Chronic Myelogenous LeukemiaPhase 2ENESTfreedomNCT01784068
Nilotinib Treatment-free Remission Study in CML (Chronic Myeloid Leukemia) Patients
A Phase 2 study testing Nilotinib followed by treatment-free in people with Chronic Myelogenous Leukemia, run by Novartis Pharmaceuticals at 113 sites in 19 countries.
Trial summary
The main purpose of the study was to investigate whether nilotinib treatment can be safely suspended with no recurrence of CML in selected patients who responded optimally on this treatment Read more about this study
- Who is it for?
- Ages 18 to 100 years
- Conditions the study is for
- Chronic Myelogenous Leukemia
- What is being tested?
- Nilotinib followed by treatment-free
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 215 participants
- Where
- 113 sitesin 19 countries
- Study dates
- 19 Mar 2013to 23 Jan 2025
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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 to 100 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male or female patients ≥ 18 years of age
- Minimum of 2 calendar years of nilotinib treatment with at least the last 12 months of nilotinib treatment prior to pre-screening at approved total daily dose of 600 mg BID or at a reduced dose of 400 mg QD if required from the perspective of tolerance for BCR-ABL positive CML in documented chronic phase at the time of diagnosis
- Evidence of typical BCR-ABL transcripts (b3a2 and/or b2a2) at the time of CML-CP diagnosis i.e. prior to first start of TKI treatment which are amenable to standardized RT-PCR quantification"
- Patient in MR4.5 at prescreening at Novartis designated lab
- ECOG performance status of 0-2
- Adequate end organ function as defined by:
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- Direct bilirubin ≤ 1.5 x ULN except for i) patients with documented Gilbert's syndrome for whom any bilirubin value is allowed and ii) for patients with asymptomatic hyperbilirubinemia (liver transaminases and alkaline phosphatase within normal range).
- SGOT(AST) and SGPT(ALT) ≤ 3 x ULN i.e. equivalent to ≤ Grade 1 NCI-CTCAE v.4.03
- Serum lipase ≤ 2 x ULN i.e. equivalent to ≤ Grade 2 NCI-CTCAE v.4.03
- Alkaline phosphatase ≤ 2.5 x ULN
- Serum creatinine < 1.5 x ULN
- Patients must have the following electrolyte values within normal limits or corrected to be within normal limits with supplements prior to first dose of study medication:
- Potassium (suggested keep to prevent issues with QT and/or rhythm abnormalities)
- Magnesium (suggested keep to prevent issues with QT and/or rhythm abnormalities)
- Total calcium (corrected for serum albumin)
- Patients must have normal marrow function as defined:
- Absolute Neutrophil Count (ANC) ≥ 1.5 x 10E9/L
- Hemoglobin ≥ 9.0 g/dL
- Platelets ≥ 100 x 10E9/L
- Documented chronic phase CML must meet all the criteria defined by:
- < 15% blasts in peripheral blood and bone marrow,
- < 30% blasts plus promyelocytes in peripheral blood and bone marrow,
- < 20% basophils in the peripheral blood,
- ≥ 100 x 109/L (≥ 100,000/mm3) platelets,
- No evidence of extramedullary leukemic involvement, with the exception of hepatosplenomegaly
- Patients must tolerate a minimum total daily dose of nilotinib of 400 mg
Who cannot join
- Previous treatment with BCR-ABL inhibitors other than nilotinib for more than a total cumulative duration of 4 weeks
- Previous treatment with alpha-interferon of any duration
- Previous anticancer agents for CML other than nilotinib except for cytoreduction after CML diagnosis until up to 4 weeks after first dose of nilotinib
- Known second chronic phase of CML after previous progression to AP/BC
- Poorly controlled diabetes mellitus (defined as HbA1c > 9%)
- Impaired cardiac function including any one of the following:
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- LVEF < 45% or below the institutional lower limit of the normal range (whichever is higher)
- Inability to determine the QT interval on ECG, except for patients with evidence of measurable QT interval at the time of CML diagnosis (e.g. prior to first start of TKI treatment) and who have no documented clinical signs of cardiovascular disease and/or clinical signs of conduction abnormality.
- Complete left bundle branch block
- Right bundle branch block plus left anterior or posterior hemiblock
- Use of a ventricular-paced pacemaker
- Congenital long QT syndrome or a known family history of long QT syndrome
- History of or presence of clinically significant ventricular or atrial tachyarrhythmias
- Clinically significant resting bradycardia
- QTc > 450 msec on the average of three serial baseline ECG (using the QTcF formula). If QTcF > 450 msec and electrolytes are not within normal ranges, electrolytes should be corrected and then the patient re-tested for QTc.This exclusion criterion is not applicable for patients with non-measurable QT interval who have evidence of measurable QT interval at the time of CML diagnosis (e.g. prior to first start of TKI treatment) and who have no documented clinical signs of cardiovascular disease and/or clinical signs of conduction abnormality.
