Clinical trial · Interventional
Protein Tyrosine Kinases (PTK) in Multiple Myeloma
Phase II Study of PTK787/ZK222584 in Multiple Myeloma
NCT00165347CI-TRIAL-00001041completedPhase 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)
The purpose of this study is to determine whether or not cancer cells in the body are affected by PTK and whether it affects the growth of these cells.
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 |
|---|---|---|---|
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PTK787/ZK222584 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- To determine the effectiveness of PTK in treating patients with relapsed or refractory myeloma
Secondary outcomes (2)
- measure
- To evaluate the progression free survival of patients treated with PTK
- measure
- to investigate the safety of PTK in patients with relapsed/refractory multiple myeloma
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Older than 18 years of age. * Confirmed diagnosis of active progressive multiple myeloma * History of \> 2 prior cytotoxic treatment regimens. Bone marrow transplantation will be considered as one regimen. * Current measurable disease based on serum and/or urine M protein and/or measurable plasmacytoma. * Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 * Absolute neutrophil count (ANC) \> 1,500 mm3 * Platelets \> 100,000 mm3 * Serum creatinine \< 1.5 upper limit of normal (ULN) * Serum bilirubin \< 1.5 ULN * AST/AGOT and ALT/SGPT \< 3.0 ULN * Life expectancy \> 12 weeks Exclusion Criteria: * Chemotherapy \< 3 weeks prior to registration. * Biologic or immunotherapy \< 2 weeks prior to registration * Full field radiotherapy \< 4 weeks or limited field radiotherapy \< 2 weeks prior to registration. * History or presence of central nervous system (CNS) disease * History of leukemia * History of another primary malignancy with the exception of inactive basal or squamous cell carcinoma of the skin * Major surgery \< 4 weeks prior to registration * Prior therapy with anti-vascular endothelial growth factor (VEGF) agents excluding thalidomide, Revimid, velcade and arsenic trioxide * Interstitial pneumonia or extensive and symptomatic interstitial fibrosis of the lung * Pleural effusion or ascites that cause respiratory compromise * Female patients that are pregnant or breast feeding * Uncontrolled high blood pressure, history of labile hypertension or history of poor compliance with an antihypertensive regimen * Unstable angina pectoris * Symptomatic congestive heart failure * Myocardial infarction \< 6 months prior to registration * Serious uncontrolled cardiac arrhythmia * Uncontrolled diabetes * Active or uncontrolled infection * Acute or chronic liver disease * Impairment of gastrointestinal (GI) function or GI disease * Confirmed HIV infection
References
Publications (0)
Data not yet available
No reference posted for this study.