Study of Oral Ixazomib Maintenance Therapy After Initial Therapy in Participants With Newly Diagnosed Multiple Myeloma Not Treated With Stem Cell Transplantation (SCT)

Multiple Myeloma Clinical Trial

Official title:

China Continuation: A Single-Arm, Open-Label Study of Oral Ixazomib Maintenance Therapy After Initial Therapy in Patients With Newly Diagnosed Multiple Myeloma Not Treated With Stem Cell Transplantation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03748953
• Other study ID #: C16021 CCS
• Secondary ID: 2014-001394-13
• Status: Completed
• Phase: Phase 3
• Start date: January 24, 2019
• Est. completion date: November 29, 2023

Study information

• Verified date: December 2023
• Source: Takeda
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the long-term safety and tolerability of ixazomib maintenance therapy.

Description:

The drug being tested in this study is called ixazomib. Ixazomib is being tested to slow disease progression and improve overall survival in Chinese participants who have newly diagnosed multiple myeloma (NDMM) who have had a major positive response to initial therapy and have not undergone stem cell transplantation (SCT). This study will look at the effect of ixazomib has on the length of time that participants are free of disease progression and their overall survival. After the implementation of Amendment 8, participants who received placebo-matching capsules before unblinding and have not yet experienced disease progression will cross over to receive ixazomib. The study will enroll approximately 31 patients. Participants will be assigned to a single treatment group • Ixazomib All participants will be asked to take one capsule on Days 1, 8, and 15 of every 28-day cycle, for up to approximately 24 months (equivalent to 26 cycles [if no cycle delays], to the nearest complete cycle) or until documented progressive disease (PD) or intolerable toxicity, whichever occurs first. This multi-center trial will be conducted in China. The overall time to participate in this study is until a total of approximately up to 60 months. Participants will make multiple visits to the clinic, and every 4 weeks until the next line of therapy begins for a follow-up assessment.

Other known NCT identifiers

• NCT04371770

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: November 29, 2023
• Est. primary completion date: November 29, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Adult male or female participants aged 18 years or older with a confirmed diagnosis of symptomatic NDMM according to standard criteria.

2. Has completed 6 to 12 months (±2 weeks) of initial therapy, during which the participant was treated to best response, defined as the best response maintained for 2 cycles after the M-protein nadir is reached.

3. Has documented major response (partial response [PR], very good partial response [VGPR], complete response [CR]) according to the international myeloma working group (IMWG) uniform response criteria, version 2011, after this initial therapy.

4. Female participants who:

Are postmenopausal for at least 1 year before the screening visit, OR Are surgically sterile, OR If they are of childbearing potential, agree to practice 2 effective methods of contraception, at the same time, from the time of signing the informed consent through 90 days after the last dose of study drug, or Agree to practice true abstinence, when this is in line with the preferred and usual lifestyle of the participant. (Periodic abstinence [e.g., calendar, ovulation,symptothermal, postovulation methods] and withdrawal are not acceptable methods of contraception.) Male participants, even if surgically sterilized (i.e., status postvasectomy), who: Agree to practice effective barrier contraception during the entire study Treatment period and through 90 days after the last dose of study drug, or Agree to practice true abstinence, when this is in line with the preferred and usual lifestyle of the participant. (Periodic abstinence [e.g., calendar, ovulation, symptothermal, postovulation methods for the female partner] and withdrawal are not acceptable methods of contraception.)

5. Voluntary written consent must be given before performance of any study-related procedure not part of standard medical care, with the understanding that consent may be withdrawn by the participant at any time without prejudice to future medical care.

6. Has availability of complete documentation for:

1. Details of initial disease state, initial therapy, and response

2. Cytogenetic assessment at diagnosis (cytogenetic assessment performed after diagnosis must be approved by a Takeda project clinician or designee)

3. International Staging System (ISS) staging at diagnosis (requiring beta 2-microglobulin and serum albumin results).

7. Has Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 2.

8. Suitable venous access for the study-required blood sampling and consent for the specific amounts that will be taken.

9. Participant is willing and able to adhere to the study visit schedule and other protocol requirements including blood sampling and bone marrow aspiration.

