Study of Efficacy of CML-CP Patients Treated With ABL001 Versus Bosutinib, Previously Treated With 2 or More TKIs

• ClinicalTrials.gov Identifier: NCT03106779
• Recruitment Status: Active, not recruiting
• First Posted: April 10, 2017
• Results First Posted: February 15, 2022
• Last Update Posted: April 24, 2024
• Sponsor: Novartis Pharmaceuticals
• Information provided by (Responsible Party): Novartis ( Novartis Pharmaceuticals )

Tracking Information

• First Submitted Date: March 9, 2017
• First Posted Date: April 10, 2017
• Results First Submitted Date: November 27, 2021
• Results First Posted Date: February 15, 2022
• Last Update Posted Date: April 24, 2024
• Actual Study Start Date: November 29, 2016
• Actual Primary Completion Date: May 25, 2020 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: January 21, 2022)

Number of Participants With Major Molecular Response (MMR) Rate at 24 Weeks [ Time Frame: 24 weeks ]

MMR was defined as a ≥ 3.0 log reduction in BCR-ABL1 transcripts compared to the standardized baseline equivalent to ≤ 0.1% BCR-ABL1/ABL% by IS as measured by RQ-PCR.

Original Primary Outcome Measures (submitted: April 4, 2017)

Major Molecular Response (MMR) rate [ Time Frame: at 24 weeks ]

To compare the MMR rate of ABL001 versus bosutinib

Current Secondary Outcome Measures (submitted: January 21, 2022)

• Number of Participants With Major Molecular Response (MMR) Rate [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy asciminib versus bosutinib
• Complete Cytogenetic Response Rate [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of asciminib versus bosutinib. Cytogenic response will include Complete, Partial, Major, Minor, Minimal and no response.
• Time to MMR [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of asciminib versus bosutinib
• Duration of MMR [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of asciminib versus bosutinib
• Time to CCyR [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of asciminib versus bosutinib
• Duration of CCyR [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of asciminib versus bosutinib
• Time to Treatment Failure [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of asciminib versus bosutinib
• Progression Free Survival [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of asciminib versus bosutinib
• Overall Survival [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of asciminib versus bosutinib
• Trough Plasma Concentrations [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of asciminib in the CML-CP population
• PK Parameter: Cmax, [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of asciminib in the CML-CP population
• PK Parameter: Tmax [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of asciminib in the CML-CP population
• PK Parameter: AUC0-12h [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of asciminib in the CML-CP population
• PK Parameter: CL/F [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of asciminib in the CML-CP population

Original Secondary Outcome Measures (submitted: April 4, 2017)

• Major Molecular Response (MMR) rate [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib
• Complete Cytogenetic response rate [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib. Cytogenic response will include Complete, Partial, Major, Minor, Minimal and no response.
• Time to MMR [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib
• Duration of MMR [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib
• Time to CCyR [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib
• Duration of CCyR [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib
• Time to treatment failure [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib
• Progression free survival [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib
• Overall survival [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To compare additional parameters of the efficacy of ABL001 versus bosutinib
• Trough plasma concentrations [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of ABL001 in the CML-CP population
• PK parameter: Cmax, [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of ABL001 in the CML-CP population
• PK parameter: Tmax [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of ABL001 in the CML-CP population
• PK parameter: AUC0-12h [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of ABL001 in the CML-CP population
• PK parameter: CL/F [ Time Frame: 96 weeks after the last patient received the first study dose ]
  To characterize the PK of ABL001 in the CML-CP population

• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Study of Efficacy of CML-CP Patients Treated With ABL001 Versus Bosutinib, Previously Treated With 2 or More TKIs
• Official Title: A Phase 3, Multi-center, Open-label, Randomized Study of Oral ABL001 Versus Bosutinib in Patients With Chronic Myelogenous Leukemia in Chronic Phase (CML-CP), Previously Treated With 2 or More Tyrosine Kinase Inhibitors

Brief Summary

The purpose of this pivotal study was to compare the efficacy of asciminib (ABL001) with that of bosutinib in the treatment of patients with CML-CP having previously been treated with a minimum of two prior ATP-binding site TKIs.

Patients intolerant to the most recent TKI therapy must have had BCR-ABL1 ratio > 0.1% IS at screening and patients failing their most recent TKI therapy must have met the definition of treatment failure as per the 2013 European LeukemiaNet (ELN) recommendations.

Patients with documented treatment failure as per 2013 ELN recommendations while on bosutinib treatment had the option to switch to asciminib treatment within 96 weeks after the last patient has been randomized on study.