- History or clinical signs of myocardial infarction within 1 year of study entry
- History of unstable angina within 1 year of study entry
- Other clinically significant heart disease (e.g. congestive heart failure, cardiomyopathy or uncontrolled hypertension)
- History of acute pancreatitis within 1 year of study entry or past medical history of chronic pancreatitis
- Known presence of significant congenital or acquired bleeding disorder unrelated to cancer
- Severe and/or uncontrolled concurrent medical disease that in the opinion of the investigator could cause unacceptable safety risks or compromise compliance with the protocol (e.g. uncontrolled diabetes, uncontrolled infection)
- History of another active malignancy within 5 years prior to study entry with the exception of previous or concomitant basal cell skin cancer and previous carcinoma in situ treated curatively
- Treatment with other investigational agents (defined as not used in accordance with the approved indication) within 4 weeks of Day 1
- Patients who have not recovered from prior surgery
- Patients actively receiving therapy with strong CYP3A4 inhibitors and/or inducers, and the treatment cannot be either discontinued or switched to a different medication prior to starting study drug.
- Patients actively receiving therapy with herbal medicines that are strong CYP3A4 inhibitors and/or inducers, and the treatment cannot be either discontinued or switched to a different medication prior to starting study drug. These herbal medicines may include Echinacea, (including E. purpurea, E. angustifolia and E. pallida), Piperine, Artemisinin, St. John's Wort, and Ginkgo.
- Patients who are currently receiving treatment with any medications that have the potential to prolong the QT interval and the treatment cannot be either safely discontinued or switched to a different medication prior to starting study drug. (see http://www.torsades.org/medical-pros/drug-lists/printable-drug-list.cfm for a list of agents that prolong the QT interval)
- Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of study drug (e.g. ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, small bowel resection, or gastric bypass surgery)
- Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test.
- Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during the study and for 14 days after the final dose of nilotinib. Highly effective contraception is defined as either:
- Total abstinence (when this is in line with the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception
- Female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before taking study treatment. In case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment.
- Male sterilization (at least 6 months prior to enrolling). For female patients on the study the vasectomized male partner should be the sole partner for that patient.
- Use of a combination of any two of the following:
- Use of oral, injected or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate <1%), for example hormone vaginal ring or transdermal hormone contraception.
- Placement of an intrauterine device (IUD) or intrauterine system (IUS)
- Barrier methods of contraception: Condom or Occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository.
- In case of use of oral contraception women should have been stable on the same pill for a minimum of 3 months before taking study treatment Women are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g. age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks prior to enrolling. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment is she considered not of child bearing potential.
- If a study patient becomes pregnant or suspects being pregnant during the study or within 30 days after the final dose of nilotinib, the Study Doctor needs to be informed immediately and ongoing study treatment with nilotinib has to be stopped immediately.
Trial locations and contacts
113 sites in 19 countries.
113 sites in 19 countries
Germany21 sites
Novartis Investigative Site
Aachen, 52074
Novartis Investigative Site
Bayreuth, 95445
Novartis Investigative Site
Berlin, 13353
Novartis Investigative Site
Bonn, 53105
Novartis Investigative Site
Bottrop, 46236
Novartis Investigative Site
Dresden, 01307
Novartis Investigative Site
Düsseldorf, North Rhine-Westphalia, 40225
Novartis Investigative Site
Düsseldorf, 40479
Novartis Investigative Site
Frankfurt am Main, Hesse, 60590
Novartis Investigative Site
Freiburg im Breisgau, Baden-Wurttemberg, 79106
Novartis Investigative Site
Goslar, 38642
Novartis Investigative Site
Hamburg, 20246
Novartis Investigative Site
Hamburg, 22417
Novartis Investigative Site
Jena, Thuringia, 07740
Novartis Investigative Site
Leipzig, Saxony, 04103
Novartis Investigative Site
Lübeck, Schleswig-Holstein, 23563
Novartis Investigative Site
Magdeburg, 39104
Novartis Investigative Site
Mainz, 55131
Novartis Investigative Site