10. Participants must meet the following clinical laboratory criteria at study entry:

1. Absolute neutrophil count (ANC) =1,000/mm^3 without growth factor support and platelet count = 75,000/mm^3. Platelet transfusions to help participants meet eligibility criteria are not allowed within 3 days before enrollment.

2. Total bilirubin =1.5*the upper limit of the normal range (ULN). 3. Alanine aminotransferase and aspartate aminotransferase =3*ULN. 4. Calculated creatinine clearance =30 mL/min (using the Cockroft-Gault equation).

Exclusion Criteria:

1. Has multiple myeloma that relapsed after, or was not responsive to, initial therapy.

2. Had prior stem-cell transplantation (SCT).

3. Has radiotherapy within 14 days before enrollment.

4. Had been diagnosed or treated for another malignancy within 5 years before enrollment or previously diagnosed with another malignancy with evidence of residual disease. Participants with nonmelanoma skin cancer or carcinoma in situ of any type are not excluded if they have undergone complete resection.

5. Female participants who are lactating and breastfeeding or have a positive serum pregnancy test during the Screening period.

6. Has major surgery within 14 days before enrollment.

7. Has central nervous system involvement.

8. Infection requiring intravenous (IV) antibiotic therapy or other serious infection within 14 days before enrollment.

9. Has diagnosis of Waldenstrom's macroglobulinemia, polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome, plasma cell leukemia, primary amyloidosis, myelodysplastic syndrome, or myeloproliferative syndrome.

10. Evidence of current uncontrolled cardiovascular conditions, including uncontrolled hypertension, uncontrolled cardiac arrhythmias, uncontrolled congestive heart failure, unstable angina, or myocardial infarction within the past 6 months.

11. Systemic treatment with strong cytochrome P450 (CYP3A) inducers (rifampin, rifapentine, rifabutin, carbamazepine, phenytoin, phenobarbital) or use of St. John's wort within 14 days before enrollment.

12. Ongoing or active infection, known human immunodeficiency virus positive, active hepatitis B or C infection.

13. Has comorbid systemic illnesses or other severe concurrent disease that, in the judgment of the investigator, would make the participant inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens (e.g., peripheral neuropathy (PN) that is Grade 1 with pain or Grade 2 or higher of any cause).

14. Psychiatric illness/social situation that would limit compliance with study requirements.

15. Known allergy to any of the study medications, their analogues, or excipients in the various formulations of any agent.

16. Inability to swallow oral medication, inability or unwillingness to comply with the drug administration requirements, or gastrointestinal (GI) procedure that could interfere with the oral absorption or tolerance of treatment.

17. Treatment with any investigational products within 30 days before enrollment.

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell

Intervention

Drug:
• Ixazomib
Ixazomib Capsules

Locations

Country	Name	City	State
China	Beijing Chaoyang Hospital Capital Medical University	Beijing	Beijing
China	Peking Union Medical College Hospital	Beijing	Beijing
China	Peking University Third Hospital	Beijing	Beijing
China	1st Affiliated Hospital of Zhejiang University	Hangzhou	Zhejiang
China	Jiangsu Province Hospital (the First Affiliated Hospital With Nanjing Medical University)	Nanjing	Jiangsu
China	Renji Hospital Shanghai Jiaotong University School of Medicine	Shanghai	Shanghai
China	Ruijin Hospital Shanghai Jiaotong University School of Medicine	Shanghai	Shanghai
China	Shanghai Chang Zheng Hospital	Shanghai	Shanghai
China	Shengjing Hospital of China Medical University	Shenyang	Liaoning
China	Tongji Hospital Tongji Medical College Huazhong University of Science and Technology	Wuhan	Hubei

Sponsors (1)

