An Open-Label Study of a Novel JAK-inhibitor, INCB052793, Given to Patients With Advanced Malignancies
Status: | Active, not recruiting |
---|---|
Conditions: | Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/19/2018 |
Start Date: | August 2014 |
End Date: | June 2019 |
A Phase 1/2, Open-Label, Dose-Escalation, Safety and Tolerability Study of INCB052793 in Subjects With Advanced Malignancies
This is a study of INCB052793 given to patients with advanced malignancies that will be
conducted in three phases; Phase 1a (Monotherapy) and Phase 1b (Combination Therapy) and
Phase 2 (Combination therapy of INCB052793 with azacitidine and itacitinib with azacitidine).
Phase 1 will have two parts; a dose escalation (Part 1) and an expansion (Part 2).
conducted in three phases; Phase 1a (Monotherapy) and Phase 1b (Combination Therapy) and
Phase 2 (Combination therapy of INCB052793 with azacitidine and itacitinib with azacitidine).
Phase 1 will have two parts; a dose escalation (Part 1) and an expansion (Part 2).
Inclusion Criteria:
Phase 1a
- Aged 18 years or older
- Histologically or cytologically confirmed solid tumor or hematologic malignancy
- Life expectancy of 12 weeks or longer
- Must have received ≥ 1 prior treatment regimen
- Must not be a candidate for potentially curative or standard of care approved therapy
Phase 1b
- Aged 18 years or older
- Cohort A: Histologically or cytologically confirmed pancreatic adenocarcinoma,
triple-negative breast cancer, urothelial cancer with at least 1 measurable or
evaluable target lesion
- Cohorts B, C, D, E and G: Histologically confirmed multiple myeloma and
measureable/evaluable disease
- Cohort F: Confirmed acute myeloid leukemia or myelodysplastic syndrome
- Cohort H: Individuals diagnosed with lymphoma
- Prior therapy:
- Cohort A: No more than 1 prior chemotherapy regimen for advanced or metastatic
disease (not including neoadjuvant and/or adjuvant therapy)
- Cohorts B, C, D, E and G: Must have relapsed from or have been refractory to ≥ 2
prior treatment regimens
- Cohort F: May have received any number of prior treatment regimens or be
treatment-naïve
- Cohort H: Must have relapsed from or have been refractory to available treatments
Phase 2
- Aged 18 years or older
- Cohorts I and J: Confirmed acute myeloid leukemia or high risk myelodysplastic
syndrome
- Prior therapy:
- Cohorts I and J: Must have failed prior therapy with a hypomethylating agent
(HMA)
Exclusion Criteria:
- Prior receipt of a JAK1 inhibitor (Phase 1a only)
- Known active central nervous system metastases and/or carcinomatous meningitis
- Eastern Cooperative Oncology Group (ECOG) performance status > 2
- Any known contraindications to the use of gemcitabine, nab-paclitaxel, dexamethasone,
carfilzomib, bortezomib, lenalidomide, azacitidine, pomalidomide or PI3Kδ inhibitor
(Phase 1b and Phase 2 only, as appropriate to treatment cohort)
- Known human immunodeficiency virus infection, or evidence of hepatitis B virus (HBV)
or hepatitis C virus (HCV) infection or risk of reactivation
We found this trial at
9
sites
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