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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT01482962




Registration number
NCT01482962
Ethics application status
Date submitted
28/11/2011
Date registered
1/12/2011
Date last updated
31/07/2018

Titles & IDs
Public title
Alisertib (MLN8237) or Investigator's Choice in Patients With Relapsed/Refractory Peripheral T-Cell Lymphoma
Scientific title
A Phase 3, Randomized, Two-Arm, Open-Label, Multicenter, International Trial of Alisertib (MLN8237) or Investigator's Choice (Selected Single Agent) in Patients With Relapsed or Refractory Peripheral T-Cell Lymphoma
Secondary ID [1] 0 0
2011-003545-18
Secondary ID [2] 0 0
C14012
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Relapsed Peripheral T-Cell Lymphoma 0 0
Refractory Peripheral T-Cell Lymphoma 0 0
Condition category
Condition code
Cancer 0 0 0 0
Lymphoma (non Hodgkin's lymphoma) - High grade lymphoma
Cancer 0 0 0 0
Lymphoma (non Hodgkin's lymphoma) - Low grade lymphoma

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Alisertib
Treatment: Drugs - Pralatrexate
Treatment: Drugs - Gemcitabine
Treatment: Drugs - Romidepsin

Experimental: Alisertib - Alisertib 50 mg, enteric-coated tablet formulation, orally, twice daily for 7 consecutive days (Cycle Days 1-7) in a 21-day cycle (Up to 148 Weeks).

Active comparator: Pralatrexate, or Romidepsin, or Gemcitabine - Pralatrexate 30 mg/m\^2, intravenous (IV) push over 3 to 5 minutes, once weekly, for 6 weeks in 7-week cycles with concurrent vitamin B12 and folic acid supplementation. Cycles were repeated every 7-weeks provided the participant continued to benefit from and tolerate the therapy (Up to 115 Weeks), or Gemcitabine 1,000 mg/m\^2 over 30 minutes, intravenously, on Days 1, 8, and 15 of a 28-day cycle until the absence of disease progression or unacceptable toxicity (Up to 32 Weeks), or Romidepsin 14 mg/m\^2, intravenously over a 4-hour period, on Days 1, 8, and 15 of a 28-cycle. Cycles were repeated every 28 days provided the patient continued to benefit from and tolerate the therapy (Up to 30 Weeks).


