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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT01324947




Registration number
NCT01324947
Ethics application status
Date submitted
27/03/2011
Date registered
29/03/2011
Date last updated
19/11/2019

Titles & IDs
Public title
Study to Evaluate the Safety and Efficacy of Pomalidomide Monotherapy in Subjects With Refractory or Relapsed Refractory Multiple Myeloma
Scientific title
Open-label, Multi-center, Single Arm Study For The Safety And Efficacy Of Pomalidomide Monotherapy For Subjects With Refractory Or Relapsed And Refractory Multiple Myeloma. A Companion Study For Clinical Trial CC-4047-MM003
Secondary ID [1] 0 0
2010-023343-16
Secondary ID [2] 0 0
CC-4047-MM-003/C
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Multiple Myeloma 0 0
Condition category
Condition code
Cancer 0 0 0 0
Other cancer types

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - pomalidomide

Experimental: Pomalidomide - Oral pomalidomide 4 mg on Days 1-21 of 28-day cycle until progressive disease (PD) or unacceptable toxicity


Treatment: Drugs: pomalidomide
Oral pomalidomide 4 mg on Days 1-21 of 28-day cycle until progressive disease (PD) or unacceptable toxicity
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Percentage of Participants With an Objective Response According to International Myeloma Working Group (IMWG) Uniform Response Criteria Based on Investigator Assessment
Timepoint [1] 0 0
From randomization through the study follow-up phase; up to the data cut-off of 31 July 2014; Maximum time on follow-up was 141.1 weeks.
Secondary outcome [1] 0 0
Percentage of Participants With Objective Response According to European Group for Blood and Marrow Transplantation (EBMT) Criteria Based on Investigator Assessment
Timepoint [1] 0 0
From randomization through the study follow-up phase; up to the data cut-off of 31 July 2014; Maximum time on follow-up was 141.1 weeks.
Secondary outcome [2] 0 0
Number of Participants With Adverse Events and Type of Adverse Events
Timepoint [2] 0 0
From first dose of study drug through to 30 days after the last dose, until the data cut-off date of 31 July 2014. Maximum time on treatment was 94.1 weeks.
Secondary outcome [3] 0 0
Kaplan Meier Estimates for Progression Free Survival (PFS) by Investigator Based on IMWG
Timepoint [3] 0 0
From randomization through the follow-up phase; Maximum duration of follow-up for PFS was 90.3 weeks.
Secondary outcome [4] 0 0
Kaplan-Meier Estimate for Time to Progression (TTP) Based on Investigator Assessment Using IMWG Criteria
Timepoint [4] 0 0
From randomization through the follow-up phase; up to the data-cut off of 31 July 2014; Maximum time to progression follow-up was 90.3 weeks.
Secondary outcome [5] 0 0
Kaplan-Meier Estimate Duration of Response Based on Investigator Assessment Using IMWG Criteria
Timepoint [5] 0 0
From randomization through the study follow-up phase; up to the data cut-off of 31 July 2014; Maximum duration of response follow-up was 90.3 weeks.
Secondary outcome [6] 0 0
Kaplan-Meier Estimate for Overall Survival
Timepoint [6] 0 0
From randomization through the follow-up phase; Maximum time on follow-up was 141.1 weeks.
Secondary outcome [7] 0 0
Time to Response Based on IMWG and Assessed by the Investigator
Timepoint [7] 0 0
From randomization through the follow-up phase; up to the data-cut off of 31 July 2014; Maximum time to response was 23.1 weeks

Eligibility
Key inclusion criteria
1. Subjects with refractory or relapsed and refractory multiple myeloma who were enrolled in Study CC-4047-MM-003 and discontinued study therapy with dexamethasone alone (Treatment Arm B) after at least starting the second cycle of dexamethasone treatment and due to development of documented disease progression according to the International Myeloma Working Group (IMWG) criteria and as decided by an Independent Review Adjudication Committee (IRAC).
2. Must be = 18 years at the time of signing the informed consent form.
3. The subject must understand and voluntarily sign an informed consent document prior to any study related assessments/procedures being conducted. The only exception is if a skeletal survey was performed within 90 days prior to the start of Cycle 1, then a new survey will not be required.
4. Must be able to adhere to the study visit schedule and other protocol requirements.
5. Subjects must have documented diagnosis of multiple myeloma and have measurable disease (serum M-protein = 0.5g/dL or urine M-protein = 200 mg/24 hours).
6. Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1, or 2.
7. Females of childbearing potential (FCBP†) must agree to utilize two reliable forms of contraception simultaneously or practice true 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]from heterosexual contact for at least 28 days before starting study drug, while participating in the study (including dose interruptions), and for at least 28 days after study treatment discontinuation and must agree to regular pregnancy testing during this timeframe.
8. Females must agree to abstain from breastfeeding during study participation and 28 days after study discontinuation.
9. Males must agree to either use a latex condom during any sexual contact with FCBP or practice true 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] while participating in the study and for 28 days following discontinuation from this study, even if he has undergone a successful vasectomy. .
10. Males must also agree to refrain from donating semen or sperm while on pomalidomide and for 28 days after discontinuation from this study treatment.
11. All subjects must agree to refrain from donating blood while on study drug and for 28 days after discontinuation from this study treatment.
12. All subjects must agree not to share study medication
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Exclusion Criteria

