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Trial record 31 of 37 for:    Recruiting Studies | Multiple Myeloma | Spain | ( Map: Spain )

Dose Escalation Study of JNJ-64407564 in Participants With Relapsed or Refractory Multiple Myeloma

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ClinicalTrials.gov Identifier: NCT03399799
Recruitment Status : Recruiting
First Posted : January 16, 2018
Last Update Posted : July 31, 2019
Sponsor:
Information provided by (Responsible Party):
Janssen Research & Development, LLC

Brief Summary:
The purpose of this study is to characterize the safety of JNJ-64407564 and to determine the recommended Phase 2 dose(s) (RP2Ds) and dosing schedule assessed to be safe for JNJ-64407564 (Part 1 [Dose Escalation]) and to further characterize the safety of JNJ-64407564 at the recommended Phase 2 dose(s) (RP2Ds) (Part 2 [Dose Expansion]).

Condition or disease Intervention/treatment Phase
Hematological Malignancies Drug: JNJ-64407564 Phase 1

Detailed Description:
The study will be conducted in 2 parts, separately for intravenous (IV) and subcutaneous (SC) administration: dose escalation and dose expansion. The study will evaluate safety, tolerability, pharmacokinetics and preliminary antitumor activity of JNJ-64407564 administered to adult participants with relapsed or refractory multiple myeloma. The overall safety of the study drug will be assessed by physical examinations, Eastern Cooperative Oncology Group performance status, laboratory tests, vital signs, electrocardiograms, adverse event monitoring, and concomitant medication usage. Disease evaluations will include peripheral blood and bone marrow assessments at screening (performed within 28 days) and to confirm stringent complete response (sCR), complete response (CR), or relapse from CR. The end of study (study completion) is defined as the last study assessment for the last participant in the study.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 87 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1, First-in-Human, Open-Label, Dose Escalation Study of JNJ-64407564, a Humanized DuoBody® Antibody, in Subjects With Relapsed or Refractory Multiple Myeloma
Actual Study Start Date : December 16, 2017
Estimated Primary Completion Date : June 15, 2020
Estimated Study Completion Date : April 13, 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Multiple Myeloma

Arm Intervention/treatment
Experimental: Part 1: Dose Escalation (JNJ-64407564) - Intravenous (IV)
Participants will receive IV infusion of JNJ-64407564 at minimum anticipated biologic effect level (MABEL)-based starting dose until the completion of the end of treatment visit. Subsequent dose levels will be selected based on the review of all available data including, but not limited to, pharmacokinetic, pharmacodynamic, safety, and preliminary antitumor activity data.
Drug: JNJ-64407564
Participants will receive IV infusion or SC injection of JNJ-64407564.

Experimental: Part 1: Dose Escalation (JNJ-64407564) - Subcutaneous (SC)
Participants will receive JNJ-64407564 SC. The dose levels will be selected to identify safe and tolerable putative RP2D(s).
Drug: JNJ-64407564
Participants will receive IV infusion or SC injection of JNJ-64407564.

Experimental: Part 2: Dose Expansion (JNJ-64407564)
Participants will receive IV infusion or SC injection of JNJ-64407564 at each putative recommended Phase 2 dose(s) (RP2D[s]) as determined in Part 1.
Drug: JNJ-64407564
Participants will receive IV infusion or SC injection of JNJ-64407564.




Primary Outcome Measures :
  1. Part 1: Dose-limiting Toxicity (DLT) [ Time Frame: Up to Day 28 ]
    The Dose Limiting Toxicities (DLTs) are based on drug related adverse events and defined as any of the following events: hematological / non-hematological toxicity of Grade 3 or higher.

  2. Part 1 and Part 2: Number of Participants with Adverse Events (AEs) as a Measure of Safety and Tolerability [ Time Frame: From signing of Informed Consent Form (ICF) up to follow up (until 100 days after the last dose of study drug or until the start of subsequent anticancer therapy, if earlier [approximately 2.10 years]) ]
    An AE is any untoward medical occurrence in a participant participating in a clinical study that does not necessarily have a causal relationship with the pharmaceutical/biological agent under study.


Secondary Outcome Measures :
  1. Part 1: JNJ-64407564 Serum Concentrations [ Time Frame: Up to 8 weeks ]
    Serum concentrations will be calculated for JNJ-64407564.

  2. Part 1 and Part 2: Biomarker Assessment [ Time Frame: Up to Cycle 7 Day 1 (each cycle of 21-days) ]
    Serum cytokine concentrations will be measured pre- and post-infusion of JNJ-64407564 for biomarker assessment.

  3. Part 1: Number of Participants with JNJ-64407564 Antibodies [ Time Frame: Up to 8 weeks ]
    Antibodies to JNJ-64407564 will be assessed to evaluate potential immunogenicity.

  4. Part 2: Overall Response Rate (ORR) [ Time Frame: Approximately 2.10 years ]
    ORR is defined as the proportion of participants who have a partial response (PR) or better according to the international myeloma working group (IMWG) criteria.