Mannheim, Baden-Wurttemberg, 68305
Novartis Investigative Site
Stuttgart, 70376
Novartis Investigative Site
Ulm, 89081
Spain14 sites
Novartis Investigative Site
Barakaldo, Vizcaya, 48903
Novartis Investigative Site
Barcelona, 08041
Novartis Investigative Site
Las Palmas de Gran Canaria, 35010
Novartis Investigative Site
Madrid, 28006
Novartis Investigative Site
Madrid, 28034
Novartis Investigative Site
Madrid, 28040
Novartis Investigative Site
Madrid, 28041
Novartis Investigative Site
Madrid, 28046
Novartis Investigative Site
Ourense, 32005
Novartis Investigative Site
Oviedo, Principality of Asturias, 33011
Novartis Investigative Site
Pamplona, Navarre, 31008
Novartis Investigative Site
San Cristóbal de La Laguna, Santa Cruz De Tenerife, 38320
Novartis Investigative Site
Tarragona, 43005
Novartis Investigative Site
Terrassa, Catalonia, 08221
Italy13 sites
Novartis Investigative Site
Ancona, AN, 60126
Novartis Investigative Site
Brescia, BS, 25123
Novartis Investigative Site
Cona, FE, 44124
Novartis Investigative Site
Florence, FI, 50134
Novartis Investigative Site
Genova, GE, 16132
Novartis Investigative Site
Naples, 80131
Novartis Investigative Site
Novara, 28100
Novartis Investigative Site
Nuoro, NU, 08100
Novartis Investigative Site
Orbassano, TO, 10043
Novartis Investigative Site
Perugia, PG, 06129
Novartis Investigative Site
Reggio Calabria, RC, 89124
Novartis Investigative Site
Roma, RM, 00161
Novartis Investigative Site
Terni, TR, 05100
France12 sites
Novartis Investigative Site
Bayonne, Bayonne Cedex, 64109
Novartis Investigative Site
Bordeaux, 33076
Novartis Investigative Site
Brest, 29609
Novartis Investigative Site
Corbeil-Essonnes, 91100
Novartis Investigative Site
Dunkirk, 59240
Novartis Investigative Site
Grenoble, 38043
Novartis Investigative Site
Nantes, 44093
Novartis Investigative Site
Rouen, 76038
Novartis Investigative Site
Saint Priest Jarez, Pays de la Loire Region, 42270
Novartis Investigative Site
Strasbourg, 67000
Novartis Investigative Site
Strasbourg, 67085
Novartis Investigative Site
Toulouse, 31059
Japan12 sites
Novartis Investigative Site
Akita, 0108543
Novartis Investigative Site
Bunkyo-ku, Tokyo, 1138519
Novartis Investigative Site
Kashiwa, Chiba, 277-8567
Novartis Investigative Site
Kawagoe, Saitama, 3508550
Novartis Investigative Site
Kumamoto, Kumamoto, 860-8556
Novartis Investigative Site
Saga, Saga-ken, 849-8501
Novartis Investigative Site
Sagamihara, Kanagawa, 252-0375
Novartis Investigative Site
Sakai, Osaka, 590-0197
Novartis Investigative Site
Sapporo, Hokkaido, 060-8648
Novartis Investigative Site
Shimotsuga Gun, Tochigi, 3210293
Novartis Investigative Site
Shinjuku Ku, Tokyo, 160-0023
Novartis Investigative Site
Suita, Osaka, 565-0871
United States10 sites
Dana Farber Cancer Institute
Boston, Massachusetts, 02215
Tennessee Oncology PLLC
Chattanooga, Tennessee, 37404
Florida Cancer Specialists
Fort Myers, Florida, 33901
Cancer Centers of the Carolinas
Greenville, South Carolina, 29605
Lakes Research
Miami Lakes, Florida, 33014
Memorial Sloan Kettering
New York, New York, 10017
Community Cancer Trials of Utah
Ogden, Utah, 84405
Oregon Health Sciences University
Portland, Oregon, 97239
H Lee Moffitt Cancer Center and Research Institute
Tampa, Florida, 33612
Cancer Center of Kansas
Wichita, Kansas, 67214-3728
Belgium7 sites
Novartis Investigative Site
Brussels, 1090
Novartis Investigative Site
Brussels, 1200
Novartis Investigative Site
Charleroi, 6000
Novartis Investigative Site
Ghent, 9000
Novartis Investigative Site
Kortrijk, West-Vlaanderen, 8500
Novartis Investigative Site
Liège, 4000
Novartis Investigative Site
Sint-Niklaas, Oost Vlaanderen, 9100
Austria5 sites
Novartis Investigative Site
Graz, 8036
Novartis Investigative Site
Rankweil, A-6830
Novartis Investigative Site
Salzburg, 5020
Novartis Investigative Site
Vienna, 1140
Novartis Investigative Site
Vienna, A-1130
Sweden3 sites
Novartis Investigative Site
Lund, SE-221 85
Novartis Investigative Site
Stockholm, SE-171 76
Novartis Investigative Site
Uppsala, SE-751 85
Colombia2 sites
Novartis Investigative Site
Bogota, Cundinamarca, 111411
Novartis Investigative Site
Montería, 230004
Greece2 sites
Novartis Investigative Site
Athens, 106 76
Novartis Investigative Site
Athens, 115 27
Hungary2 sites
Novartis Investigative Site
Budapest, H-1083
Novartis Investigative Site
Szeged, 6725
Ireland2 sites
Novartis Investigative Site
Dublin, D03 VX82
Novartis Investigative Site
Galway, 12074
Poland2 sites
Novartis Investigative Site
Gdansk, 80-952
Novartis Investigative Site
Warsaw, 02-172
United Kingdom2 sites
Novartis Investigative Site
Cardiff, CF14 4XW
Novartis Investigative Site
Oxford, OX3 7LE
About this study
Official title: A Single-arm, Multicenter, Nilotinib Treatment-free Remission Study in Patients With BCR-ABL1 Positive Chronic Myelogenous Leukemia in Chronic Phase Who Have Achieved Durable Minimal Residual Disease (MRD) Status on First Line Nilotinib Treatment.