* The presence of any of the following will exclude a subject from enrollment:

1. Subjects with multiple myeloma who were not treated as a part of Study CC-4047-MM-003 (Arm B).
2. Subjects who received any anti-myeloma or anti-cancer therapies within the last 14 days of wash-out period before initiation of study treatment.
3. Subjects who discontinued CC-4047-MM-003 study =120 days.
4. Subjects who initiate another anti-myeloma therapy from the time of disease progression on study CC-4047-MM-003 to the time of treatment initiation in the companion study.
5. Any of the following laboratory abnormalities:

* Absolute neutrophil count (ANC) < 1,000/µL.
* Platelet count < 75,000/µL for subjects in whom < 50% of bone marrow nucleated cells are plasma cells; or a platelet count < 30,000/µL for subjects in whom = 50% of bone marrow nucleated cells are plasma cells
* Creatinine Clearance < 45 mL/min according to Cockcroft-Gault formula (If creatinine clearance calculated from the 24-hour urine sample is =45 ml/min, patient will qualify for the trial)
* Corrected serum calcium > 14 mg/dL (> 3.5 mmol/L);
* Hemoglobin < 8 g/dL (< 4.9 mmol/L; prior RBC transfusion or recombinant human erythropoietin use is permitted)
* Serum SGOT/AST or SGPT/ALT > 3.0 x upper limit of normal (ULN)
* Serum total bilirubin > 2.0 mg/dL (34.2 µmol/L); or > 3.0 x ULN for subjects with hereditary benign hyperbilirubinaemia
6. Prior history of malignancies, other than Multiple Myeloma (MM), unless the subject has been free of the disease for = 5 years. Exceptions include the following:

* Basal or Squamous cell carcinoma of the skin
* Carcinoma in situ of the cervix or breast
* Incidental histologic finding of prostate cancer (TNM stage of T1a or T1b)
7. Hypersensitivity to thalidomide or lenalidomide. (This includes = Grade 3 rash during prior thalidomide or lenalidomide therapy).
8. Peripheral neuropathy = Grade 2.
9. Subjects who received an allogeneic bone marrow or allogeneic peripheral blood stem cell transplant less than 12 months prior to initiation of study treatment and who have not discontinued immunosuppressive treatment for at least 4 weeks prior to initiation of study treatment and are currently dependent on such treatment.
10. Subjects who are planning for or who are eligible for stem cell transplant.
11. Subjects with any one of the following:

* Congestive heart failure (NY Heart Association Class III or IV)
* Myocardial infarction within 12 months prior to starting study treatment
* Unstable or poorly controlled angina pectoris, including Prinzmetal variant angina pectoris
12. Subjects who received any of the following within the last 14 days of initiation of study treatment:

* Plasmapheresis
* Major surgery (kyphoplasty is not considered major surgery)
* Radiation therapy
13. Use of any investigational agents within 28 days or 5 half lives (whichever is longer) of treatment.
14. Subjects with chronic conditions such as rheumatoid arthritis, multiple sclerosis and lupus, which likely need additional steroid or immunosuppressive treatments in addition to the study treatment.
15. Any condition including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study.
16. Incidence of gastrointestinal disease that may significantly alter the absorption of pomalidomide.
17. Subjects unable or unwilling to undergo antithrombotic prophylactic treatment.
18. Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.
19. Pregnant or breastfeeding females.
20. Known human immunodeficiency virus (HIV) positivity or active infectious hepatitis A, B or C.

