Clinical trial · Interventional
Cyclin Dependent Kinase (CDK)4/6 Inhibitor, PD0332991 in Advanced Non-small Cell Lung Cancer NSCLC.
A Phase II Clinical Trail of the Cyclin Dependent Kinase (CDK)4/6 Inhibitor, PD0332991 in Previously Treated, Advanced NSCLC Patients With Wildtype Retinoblastoma Protein (RB) and Inactive Cyclin Dependent Kinase (CDK)N2a
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to determine the efficacy and the toxicities of the study drug PD0332991 in the treatment of patients with Stage IV non-small cell lung cancer with wildtype retinoblastoma protein (RB) and inactivated cyclin dependent kinase (CDK) N2A in the tumor.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PD0332991 | Drug | Palbociclib | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- PD0332991
- description
- PD0332991 125 mg PO days 1 - 21
- interventionNames
- Drug: PD0332991
Primary outcomes (1)
- measure
- Tumor Response by Direct RECIST Measurement
- timeFrame
- 6 months
- description
- Response is a decrease in the sum of the longest diameters of the target lesions by more than 30% compared to the baseline.
Secondary outcomes (4)
- measure
- Overall Survival
- timeFrame
- 14 months
- description
- Median overall survival
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically or cytologically proven non small cell lung cancer * Stage IV (M1a or M1b) disease. Patients may also have recurrence of early-stage disease or locally advanced disease with the presence of new distant metastases. * Cyclin dependent kinase (CDK)N2a (p16) protein absent or expressed at a low level in tumor biopsy specimen * Failed or intolerant of at least one prior systemic chemotherapy regimen (there is no maximum number of prior chemotherapy regimens) * Eastern cooperative oncology group (ECOG) performance status 0-2 * Age \>18 years. * Adequate organ and bone marrow function * Measurable disease by standard RECIST v1.1 criteria * Life expectancy of greater than 3 months Exclusion Criteria: * Inability to understand or sign the informed consent document * Inability or unwillingness to take oral medications * No available tissue specimen for p16 analysis * Chemotherapy or radiotherapy within 3 weeks prior to beginning the study drug * Other investigational agents within 4 weeks prior to beginning the study drug * All side effects from previous chemotherapy, radiotherapy or investigational agents not resolved, returned to baseline or returned to Grade 1 toxicity (exceptions are grade 2 alopecia and grade 2 peripheral neuropathy) * Major surgery within 4 weeks prior to beginning the study drug * Surgical scar from previous surgery not healed prior to beginning the study drug * High-dose or chronic steroid use * High-dose statins within 7 days * History of rhabdomyolysis * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, uncontrolled diabetes, stroke or myocardial infarction within 3 months, or psychiatric illness/social situations that would limit compliance with study requirements. * Baseline corrected QT interval (QTc) \>470ms * Pre-existing clinically significant cardiac, hepatic or renal dysfunction at the discretion of the treating physician * Untreated or uncontrolled (symptomatic or asymptomatic) brain metastases * Leptomeningeal carcinomatosis * Inability or unwillingness to use contraception during the treatment period by patients with reproductive potential. * Pregnant or breastfeeding women * HIV-positive patients on combination antiretroviral therapy
References
Publications (0)
Data not yet available