The main purpose of the study was to investigate whether nilotinib treatment can be safely suspended with no recurrence of CML in selected patients who responded optimally on this treatment
Read the detailed description
The Primary objective of this study was to determine the percentage of patients who were in Major Molecular Response (MMR) at 48 weeks after starting the Treatment-Free Remission (TFR) phase (patients who required re-initiation of treatment were considered as non-responders).
Nilotinib treatment consolidation phase (NTCS): Patients who satisfied all inclusion/exclusion criteria were enrolled in the consolidation phase and continued to receive nilotinib for 52 weeks. All patients were treated with the planned nilotinib dose 300 mg BID (or at a reduced dose level of 400 mg QD if required from the perspective of toxicity). In order for patients to be eligible for the TFR phase, they had to fulfill the protocol specific definition of durable MRD. The four last quarterly performed PCR assessments must have fulfilled the following criteria:
- The last assessment was MR4.5 (BCR-ABL ≤ 0.0032% IS)
- No assessment worse than MR4.0 (BCR-ABL >0.01% IS) and
- No more than two assessments between MR4.0 and MR4.5 (0.0032% IS<BCR-ABL ≤ 0.01% IS)
Nilotinib Treatment-Free Remission (TFR) phase: Patients who were eligible to enter in the TFR phase after completing the 52 weeks consolidation phase, stopped taking nilotinib on the first day of the TFR phase. Duration of this phase was up to 10 years after the last patient enters in the TFR phase. BCR-ABL levels were monitored every four weeks during the first 48 weeks, every six weeks for the following 48 weeks and every 12 weeks during the last period.
Nilotinib treatment re-initiation (NTRI) phase: If a patient had a loss of MMR (BCR-ABL >0.1% IS) in the TFR phase, the patient restarted nilotinib treatment. Patients were on nilotinib treatment for up to 10 years after the last patient entered the nilotinib TFR phase. Patients who required re-initiation of nilotinib treatment were monitored for the BCR-ABL level every four weeks for the first 24 weeks and then every 12 weeks thereafter in patients who regained MMR. The frequency of BCR-ABL monitoring in patients not regaining MMR within the first 24 weeks after re-initiation of treatment was at least every 12 weeks or more frequently as clinically indicated.
- Conditions
- Chronic Myelogenous Leukemia
- Being tested
- Nilotinib followed by treatment-free
- Keywords
- AMN107, Ph+ CML-CP, chronic phase, nilotinib treatment, 2 years treatment, MR 4.5, Loss of MR 4, Loss of MMR, CML
- 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 followed by treatment-freeDrug
Also called AMN107
Nilotinib is being used as commercial available capsules (except in Japan where clinical supplies is used) of 150 mg and 200 mg strength. Treatment occurs during consolidation, continuation, prolonged continuation, re-initiation and re-initiation-2 phases of the study.
| Study group | Role | What they receive |
|---|---|---|
| Nilotinib followed by treatment-free | Experimental | Patients who received a minimum of 2 years of first line nilotinib treatment and with pre-screen PCR results in ≥ MR4.5 entered the consolidation phase of the study (52 weeks - nilotinib 300 mg BID). Patients with Minimal Residual Disease (MRD) at the end of this phase entered the Treatment-Free Remission (TFR) phase where no treatment was given. Non eligible patients will enter the continuation phase of the study. Patients with MRD at the end of the continuation phase will enter the TFR-2 phase of the study where no treatment is given. Non eligible patients will enter the prolonged continuation phase of the study. If at any time during TFR or TFR-2 the patient loses MMR, nilotinib treatment will be immediately re-initiated (nilotinib 300 mg BID). Receives: Drug: Nilotinib followed by treatment-free |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants in Major Molecular Response at 48 Weeks After Start of Treatment-Free Remission (TFR) Phase
The primary endpoint was the percentage of participants in major molecular response (MMR) at 48 weeks after initiation of the treatment-free remission (TFR) phase. Participants who required re-initiation of treatment were considered as non-responders.
Measured: 48 weeks in TFR
Secondary outcomes (16)
Percentage of Participants in MR4.5 (BCR-ABL ≤ 0.0032% IS) at 48 Weeks After Start of TFR Phase
The outcome measure was the percentage of participants in molecular response 4.5 (MR4.5) at 48 weeks after initiation of the treatment-free remission (TFR) phase. Participants who required reinitiation of treatment were considered non-responders. MR4.5 corresponds to a BCR-ABL transcript level ≤0.0032% on the International Scale (IS), representing a deep molecular response.