Study design
Purpose of the study
Treatment
Allocation to intervention
NA
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/03/2011
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
31/07/2014
Sample size
Target
Accrual to date
Final
74
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Royal Adelaide Hospital - SA Pathology Haematology - Adelaide
Recruitment hospital [2] 0 0
Princess Alexandra Hospital - Haematology - Brisbane
Recruitment hospital [3] 0 0
Royal Prince Alfred Hospital - Institute of Haematology - Camperdown
Recruitment hospital [4] 0 0
Peter McCallum Cancer Institute - Directorate of Cancer Medicine - East Melbourne
Recruitment hospital [5] 0 0
Frankston Hospital-Peninsula Health - Oncology Day Unit - Frankston
Recruitment hospital [6] 0 0
The Alfred Hospital - Malignant Haematology & Stem Cell Transplantation - Melbourne
Recruitment hospital [7] 0 0
Calvary Mater Newcastle - Haematology - Waratah
Recruitment hospital [8] 0 0
Border Medical Oncology - Wodonga
Recruitment hospital [9] 0 0
Wollongong Hospital - Haematology - Wollongong
Recruitment postcode(s) [1] 0 0
5000 - Adelaide
Recruitment postcode(s) [2] 0 0
4102 - Brisbane
Recruitment postcode(s) [3] 0 0
2050 - Camperdown
Recruitment postcode(s) [4] 0 0
3002 - East Melbourne
Recruitment postcode(s) [5] 0 0
3199 - Frankston
Recruitment postcode(s) [6] 0 0
3004 - Melbourne
Recruitment postcode(s) [7] 0 0
2298 - Waratah
Recruitment postcode(s) [8] 0 0
3690 - Wodonga
Recruitment postcode(s) [9] 0 0
2500 - Wollongong
Recruitment outside Australia
Country [1] 0 0
Belgium
State/province [1] 0 0
Gent
Country [2] 0 0
Belgium
State/province [2] 0 0
Leuven
Country [3] 0 0
Belgium
State/province [3] 0 0
Yvoir
Country [4] 0 0
Canada
State/province [4] 0 0
Alberta
Country [5] 0 0
Canada
State/province [5] 0 0
British Columbia
Country [6] 0 0
Canada
State/province [6] 0 0
Nova Scotia
Country [7] 0 0
Canada
State/province [7] 0 0
Ontario
Country [8] 0 0
Canada
State/province [8] 0 0
Quebec
Country [9] 0 0
Czechia
State/province [9] 0 0
Prague
Country [10] 0 0
Denmark
State/province [10] 0 0
Aalborg
Country [11] 0 0
Denmark
State/province [11] 0 0
Aarhus
Country [12] 0 0
Denmark
State/province [12] 0 0
Odense
Country [13] 0 0
Denmark
State/province [13] 0 0
Vejle
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France
State/province [14] 0 0
Angers
Country [15] 0 0
France
State/province [15] 0 0
Bayonne
Country [16] 0 0
France
State/province [16] 0 0
La Roche
Country [17] 0 0
France
State/province [17] 0 0
Lille
Country [18] 0 0
France
State/province [18] 0 0
Marseille
Country [19] 0 0
France
State/province [19] 0 0
Nantes
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France
State/province [20] 0 0
Paris
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France
State/province [21] 0 0
Pessac
Country [22] 0 0
France
State/province [22] 0 0
Pierre-Benite
Country [23] 0 0
France
State/province [23] 0 0
Toulouse
Country [24] 0 0
France
State/province [24] 0 0
Tours
Country [25] 0 0
France
State/province [25] 0 0
Vandoeuvre-les-Nancy
Country [26] 0 0
Germany
State/province [26] 0 0
Dresden
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Germany
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Essen
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Germany
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Hamburg
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Germany
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Heidelberg
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Germany
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Jena
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Germany
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Leipzig
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Germany
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Münster
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Germany
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Tübingen
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Germany
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Ulm
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Germany
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Würzburg
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Greece
State/province [36] 0 0
Athens
Country [37] 0 0
Italy
State/province [37] 0 0
Bologna
Country [38] 0 0
Italy
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Genova
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Italy
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Napoli
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Italy
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Orbassano
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Italy
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Padova
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Italy
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Piacenza
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Italy
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Reggio Emilia
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Italy
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Roma
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Italy
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Torino
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Amsterdam
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Netherlands
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Rotterdam
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Netherlands
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Utrecht
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Russian Federation
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Moscow
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Russian Federation
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St. Petersburg
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Badalona
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Barcelona
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Guipúzcoa
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Madrid
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Spain
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Salamanca
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Spain
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Santander
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Spain
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Valencia
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Sweden
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Goteborg
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Sweden
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Stockholm
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Sweden
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Uppsala
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Switzerland
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Bern
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Switzerland
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Genève
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Switzerland
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Zürich
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United Kingdom
State/province [64] 0 0
Bournemouth
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United Kingdom
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Leeds
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United Kingdom
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London
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United Kingdom
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Newcastle Upon Tyne
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United Kingdom
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Nottingham
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United Kingdom
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Plymouth
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United Kingdom
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Sheffield
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United Kingdom
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Surrey
Country [72] 0 0
United Kingdom
State/province [72] 0 0
Wolverhampton

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Celgene
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Mohamed Zaki, MD, PhD
Address 0 0
Celgene Corporation
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results are available at https://clinicaltrials.gov/study/NCT01324947