NCT02807454 · REGISTRY CONDITION SEARCH

A Study to Determine the Safety and Efficacy for the Combination of Durvalumab and Daratumumab in Relapsed and Refractory Multiple Myeloma

Found through the registry condition index, not selected as a treatment recommendation. This discovery collection was restricted to studies with posted results.

Phase: PHASE2
Status at capture: TERMINATED
Registry last update: 2023-02-21

This is an open-label, multicenter study to confirm the safety and efficacy of durvalumab + daratumumab (D2) in subjects with relapsed and refractory multiple myeloma. This study will also explore the safety and efficacy of the addition of pomalidomide + dexamethasone to durvalumab + daratumumab (PD3). On 05 Sep 2017, a Partial Clinical Hold was placed on this study by the United States (US) Food and Drug Administration (FDA). The decision by the FDA was based on data related to risks of anti-programmed cell death-1 (PD-1) antibody, pembrolizumab, in combination with IMiDs® immunomodulatory drugs in patients with multiple myeloma. As a result, enrollment into this study has been discontinued. Subjects who are receiving clinical benefit, based on the discretion of the investigator, may remain on study treatment after being reconsented.

Open the original ClinicalTrials.gov record → · Download preserved record

What did the study report?

Outcomes, safety and baseline populations are separate source sections. Quality-of-life measures appear under their original outcome titles.

flow

Participant flow

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baseline

Baseline characteristics

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outcome · POSTED

Overall Response Rate (ORR)

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outcome · POSTED

Number of Participants With Adverse Events (AEs)

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outcome · POSTED

Number of Participants With Serious Adverse Events (SAEs)

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outcome · POSTED

Time-To-Response (TTR)

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outcome · POSTED

Kaplan-Meier Estimate of Duration of Response (DOR) - Simon Stage 1: D2 Arm

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outcome · POSTED

Kaplan-Meier Estimate of Duration of Response (DOR) - PD3 Arm

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outcome · POSTED

Kaplan-Meier Estimate of Progression-Free Survival (PFS) - Simon Stage 1: D2 Arm

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outcome · POSTED

Kaplan-Meier Estimate of Progression-Free Survival (PFS) - PD3 Arm

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outcome · POSTED

Maximum Observed Plasma Concentration (Cmax) - Simon Stage 1: D2 Arm

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outcome · POSTED

Time of Maximum Observed Concentration (Tmax) - Simon Stage 1: D2 Arm

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outcome · POSTED

Area Under the Plasma Concentration-Time Curve to the Last Measurable Plasma Concentration [AUC(0-Last)] - Simon Stage 1: D2 Arm

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outcome · POSTED

Area Under the Plasma Concentration-Time Curve in 1 Dosing Interval [AUC(TAU)] - Simon Stage 1: D2 Arm

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adverse events

Adverse events

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more info

Limitations, agreements, and source contact

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Who could take part

eligibility Criteria: Inclusion Criteria: * Must have measurable disease as defined by m-protein or serum free light chain. * Must have failed last line of treatment (refractory to last line of treatment). * Must have achieved at least a minimal response (MR) to at least 1 prior anti-myeloma regimen before developing PD (relapsed) * Has performance status of 0, 1, or 2 on the Eastern Cooperative Oncology Group (ECOG) Performance Scale * Must be at least 18 years of age Exclusion Criteria: * Has non-secretory multiple myeloma * Has had prior anti-myeloma therapy within 2 weeks prior to study Day 1 * Has received prior therapy with an anti-programmed cell death 1 receptor (anti-PD-1), antiprogrammed death-ligand 1 (anti-PD-L1), anti-PD-L2, anti-CD137, or anti-cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) antibody (including ipilimumab or any other antibody or drug specifically targeting T-cell costimulation or checkpoint pathways). * Has received prior treatment with daratumumab or other anti-CD38 therapies previously * Has undergone prior organ or allogeneic hematopoetic stem cell transplantation * Has received autologous stem cell transplantation (ASCT) within 12 weeks before the date of randomization. * Has received prior treatment with a monoclonal antibody within 5 half-lives of Study Day 1 * Has received investigational agents within 28 days or 5 half-lives (whichever is longer) of Study Day 1 * Has received live, attenuated vaccine within 30 days prior to Study Day 1 * Has chronic obstructive pulmonary disease (COPD) with a forced expiratory volume in 1 second (FEV1) 50% of predicted normal * Has moderate or severe persistent asthma within the past 2 years or uncontrolled asthma of any classification. * Is positive for human immunodeficiency virus (HIV), chronic or active hepatitis B or active hepatitis A or C * Has a prior history of malignancies, other than MM, unless the subject has been free of the disease for ≥ 5 years (with the exception Basal cell carcinoma of the skin, Squamous cell carcinoma of the skin, Carcinoma in situ of the cervix, Carcinoma in situ of the breast, Incidental histologic finding of prostate cancer \[T1a or T1b\] or prostate cancer that is curative) * Has clinical evidence of central nervous system (CNS) or pulmonary leukostasis, disseminated intravascular coagulation, or CNS multiple myeloma * Has clinically significant cardiac disease * Is a female who is pregnant, nursing, or breastfeeding, or who intends to become pregnant during the participation in the study
healthy Volunteers: false
minimum Age: 18 Years
sex: ALL
std Ages: ADULT
OLDER_ADULT