• Detailed Description: Patients were randomized in a 2:1 ratio to asciminib 40 mg BID or bosutinib 500 mg QD. Randomization was stratified by major cytogenetic response (MCyR) at screening. Patients with documented treatment failure (specifically meeting lack of efficacy criteria adapted from the 2013 ELN recommendations) while on bosutinib treatment were offered the option to switch to asciminib treatment within 96 weeks after the last patient was randomized to the study.
• Study Type: Interventional
• Study Phase: Phase 3
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: None (Open Label); Primary Purpose: Treatment
• Condition: Chronic Myelogenous Leukemia

Intervention

• Drug: Asciminib
  40 mg tablets was taken orally twice a day (BID)
  Other Name: ABL001
• Drug: Bosutinib
  500 mg tablets was taken orally once daily (QD)

Study Arms

• Experimental: Asciminib
  Patients were randomized to asciminib 40mg BID
  Intervention: Drug: Asciminib
• Active Comparator: Bosutinib
  Patients were randomized to bosutinib 500mg QD
  Intervention: Drug: Bosutinib

Publications *

• Yuda J, Doki N, Matsuoka H, Yokota T, Tomita A, Takahashi N, Matsumura I, Kubo K, Goto T, Kirito K, Maki A, Aoki M, Allepuz A, Minami Y. Asciminib vs bosutinib in CML patients pretreated with >/=2 tyrosine kinase inhibitors: Results from the Japanese subgroup analysis of ASCEMBL study. Cancer Med. 2023 Feb;12(3):2990-2998. doi: 10.1002/cam4.5212. Epub 2022 Sep 27.
• Li YF, Combes FP, Hoch M, Lorenzo S, Sy SKB, Ho YY. Population Pharmacokinetics of Asciminib in Tyrosine Kinase Inhibitor-Treated Patients with Philadelphia Chromosome-Positive Chronic Myeloid Leukemia in Chronic and Acute Phases. Clin Pharmacokinet. 2022 Oct;61(10):1393-1403. doi: 10.1007/s40262-022-01148-9. Epub 2022 Jun 28. Erratum In: Clin Pharmacokinet. 2022 Aug 17;:
• Rea D, Mauro MJ, Boquimpani C, Minami Y, Lomaia E, Voloshin S, Turkina A, Kim DW, Apperley JF, Abdo A, Fogliatto LM, Kim DDH, le Coutre P, Saussele S, Annunziata M, Hughes TP, Chaudhri N, Sasaki K, Chee L, Garcia-Gutierrez V, Cortes JE, Aimone P, Allepuz A, Quenet S, Bedoucha V, Hochhaus A. A phase 3, open-label, randomized study of asciminib, a STAMP inhibitor, vs bosutinib in CML after 2 or more prior TKIs. Blood. 2021 Nov 25;138(21):2031-2041. doi: 10.1182/blood.2020009984.

Recruitment Information

• Recruitment Status: Active, not recruiting
• Actual Enrollment (submitted: November 16, 2021): 233
• Original Estimated Enrollment (submitted: April 4, 2017): 222
• Estimated Study Completion Date: December 18, 2024
• Actual Primary Completion Date: May 25, 2020 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

Male or female patients with a diagnosis of CML-CP ≥ 18 years of age

Patients must meet all of the following laboratory values at the screening visit:

• < 15% blasts in peripheral blood and bone marrow
• < 30% blasts plus promyelocytes in peripheral blood and bone marrow
• < 20% basophils in the peripheral blood
• ≥ 50 x 109/L (≥ 50,000/mm3) platelets
• Transient prior therapy related thrombocytopenia (< 50,000/mm3 for ≤ 30 days prior to screening) is acceptable
• No evidence of extramedullary leukemic involvement, with the exception of hepatosplenomegaly

BCR-ABL1 ratio > 0.1% IS according to central laboratory at the screening examination for patients intolerant to the most recent TKI therapy

Prior treatment with a minimum of 2 prior ATP-binding site TKIs (i.e. imatinib, nilotinib, dasatinib, radotinib or ponatinib)

Failure (adapted from the 2013 ELN Guidelines Bacarrani 2013) or intolerance to the most recent TKI therapy at the time of screening

