Trial Review

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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT04442022




Registration number
NCT04442022
Ethics application status
Date submitted
10/06/2020
Date registered
22/06/2020
Date last updated
3/10/2023

Titles & IDs
Public title
A Study of Rituximab-Gemcitabine-Dexamethasone-Platinum (R-GDP) With or Without Selinexor in Patients With Relapsed/Refractory Diffuse Large B-cell Lymphoma
Scientific title
A Phase 2/3, Multicenter Randomized Study of Rituximab-Gemcitabine-Dexamethasone-Platinum (R-GDP) With or Without Selinexor in Patients With Relapsed/Refractory Diffuse Large B-cell Lymphoma (RR DLBCL)
Secondary ID [1] 0 0
2020-000605-84
Secondary ID [2] 0 0
XPORT-DLBCL-030
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
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 - Selinexor (combination therapy)
Treatment: Drugs - Selinexor (combination therapy)
Treatment: Drugs - Selinexor (combination therapy)
Treatment: Drugs - Placebo matching for Selinexor (combination therapy)
Treatment: Drugs - Rituximab (combination therapy)
Treatment: Drugs - Rituximab (combination therapy)
Treatment: Drugs - Gemcitabine (combination therapy)
Treatment: Drugs - Dexamethasone (combination therapy)
Treatment: Drugs - Cisplatin (combination therapy)
Treatment: Drugs - Selinexor (continuous therapy)
Treatment: Drugs - Placebo matching for Selinexor (continuous therapy)

Experimental: Phase 2: Selinexor 40 mg + R-GDP - Patients with RR DLBCL will receive combination therapy of selinexor 40 mg orally at Day 1, and Day 8 of each 21-day cycle for up to 6 cycles in combination with R-GDP followed by single-agent continuous therapy with selinexor 60 mg orally once weekly (QW) for each 28-day cycle until progressive disease (PD) or unacceptable toxicity.

Experimental: Phase 2: Selinexor 60 mg + R-GDP - Patients with RR DLBCL will receive combination therapy of selinexor 60 mg orally at Day 1 and Day 8 of each 21-day cycle for up to 6 cycles in combination with R-GDP followed by single-agent continuous therapy with selinexor 60 mg orally QW for each 28-day cycle until PD or unacceptable toxicity.

Active Comparator: Phase 2: R-GDP - Patients with RR DLBCL will receive R-GDP on specified days (Days 1, 2, 3, 4, and 8) for each 21-day cycle for up to 6 cycles.

Experimental: Phase 3: Selinexor (Selected Dose) + R-GDP followed by Selinexor 60 mg - Patients with RR DLBCL will receive combination therapy of selinexor (selected dose from Phase 2) at Day 1 and Day 8 of each 21-day cycle for up to 6 cycles in combination with R-GDP followed by selinexor 60 mg orally QW for each 28-day cycle until PD or unacceptable toxicity.

Experimental: Phase 3: Selinexor (Selected Dose) + R-GDP followed by Placebo - Patients with RR DLBCL will receive combination therapy of selinexor (selected dose from Phase 2) at Day 1 and Day 8 of each 21-day cycle for up to 6 cycles in combination with R-GDP followed by matching placebo for selinexor orally QW for each 28-day cycle until PD or unacceptable toxicity.

Placebo Comparator: Phase 3: Placebo + R-GDP followed by Placebo - Patients with RR DLBCL will receive combination therapy of placebo matching for selinexor (selected dose from Phase 2) at Day 1 and Day 8 of each 21-day cycle for up to 6 cycles in combination with R-GDP followed by matching placebo for selinexor orally QW for each 28-day cycle until PD or unacceptable toxicity.


Treatment: Drugs: Selinexor (combination therapy)
Dose: 40 mg on Days 1 and 8 of each 21-day cycle for up to 6 cycles; Route of administration: oral

Treatment: Drugs: Selinexor (combination therapy)
Dose: 60 mg on Days 1 and 8 of each 21-day cycle for up to 6 cycles; Route of administration: oral

Treatment: Drugs: Selinexor (combination therapy)
Dose: Selected dose of selinexor (from Phase 2) on Days 1 and 8 of each 21-day cycle for up to 6 cycles; Route of administration: oral

Treatment: Drugs: Placebo matching for Selinexor (combination therapy)
Dose: Placebo matching for selected dose of selinexor (from Phase 2) on Days 1 and 8 of each 21-day cycle for up to 6 cycles; Route of administration: oral

Treatment: Drugs: Rituximab (combination therapy)
Dose: 375 milligram per meter square (mg/m^2) on Day 1; Route of administration: intravenous (IV)

Treatment: Drugs: Rituximab (combination therapy)
Dose: 375 mg/m^2 on Day 1; Route of administration: IV

