A Study of Daratumumab, Carfilzomib, Lenalidomide, and Dexamethasone in Patients With Newly-Diagnosed Multiple Myeloma

NCT ID: NCT04268498

Last Updated: 2025-05-29

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 310 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-02-11
• Study Completion Date: 2027-02-01

Brief Summary

This study is being done to find out whether carfilzomib, lenalidomide, and dexamethasone (KRD) or KRD and Daratumumab (KRD+DARA) might be safer and more effective ways of controlling multiple myeloma than the standard of care treatment, which is lenalidomide, bortezomib, and dexamethasone (VRD).

Detailed Description

Per protocol amendment version 4.0 (May 23, 2022), Arm A will be closed and no additional participants will be enrolled in this arm.

Conditions

Multiple Myeloma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm A - Bortezomib, Lenalidomide and Dexamethasone (VRD)

Participants in this group will receive Bortezomib, Lenalidomide and Dexamethasone on a 21 day treatment cycle. Participants achieving a PR or better at the end of 4 cycles will continue to receive a total of 8 cycles of combination therapy. Participants with less than PR after completing 4 cycles will go off study therapy. After 8 cycles of therapy, participants who are MRD positive will have the option to receive an ASCT if stem cells were able to be extracted, before initiating maintenance therapy with Lenalidomide for up to 2 years, and patients who are MRD negative will go directly on to receive maintenance therapy with Lenalidomide for up to 2 years.

Group Type: EXPERIMENTAL

Bortezomib

Intervention Type: DRUG

1.3 mg/m2 administered Subcutaneous (SC) or intravenous (IV) on days 1, 4, 8 and 11 of a 21 day treatment cycle for participants randomized to Arm A.

Dexamethasone

Intervention Type: DRUG

20 mg or 40 mg per dose administered by mouth (PO) or IV.

Participants randomized in Arm A:

20 mg/dose on days 1, 4, 8 and 11 on a 21 day treatment cycle;

Participants randomized in Arm B:

Cycles 1 through 8 - 40mg/dose on days 1, 8 and 15 on a 28-day cycle

Participants randomized in Arm C:

Cycle 1-2 - 40 mg/dose on days 1, 8, 15 and 22 on a 28-day cycle; Cycles 3-8 - 40mg/dose on Days 1, 8, 15 on a 28-day cycle;

Lenalidomide

Intervention Type: DRUG

10 or 25 mg/day capsules administered PO.

Participants randomized in Arm A:

25 mg/day capsules on Days 1 through 14 of a 21 day cycle.;

Participants randomized in Arm B:

Cycles 1 through 8 - 25 mg/day capsules on Days 1 through 21 of a 28 day cycle;

Participants randomized in Arm C:

Cycles 1 - 25 mg/day capsules on Days 2 through 21 of a 28 day cycle; Cycles 2 through 8 - 25 mg/day capsules on Days 1 through 21 of a 28 day cycle;

Maintenance Therapy:

10 mg capsules on Days 1 through 21 on a 28 days cycle.

Autologous Stem Cell Transplant (ASCT)

Intervention Type: BIOLOGICAL

Participants who are MRD positive at the conclusion of 8 cycles of study treatment, and were able to have their stem cells that were extracted, will receive ASCT from participants' bone marrow samples.

Arm B - Carfilzomib, Lenalidomide and Dexamethasone (KRD)

Participants in this group will receive Carfilzomib, Lenalidomide and Dexamethasone on a 28 day cycle. Participants achieving a PR or better at the end of 4 cycles will continue to receive a total of 8 cycles of combination therapy. Participants with less than PR after completing 4 cycles will go off study therapy. After 8 cycles of therapy, participants who are MRD positive will have the option to receive an ASCT if stem cells were able to be extracted, before initiating maintenance therapy with Lenalidomide for up to 2 years, and patients who are MRD negative will go directly on to receive maintenance therapy with Lenalidomide for up to 2 years.

Group Type: EXPERIMENTAL

Dexamethasone

Intervention Type: DRUG

20 mg or 40 mg per dose administered by mouth (PO) or IV.

Participants randomized in Arm A:

20 mg/dose on days 1, 4, 8 and 11 on a 21 day treatment cycle;

Participants randomized in Arm B:

Cycles 1 through 8 - 40mg/dose on days 1, 8 and 15 on a 28-day cycle

Participants randomized in Arm C:

Cycle 1-2 - 40 mg/dose on days 1, 8, 15 and 22 on a 28-day cycle; Cycles 3-8 - 40mg/dose on Days 1, 8, 15 on a 28-day cycle;

Lenalidomide

Intervention Type: DRUG

10 or 25 mg/day capsules administered PO.