Treatment: Drugs: Alisertib
Alisertib enteric coated tablets

Treatment: Drugs: Pralatrexate
Pralatrexate IV infusion

Treatment: Drugs: Gemcitabine
Gemcitabine IV infusion

Treatment: Drugs: Romidepsin
Romidepsin IV infusion

Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Overall Response Rate (ORR) Based on Independent Review Committee (IRC) Assessment
Timepoint [1] 0 0
Every 8 weeks from date of first dose treatment; every 12 weeks after 40 week assessment; at end of treatment visit until progressive disease. Duration is approximately 3 years
Primary outcome [2] 0 0
Progression-Free Survival (PFS) Based on IRC Assessment
Timepoint [2] 0 0
Every 8 weeks from date of first dose treatment; every 12 weeks after 40 week assessment; at end of treatment visit until progressive disease. Duration is approximately 3 years
Secondary outcome [1] 0 0
Overall Survival (OS)
Timepoint [1] 0 0
Participants were followed for survival for 2 years from date of last participant off study treatment, or death, whichever occurs first. Contacts were every 4 months (Median follow-up 519 days in the alisertib arm and 586 days in the comparative arm)
Secondary outcome [2] 0 0
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
Timepoint [2] 0 0
First dose to 30 days after last dose of study drug or comparator (Up to 152 Weeks)
Secondary outcome [3] 0 0
Number of Participants With Clinically Important Abnormal Laboratory Values Reported as AEs
Timepoint [3] 0 0
First dose to 30 days after last dose of study drug or comparator (Up to 152 Weeks)
Secondary outcome [4] 0 0
Number of Participants With Clinically Important Vital Sign Measurements Reported as AEs
Timepoint [4] 0 0
First dose to 30 days after last dose of study drug or comparator (Up to 152 Weeks)
Secondary outcome [5] 0 0
Complete Response (CR) Rate
Timepoint [5] 0 0
At the end of every 8 weeks from date of first dose treatment; every 12 weeks after 40 week assessment; at end of treatment visit until PD (approximately 3 years)
Secondary outcome [6] 0 0
Time to Disease Progression (TTP)
Timepoint [6] 0 0
At the end of every 8 weeks from date of first dose treatment; every 12 weeks after 40 week assessment; at end of treatment visit until progressive disease. Duration is approximately 3 years
Secondary outcome [7] 0 0
Duration of Response (DOR)
Timepoint [7] 0 0
At the end of every 8 weeks from date of first dose treatment; every 12 weeks after 40 week assessment; at end of treatment visit until progressive disease. Duration is approximately 3 years
Secondary outcome [8] 0 0
Time to Response
Timepoint [8] 0 0
At the end of every 8 weeks from date of first dose treatment; every 12 weeks after 40 week assessment; at end of treatment visit until progressive disease. Duration is approximately 3 years
Secondary outcome [9] 0 0
Time to Subsequent Antineoplastic Therapy
Timepoint [9] 0 0
From date of last study drug to date of subsequent antineoplastic therapy, if required; approximately 3 years
Secondary outcome [10] 0 0
Plasma Concentration-time Data to Contribute to Future Population Pharmacokinetics (PK) Analysis
Timepoint [10] 0 0
Cycle 1, Days 1 and 7; Cycle 2, Day 8; Cycle 3, Day 8; Cycle 4, Day 8. Duration is approximately 4 months.
Secondary outcome [11] 0 0
Change Form Baseline in Reported Symptoms and Quality of Life (QoL) Assessment Per Functional Assessment of Cancer Therapy-Lymphoma (FACT-LYM) for Functioning and Symptoms
Timepoint [11] 0 0
Baseline and End of Treatment (EOT) (Up to 152 Weeks)

Eligibility
Key inclusion criteria
* Male or female participants age 18 or older
* Participants with Peripheral T cell lymphoma (PTCL) (selected subtypes) according to World Health Organization (WHO) criteria and have relapsed or are refractory to at least 1 prior systemic, cytotoxic therapy for PTCL. Participants must have received conventional therapy as a prior therapy. Cutaneous-only disease is not permitted. Participants must have documented evidence of progressive and measurable disease.
* Tumor biopsy available for central hematopathologic review
* Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
* Female participants who are post menopausal for at least 1 year, surgically sterile, or agree to practice 2 effective methods of contraception through 30 days after the last dose of study drug or agree to abstain from heterosexual intercourse.
* Male participants who agree to practice effective barrier contraception through 6 months after the last dose of alisertib or agree to abstain from heterosexual intercourse
* Suitable venous access
* Voluntary written consent
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Exclusion Criteria

* Known central nervous system lymphoma
* Systemic antineoplastic therapy, immunotherapy, investigational agent or radiation therapy within 4 weeks of first dose of study treatment or concomitant use during study
* Prior administration of an Aurora A kinase-targeted agent, including alisertib; or all of the 3 comparator drugs (pralatrexate, or romidepsin or gemcitabine; or known hypersensitivity)
* History of uncontrolled sleep apnea syndrome or other conditions that could result in excessive daytime sleepiness
* Cardiac condition as specified in study protocol, including left ventricular ejection fraction (LVEF) <40%
* Concomitant use of other medicines as specified in study protocol
* Participants with abnormal gastric or bowel function who require continuous treatment with H2-receptor antagonists or proton pump inhibitors
* Known active infection with human immunodeficiency virus (HIV), hepatitis B virus, or hepatitis C
* Autologous stem cell transplant less than 3 months prior to enrollment
* Participants who have undergone allogeneic stem cell or organ transplantation any time
* Inadequate blood levels, bone marrow or other organ function as specified in study protocol
* The participant must have recovered to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Grade = 1 toxicity, to participant's baseline status (except alopecia), or deemed irreversible from the effects of prior cancer therapy
* Major surgery, serious infection, or infection requiring systemic antibiotic therapy within 14 days prior to the first dose of study treatment
* Female participants who are breastfeeding or pregnant
* Coexistent second malignancy or history of prior solid organ malignancy within previous 3 years
* Serious medical or psychiatric illness or laboratory abnormality that could, in the investigator's opinion, potentially interfere with the completion of treatment according to the protocol

