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INCMGA00012 in Combination With Other Therapies in Patients With Advanced Solid Tumors

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03589651
Recruitment Status : Completed
First Posted : July 18, 2018
Last Update Posted : February 21, 2023
Sponsor:
Information provided by (Responsible Party):
Incyte Corporation

Study Description
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Brief Summary:
The purpose of this study is to determine the safety, preliminary evidence of clinical activity, and recommended Phase 2 dose (RP2D) of INCMGA00012 in combination with other agents that may improve the therapeutic efficacy of anti-PD-1 monotherapy.

Condition or disease Intervention/treatment Phase
Unresectable or Metastatic Solid Tumors Drug: Retifanlimab Drug: Epacadostat Drug: INCB050465 Phase 1

Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 83 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1b Study of INCMGA00012 in Combination With Other Therapies in Patients With Advanced Solid Tumors
Actual Study Start Date : August 17, 2018
Actual Primary Completion Date : November 21, 2022
Actual Study Completion Date : November 21, 2022
Arms and Interventions
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Arm Intervention/treatment
Experimental: Group A
INCMGA00012 with epacadostat.
 Drug: Retifanlimab

Part 1: INCMGA00012 at the protocol-defined starting dose administered intravenously every 4 weeks, with dose escalation to determine the maximum tolerated dose.

Part 2: INCMGA00012 at the recommended dose from Part 1.


Drug: Epacadostat

Part 1: Epacadostat at the protocol-defined starting dose administered orally twice daily, with dose escalation to determine the maximum tolerated dose.

Part 2: Epacadostat at the recommended dose from Part 1.

Other Names:
  • INCB024360
  • INCMGA00012
Experimental: Group B
INCMGA00012 with INCB050465.
 Drug: Retifanlimab

Part 1: INCMGA00012 at the protocol-defined starting dose administered intravenously every 4 weeks, with dose escalation to determine the maximum tolerated dose.

Part 2: INCMGA00012 at the recommended dose from Part 1.


Drug: INCB050465
Part 1: INCB050465 at the protocol-defined starting dose administered orally once daily, with dose escalation to determine the maximum tolerated dose. Part 2: INCB050465 at the recommended dose from Part 1.


Outcome Measures
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Primary Outcome Measures :
  1. Number of treatment-emergent adverse events [ Time Frame: Up to approximately 30 months ]
    Defined as any adverse event either reported for the first time or worsening of a pre-existing event after first dose of study drug.


Secondary Outcome Measures :
  1. Cmax of INCMGA00012 when given in combination with immune therapies [ Time Frame: Up to approximately 4 months ]
    Defined as maximum observed plasma or serum concentration. Other pharmacokinetic measures (including Cmin and AUC0-t) will also be evaluated.

  2. Tmax of INCMGA00012 when given in combination with immune therapies [ Time Frame: Up to approximately 4 months ]
    Defined as time to maximum concentration. Other pharmacokinetic measures (including Cmin and AUC0-t) will also be evaluated.

  3. Cmax of epacadostat when given in combination with INCMGA00012 [ Time Frame: Up to approximately 4 months ]
    Defined as maximum observed plasma or serum concentration. Other pharmacokinetic measures (including Cmin and AUC0-t) will also be evaluated.

  4. Tmax of epacadostat when given in combination with INCMGA00012 [ Time Frame: Up to approximately 4 months ]
    Defined as time to maximum concentration. Other pharmacokinetic measures (including Cmin and AUC0-t) will also be evaluated.

  5. Cmax of INCB050645 when given in combination with INCMGA00012 [ Time Frame: Up to approximately 4 months ]
    Defined as maximum observed plasma or serum concentration. Other pharmacokinetic measures (including Cmin and AUC0-t) will also be evaluated.

  6. Tmax of INCB050645 when given in combination with INCMGA00012 [ Time Frame: Up to approximately 4 months ]
    Defined as time to maximum concentration. Other pharmacokinetic measures (including Cmin and AUC0-t) will also be evaluated.

  7. Overall response rate [ Time Frame: Up to approximately 30 months ]
    Defined as the percentage of participants having complete response (CR) or partial response (PR) as determined by investigator assessment of radiographic disease per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 and modified RECIST v1.1 for immune-based therapeutics.

  8. Duration of response [ Time Frame: Up to approximately 30 months ]
    Defined as the time from the earliest date of CR or PR until the earliest date at which progression criteria are met or date of death due to any cause, whichever occurs first.

  9. Progression-free survival [ Time Frame: Up to approximately 30 months ]
    Defined as the time from the start of therapy until the earliest date at which progression criteria are met or date of death due to any cause, whichever occurs first.

  10. Overall survival [ Time Frame: Up to approximately 30 months ]
    Defined as the time from randomization to death due to any cause.


Eligibility Criteria
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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:

  • Histologically proven, locally advanced unresectable or metastatic solid tumors for whom no approved therapy with demonstrated clinical benefit is available or participants who are intolerant to or have declined standard therapy
  • Measurable or nonmeasurable tumor lesions per RECIST v 1.1.
  • Willing to provide fresh or archival tumor tissue for correlative studies.
  • Eastern Cooperative Oncology Group performance status 0 to 1.
  • Willingness to avoid pregnancy or fathering children based on protocol-defined criteria.

Exclusion Criteria:

  • Receipt of anticancer therapy within 21 days of the first administration of study treatment, with the exception of localized radiotherapy.
  • Toxicity of prior therapy that has not recovered to ≤ Grade 1 or baseline (with the exception of alopecia and anemia not requiring transfusional support).
  • Laboratory values outside the protocol-defined range at screening.
  • Active autoimmune disease requiring systemic immunosuppression in excess of physiologic maintenance doses of corticosteroids.
  • Known hypersensitivity to any of the study drugs, excipients, or another monoclonal antibody which cannot be controlled with standard measures (eg, antihistamines and corticosteroids).
  • Evidence of interstitial lung disease or active, noninfectious pneumonitis.
Contacts and Locations
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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): NCT03589651


Locations
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United States, California
The Angeles Clinic and Research Institute
Los Angeles, California, United States, 90025
United States, Connecticut
Yale New Haven Hospital
New Haven, Connecticut, United States, 06510
United States, Florida
University of Florida - Shands Cancer Center
Gainesville, Florida, United States, 32610
United States, Illinois
University of Chicago Medical Center
Chicago, Illinois, United States, 60637
United States, New Jersey
Rutgers Cancer Institute of Nj
New Brunswick, New Jersey, United States, 08901
United States, New York
Roswell Park Cancer Institute
Buffalo, New York, United States, 14263
United States, Pennsylvania
Hospital of the University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Upmc Cancercenter
Pittsburgh, Pennsylvania, United States, 15232
United States, Texas
South Texas Accelerated Research Therapeutics
San Antonio, Texas, United States, 78229
Sponsors and Collaborators
Incyte Corporation
More Information
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Responsible Party: Incyte Corporation
ClinicalTrials.gov Identifier: NCT03589651    
Other Study ID Numbers: INCMGA 0012-102
First Posted: July 18, 2018    Key Record Dates
Last Update Posted: February 21, 2023
Last Verified: February 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Incyte Corporation:
Solid tumors
locally advanced unresectable tumor
metastatic solid tumors
Additional relevant MeSH terms:
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Neoplasms