Participants randomized in Arm A:

25 mg/day capsules on Days 1 through 14 of a 21 day cycle.;

Participants randomized in Arm B:

Cycles 1 through 8 - 25 mg/day capsules on Days 1 through 21 of a 28 day cycle;

Participants randomized in Arm C:

Cycles 1 - 25 mg/day capsules on Days 2 through 21 of a 28 day cycle; Cycles 2 through 8 - 25 mg/day capsules on Days 1 through 21 of a 28 day cycle;

Maintenance Therapy:

10 mg capsules on Days 1 through 21 on a 28 days cycle.

Carfilzomib

Intervention Type: DRUG

20 mg or 56 mg/m2 per dose administered via IV.

Participants randomized to Arm B:

Cycle 1 - 20 mg/m2 per dose on Day 1 and 56 mg/m2 per dose on days 8 and 15 of a 28 day cycle; Cycles 2 through 8 - 56 mg/m2 per dose on days 1, 8 and 15 of a 28 day cycle;

Participants randomized to Arm C:

Cycle 1 - 20 mg/m2 per dose on Day 2 and 56 mg/m2 per dose on days 8 and 15 of a 28 day cycle; Cycles 2 through 8 - 56 mg/m2 per dose on days 1, 8 and 15 of a 28 day cycle

Autologous Stem Cell Transplant (ASCT)

Intervention Type: BIOLOGICAL

Participants who are MRD positive at the conclusion of 8 cycles of study treatment, and were able to have their stem cells that were extracted, will receive ASCT from participants' bone marrow samples.

Arm C- Carfilzomib, Lenalidomide and Dexamethasone with Daratumumab (DKrd)

Participants in this group will receive Carfilzomib, Lenalidomide, Dexamethasone with Daratumumab, Acetaminophen, Diphenhydramine and Montelukast on a 28 day cycle. Participants achieving a PR or better at the end of 4 cycles will continue to receive a total of 8 cycles of combination therapy. Participants with less than PR after completing 4 cycles will go off study therapy. After 8 cycles of therapy, participants who are MRD positive will have the option to receive an ASCT if stem cells were able to be extracted, before initiating maintenance therapy with Lenalidomide for up to 2 years, and patients who are MRD negative will go directly on to receive maintenance therapy with Lenalidomide for up to 2 years.

Group Type: EXPERIMENTAL

Dexamethasone

Intervention Type: DRUG

20 mg or 40 mg per dose administered by mouth (PO) or IV.

Participants randomized in Arm A:

20 mg/dose on days 1, 4, 8 and 11 on a 21 day treatment cycle;

Participants randomized in Arm B:

Cycles 1 through 8 - 40mg/dose on days 1, 8 and 15 on a 28-day cycle

Participants randomized in Arm C:

Cycle 1-2 - 40 mg/dose on days 1, 8, 15 and 22 on a 28-day cycle; Cycles 3-8 - 40mg/dose on Days 1, 8, 15 on a 28-day cycle;

Lenalidomide

Intervention Type: DRUG

10 or 25 mg/day capsules administered PO.

Participants randomized in Arm A:

25 mg/day capsules on Days 1 through 14 of a 21 day cycle.;

Participants randomized in Arm B:

Cycles 1 through 8 - 25 mg/day capsules on Days 1 through 21 of a 28 day cycle;

Participants randomized in Arm C:

Cycles 1 - 25 mg/day capsules on Days 2 through 21 of a 28 day cycle; Cycles 2 through 8 - 25 mg/day capsules on Days 1 through 21 of a 28 day cycle;

Maintenance Therapy:

10 mg capsules on Days 1 through 21 on a 28 days cycle.

Acetaminophen

Intervention Type: DRUG

650 mg administered PO.

Participants randomized to Arm C:

Cycles 1 through 8 - 650 mg administered on Days 1, 8 and 15.

Diphenhydramine

Intervention Type: DRUG

25 mg administered via IV

Participants randomized to Arm C:

Cycles 1 through 8 - 25 mg administered on Days 1, 8 and 15.

Montelukast

Intervention Type: DRUG

10 mg administered PO to participants randomized to Arm C prior to the first 4 doses of Daratumumab.

Carfilzomib

Intervention Type: DRUG

20 mg or 56 mg/m2 per dose administered via IV.