Treatment: Drugs: Gemcitabine (combination therapy)
Dose: 1000 mg/m^2 on Days 1 and 8; Route of administration: IV

Treatment: Drugs: Dexamethasone (combination therapy)
Dose: 40 mg (20 mg if patient is more than 70 years old) on Days 1, 2, 3, and 4; Route of administration: oral or IV

Treatment: Drugs: Cisplatin (combination therapy)
Dose: 75 mg/m^2 on Day 1; Route of administration: IV

Treatment: Drugs: Selinexor (continuous therapy)
Dose: 60 mg QW for each 28-day cycle until PD; Route of administration: oral

Treatment: Drugs: Placebo matching for Selinexor (continuous therapy)
Dose: Placebo matching for 60 mg selinexor QW for each 28-day cycle until PD; Route of administration: oral
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Phase 2: Overall Response Rate (ORR): Based on Lugano Criteria 2014
Timepoint [1] 0 0
From date of initial randomization to the date of disease progression or initiating a new DLBCL treatment (maximum of 5 years from randomization)
Primary outcome [2] 0 0
Phase 3: Progression-free Survival (PFS): Based on Lugano Criteria 2014
Timepoint [2] 0 0
From date of initial randomization to the date of disease progression or death (maximum of 5 years from randomization)
Secondary outcome [1] 0 0
Phase 2: Progression-free Survival: Based on Lugano Criteria 2014
Timepoint [1] 0 0
From date of initial randomization to the date of disease progression or death (maximum of 5 years from randomization)
Secondary outcome [2] 0 0
Phase 2: Overall Survival (OS)
Timepoint [2] 0 0
From date of initial randomization until death (maximum of 5 years from randomization)
Secondary outcome [3] 0 0
Phase 3: Overall Response Rate: Based on Lugano Criteria 2014
Timepoint [3] 0 0
From date of initial randomization to the date of disease progression or initiating a new DLBCL treatment (maximum of 5 years from randomization)
Secondary outcome [4] 0 0
Phase 3: Overall Survival
Timepoint [4] 0 0
From date of initial randomization until death (maximum of 5 years from randomization)
Secondary outcome [5] 0 0
Phase 2: Overall Response Rate at the End of Combination Therapy (ORR-EoC): Based on Lugano Criteria 2014
Timepoint [5] 0 0
From C1D1 (Cycles 1 up to 6; 21 days per cycle) up to 28 days after EoC therapy
Secondary outcome [6] 0 0
Phase 2: Overall Response Rate at the End of Combination Therapy: Based on Modified Lugano Criteria
Timepoint [6] 0 0
From C1D1 (Cycles 1 up to 6; 21 days per cycle) up to 28 days after EoC therapy
Secondary outcome [7] 0 0
Phase 2: Duration of Response (DOR): Based on Lugano Criteria 2014
Timepoint [7] 0 0
From time of first response until disease progression or death (maximum of 5 years from randomization)
Secondary outcome [8] 0 0
Phase 2: Number of Patients with Adverse Events (AEs)
Timepoint [8] 0 0
Up to 30 days after last dose of study drug (maximum of 5 years from randomization)
Secondary outcome [9] 0 0
Phase 3: Overall Response Rate at the End of Combination Therapy: Based on Lugano Criteria 2014
Timepoint [9] 0 0
From C1D1 (Cycles 1 up to 6; 21 days per cycle) up to 28 days after EoC therapy
Secondary outcome [10] 0 0
Phase 3: Overall Response Rate at the End of Combination Therapy: Based on Modified Lugano Criteria
Timepoint [10] 0 0
From C1D1 (Cycles 1 up to 6; 21 days per cycle) up to 28 days after EoC therapy
Secondary outcome [11] 0 0
Phase 3: Duration of Response: Based on Lugano Criteria 2014
Timepoint [11] 0 0
From time of first response until disease progression or death (maximum of 5 years from randomization)
Secondary outcome [12] 0 0
Phase 3: Progression-free Survival: Based on Modified Lugano Criteria
Timepoint [12] 0 0
From date of initial randomization to the date of disease progression or death (maximum of 5 years from randomization)
Secondary outcome [13] 0 0
Phase 3: Number of Patients with Adverse Events
Timepoint [13] 0 0
Up to 30 days after last dose of study drug (maximum of 5 years from randomization)

Eligibility
Key inclusion criteria
- Have pathologically confirmed de novo DLBCL or DLBCL transformed from previously
diagnosed indolent lymphoma (e.g., follicular lymphoma). Patient with high-grade
lymphoma with c-MYC, Bcl2 and/or Bcl6 rearrangements are eligible (only for Phase 2).
(Documentation to be provided).

- Have received at least 1 but no more than 3 prior lines of systemic therapy for the
treatment of DLBCL with relapsed or refractory disease following their most recent
regimen.

