Clinical trial · Interventional
Safety of MP470 in Combination With Standard-of-Care Chemotherapy Regimens to Treat Solid Tumors
Safety and Dose Finding Study of Oral MP470, a Multi-targeted Tyrosine Kinase Inhibitor, in Combination With Standard-of-Care Chemotherapy Regimens
- 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)
Adult subjects with malignant disease appropriate for treatment with carboplatin/paclitaxel, carboplatin/etoposide, topotecan, docetaxel or erlotinib according to the standard dosing regimen will be enrolled in each treatment arm. Primary objective: Determine the MTD. Secondary objectives: Response rates, PK, quantify MP-470 on PK of SOC, and collect pharmacodynamic information. Evaluate the overall safety of MP-470 when co-administered with specific SOC treatments.
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 |
|---|---|---|---|
| Malignant Disease | — | UNRESOLVED | — |
Interventions
Interventions (5)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| MP-470 + carboplatin/etoposide | Drug | — | UNRESOLVED |
| MP-470 + docetaxel | Drug | — | UNRESOLVED |
| MP-470 + erlotinib | Drug | — | UNRESOLVED |
| MP-470 + paclitaxel/carboplatin | Drug | — | UNRESOLVED |
| MP-470 + topotecan | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (5)
- type
- EXPERIMENTAL
- label
- 1
- description
- oral MP-470 + paclitaxel/carboplatin
- interventionNames
- Drug: MP-470 + paclitaxel/carboplatin
- type
- EXPERIMENTAL
- label
- 2
- description
- oral MP-470 + carboplatin/etoposide
- interventionNames
- Drug: MP-470 + carboplatin/etoposide
- type
- EXPERIMENTAL
- label
- 3
- description
- oral MP-470 + topotecan
- interventionNames
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Malignant disease appropriate for initiating treatment with carboplatin/paclitaxel, carboplatin/etoposide, topotecan, docetaxel, or erlotinib. 2. Must be able to read, understand, and sign the IRB approved Informed Consent Form. 3. At least 18 years old. 4. Eastern Cooperative Oncology Group (ECOG) performance status 0-2. 5. Adequate bone marrow function; normal renal and hepatic function, normal cardiac function. Exclusion Criteria: 1. Any other active invasive malignancy except non-melanoma skin cancers or cervical carcinoma in situ. 2. History of significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, congestive heart failure and/or myocardial infarction. 3. 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 LHRH agonists. 4. Received prior radiation therapy within the past 4 weeks. 5. Any serious, uncontrolled active infection that requires systemic treatment or known infection with HIV, HCV or HBV. 6. Patient requires treatment with immunosuppressive agents other than corticosteroids appropriate for the SOC chemotherapy regimen or those at stable doses for at least 2 weeks.
References
Publications (1)
- DERIVEDMita M, Gordon M, Rosen L, Kapoor N, Choy G, Redkar S, Taverna P, Oganesian A, Sahai A, Azab M, Bristow R, Tolcher AW. Phase 1B study of amuvatinib in combination with five standard cancer therapies in adults with advanced solid tumors. Cancer Chemother Pharmacol. 2014 Jul;74(1):195-204. doi: 10.1007/s00280-014-2481-1. Epub 2014 May 22. PMID 24849582