Participants randomized to Arm B:

Cycle 1 - 20 mg/m2 per dose on Day 1 and 56 mg/m2 per dose on days 8 and 15 of a 28 day cycle; Cycles 2 through 8 - 56 mg/m2 per dose on days 1, 8 and 15 of a 28 day cycle;

Participants randomized to Arm C:

Cycle 1 - 20 mg/m2 per dose on Day 2 and 56 mg/m2 per dose on days 8 and 15 of a 28 day cycle; Cycles 2 through 8 - 56 mg/m2 per dose on days 1, 8 and 15 of a 28 day cycle

Daratumumab

Intervention Type: DRUG

16 mg/kg administered via IV or 1800 mg SC, per treating physician discretion.

Participants randomized to Arm C:

Cycles 1 though 2 - 16 mg/kg IV or 1800 mg SC on days 1, 8, 15, and 22 of a 28 day cycle; Cycles 3 through 6- 16 mg/kg IV or 1800 mg SC on days 1 and 15 of a 28 day cycle; Cycles 7 through 8 - 16 mg/kg IV or 1800 mg SC on day 1 of a 28 day cycle

Autologous Stem Cell Transplant (ASCT)

Intervention Type: BIOLOGICAL

Participants who are MRD positive at the conclusion of 8 cycles of study treatment, and were able to have their stem cells that were extracted, will receive ASCT from participants' bone marrow samples.

Interventions

Bortezomib

1.3 mg/m2 administered Subcutaneous (SC) or intravenous (IV) on days 1, 4, 8 and 11 of a 21 day treatment cycle for participants randomized to Arm A.

Intervention Type: DRUG

Dexamethasone

20 mg or 40 mg per dose administered by mouth (PO) or IV.

Participants randomized in Arm A:

20 mg/dose on days 1, 4, 8 and 11 on a 21 day treatment cycle;

Participants randomized in Arm B:

Cycles 1 through 8 - 40mg/dose on days 1, 8 and 15 on a 28-day cycle

Participants randomized in Arm C:

Cycle 1-2 - 40 mg/dose on days 1, 8, 15 and 22 on a 28-day cycle; Cycles 3-8 - 40mg/dose on Days 1, 8, 15 on a 28-day cycle;

Intervention Type: DRUG

Lenalidomide

10 or 25 mg/day capsules administered PO.

Participants randomized in Arm A:

25 mg/day capsules on Days 1 through 14 of a 21 day cycle.;

Participants randomized in Arm B:

Cycles 1 through 8 - 25 mg/day capsules on Days 1 through 21 of a 28 day cycle;

Participants randomized in Arm C:

Cycles 1 - 25 mg/day capsules on Days 2 through 21 of a 28 day cycle; Cycles 2 through 8 - 25 mg/day capsules on Days 1 through 21 of a 28 day cycle;

Maintenance Therapy:

10 mg capsules on Days 1 through 21 on a 28 days cycle.

Intervention Type: DRUG

Acetaminophen

650 mg administered PO.

Participants randomized to Arm C:

Cycles 1 through 8 - 650 mg administered on Days 1, 8 and 15.

Intervention Type: DRUG

Diphenhydramine

25 mg administered via IV

Participants randomized to Arm C:

Cycles 1 through 8 - 25 mg administered on Days 1, 8 and 15.

Intervention Type: DRUG

Montelukast

10 mg administered PO to participants randomized to Arm C prior to the first 4 doses of Daratumumab.

Intervention Type: DRUG

Carfilzomib

20 mg or 56 mg/m2 per dose administered via IV.

Participants randomized to Arm B:

Cycle 1 - 20 mg/m2 per dose on Day 1 and 56 mg/m2 per dose on days 8 and 15 of a 28 day cycle; Cycles 2 through 8 - 56 mg/m2 per dose on days 1, 8 and 15 of a 28 day cycle;

Participants randomized to Arm C:

Cycle 1 - 20 mg/m2 per dose on Day 2 and 56 mg/m2 per dose on days 8 and 15 of a 28 day cycle; Cycles 2 through 8 - 56 mg/m2 per dose on days 1, 8 and 15 of a 28 day cycle

Intervention Type: DRUG

Daratumumab

16 mg/kg administered via IV or 1800 mg SC, per treating physician discretion.

Participants randomized to Arm C:

Cycles 1 though 2 - 16 mg/kg IV or 1800 mg SC on days 1, 8, 15, and 22 of a 28 day cycle; Cycles 3 through 6- 16 mg/kg IV or 1800 mg SC on days 1 and 15 of a 28 day cycle; Cycles 7 through 8 - 16 mg/kg IV or 1800 mg SC on day 1 of a 28 day cycle

Intervention Type: DRUG

Autologous Stem Cell Transplant (ASCT)

Participants who are MRD positive at the conclusion of 8 cycles of study treatment, and were able to have their stem cells that were extracted, will receive ASCT from participants' bone marrow samples.

