed description

Imatinib mesylate (imatinib) binds to the inactive conformation of Bcr-Abl tyrosine kinase suppressing the Ph+ clone in CML (Giles et al, 2005). It is effective in CML and is a major advance in therapy. With standard dose imatinib, the MMR and complete molecular response (CMR) rates are 35% to 40% and 6% to 10% respectively at 12 months. These surrogate endpoints have been associated with high long term survival rates (Kantarjian et al, 2004).

For patients who had a CCyR and MMR (defined as a reduction in Bcr-Abl transcript levels of at least 3 log at 12 months following imatinib therapy), the probability of remaining progression-free was 100 percent at 24 months, compared with 95% for patients achieved a CCyR but no MMR and 85% for patients who did not achieve a CCyR (P<0.001) (Hughes et al, 2003/Druker et al, 2006).

With continued doses of imatinib 400 mg/day, MMR at 24 months is 54% (IRIS SmPC data), however with high dose imatinib 800 mg/day, MMR may be 70%. Higher doses of imatinib improved the CCyR rates to 90% both in patients who failed prior IFN-alfa therapy and in those previously untreated (Cortes et al, 2005). Higher doses are expected to yield higher MMR rates at 24 months (Cortes et al, ASH 2004 poster). There is also a continued increase in the cumulative major/complete cytogenetic and molecular response rates with therapy, even after 2 years (Kantarjian 2004).

Nilotinib is a novel, oral tyrosine kinase inhibitor with improved potency compared with imatinib. In pre-clinical models of imatinib-sensitive CML cell lines, nilotinib was 20-50 times more potent than imatinib, and 3-7 times more potent in imatinib-resistant cell lines. In a Phase I dose-escalation trial [Study CAMN107A2101], 119 imatinib-resistant Ph+ CML and ALL patients were treated with single oral doses of nilotinib ranging from 50-1200 mg daily or 400 mg and 600 mg given twice daily. Nilotinib produced high hematologic and cytogenetic response rates of 92% and 53%, respectively (CCyR in 35%), in patients with chronic phase CML, who were resistant to imatinib. Nilotinib was found to have an acceptable tolerability profile (Kantarjian et al, 2005). Preliminary results from an ongoing Phase II study appear to confirm the efficacy and safety profile of nilotinib (Kantarjian et al, 2006).

Achievement of a major molecular response is an important short-term goal in CML therapy as it appears to predict for long-term event-free survival. This study is designed to compare the efficacy of nilotinib 400 mg twice daily with patients' maximum tolerated doses of imatinib (optimally 800 mg/day) in producing a major molecular response after 12 months of treatment in individuals previously not in major molecular remission. It will also examine the rates of major molecular and complete molecular response in each of the treatment arms, as achievement of these endpoints may also be of prognostic significance.

Being tested
Nilotinib, Imatinib
Medical subject headings
Leukemia, Myelogenous, Chronic, BCR-ABL Positive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nilotinib, ImatinibDrug

    Also called Nilotinib (AMN107): Tasigna, Imatinib (STI571): Gleevec

    Nilotinib: 400 mg twice daily Imatinib: 400 mg twice daily

Study groups in NCT01400074
Study groupRoleWhat they receive
NilotinibActive comparator400 mg twice daily
Receives: Drug: Nilotinib, Imatinib
ImatinibActive comparator400 mg twice daily
Receives: Drug: Nilotinib, Imatinib

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. the cumulative rate of MMR

    To evaluate the cumulative rate of MMR at 12 months of nilotinib compared to imatinib in adult patients with Ph+ CML in early CP who have suboptimal molecular response to imatinib

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jul 2011 (estimated)
  2. Study startJan 2009
  3. Primary completionJun 2014 (estimated)
  4. Study completionJun 2014 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01400074
Sponsor's protocol ID
CAMN107AKR01T
Acronym
RE-NICE
Status last verified
Jan 2014
First submitted
21 Jul 2011
Last updated
13 Jan 2014
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Nilotinib, Imatinib in people with Chronic Myeloid Leukemia, run by Seoul St. Mary's Hospital at 1 site in South Korea.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 14 inclusion and 23 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 13 Jan 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Sahee Park, MS (+82-2-2258-7030, saheepark@catholic.ac.kr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

the cumulative rate of MMR (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jan 2014.

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