Measured: 48 weeks in TFR
Percentage of Participants in Major Molecular Response (MMR) at Multiple Time Points After Start of the Treatment-Free Remission (TFR) Phase
This outcome measure was the percentage of participants in major molecular response (MMR) assessed at multiple timepoints after initiation of the treatment-free remission (TFR) phase. Participants who required re-initiation of treatment at any time prior to the respective assessment were considered non-responders.
Measured: Weeks 96, 144, 192, and 264, and End of Years 6, 7, 8, 9, and 10
Percentage of Participants in Molecular Response 4.5 (MR4.5) at Multiple Time Points After Start of the Treatment-Free Remission (TFR) Phase
This secondary outcome measure was the percentage of participants in molecular response 4.5 (MR4.5) assessed at multiple timepoints after initiation of the treatment-free remission (TFR) phase. Participants who required reinitiation of treatment at any time prior to the respective assessment were considered non-responders. MR4.5 corresponds to a BCR-ABL transcript level ≤0.0032% on the International Scale (IS).
Measured: Weeks 96, 144, 192, and 264, and End of Years 6, 7, 8, 9, and 10
Number of Participants in Major Molecular Response (MMR) at Multiple Time Points After Start of the Treatment-Free Remission (TFR) Phase
This outcome measure was the number of participants in major molecular response (MMR) assessed at multiple timepoints after initiation of the treatment-free remission (TFR) phase of nilotinib. At each assessment time point, participants with available MMR data were counted. Participants who reinitiated nilotinib treatment for less than 12 weeks prior to the respective assessment time point were excluded from the analysis at that time point.
Measured: Weeks 48, 96, 144, 192, and 264, and End of Years 6, 7, 8, 9, and 10
Number of Participants in Molecular Response 4.5 (MR4.5) at Multiple Time Points After Start of the Treatment-Free Remission (TFR) Phase
This outcome measure was the number of participants in molecular response 4.5 (MR4.5) assessed at multiple timepoints after initiation of the treatment-free remission (TFR) phase of nilotinib. At each assessment time point, participants with available MR4.5 data were counted. Participants who reinitiated nilotinib treatment for less than 12 weeks prior to the respective assessment time point were excluded from the analysis at that time point. MR4.5 corresponds to a BCR-ABL transcript level ≤0.0032% on the International Scale (IS).
Measured: Weeks 48, 96, 144, 192, and 264, and End of Years 6, 7, 8, 9, and 10
Percentage of Participants Who Achieved Major Molecular Response (MMR) Within 12 Weeks of Reinitiation of Nilotinib Treatment
Percentage of patients who achieved MMR within 12 weeks of re-initiation of treatment with nilotinib defined as the number of patients who were in MMR at least at 1 assessment within 12 weeks after re-start of nilotinib treatment divided by the number of patients who were re-initiated for at least 12 weeks.
Measured: 12 weeks after reinitiation of nilotinib treatment
Percentage of Participants With Stable Major Molecular Response (MMR) at Multiple Time Points After First Achievement of MMR During Nilotinib Re-Initiation
The percentage of patients who were in stable MMR after achieving a response in the NTRI phase at multiple timepoints was calculated by dividing the number of participants achieving MMR any time during the NTRI phase and having the same response at those timepoints after the first achievement of MMR, irrespective of whether there was loss of MMR in between, by the number of patients who achieved MMR at any time during the NTRI phase.
Measured: Weeks 48, 96, 144, 192, 240, 288, 336, 384, and 432 after first achievement of MMR during the nilotinib re-initiation phase
Percentage of Participants With Stable Molecular Response 4.5 (MR4.5) at Multiple Time Points After First Achievement During Nilotinib Re-Initiation
The proportion of patients who were in stable MR4.5 after achieving a response in the NTRI phase at multiple timepoints was calculated by dividing the number of participants achieving MR4.5 any time during the NTRI phase and having the same response at those timepoints after the first achievement of MR4.5, irrespective of whether there was loss of MR4.5 in between, by the number of patients who achieved MR4.5 at any time during the NTRI phase.
Measured: Weeks 48, 96, 144, 192, 240, 288, 336, 384, and 432 after first achievement of MR4.5 during the nilotinib re-initiation phase
BCR-ABL Ratio (%) Over Time in Nilotinib Treatment Re-initiation Phase (NTRI)
The BCR-ABL ratio (%) represents the level of BCR-ABL fusion gene transcripts relative to a control gene (ABL) measured in peripheral blood samples using quantitative reverse transcription polymerase chain reaction (RT-PCR). Results are expressed as a percentage on the International Scale (IS), a standardized reporting method that allows comparison across laboratories. The BCR-ABL ratio is used to assess the molecular response to treatment, with lower values indicating a reduced disease burden.
