Clinical trial · Interventional
A Randomized Phase 2 Study of AT-101 in Combination With Docetaxel in Relapsed/Refractory Non-Small Cell Lung Cancer
A Phase 2, Randomized, 2-Arm, Double-Blind Study of AT-101 in Combination With Docetaxel Versus Docetaxel Plus Placebo in Patients With Relapsed or Refractory Non-Small Cell Lung Cancer (NSCLC)
NCT00544960CI-TRIAL-00003852completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- 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)
This is a double- blind, multicenter, randomized Phase II study to evaluate the efficacy and safety of AT-101 in combination with docetaxel in relapsed/refractory non-small cell lung cancer
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 (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| AT-101 and docetaxel | Drug | — | UNRESOLVED |
| placebo and docetaxel | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- 1
- description
- AT-101 and docetaxel
- interventionNames
- Drug: AT-101 and docetaxel
- type
- PLACEBO_COMPARATOR
- label
- 2
- description
- placebo and docetaxel
- interventionNames
- Drug: placebo and docetaxel
Primary outcomes (1)
- measure
- duration of disease remission
- timeFrame
- 12 months
Secondary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically or cytologically confirmed Stage IIIb with pleural/pericardial effusion or Stage IV non-small cell lung cancer (NSCLC). * Progression of disease after one prior systemic chemotherapeutic regimen for locally advanced or metastatic NSCLC. (Systemic therapies given in the adjuvant setting are counted only if the patient relapses within 6 months of the last cycle of therapy.) In addition to the one prior chemotherapeutic regimen, patients may have received erlotinib in any setting. * All patients must have measurable disease. * No unstable or progressive brain metastases. * Patients may have received prior radiation therapy but they must have recovered from all treatment-related toxicities. * ECOG performance status 0-1 * Adequate hematologic function * Adequate liver and renal function * Ability to swallow oral medication Exclusion Criteria: * Prior chemotherapy regimen containing docetaxel. * Active secondary malignancy. * Uncontrolled concurrent illness including, but not limited to: serious uncontrolled infection, symptomatic congestive heart failure (CHF), unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with the study requirements. * Failure to recover from toxicities related to prior therapy (e.g., surgery, radiation, chemotherapy).
References
Publications (0)
Data not yet available
No reference posted for this study.