- Salvage chemoimmunotherapy followed by stem cell transplantation will be
considered as 1 line of systemic therapy.

- Maintenance therapy will not be counted as a separate line of systemic therapy.

- Radiation with curative intent for localized DLBCL will not be counted as 1 line
of systemic therapy.

- Positron emission tomography (PET) positive measurable disease with at least 1 node
having the longest diameter (LDi) greater than (>) 1.5 centimeter (cm) or 1 extranodal
lesion with LDi >1 cm (per the Lugano Criteria 2014). The Deauville 5-point scale
(D5PS) score assessed on the FDG PET/CT should be between 3 to 5.

- Not intended for HSCT or CAR-T cell therapy based on objective clinical criteria
determined by the treating physician. Patients who cannot receive HSCT due to active
disease are allowed on study (up to approximately 15 percent [%] of patients enrolled
in each Phase). Documentation on lack of intention to proceed to receive HSCT or CAR-T
therapy must be provided by the treating physician.

- Adequate bone marrow function at screening, defined as:

- Absolute neutrophil count (ANC) =1*10^9 per liter (/L).

- Platelet count =100*10^9/L (without platelet transfusion less than [<] 14 days
prior to Cycle 1 Day 1 [C1D1]).

- Hemoglobin =8.5 gram per deciliter (g/dL) (without red blood cell transfusion <14
days prior to C1D1).

- Circulating lymphocytes less than or equal to (=) 50*10^9/L.

- Adequate liver and kidney function, defined as:

- Aspartate transaminase (AST) or alanine transaminase (ALT) =2.5*upper limit of
normal (ULN), or =5*ULN in cases with known lymphoma involvement in the liver.

- Serum total bilirubin =2*ULN, or =5*ULN if due to Gilbert syndrome or in cases
with known lymphoma involvement in the liver.

- Calculated creatinine clearance (CrCl) =30 milliliter per minute (mL/min) based
on Cockcroft-Gault formula.

- Eastern Cooperative Oncology Group (ECOG) performance status of =2.

- An estimated life expectancy of >3 months at Screening.

- Patients with primary refractory DLBCL defined as no response or relapse within 6
months after ending first-line treatment, will be allowed in the study.

- Agree to highly effective contraception during the duration of the study with
contraception use continuing for 12 months after the last dose of study treatment

- Female patients of childbearing potential must have a negative serum pregnancy test at
Screening and agree to use highly effective methods of contraception throughout the
study and for 12 months following the last dose of study treatment (except patients
with Non-Childbearing potential: Age >50 years and naturally amenorrhoeic for >1 year,
or previous bilateral salpingo-oophorectomy, or hysterectomy).

- Male patients who are sexually active must use highly effective methods of
contraception throughout the study and for 12 months following the last dose of study
treatment. Male patients must agree not to donate sperm during the study treatment
period and for 12 months following the last dose of study treatment.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- DLBCL with mucosa-associated lymphoid tissue (MALT) lymphoma, composite lymphoma
(Hodgkin's lymphoma + non-Hodgkin's lymphoma [NHL]), DLBCL transformed from diseases
other than indolent NHL; primary mediastinal (thymic) large B-cell lymphoma (PMBL);
T-cell rich large B-cell lymphoma.

- Previous treatment with selinexor or other XPO1 inhibitors.

- Contraindication to any drug contained in the combination therapy regimen (SR-GDP).

- Known active central nervous system or meningeal involvement by DLBCL at time of
Screening.

- Use of any standard or experimental anti-DLBCL therapy (including nonpalliative
radiation, chemotherapy, immunotherapy, radio-immunotherapy, or any other anticancer
therapy) <21 days prior to C1D1 (prednisone <30 mg or equivalent is permitted;
palliative radiation is permitted only if on non-target lesions).

- Any AE, by C1D1, which has not recovered to Grade =1 (Common Terminology Criteria for
Adverse Events [CTCAE], v.5.0), or returned to baseline, related to the previous DLBCL
therapy, except hematological abnormalities (as specified in the inclusion criteria)
and alopecia.

- Major surgery <14 days of Cycle 1 Day 1.

- Hematopoietic stem cell transplantation/CAR-T therapy as follows:

- Autologous stem cell transplant (SCT) <100 days or allogeneic-SCT <180 days prior
to C1D1

- Active graft-versus-host disease (GVHD) after allogeneic SCT (or cannot
discontinue GVHD treatment or prophylaxis)

- CAR-T cell infusion <90 days prior to Cycle 1

- Neuropathy Grade =2 (CTCAE, v.5.0).

- Any life-threatening illness, medical condition, or organ system dysfunction which, in
the Investigator's opinion, could compromise the patient's safety, or being compliant
with the study procedures.