Measured: Baseline; every 4 weeks up to Week 24; and every 12 weeks thereafter, up to Week 528
Duration of Re-Initiated Nilotinib Treatment Required to Regain Major Molecular Response (MMR) After Loss of MMR
This outcome measure was defined as the time from the date of reinitiation of nilotinib treatment following loss of major molecular response (MMR) to the date of first documented achievement of MMR. Participants who did not regain MMR after reinitiation of treatment on or before the data cut-off date were censored at the date of their last available BCR-ABN PCR assessment.
Measured: Every 4 weeks up to Week 24, and every 12 weeks thereafter, up to Week 528
Duration of Re-Initiated Nilotinib Treatment Required to Regain Molecular Response 4.5 (MR4.5) After Loss of MMR
This outcome measure was defined as the time from the date of reinitiation of nilotinib treatment following loss of major molecular response (MMR) to the date of first documented achievement of molecular response 4.5 (MR4.5). Participants who did not regain MR4.5 after reinitiation of treatment on or before the data cut-off date were censored at the date of their last available BCR-ABN PCR assessment. MR4.5 corresponds to a BCR-ABN transcript level ≤0.0032% on the International Scale (IS).
Measured: From start of Nilotinib treatment re-initiation up to Week 528
Treatment-Free Survival (TFS) After Start of the Treatment-Free Remission (TFR) Phase
Treatment-free survival (TFS) was defined as the time from the start of the treatment-free remission (TFR) phase to the earliest occurrence of loss of major molecular response (MMR), reinitiation of treatment for any reason, progression to accelerated phase (AP) or blast crisis (BC), or death due to any cause. Participants without an event on or before the data cut-off date were censored at the date of their last available disease assessment (polymerase chain reaction, cytogenetic, hematologic, or extramedullary assessment).
Measured: From start of the treatment-free remission (TFR) phase up to Week 528
Progression-Free Survival (PFS) After Start of the Treatment-Free Remission (TFR) Phase
Progression-free survival (PFS) was defined as the time from the start of the treatment-free remission (TFR) phase to the earliest occurrence of disease progression to accelerated phase (AP) or blast crisis (BC), or death due to any cause. Participants without an event on or before the data cut-off date were censored at the date of their last available disease assessment (cytogenetic, hematologic, or extramedullary assessment) or last contact for participants in follow-up.
Measured: From start of the treatment-free remission (TFR) phase up to Week 528
Overall Survival (OS) After Start of the Treatment-Free Remission (TFR) Phase
Overall survival (OS) was defined as the time from the start of the treatment-free remission (TFR) phase to death due to any cause. Participants who were alive on or before the data cut-off date were censored at the date of their last assessment or last known alive date for participants in follow-up.
Measured: From start of the treatment-free remission (TFR) phase up to Week 528
Percentage of Participants With Treatment-emergent Adverse Events During the Entire Study
This outcome measure summarized the overall occurrence of adverse events related to nilotinib during the study. A study drug-related adverse event was defined as any adverse event assessed by the investigator as related to nilotinib and reported during the nilotinib treatment consolidation (NTCS) phase, the treatment-free remission (TFR) phase, or the nilotinib treatment re-initiation (NTRI) phase.
Measured: From first dose of nilotinib through up to approximately 11 years of study participation, including the NTCS, TFR, and NTRI phases
Number of Participants With BCR-ABL1 Mutations Associated With Resistance to Nilotinib After Loss of Major Molecular Response
This outcome measure was the number of participants who developed BCR-ABL1 mutations associated with resistance to nilotinib following loss of major molecular response (MMR) after suspension of nilotinib treatment. Mutations assessed included, but were not limited to, T315I, E255K, Y253H, F359V, F359C, and F359I. The endpoint was calculated as the number of participants with at least one detected BCR-ABL1 mutation divided by the number of participants who experienced loss of MMR after nilotinib suspension.
Measured: From loss of major molecular response after nilotinib suspension through up to 528 weeks of study participation
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Feb 2013 (estimated)
- Study start19 Mar 2013
- Primary completion31 May 2016
- Study completion23 Jan 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Chronic Myelogenous LeukemiaStudies of the same condition, open and under way.
- More trials run by Novartis PharmaceuticalsThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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 2
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 215 participants (actual)
Sponsor and investigators
- Lead sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Novartis Pharmaceuticals, Study director, Novartis Pharmaceuticals
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01784068
- Sponsor's protocol ID
- CAMN107I2201
- Other IDs
- 2012-004092-40
- Acronym
- ENESTfreedom
- Status last verified
- Jul 2026
- First submitted
- 30 Jan 2013
- Last updated
- 13 Aug 2026
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Yes: Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations. This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com
Study at a glance
From the registry record, last updated by the sponsor on 13 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Single-arm, Multicenter, Nilotinib Treatment-free Remission Study in Patients With BCR-ABL1 Positive Chronic Myelogenous Leukemia in Chronic Phase Who Have Achieved Durable Minimal Residual Disease (MRD) Status on First Line Nilotinib Treatment.
