Clinical trial · Interventional
MP470 in Treating Patients With Unresectable or Metastatic Solid Tumor or Lymphoma
Safety Study to Determine the Maximum Tolerated Dose, Pharmacokinetics and Pharmacodynamics of Oral MP470, a Multi-Targeted Tyrosine Kinase Inhibitor, in Patients With Solid Malignancies
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Withdrawn as trial was never activated by SuperGen
Summary
Brief summary (as posted)
RATIONALE: MP470 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. PURPOSE: This clinical trial is studying the side effects and best dose of MP470 in treating patients with unresectable or metastatic refractory solid tumor, Hodgkin's lymphoma, or non-Hodgkin's lymphoma.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lymphoma | Lymphoma | ONTOLOGY_EXACT | 0.90 |
| Unspecified Adult Solid Tumor, Protocol Specific | Adult Solid Neoplasm | ALIAS | 0.85 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| laboratory biomarker analysis | Other | — | UNRESOLVED |
| multitargeted receptor tyrosine kinase inhibitor MP470 | Drug | — | UNRESOLVED |
| pharmacological study | Other | — | UNRESOLVED |
| positron emission tomography | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (3)
- measure
- Safety
- measure
- Response to treatment according to RECIST criteria
- measure
- Pharmacodynamic assessments (e.g., changes in phosphorylation of ERK, Rad51 expression, number of CTCs, and tumor glucose metabolism measured by FDG-PET)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: Inclusion criteria: * Histological or cytological diagnosis of unresectable or metastatic solid-tumor cancer that is refractory to standard therapies OR for which no standard therapy exists * Patients with refractory lymphoma (Hodgkin or non-Hodgkin) are also permitted to participate Exclusion criteria: * Active CNS metastases (primary brain tumors are permitted) PATIENT CHARACTERISTICS: Inclusion criteria: * Karnofsky performance status ≥ 70% * Hemoglobin ≥ 9 g/dL * ANC ≥ 1.5 × 10\^9/L * Platelet count ≥ 100 × 10\^9/L * Total serum bilirubin ≤ 2 mg/dL * AST and ALT ≤ 2.5 × ULN (upper limit of normal for the clinical laboratory), but ≤ 5 × ULN is acceptable if due to hepatic metastases * Serum albumin ≥ 2 g/dL * Serum creatinine ≤ 2 mg/dL * LVEF ≥ 50% on ECHO * No significant abnormalities on the screening ECG (e.g., left bundle branch block, 3rd degree AV block, acute myocardial infarction or QTc interval \> 450 msec) * No history of additional risk factors for torsade de pointes (e.g., heart failure, hypokalemia or family history of Long QT Syndrome) * Able to swallow MP470 capsules * Capable of fasting for 6 hours * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception during and for 3 months following completion of study treatment Exclusion criteria: * Life-threatening illness, medical condition, or organ system dysfunction which, in the investigator's opinion, could compromise the patient's safety, interfere with the absorption or metabolism of oral MP470, or put the study outcomes at risk * Any serious, uncontrolled active infection that requires systemic treatment * History of significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, congestive heart failure, and/or myocardial infarction PRIOR CONCURRENT THERAPY: Inclusion criteria: * Recuperated from any prior surgical procedures including at least 4 weeks rest since a major surgery Exclusion criteria: * Patient has received any anticancer agent(s) within the past 3 weeks, including investigational agents, chemotherapy (6 weeks for nitrosoureas or mitomycin), immunotherapy, biologic, or hormonal therapy other than luteinizing hormone-releasing hormone (LHRH) agonists * Patient has received radiation therapy within the past 4 weeks * Patient has a grade 2 or more severe toxicity (other than alopecia) continuing from prior anticancer therapy * Patient requires treatment with immunosuppressive agents other than corticosteroids that have been at stable doses for at least 2 weeks
References
Publications (0)
Data not yet available