Intervention Type: BIOLOGICAL

Other Intervention Names

Revlimid

Eligibility Criteria

Inclusion Criteria

1. Newly diagnosed patients with histologically confirmed Multiple Myeloma (MM) based on the IMWG diagnostic criteria and measurable disease within the past 4 weeks (or past 8 weeks if patient received pre-study MM therapy) based on one of the following:

• Serum monoclonal protein ≥ 1.0 g/dL
• Urine monoclonal protein ≥ 200 mg/24 hour
• Involved serum immunoglobulin free light chain ≥ 10 mg/dL and abnormal kappa/lambda ratio.

2. Evidence of underlying end organ damage and/or myeloma defining event attributed to underlying plasma cell proliferative disorder meeting at least one of the following (Note: Myeloma defining event does not need to be based on repeat testing done at screening, if previous pathology, radiology, etc., confirm diagnosis of myeloma per IMWG)

• Hypercalcemia: serum calcium >0.25 mmol/L (> 1 mg/dL) above upper limit of normal or ≥ 2.75 mmol/L (11 mg/dL)
• Anemia: hemoglobin value <10 g/dL or > 2 g/dL below lower limit of normal
• Bone disease: ≥ 1 lytic lesions on skeletal X-ray, CT, or Positron Emission Tomography (PET)-C. For patients with 1 lytic lesion, bone marrow should demonstrate ≥10% clonal plasma cells
• Clonal bone marrow plasma cell percentage ≥60%
• Involved/un-involved serum free light chain ratio ≥100 and involved free light chain

≥100 mg/L.

• > 1 focal lesion on magnetic resonance imaging study (lesion must be >5 mm) in size
• For patients with 1 lytic lesion, bone marrow should demonstrate ≥10% clonal plasma cells

3. Creatinine Clearance (CrCl) ≥ 60 ml/min. CrCl can be measured or estimated using Cockcroft-Gault method, Modification of Diet in Renal Disease (MDRD), or Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formulae

4. Age ≥ 18 years at the time of signing the informed consent documentation. Age limit of ≤ 75 years.

5. Eastern Cooperative Oncology Group (ECOG) performance status 0-2

6. Absolute neutrophil count (ANC) ≥ 1.0 K/microliter (uL), hemoglobin ≥ 8 g/dL, and platelet count ≥ 75 K/uL, unless if cytopenias are deemed to be due disease at discretion of clinical investigator. Transfusions and growth factors are permissible.

7. Adequate hepatic function, with bilirubin < 1.5 x the pper Limit of Normal (ULN), and Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) < 3.0 x ULN.

8. All study participants must be able to tolerate one of the following thromboprophylactic strategies: aspirin, oral facto Xa inhibitors, low molecular weight heparin, warfarin (coumadin), or alternative anti-coagulant.

9. All study participants must be registered into the mandatory electronic REMS (eREMS) program and be willing and able to comply with the requirements of Risk Evaluation Management and Safety (REMS).

10. Females of childbearing potential (FCBP) must have a negative serum or urine pregnancy test within 10 - 14 days and again within 24 hours prior to prescribing lenalidomide for Cycle 1 (prescriptions must be filled within 7 days) and must either commit to continued abstinence from heterosexual intercourse or begin two acceptable methods of birth control, one highly effective method and one additional effective method at the same time, at least 28 days before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy.

A female of childbearing potential is a sexually mature female who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).

Exclusion Criteria

1. Patients receiving >1 cycle of prior treatment or concurrent systemic treatment for multiple myeloma:

• Treatment of hypercalcemia or spinal cord compression or aggressively progressing myeloma with current or prior corticosteroids is permitted
• Bone targeting agents are permitted
• Concurrent or prior treatment with corticosteroids for indications other than multiple myeloma is permitted
• Prior treatment with radiotherapy is permitted
• Prior MM treatments, such as Immunomodulating Drugs (IMIDs) or non-MM drugs in clinical trials for smoldering myeloma is permitted with a washout period of 2 weeks from last dose. Smoldering patients previously treated with carfilzomib are excluded.
• Patients with measurable disease who received up to one cycle of any therapy within 60 days with a washout period of 2 weeks from last dose (on a trial or outside a trial) are eligible (Note: Measurable disease is defined as one or more of the following: Serum monoclonal protein ≥ 1.0 g/dL, Urine monoclonal protein ≥ 200 mg/24 hour and/ or Involved serum immunoglobulin free light chain ≥ 10 mg/dL AND abnormal kappa/lambda ratio)

2. Prior or current exposure to any of the following:

• To daratumumab or other anti- Cluster of Differentiation (CD) -38 therapies (unless a re-treatment study)
• Exposure to an investigational drug (including investigational vaccine) or invasive investigational medical device for any indication within 4 weeks or 5 pharmacokinetic half-lives, whichever is longer.
• Focal radiation therapy within 14 days prior to randomization with the exception of palliative radiotherapy for symptomatic management but not on measurable extramedullary plasmacytoma.