Lead Sponsor	Collaborator
Millennium Pharmaceuticals, Inc.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants for Each of the Eastern Cooperative Oncology Group (ECOG) Performance Status	ECOG performance status will assess participant's performance status on 5 point scale: 0=Fully active/able to carry on all pre-disease activities without restriction; 1=restricted in physically strenuous activity, ambulatory/able to carry out light or sedentary work; 2=ambulatory (>50% of waking hours), capable of all self-care, unable to carry out any work activities; 3=capable of only limited self-care, confined to bed/chair >50% of waking hours; 4=completely disabled, cannot carry on any self-care, totally confined to bed/chair; 5=dead.	From the date of first dose of study drug to every 4 weeks after progressive disease (PD) until next line therapy or death from any cause (approximately 60 months)
Primary	Percentage of Participants with Adverse Events (AEs)	Adverse events are defined as any unfavorable and unintended sign, symptom or disease temporally associated with the use of a medicinal product reported from first dose of study drug through 30 days after the last dose of study drug.	From the date of first dose of study drug through 30 days after last dose of study drug (approximately 25 months)
Primary	Percentage of Participants with Serious Adverse Event (SAE)	A serious adverse event is any experience that suggests a significant hazard, contraindication, side effect or precaution that: results in death, is life-threatening, required in-patient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or is medically significant.	From the date of first dose through 30 days after last dose of study drug (approximately 25 months)
Primary	Number of Participants with Any Markedly Abnormal Standard Safety Laboratory Values	Clinical laboratory evaluations will be performed by a central laboratory. The number of participants with any markedly abnormal standard safety laboratory values collected throughout study will be reported.	From the date of first dose of study drug to every 4 weeks after progressive disease (PD) until next line therapy or death from any cause (approximately 60 months)
Secondary	Progression-Free Survival (PFS)	PFS is defined as the time from the date of first dose of study drug to the first occurrence of PD as evaluated by the investigator or death from any cause, whichever occurs first. PD is defined as >=25% increase from lowest value in serum M component or urine M-component; difference between involved and uninvolved free light chain (FLC) levels (absolute increase >10 mg/dL); bone marrow plasma cell percent >/=10%; new bone lesions or soft tissue plasmacytomas development or definite increase in existing bone lesions/soft tissue plasmacytomas size; hypercalcaemia development.	From the date of first dose of study drug to every 4 weeks until PD or death from any cause (approximately 60 months)
Secondary	Overall Survival (OS)	OS is measured as the time from the date of first dose of study drug to the date of death.	From the date of first dose of study drug to every 12 weeks during follow-up after PD or next line therapy or death whichever occurs later (approximately 60 months)
Secondary	Percentage of Participants who Achieve or Maintain Best Response Before PD or up to Subsequent Therapy	Response will be assessed as per the International Myeloma Working Group (IMWG) criteria. Best response will include partial responses (PR), very good partial response (VGPR) and complete response (CR). PR is defined as >=50% reduction of serum M-component, urinary M- component by >=90% to <200 mg/24-hour reduction; >=50% in the difference between involved and uninvolved FLC; bone marrow plasma cells (PC) >/=30%; reduction >/=50% reduction in the soft tissue size. VGPR is defined as serum or urine M-component detectable by immunofixation but not on electrophoresis; >=90% reduction in serum or urine M-component level <100 mg/24 hour. CR is defined as negative immunofixation on the serum and urine; soft tissue plasmacytomas disappearance; <5% PCs in bone marrow.	From the date of first dose of study drug to every 4 weeks after PD or next line therapy or death from any cause (approximately 60 months)
Secondary	Duration of Complete Response (CR)	Duration of CR is defined as the time from the date of first dose of study drug or the date of CR to the date of first documentation of PD. CR is defined as negative immunofixation on the serum and urine; soft tissue plasmacytomas disappearance; <5% PCs in bone marrow.	From the date of first dose of study drug to every 4 weeks after PD or next line therapy or death from any cause (approximately 60 months)