• Failure is defined for CML-CP patients (CP at the time of initiation of last therapy) as follows. Patients must meet at least 1 of the following criteria.
• Three months after the initiation of therapy: No CHR or > 95% Ph+ metaphases
• Six months after the initiation of therapy: BCR-ABL1 ratio > 10% IS and/or > 65% Ph+ metaphases
• Twelve months after initiation of therapy: BCR-ABL1 ratio > 10% IS and/or > 35% Ph+ metaphases
• At any time after the initiation of therapy, loss of CHR, CCyR or PCyR
• At any time after the initiation of therapy, the development of new BCR-ABL1 mutations which potentially cause resistance to study treatment
• At any time after the initiation of therapy, confirmed loss of MMR in 2 consecutive tests, of which one must have a BCR-ABL1 ratio ≥ 1% IS
• At any time after the initiation of therapy, new clonal chromosome abnormalities in Ph+ cells: CCA/Ph+
• Intolerance is defined as:
• Non-hematologic intolerance: Patients with grade 3 or 4 toxicity while on therapy, or with persistent grade 2 toxicity, unresponsive to optimal management, including dose adjustments (unless dose reduction is not considered in the best interest of the patient if response is already suboptimal)
• Hematologic intolerance: Patients with grade 3 or 4 toxicity (absolute neutrophil count [ANC] or platelets) while on therapy that is recurrent after dose reduction to the lowest doses recommended by manufacturer

Exclusion Criteria:

Known presence of the T315I or V299L mutation at any time prior to study entry Known second chronic phase of CML after previous progression to AP/BC Previous treatment with a hematopoietic stem-cell transplantation Patient planning to undergo allogeneic hematopoietic stem cell transplantation

Cardiac or cardiac repolarization abnormality, including any of the following:

• History within 6 months prior to starting study treatment of myocardial infarction (MI), angina pectoris, coronary artery bypass graft (CABG)
• Clinically significant cardiac arrhythmias (e.g., ventricular tachycardia), complete left bundle branch block, high-grade AV block (e.g., bifascicular block, Mobitz type II and third degree AV block)
• QTcF at screening ≥450 msec (male patients), ≥460 msec (female patients)
• Long QT syndrome, family history of idiopathic sudden death or congenital long QT syndrome, or any of the following:
• Risk factors for Torsades de Pointes (TdP) including uncorrected hypokalemia or hypomagnesemia, history of cardiac failure, or history of clinically significant/symptomatic bradycardia
• Concomitant medication(s) with a known risk of Torsades de Pointes per www.crediblemeds.org that cannot be discontinued or replaced 7 days prior to starting study drug by safe alternative medication.
• Inability to determine the QTcF interval
• 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, active or uncontrolled infection, pulmonary hypertension)
• History of acute pancreatitis within 1 year of study entry or past medical history of chronic pancreatitis
• History of acute or chronic liver disease
• Treatment with medications that meet one of the following criteria and that cannot be discontinued at least one week prior to the start of treatment with study treatment
• Moderate or strong inducers of CYP3A
• Moderate or strong inhibitors of CYP3A
• Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during dosing and for 3 days after last dose of ABL001 and one month after last dose of bosutinib. Highly effective contraception methods include:
• Total abstinence (when this is in line with the preferred and usual lifestyle of the subject. 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) total hysterectomy or bilateral 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 screening). The vasectomized male partner should be the sole partner for that subject.
• Use of oral, injected or implanted hormonal methods of contraception or placement of an intrauterine device (IUD) or intrauterine system (IUS) or other forms of hormonal contraception that have comparable efficacy (failure rate <1%), for example hormone vaginal ring or transdermal hormone contraception.
• 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), total hysterectomy or bilateral tubal ligation at least six weeks before taking study medication. In the case of oophorectomy alone, women are considered post-menopausal and not of child bearing potential only when the reproductive status of the woman has been confirmed by follow up hormone level assessment.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Argentina, Australia, Brazil, Bulgaria, Canada, Czechia, France, Germany, Hungary, Israel, Italy, Japan, Korea, Republic of, Lebanon, Mexico, Netherlands, Romania, Russian Federation, Saudi Arabia, Serbia, Spain, Switzerland, Turkey, United Kingdom, United States
• Removed Location Countries: Belgium

Administrative Information

• NCT Number: NCT03106779
• Other Study ID Numbers: CABL001A2301
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: Yes

Plan Description

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 expert 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 is currently available according to the process described on www.clinicalstudydatarequest.com

• URL: https://www.clinicalstudydatarequest.com

• Current Responsible Party: Novartis ( Novartis Pharmaceuticals )
• Original Responsible Party: Same as current
• Current Study Sponsor: Novartis Pharmaceuticals
• Original Study Sponsor: Same as current
• Collaborators: Not Provided

Investigators

• Study Director: Novartis Pharmaceuticals; Novartis Pharmaceuticals

• PRS Account: Novartis
• Verification Date: April 2024