3. Patients with plasma cell leukemia

4. Patients with Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal protein, Skin changes syndrome (POEMS syndrome)

5. Patients with amyloidosis

6. Patients with known Chronic Obstructive Pulmonary Disorder (COPD) with a forced expiratory volume in 1 second (FEV1) < 50% of predicted normal. Note that FEV1 testing is required for subjects suspected of having COPD, and subjects must be excluded if FEV1 <50% of predicted normal.

7. Moderate or severe persistent asthma within the past 2 years, or uncontrolled asthma of any classification. Note that participants who currently have controlled intermittent asthma or controlled mild persistent asthma are allowed to participate in the study.

8. Pregnant or lactating females. Because there is a potential risk for AEs in nursing infants secondary to treatment of the mother with carfilzomib in combination with lenalidomide, pregnant or lactating females are excluded from study participation. These potential risks may also apply to other agents used in this study.

9. Uncontrolled hypertension (i.e., systolic blood pressure (BP) >160 mmHg, diastolic BP > 100 mmHg)

10. Uncontrolled diabetes (i.e., two independent glucose readings >200 mg/dL)

11. Active hepatitis B or C infection

12. Subject is:

• Seropositive for human immunodeficiency virus (HIV)
• Seropositive for hepatitis B (defined by a positive test for hepatitis B surface antigen [HBsAg]). Subjects with resolved infection (i.e., subjects who are HBsAg negative but positive for antibodies to hepatitis B core (HBc) antigen [anti-HBc] and/or antibodies to hepatitis B surface antigen [anti-HBs]) must be screened using real-time polymerase chain reaction (RT-PCR) measurement of hepatitis B virus (HBV) DNA levels. Those who are PCR positive will be excluded. EXCEPTION: Subjects with serologic findings suggestive of HBV vaccination (anti-HBs positivity as the only serologic marker) AND a known history of prior HBV vaccination do not need to be tested for HBV DNA by PCR.
• Seropositive for hepatitis C (except in the setting of a sustained virologic response (SVR), defined as aviremia at least 12 weeks after completion of antiviral therapy).
• Patients with active Coronavirus Disease of 2019 (COVID-19) infection are not to be enrolled until 10 days have passed from the initial positive test, and the patient is symptom-free. COVID-19 vaccinations following national guidelines (i.e., CDC) are encouraged; however, the series should be completed prior to the first day of study treatment. If this is not possible, every effort should be made to administer vaccines at a time when patient is not scheduled to receive study treatment (e.g., "off-weeks").

13. Clinically significant cardiac disease, including:

• Myocardial infarction within 6 months before randomization, or unstable or uncontrolled disease/condition related to or affection cardiac function (e.g., unstable angina, congestive heart failure, New York Heart Association (NYHA) Class III-IV) or a left ventricular ejection fraction of <40%.
• Uncontrolled cardiac arrhythmia
• Intolerance to hydration due to pre-existing pulmonary or cardiac impairment.

14. Pulmonary hypertension

15. Has refractory gastrointestinal (GI) disease with refractory nausea/vomiting, inflammatory bowel disease, or bowel resection that would prevent absorption of oral agents

16. Uncontrolled intercurrent illness including but not limited to active infection or psychiatric illness/social situations that would compromise compliance with study requirements

17. Significant neuropathy ≥ Grade 3 or Grade 2 neuropathy with pain at baseline

18. Contraindication to any concomitant medication, including antivirals or anticoagulation

19. Major surgery within 3 weeks prior to first dose

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Amgen

INDUSTRY

Sponsor Role: collaborator

Janssen Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

University of Miami

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Carl Landgren, MD

Role: PRINCIPAL_INVESTIGATOR

University of Miami

Locations

University of Miami

Miami, Florida, United States

Moffitt Cancer Center

Tampa, Florida, United States

Roswell Park Comprehensive Cancer Center

Buffalo, New York, United States

Memorial Sloan Kettering Cancer Center

New York, New York, United States

Stony Brook University

Stony Brook, New York, United States

MD Anderson Cancer Center

Houston, Texas, United States

Huntsman Cancer Institue

Salt Lake City, Utah, United States

Countries

United States

Other Identifiers

2019-001645-41

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

19-339

Identifier Type: OTHER

Identifier Source: secondary_id

20201316

Identifier Type: -

Identifier Source: org_study_id