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
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
Parallel
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
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
- Adelaide
Recruitment hospital [2] 0 0
- Concord
Recruitment hospital [3] 0 0
- Gosford
Recruitment hospital [4] 0 0
- Hobart
Recruitment hospital [5] 0 0
- St Leonards
Recruitment postcode(s) [1] 0 0
- Adelaide
Recruitment postcode(s) [2] 0 0
- Concord
Recruitment postcode(s) [3] 0 0
- Gosford
Recruitment postcode(s) [4] 0 0
- Hobart
Recruitment postcode(s) [5] 0 0
- St Leonards
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Alabama
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United States of America
State/province [2] 0 0
California
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United States of America
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Florida
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United States of America
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Indiana
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Iowa
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Massachusetts
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Michigan
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Minnesota
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Missouri
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New Hampshire
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New Jersey
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New York
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North Carolina
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Ohio
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South Carolina
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Texas
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Vermont
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Washington
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United States of America
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West Virginia
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Austria
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Graz
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Austria
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Innsbruck
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Austria
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Salzburg
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Austria
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Wien
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Belarus
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Minsk Didtrict
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Belarus
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Vitebsk
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Belgium
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Brugge
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Belgium
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Brussels
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Belgium
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Gent
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Belgium
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Kortrijk
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Belgium
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Turnhout
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Belgium
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Yvoir
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Brazil
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Belo Horizonte
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Brazil
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Campianas
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Brazil
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Caxias Do Sul
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Curitiba
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Goiania
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Porto Alegre/rs
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Rio de Janeiro
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Brazil
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Salvador
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Brazil
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SAO Paulo - SP
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Brazil
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Sao Paulo
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Bulgaria
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Pleven
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Sofia
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Varna
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Canada
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Ontario
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Concepcion
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Santiago
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Praha 2
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Arhus C
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Kobenhavn O
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Alexandria
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Pessac
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Pierre Benite
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Tours
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Berlin
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Essen
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Freiburg
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Goettingen
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Homburg/saar
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Mainz
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Muenchen
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Munchen
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ULM
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Budapest
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Debrecen
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Kaposvar
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Pecs
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Haifa
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Jerusalem
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Petach Tikva
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Bologna
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Italy
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Firenze
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Italy
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Meldola
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Italy
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Modena
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Italy
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Ravenna
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Italy
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Rimini
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Italy
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Roma
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Italy
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Torino
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Mexico
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Durango Durango
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Mexico
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Mexico
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Mexico
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Monterrey Nuevo LEON
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Mexico
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Monterrey
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Mexico
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San Luis Potosi
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Netherlands
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Maastricht
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Netherlands
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Nieuwegein
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New Zealand
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Auckland
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New Zealand
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Christchurch
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New Zealand
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Takapuna
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Peru
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Arequipa
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Peru
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Lima
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Poland
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Bydgoszcz
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Chorzow
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Lodz
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Warszawa
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Wroclaw
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Portugal
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Braga
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Portugal
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Coimbra
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Portugal
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Porto
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Puerto Rico
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San Juan
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Romania
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Bucuresti
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Russian Federation
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Chelyabinsk
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Russian Federation
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Moscow
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Russian Federation
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Petrozavodsk
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Russian Federation
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St Petersburg
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Slovakia
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Bratislava
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Martin
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Barcelona
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Girona
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Madrid
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Pamplona
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Spain
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Salamanca
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Spain
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Sevilla
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Spain
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Valencia
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Sweden
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Linkoping
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Sweden
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Lund
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Sweden
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Solna
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Turkey
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Ankara
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Turkey
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Denizli
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Turkey
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Istanbul
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Turkey
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Kayseri
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Turkey
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Samsun
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United Kingdom
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Birmingham
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United Kingdom
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Cardiff
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United Kingdom
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Liverpool
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Manchester
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United Kingdom
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Newcastle Upon Tyne
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United Kingdom
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Southampton
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United Kingdom
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Truro

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Millennium Pharmaceuticals, Inc.
Address
Country

Ethics approval
Ethics application status

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

Contacts
Principal investigator
Name 0 0
Medical Monitor
Address 0 0
Takeda Oncology
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.