Multiple Myeloma Clinical Trial

INCB001158 Combined With Subcutaneous (SC) Daratumumab, Compared to Daratumumab SC, in Relapsed or Refractory Multiple Myeloma

Summary

The purpose of this study is to evaluate the safety and antitumor activity of INCB001158 in combination with daratumumab SC, compared with daratumumab SC alone, in participants with relapsed or refractory multiple myeloma.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Prior diagnosis of multiple myeloma according to IMWG diagnostic criteria.
Measurable disease at screening.
Has received at least 3 but not more than 5 prior lines of multiple myeloma treatment, including proteasome inhibitor, immunomodulatory drug, and anti-CD38 therapies.
Eastern Cooperative Oncology Group performance status of 0 or 1.
Willing to avoid pregnancy or fathering children.
Willing to provide fresh and archival bone marrow aspiration and biopsy tissue.

Exclusion Criteria:

Receipt of any of the following treatment within the indicated interval before the first administration of study drug:

Anti-myeloma treatment within 2 weeks or 5 half-lives (whichever is longer).
Investigational drug (including investigational vaccines) or invasive investigational medical device within 4 weeks.
Autologous stem cell transplant within 12 weeks, or allogeneic stem cell transplant at any time.
Plasmapheresis within 4 weeks.
Radiation therapy within 2 weeks.
Major surgery within 2 weeks, or inadequate recovery from an earlier surgery, or surgery planned during the time the participant is expected to participate in the study or within 2 weeks after the last dose of study treatment.
Toxicity ≥ Grade 2 from previous anti-myeloma therapy except for stable chronic toxicities (≤ Grade 2) not expected to resolve, such as stable Grade 2 peripheral neuropathy.
Known additional malignancy (other than multiple myeloma) that is progressing or requires active treatment, or history of other malignancy within 2 years of study entry.
Laboratory values at screening outside the protocol-defined range.
Significant concurrent, uncontrolled medical condition including but not limited to known chronic obstructive pulmonary disease (COPD), persistent asthma, or history of asthma within the past 2 years; chronic or current active infectious disease requiring systemic antibiotics, antifungal, or antiviral treatment; acute diffuse infiltrative pulmonary disease; clinically significant or uncontrolled cardiac disease.
Plasma cell leukemia, Waldenström's macroglobulinemia, POEMS syndrome, or amyloidosis.

Study is for people with:

Multiple Myeloma

Phase:

Phase 1

Estimated Enrollment:

15

Study ID:

NCT03837509

Recruitment Status:

Terminated

Sponsor:

Incyte Corporation

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There are 29 Locations for this study

See Locations Near You

Southern Cancer Center
Daphne Alabama, 36526, United States
Arizona Oncology Associates (Wilmot)
Tucson Arizona, 85711, United States
Rocky Mountain Cancer Centers
Denver Colorado, 80218, United States
Dana Farber Cancer Institute
Boston Massachusetts, 02215, United States
Comprehensive Cancer Centers of Nevada - Twain
Las Vegas Nevada, 89169, United States
New York Oncology Hematology
Albany New York, 12206, United States
Lineberger Comprehensive Cancer Center At University of North Carolina Chapel Hill
Chapel Hill North Carolina, 27514, United States
Oncology Hematology Care, Inc
Cincinnati Ohio, 45236, United States
Texas Oncology-Austin Midtown
Austin Texas, 78705, United States
Texas Oncology - Fort Worth South Henderson
Fort Worth Texas, 76104, United States
Texas Oncology San Antonio
San Antonio Texas, 78240, United States
Texas Oncology - Tyler
Tyler Texas, 75702, United States
University of Virginia
Charlottesville Virginia, 22903, United States
Virginia Cancer Specialists-Fairfax
Fairfax Virginia, 22031, United States
Charite - Universit�Tsmedizin Berlin
Berlin , 13353, Germany
University of Heidelberg
Heidelberg , 69117, Germany
Universitatsmedizin Der Johannes Gutenberg-Universitat Mainz Iii
Mainz , 55131, Germany
Universitatsklinikum Munster
Munster , 48149, Germany
Hospital General Universitari Vall D Hebron
Barcelona , 08035, Spain
Hospital Clinic I Provincial
Barcelona , 08036, Spain
Ico Institut Catala D Oncologia
Barcelona , 08908, Spain
Hospital Universitario Ramon Y Cajal
Madrid , 28034, Spain
Fundacion Jimenez Diaz University Hospital
Madrid , 28040, Spain
Hospital Universitario 12 de Octubre
Madrid , 28041, Spain
Clinica Universidad de Navarra (Cun)
Pamplona , 31008, Spain
Hospital Clinico Universitario de Salamanca
Salamanca , 37007, Spain
Hospital Universitario Marques de Valdecilla
Santander , 39008, Spain
Hospital Universitario Doctor Peset
Valencia , 46017, Spain
Hospital Universitario Y Politcnico de La Fe
Valencia , 46026, Spain

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Phase:

Phase 1

Estimated Enrollment:

15

Study ID:

NCT03837509

Recruitment Status:

Terminated

Sponsor:


Incyte Corporation

How clear is this clinincal trial information?

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