- ClinicalTrials.gov ID
- NCT01784068
- Acronym / sponsor ID
- ENESTfreedom / CAMN107I2201
- Conditions
- Chronic Myelogenous Leukemia
- Keywords
- AMN107, Ph+ CML-CP, chronic phase, nilotinib treatment, 2 years treatment, MR 4.5, Loss of MR 4, Loss of MMR
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 215 participants (actual)
- Lead sponsor
- Novartis PharmaceuticalsIndustry (pharma, biotech, devices)
- Study start
- 19 Mar 2013 (actual)
- Primary completion
- 31 May 2016 (actual)
- Study completion
- 23 Jan 2025 (actual)
- First posted
- 5 Feb 2013 (estimated)
- Results
- Posted 14 Jan 2021
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The main purpose of the study was to investigate whether nilotinib treatment can be safely suspended with no recurrence of CML in selected patients who responded optimally on this treatment
Detailed description
The Primary objective of this study was to determine the percentage of patients who were in Major Molecular Response (MMR) at 48 weeks after starting the Treatment-Free Remission (TFR) phase (patients who required re-initiation of treatment were considered as non-responders).
Nilotinib treatment consolidation phase (NTCS): Patients who satisfied all inclusion/exclusion criteria were enrolled in the consolidation phase and continued to receive nilotinib for 52 weeks. All patients were treated with the planned nilotinib dose 300 mg BID (or at a reduced dose level of 400 mg QD if required from the perspective of toxicity). In order for patients to be eligible for the TFR phase, they had to fulfill the protocol specific definition of durable MRD. The four last quarterly performed PCR assessments must have fulfilled the following criteria:
- The last assessment was MR4.5 (BCR-ABL ≤ 0.0032% IS)
- No assessment worse than MR4.0 (BCR-ABL >0.01% IS) and
- No more than two assessments between MR4.0 and MR4.5 (0.0032% IS<BCR-ABL ≤ 0.01% IS)
Nilotinib Treatment-Free Remission (TFR) phase: Patients who were eligible to enter in the TFR phase after completing the 52 weeks consolidation phase, stopped taking nilotinib on the first day of the TFR phase. Duration of this phase was up to 10 years after the last patient enters in the TFR phase. BCR-ABL levels were monitored every four weeks during the first 48 weeks, every six weeks for the following 48 weeks and every 12 weeks during the last period.
Nilotinib treatment re-initiation (NTRI) phase: If a patient had a loss of MMR (BCR-ABL >0.1% IS) in the TFR phase, the patient restarted nilotinib treatment. Patients were on nilotinib treatment for up to 10 years after the last patient entered the nilotinib TFR phase. Patients who required re-initiation of nilotinib treatment were monitored for the BCR-ABL level every four weeks for the first 24 weeks and then every 12 weeks thereafter in patients who regained MMR. The frequency of BCR-ABL monitoring in patients not regaining MMR within the first 24 weeks after re-initiation of treatment was at least every 12 weeks or more frequently as clinically indicated.
Study design
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Nilotinib followed by treatment-free | Experimental | Drug: Nilotinib followed by treatment-freePatients who received a minimum of 2 years of first line nilotinib treatment and with pre-screen PCR results in ≥ MR4.5 entered the consolidation phase of the study (52 weeks - nilotinib 300 mg BID). Patients with Minimal Residual Disease (MRD) at the end of this phase entered the Treatment-Free Remission (TFR) phase where no treatment was given. Non eligible patients will enter the continuation phase of the study. Patients with MRD at the end of the continuation phase will enter the TFR-2 phase of the study where no treatment is given. Non eligible patients will enter the prolonged continuation phase of the study. If at any time during TFR or TFR-2 the patient loses MMR, nilotinib treatment will be immediately re-initiated (nilotinib 300 mg BID). |
Who may qualify
- Ages
- 18 to 100 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (26 listed)
- Male or female patients ≥ 18 years of age
- Minimum of 2 calendar years of nilotinib treatment with at least the last 12 months of nilotinib treatment prior to pre-screening at approved total daily dose of 600 mg BID or at a reduced dose of 400 mg QD if required from the perspective of tolerance for BCR-ABL positive CML in documented chronic phase at the time of diagnosis
- Evidence of typical BCR-ABL transcripts (b3a2 and/or b2a2) at the time of CML-CP diagnosis i.e. prior to first start of TKI treatment which are amenable to standardized RT-PCR quantification"
- Patient in MR4.5 at prescreening at Novartis designated lab
- ECOG performance status of 0-2
Key exclusion criteria (39 listed)
- Previous treatment with BCR-ABL inhibitors other than nilotinib for more than a total cumulative duration of 4 weeks
- Previous treatment with alpha-interferon of any duration
- Previous anticancer agents for CML other than nilotinib except for cytoreduction after CML diagnosis until up to 4 weeks after first dose of nilotinib
- Known second chronic phase of CML after previous progression to AP/BC
- Poorly controlled diabetes mellitus (defined as HbA1c > 9%)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Nilotinib followed by treatment-freeAlso: AMN107Nilotinib is being used as commercial available capsules (except in Japan where clinical supplies is used) of 150 mg and 200 mg strength. Treatment occurs during consolidation, continuation, prolonged continuation, re-initiation and re-initiation-2 phases of the study. | Drug | Nilotinib followed by treatment-free |
Primary outcome
Percentage of Participants in Major Molecular Response at 48 Weeks After Start of Treatment-Free Remission (TFR) Phase
Time frame: 48 weeks in TFR
The primary endpoint was the percentage of participants in major molecular response (MMR) at 48 weeks after initiation of the treatment-free remission (TFR) phase. Participants who required re-initiation of treatment were considered as non-responders.