Secondary	Time to Progression (TTP)	TTP is defined as the time from the date of first dose of study drug to the date of first documentation of PD. PD is defined as >=25% increase from lowest value in serum M component or urine M-component; difference between involved and uninvolved FLC levels (absolute increase >10 mg/dL); bone marrow plasma cell percent >/=10%; new bone lesions or soft tissue plasmacytomas development or definite increase in existing bone lesions/soft tissue plasmacytomas size; hypercalcaemia development.	From the date of first dose of study drug to every 4 weeks after PD or next line therapy or death from any cause (approximately 60 months)
Secondary	Time to Next-Line Therapy (TTNT)	TTNT is defined as the time from the date of first dose of study drug to the date of the first dose of next-line of antineoplastic therapy.	From the date of first dose of study drug to every 4 weeks after PD or next line therapy or death from any cause (approximately 60 months)
Secondary	Percentage of Participants With A New Primary Malignancy	Percentage of participants with a new primary malignancy will be reported.	From the date of first dose of study drug to every 4 weeks after PD or next line therapy or death from any cause or termination of the study (approximately 60 months)
Secondary	European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC) QLQ-C30	The European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC) QLQ-C30 is completed by the participant. The EORTC QLQ-30 contains 30 questions that incorporate 5 functional scales (physical functioning, role functioning, emotional functioning, cognitive functioning, and social functioning), 1 global health status scale, 3 symptom scales (fatigue, nausea and vomiting, and pain), and 6 single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). The participant answers questions about their health during the past week. There are 28 questions answered on a 4-point scale where 1=not at all (best) to 4=very much (worst) and 2 questions answered on a 7-point scale where 1=very poor (worst) to 7= excellent (best).	From the date of first dose of study drug to every 4 weeks after PD or next line therapy or death from any cause (approximately 60 months)
Secondary	Correlation Between Frailty Status and PFS and OS	Participants frailty status will be assessed on basis of 4 components: age(<75, 75- 80, and>80 years correspond to frailty scores of 0, 1, and 2, respectively), Charlson comorbidity scoring system without age weighting (scores of = 1 and = 2 correspond to frailty scores of 0 and 1, respectively), Katz index of independence in activities of daily living (scores of >4 and =4 correspond to frailty scores of 0 and 1, respectively) and Lawton instrumental activities of daily living scale (scores of >5 and =5 correspond to frailty scores of 0 and 1, respectively). The sum of the 4 frailty scores equals the total frailty score. A total frailty score of 0 corresponds to a frailty status of fit; a total score of 1, to unfit; and a total score of 2 or more, to frail. PFS is defined as the time from the date of first dose of study drug to the first occurrence of PD as evaluated by the investigator. OS will be measured as the time from the date of first dose of study drug to the date of death.	From the date of first dose of study drug to every 12 weeks during follow-up after PD or next line therapy or death whichever occurs later (approximately 60 months)
Secondary	Plasma Concentration of Ixazomib		Cycle1 Day1(1,4 hours post-dose),pre-dose Cycle1 on Days8 and 15;pre-dose Cycle2 on Days1 and 8;pre-dose Cycles 3-5 on Day1;pre-dose Cycle5 on Day8(only for those who have dose escalated after Cycle4); pre-dose Cycles 6-10 on Day 1;each cycle of 28 days
Secondary	Time to Resolution of Peripheral Neuropathy (PN) Events	PN is defined as the treatment-emergent adverse event in the high-level term of peripheral neuropathies not elsewhere classified (NEC) according to the Medical Dictionary for Regulatory Activities (MedDRA). A PN event is considered as resolved if its final outcome is resolved with no subsequent PN event of the same preferred term occurring on the resolution date or the day before and after. Time to resolution is defined as the time from the initial onset date (inclusive) to the resolution date for resolved events.	From the date of first dose of study drug to next-line therapy or 6 months after PD (approximately 60 months)
Secondary	Time to Improvement of PN Events	PN is defined as the treatment-emergent adverse event in the high-level term of peripheral neuropathies not elsewhere classified (NEC) according to the MedDRA. A PN event is considered to be improved if the event improves from the maximum grade; that is, all the grades recorded after the maximum grade are less than the maximum grade. Time to improvement is defined as the time from the initial onset date (inclusive) of the maximum grade to the first onset date that the toxicity grade is below the maximum grade with no higher grade thereafter, or the resolution date, whichever occurs first.	From the date of first dose of study drug to next-line therapy or 6 months after PD (approximately 60 months)

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