  5. Part 2: Clinical Benefit Rate (CBR) [ Time Frame: Approximately 2.10 years ]
    CBR is defined as the proportion of participants who have a minimal response (MR) or better according to the IMWG criteria.

  6. Part 2: Duration of Response (DOR) [ Time Frame: From the date of initial documentation of a response to the date of first documented evidence of progressive disease (PD) (approximately 2.10 years) ]
    DOR is defined as time from date of initial documentation of a response (PR or better) to date of first documented evidence of PD, per IMWG criteria.

  7. Part 2: Time to Response (TTR) [ Time Frame: From the date of first dose of study drug to the date of initial documentation of a response (approximately 2.10 years) ]
    TTR is defined as the time between date of first dose of study drug and the first efficacy evaluation that the participant has met all criteria for PR or better.

  8. Part 2: Progression-Free Survival (PFS) [ Time Frame: From the date of first dose of study drug to the date of first documented progressive disease, or death, whichever occurs first (approximately 18 months) ]
    PFS is defined as time from date of first dose of study drug to date of first documented PD, per IMWG criteria, or death due to any cause, whichever occurs first.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Documented initial diagnosis of multiple myeloma according to International Myeloma Working Group (IMWG) diagnostic criteria
  • Participants with measurable multiple myeloma who have progressed on, or could not tolerate, all available established therapies
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1
  • Women of childbearing potential must have a negative pregnancy test at screening and prior to the first dose of study drug using a highly sensitive pregnancy test either serum (Beta human chorionic gonadotropin [beta-hCG]) or urine
  • Sign an informed consent form (ICF) indicating that he or she understands the purpose of and procedures required for the study, and is willing to and able participate in the study. Consent is to be obtained prior to the initiation of any study-related tests or procedures that are not part of standard-of-care for the participant's disease

Exclusion Criteria:

  • Vaccinated with live, attenuated vaccine within 4 weeks or as recommended by the product manufacturer prior to the first dose, during treatment, or within 100 days of the last dose of JNJ-64407564
  • Toxicities from previous anticancer therapies should have resolved to baseline levels or to Grade 1 or less except for alopecia or peripheral neuropathy
  • Received a cumulative dose of corticosteroids equivalent to greater than or equal to ( >=) 140 milligram (mg) of prednisone within the 14-day period before the first dose of study drug
  • An allogenic stem cell transplant within 6 months before first dose of study drug. Participants who received an allogeneic transplant must be off all immunosuppressive medications for 6 weeks without signs of graft-versus-host disease (GVHD); and/or an autologous stem cell transplant less than or equal to (<=) 12 weeks before first dose of study drug
  • Documented history of central nervous system (CNS) involvement or exhibits clinical signs of meningeal involvement of multiple myeloma. If either is suspected, whole body magnetic resonance imaging (MRI) and lumbar cytology are required

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03399799


Contacts
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Contact: Study Contact 844-434-4210 JNJ.CT@sylogent.com

Locations
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United States, California
City of Hope Recruiting
Duarte, California, United States, 91010
United States, Colorado
University of Colorado Cancer Center Recruiting
Aurora, Colorado, United States, 80045
United States, New York
Mount Sinai Medical Center Recruiting
New York, New York, United States, 10029
United States, Tennessee
Sarah Cannon Research Institute Recruiting
Nashville, Tennessee, United States, 37203
Netherlands
VU Medisch Centrum Recruiting
Amsterdam, Netherlands, 1081 HV
UMCU Not yet recruiting
Utrecht, Netherlands, 3584 CX
Spain
Hosp. Univ. Germans Trias I Pujol Recruiting
Badalona, Spain, 08916
Hosp. Univ. Fund. Jimenez Diaz Recruiting
Madrid, Spain, 28040
Clinica Univ. de Navarra Recruiting
Pamplona, Spain, 31008
Hosp. Clinico Univ. de Salamanca Recruiting
Salamanca, Spain, 37007
Sponsors and Collaborators
Janssen Research & Development, LLC
Investigators
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Study Director: Janssen Research & Development, LLC Clinical Trial Janssen Research & Development, LLC

Additional Information:
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Responsible Party: Janssen Research & Development, LLC
ClinicalTrials.gov Identifier: NCT03399799     History of Changes
Other Study ID Numbers: CR108404
2017-002400-26 ( EudraCT Number )
64407564MMY1001 ( Other Identifier: Janssen Research & Development, LLC )
First Posted: January 16, 2018    Key Record Dates
Last Update Posted: July 31, 2019
Last Verified: July 2019

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Multiple Myeloma
Neoplasms, Plasma Cell
Neoplasms by Histologic Type
Neoplasms
Hemostatic Disorders
Vascular Diseases
Cardiovascular Diseases
Paraproteinemias
Blood Protein Disorders
Hematologic Diseases
Hemorrhagic Disorders
Lymphoproliferative Disorders
Immunoproliferative Disorders
Immune System Diseases