NSCLC (Non-small Cell Lung Carcinoma)
Conditions
Keywords
Stage IIIb, IV, or Recurrent Non-Small Cell Lung Cancer
Brief summary
The primary objectives of this study were to evaluate the safety and tolerability of itacitinib in combination with docetaxel and to select doses for further evaluation (Part 1, safety run-in portion), and to evaluate and compare the overall survival of subjects with previously treated advanced or metastatic non-small cell lung cancer (NSCLC) when treated with itacitinib in combination with docetaxel versus docetaxel alone (Part 2, randomized portion).
Detailed description
The secondary objectives of this study (Part 2) were to evaluate and compare the efficacy of the 2 treatment groups with respect to progression-free survival, overall tumor response, and duration of response, and to evaluate and compare disease control, safety, and tolerability of itacitinib in combination with docetaxel versus docetaxel alone. Part 2 of the study was not conducted.
Interventions
DRUGItacitinib
Itacitinib tablets administered orally at 400 mg QD for Part 1 of the study.
DRUGdocetaxel
Administered as an intravenous infusion in the clinic at 75 mg/m\^2 Q3W for Part 1 of the study.
Sponsors
Incyte Corporation
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Histologically or cytologically confirmed diagnosis of NSCLC that is Stage IIIb, IV, or recurrent. 2. Received only 1 prior systemic chemotherapy regimen for Stage IIIb, IV, or recurrent disease not including neoadjuvant and/or adjuvant therapy. (NOTE: Exceptions may be allowed based on prior treatment regimens and tumor types in agreement with protocol requirements.) 3. Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2. 4. Life expectancy of ≥12 weeks.
Exclusion criteria
1. Received prior treatment with docetaxel. 2. Known active central nervous system (CNS) metastases. Subjects with CNS metastases who have completed a course of therapy would be eligible for the study provided they are clinically stable for at least 1 month prior to study entry, defined as: 1. No evidence of new or enlarging CNS metastasis or new neurological symptoms attributable to CNS metastases. 2. Subjects who are receiving concomitant corticosteroids must be on a stable or decreasing dose for at least 4 weeks prior to first dose of study treatment and off all anticonvulsants for at least 4 weeks prior to study entry. 3. Peripheral neuropathy ≥ Grade 3. 4. Current or previous other malignancy within 2 years of study entry, except cured basal or squamous cell skin cancer, superficial bladder cancer, prostate intraepithelial neoplasm, carcinoma in situ of the cervix, or other noninvasive malignancy. 5. Significant, concurrent, uncontrolled medical condition including but not limited to, renal, hepatic, hematological, gastrointestinal, endocrine, pulmonary, cardiac, neurological, cerebral, or psychiatric disease. 6. Unwilling to be transfused with blood components.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Dose Limiting Toxicities (DLTs) | Baseline through 21 days; the end of cycle 1. | Number of participants with DLT for the determination of the Maximum Tolerated Dose (MTD). |
Countries
United States
Contacts
STUDY_DIRECTORAmit Pande, M.D.
Incyte Corporation
Outcome results
None listed