Treatment arms and interventions

arm Groups

description
* Intravenous (IV) durvalumab at 1500mg on Day 1 or 2 of a 28-day cycle * IV daratumumab at 16mg/kg on days 1, 8, 15 and 22 at cycles 1-2; on days 1 and 15 at cycles 3-6; and on day 1 from cycle 7 onward
intervention Names
Drug: Daratumumab
Drug: Durvalumab
label
Daratumumab Plus Durvalumab Treatment
type
EXPERIMENTAL
description
* Intravenous (IV) durvalumab at 1500mg on Day 1 or 2 of a 28-day cycle * IV daratumumab at 16mg/kg on days 1, 8, 15 and 22 at cycles 1-2; on days 1 and 15 at cycles 3-6; and on day 1 from cycle 7 onward * oral POM at 4mg/day on days 1 to 21 * oral/IV dex at 40mg/day (\>75 years old) or 20mg/day (\>75 years old) on days 1, 8, 15 and 22
intervention Names
Drug: Daratumumab
Drug: Durvalumab
Drug: Pomalidomide
Drug: Dexamethasone
label
Pomalidomide+ Daratumumab+ Durvalumab+ Dexamethasone Treatment
type
EXPERIMENTAL

interventions

arm Group Labels
Daratumumab Plus Durvalumab Treatment
Pomalidomide+ Daratumumab+ Durvalumab+ Dexamethasone Treatment
name
Daratumumab
type
DRUG
arm Group Labels
Daratumumab Plus Durvalumab Treatment
Pomalidomide+ Daratumumab+ Durvalumab+ Dexamethasone Treatment
name
Durvalumab
type
DRUG
arm Group Labels
Pomalidomide+ Daratumumab+ Durvalumab+ Dexamethasone Treatment
name
Pomalidomide
type
DRUG
arm Group Labels
Pomalidomide+ Daratumumab+ Durvalumab+ Dexamethasone Treatment
name
Dexamethasone
type
DRUG

Study design

allocation

RANDOMIZED

intervention Model

PARALLEL

masking Info

masking: NONE

primary Purpose

TREATMENT

Enrollment

count: 37
type: ACTUAL

Registered outcome plans (not posted results)

primary Outcomes

description
Tumor response of partial response (PR) or better was assessed using the International Myeloma Working Group (IMWG) Uniform Response Criteria. ORR was calculated as the percent of responders (multiplied by 100). Partial response required ≥ 50% reduction of serum M-Protein and reduction in 24-hour urinary M protein by ≥ 90% or to \< 200 mg per 24 hours.
measure
Overall Response Rate (ORR)
time Frame
From first dose to up to approximately 66 months
description
Number of participants who experienced at least one adverse event. An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a participant during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values, regardless of etiology. Any worsening (i.e., any clinically significant adverse change in the frequency or intensity of a preexisting condition should be considered an AE.
measure
Number of Participants With Adverse Events (AEs)
time Frame
From first dose to 90 days after last dose (up to approximately 58 months)
description
Number of participants who experienced at least one serious adverse event. An SAE is any AE occurring at any dose that results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, constitutes an important medical event.
measure
Number of Participants With Serious Adverse Events (SAEs)
time Frame
From first dose to 90 days after last dose (up to approximately 58 months)