- Uncontrolled (i.e., clinically unstable) infection requiring parenteral antibiotics,
antivirals, or antifungals within 7 days prior to first dose of study treatment;
however, prophylactic use of these agents is acceptable (including parenteral).

- Patient with active hepatitis B virus (HBV), hepatitis C virus (HCV), or human
immunodeficiency virus (HIV) infections:

- Patient with active HBV are allowed if antiviral therapy for hepatitis B has been
given for >8 weeks and viral load is <100 International units (IU)/mL prior to
first dose of study treatment.

- Patients with known history of HCV or found to be HCV antibody positive on
screening, are allowed if there is documentation of negative viral load per
institutional standard.

- Patients with HIV are allowed if they have a negative viral load per
institutional standard, and no history of acquired immune deficiency syndrome
(AIDS)-defining opportunistic infections in the last year.

- Inability to swallow tablets, malabsorption syndrome, or any other gastrointestinal
(GI) disease or dysfunction that could interfere with absorption of study treatment.

- Breastfeeding or pregnant women.

- Inability or unwillingness to sign an informed consent form (ICF).

- In the opinion of the Investigator, patient who are significantly below their ideal
body weight.

- Patients who received a live attenuated vaccine within prior 28 days of the first dose
of study treatment.

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
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Other
Other design features
Phase
Phase 2/Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
3/09/2020
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/12/2025
Actual
Sample size
Target
501
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Arizona
Country [2] 0 0
United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
Indiana
Country [4] 0 0
United States of America
State/province [4] 0 0
Kentucky
Country [5] 0 0
United States of America
State/province [5] 0 0
Louisiana
Country [6] 0 0
United States of America
State/province [6] 0 0
Maryland
Country [7] 0 0
United States of America
State/province [7] 0 0
Nevada
Country [8] 0 0
United States of America
State/province [8] 0 0
New Mexico
Country [9] 0 0
United States of America
State/province [9] 0 0
New York
Country [10] 0 0
United States of America
State/province [10] 0 0
Ohio
Country [11] 0 0
United States of America
State/province [11] 0 0
Texas
Country [12] 0 0
United States of America
State/province [12] 0 0
Washington
Country [13] 0 0
Austria
State/province [13] 0 0
Linz
Country [14] 0 0
Austria
State/province [14] 0 0
Vienna
Country [15] 0 0
China
State/province [15] 0 0
Jiangsu
Country [16] 0 0
China
State/province [16] 0 0
Shanghai
Country [17] 0 0
China
State/province [17] 0 0
Sichuan
Country [18] 0 0
China
State/province [18] 0 0
Zhejiang
Country [19] 0 0
Israel
State/province [19] 0 0
Ashdod
Country [20] 0 0
Israel
State/province [20] 0 0
Beer Sheva
Country [21] 0 0
Israel
State/province [21] 0 0
Haifa
Country [22] 0 0
Israel
State/province [22] 0 0
Holon
Country [23] 0 0
Israel
State/province [23] 0 0
Jerusalem
Country [24] 0 0
Israel
State/province [24] 0 0
Petach Tikva
Country [25] 0 0
Israel
State/province [25] 0 0
Tel aviv
Country [26] 0 0
Israel
State/province [26] 0 0
Tel Aviv
Country [27] 0 0
Italy
State/province [27] 0 0
Napoli
Country [28] 0 0
Italy
State/province [28] 0 0
Sicilia
Country [29] 0 0
Italy
State/province [29] 0 0
Torino
Country [30] 0 0
Italy
State/province [30] 0 0
Ancona
Country [31] 0 0
Italy
State/province [31] 0 0
Bologna
Country [32] 0 0
Italy
State/province [32] 0 0
Caserta
Country [33] 0 0
Italy
State/province [33] 0 0
Novara
Country [34] 0 0
Italy
State/province [34] 0 0
Pescara
Country [35] 0 0
Italy
State/province [35] 0 0
Rome
Country [36] 0 0
Poland
State/province [36] 0 0
Lesser
Country [37] 0 0
Poland
State/province [37] 0 0
Pomerania
Country [38] 0 0
Poland
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Radeckiego
Country [39] 0 0
Poland
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Wielkopolska
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Poland
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Warsaw
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Poland
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Warszawa
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Poland
State/province [42] 0 0
Slaskie
Country [43] 0 0
Spain
State/province [43] 0 0
Barcelona
Country [44] 0 0
Spain
State/province [44] 0 0
Madrid
Country [45] 0 0
Spain
State/province [45] 0 0
Seville

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Karyopharm Therapeutics 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
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Karyopharm Medical Information
Address 0 0
Country 0 0
Phone 0 0
(888) 209-9326
Fax 0 0
Email 0 0
[email protected]
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 not provided in https://clinicaltrials.gov/ct2/show/NCT04442022