16 secondary outcomes
Percentage of Participants in MR4.5 (BCR-ABL ≤ 0.0032% IS) at 48 Weeks After Start of TFR Phase
Time frame: 48 weeks in TFR
Percentage of Participants in Major Molecular Response (MMR) at Multiple Time Points After Start of the Treatment-Free Remission (TFR) Phase
Time frame: Weeks 96, 144, 192, and 264, and End of Years 6, 7, 8, 9, and 10
Percentage of Participants in Molecular Response 4.5 (MR4.5) at Multiple Time Points After Start of the Treatment-Free Remission (TFR) Phase
Time frame: Weeks 96, 144, 192, and 264, and End of Years 6, 7, 8, 9, and 10
Number of Participants in Major Molecular Response (MMR) at Multiple Time Points After Start of the Treatment-Free Remission (TFR) Phase
Time frame: Weeks 48, 96, 144, 192, and 264, and End of Years 6, 7, 8, 9, and 10
Number of Participants in Molecular Response 4.5 (MR4.5) at Multiple Time Points After Start of the Treatment-Free Remission (TFR) Phase
Time frame: Weeks 48, 96, 144, 192, and 264, and End of Years 6, 7, 8, 9, and 10
Percentage of Participants Who Achieved Major Molecular Response (MMR) Within 12 Weeks of Reinitiation of Nilotinib Treatment
Time frame: 12 weeks after reinitiation of nilotinib treatment
Percentage of Participants With Stable Major Molecular Response (MMR) at Multiple Time Points After First Achievement of MMR During Nilotinib Re-Initiation
Time frame: Weeks 48, 96, 144, 192, 240, 288, 336, 384, and 432 after first achievement of MMR during the nilotinib re-initiation phase
Percentage of Participants With Stable Molecular Response 4.5 (MR4.5) at Multiple Time Points After First Achievement During Nilotinib Re-Initiation
Time frame: Weeks 48, 96, 144, 192, 240, 288, 336, 384, and 432 after first achievement of MR4.5 during the nilotinib re-initiation phase
BCR-ABL Ratio (%) Over Time in Nilotinib Treatment Re-initiation Phase (NTRI)
Time frame: Baseline; every 4 weeks up to Week 24; and every 12 weeks thereafter, up to Week 528
Duration of Re-Initiated Nilotinib Treatment Required to Regain Major Molecular Response (MMR) After Loss of MMR
Time frame: Every 4 weeks up to Week 24, and every 12 weeks thereafter, up to Week 528
Duration of Re-Initiated Nilotinib Treatment Required to Regain Molecular Response 4.5 (MR4.5) After Loss of MMR
Time frame: From start of Nilotinib treatment re-initiation up to Week 528
Treatment-Free Survival (TFS) After Start of the Treatment-Free Remission (TFR) Phase
Time frame: From start of the treatment-free remission (TFR) phase up to Week 528
Progression-Free Survival (PFS) After Start of the Treatment-Free Remission (TFR) Phase
Time frame: From start of the treatment-free remission (TFR) phase up to Week 528
Overall Survival (OS) After Start of the Treatment-Free Remission (TFR) Phase
Time frame: From start of the treatment-free remission (TFR) phase up to Week 528
Percentage of Participants With Treatment-emergent Adverse Events During the Entire Study
Time frame: From first dose of nilotinib through up to approximately 11 years of study participation, including the NTCS, TFR, and NTRI phases
Number of Participants With BCR-ABL1 Mutations Associated With Resistance to Nilotinib After Loss of Major Molecular Response
Time frame: From loss of major molecular response after nilotinib suspension through up to 528 weeks of study participation
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Aug 2026.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: Yes. Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations. This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Novartis Pharmaceuticals study director
Novartis Pharmaceuticals
113 sites in 19 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Nilotinib followed by treatment-free in people with Chronic Myelogenous Leukemia, run by Novartis Pharmaceuticals at 113 sites in 19 countries.
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 26 inclusion and 39 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: finished, as of the sponsor's last update on 13 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 113 sites in Germany, Spain, Italy, France, Japan and 14 more countries. 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 14 Jan 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of Participants in Major Molecular Response at 48 Weeks After Start of Treatment-Free Remission (TFR) Phase (time frame: 48 weeks in TFR). 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 Aug 2026.