secondary Outcomes

description
Time-to-response is calculated as the time from enrollment to the first date of documented response (partial response or better). Tumor response of partial response (PR) or better was assessed using the International Myeloma Working Group (IMWG) Uniform Response Criteria. Partial response required ≥ 50% reduction of serum M-Protein and reduction in 24-hour urinary M protein by ≥ 90% or to \< 200 mg per 24 hours. For those participants where POM + DEX were added, time-to-response was calculated from the date POM and DEX were added to the first date of documented response (PR or better).
measure
Time-To-Response (TTR)
time Frame
From enrollment to earliest documented response (up to approximately 66 months)
description
Duration of response was calculated as the time from the earliest date of documented response (PR or better) to the earliest date of disease progression as determined by the investigator. For those participants where POM + DEX was added, duration of response was calculated as the time from the earliest date of documented response after POM + DEX was added (PR or better) to the earliest date of disease. Tumor response of partial response (PR) or better was assessed using the International Myeloma Working Group (IMWG) Uniform Response Criteria. Partial response required ≥ 50% reduction of serum M-Protein and reduction in 24-hour urinary M protein by ≥ 90% or to \< 200 mg per 24 hours. Progressive Disease required increase of 25% from lowest response value in the serum M-component (absolute increase must be ≥ 0.5 g/dL) and/or urine M-component (absolute increase must be ≥ 200 mg/24 h).
measure
Kaplan-Meier Estimate of Duration of Response (DOR) - Simon Stage 1: D2 Arm
time Frame
From the earliest date of documented response (PR or better) to earliest date of progressive disease (up to approximately 66 months)
description
Duration of response was calculated as the time from the earliest date of documented response (PR or better) to the earliest date of disease progression as determined by the investigator. For those participants where POM + DEX was added, duration of response was calculated as the time from the earliest date of documented response after POM + DEX was added (PR or better) to the earliest date of disease progression as determined by the investigator. Participants who are alive or lost to follow-up will be censored on the last-known-to-be-alive date. Tumor response of partial response (PR) or better was assessed using the International Myeloma Working Group (IMWG) Uniform Response Criteria. Partial response required ≥ 50% reduction of serum M-Protein and reduction in 24-hour urinary M protein by ≥ 90% or to \< 200 mg per 24 hours.
measure
Kaplan-Meier Estimate of Duration of Response (DOR) - PD3 Arm
time Frame
From the earliest date of documented response (PR or better) to earliest date of progressive disease (up to approximately 66 months)
description
Progression-free survival was calculated as the time between the enrollment to the first documentation of progressive disease or death from any cause during study, whichever occurs earlier using the International Myeloma Working Group (IMWG) Uniform Response Criteria. Progressive Disease required increase of 25% from lowest response value in the serum M-component (absolute increase must be ≥ 0.5 g/dL) and/or urine M-component (absolute increase must be ≥ 200 mg/24 h).
measure
Kaplan-Meier Estimate of Progression-Free Survival (PFS) - Simon Stage 1: D2 Arm
time Frame
From enrollment to first documentation of progressive disease or death from any cause during study, whichever occurs earlier (up to approximately 66 months)
description
Progression-free survival was calculated as the time between the enrollment to the first documentation of progressive disease or death from any cause during study, whichever occurs earlier using the International Myeloma Working Group (IMWG) Uniform Response Criteria. Progressive Disease required increase of 25% from lowest response value in the serum M-component (absolute increase must be ≥ 0.5 g/dL) and/or urine M-component (absolute increase must be ≥ 200 mg/24 h).
measure
Kaplan-Meier Estimate of Progression-Free Survival (PFS) - PD3 Arm
time Frame
From enrollment to first documentation of progressive disease or death from any cause during study, whichever occurs earlier (up to approximately 66 months)
description
Pharmacokinetics of Durvalumab derived from serum concentration versus time data.
measure
Maximum Observed Plasma Concentration (Cmax) - Simon Stage 1: D2 Arm
time Frame
Cycle 1 - Days 2, 8, 15, 22
description
Pharmacokinetics of Durvalumab derived from serum concentration versus time data.
measure
Time of Maximum Observed Concentration (Tmax) - Simon Stage 1: D2 Arm
time Frame
Cycle 1 - Days 2, 8, 15, 22
description
Pharmacokinetics of Durvalumab derived from serum concentration versus time data.
measure
Area Under the Plasma Concentration-Time Curve to the Last Measurable Plasma Concentration [AUC(0-Last)] - Simon Stage 1: D2 Arm
time Frame
Cycle 1 - Days 2, 8, 15, 22
description
Pharmacokinetics of Durvalumab derived from serum concentration versus time data.
measure
Area Under the Plasma Concentration-Time Curve in 1 Dosing Interval [AUC(TAU)] - Simon Stage 1: D2 Arm
time Frame
Cycle 1 - Days 2, 8, 15, 22

Full study description

brief Summary: This is an open-label, multicenter study to confirm the safety and efficacy of durvalumab + daratumumab (D2) in subjects with relapsed and refractory multiple myeloma. This study will also explore the safety and efficacy of the addition of pomalidomide + dexamethasone to durvalumab + daratumumab (PD3). On 05 Sep 2017, a Partial Clinical Hold was placed on this study by the United States (US) Food and Drug Administration (FDA). The decision by the FDA was based on data related to risks of anti-programmed cell death-1 (PD-1) antibody, pembrolizumab, in combination with IMiDs® immunomodulatory drugs in patients with multiple myeloma. As a result, enrollment into this study has been discontinued. Subjects who are receiving clinical benefit, based on the discretion of the investigator, may remain on study treatment after being reconsented.

Source references