Clinical trial · Interventional
A Phase 1 Dose Escalation Study of VS-5584 Administered in Combination With VS-6063, in Subjects With Relapsed Malignant Mesothelioma
A Phase 1 Dose Escalation Study of VS-5584, a Dual PI3K/mTOR Inhibitor, Administered With a Fixed Dose of VS-6063, a Focal Adhesion Kinase Inhibitor, in Subjects With Relapsed Malignant Mesothelioma
- 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 evaluate rising dose levels of VS-5584 administered in combination with a fixed dose of VS-6063 in subjects with relapsed malignant mesothelioma to determine a recommended Phase 2 dose (RP2D) for further development of this combination in this indication.
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 |
|---|---|---|---|
| Relapsed Malignant Mesothelioma | Malignant Mesothelioma | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| VS-5584 and VS-6063 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- VS-5584 and VS-6063
- interventionNames
- Drug: VS-5584 and VS-6063
Primary outcomes (2)
- measure
- Incidence of dose-limiting toxicities (DLTs)
- timeFrame
- 6 months
- description
- Dose Escalation Phase: Frequency of DLTs at each dose level associated with administration of VS-5584 and VS-6063 in a 21 day cycle
- measure
- Safety and tolerability of the combination of VS-5584 and VS-6063
- timeFrame
- 16 months
- description
- Dose Escalation Phase and Expansion Phase: A composite by dose level to include incidence of AEs, SAEs (overall and severity), laboratory abnormalities, ECGs, vital signs, Karnofsky Performance Status, dose interruptions and dose reductions as a measure of safety and tolerability
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histopathologically-confirmed diagnosis of malignant mesothelioma (pleural or peritoneal). Must have disease that has relapsed following at least one prior line of chemotherapy. 2. Must have received at least 3 cycles of first-line chemotherapy. 3. Evaluable or measurable disease as assessed by Response Evaluation Criteria in Solid Tumors (RECIST). 4. Must have archival tumor tissue available for biomarker analysis. A study-specific tumor core biopsy, pleural effusion or ascites sample must be obtained prior to treatment if archival tissue is not available. 5. Performance status according to the Karnofsky Performance Scale ≥70%. 6. Fasting blood glucose of ≤ 140 mg/dL (7.8 mmol/L). 7. Adequate renal function (creatinine ≤ 1.5x upper limit of normal \[ULN\]) and/or glomerular filtration rate (GFR) of ≥50 mL/min. 8. Adequate hepatic function (total bilirubin ≤ 1.5x ULN; AST and ALT ≤ 3x ULN). 9. Adequate bone marrow function (hemoglobin ≥9.0 g/dL; platelets ≥100 x10\^9 cells/L; absolute neutrophil count ≥1.5x10\^9 cells/L) without the use of hematopoietic growth factors. Exclusion Criteria: 1. Have had a previous extra pleural pneumonectomy (EPP). 2. Gastrointestinal condition which could interfere with the swallowing or absorption of study drug. 3. Uncontrolled or severe concurrent medical condition (including uncontrolled brain metastases). 4. Known history of stroke or cerebrovascular accident within 6 months prior to the first dose of study drug. 5. Any evidence of serious active infection. 6. Undergoing active treatment for a secondary malignancy. 7. Cancer-directed therapy (chemotherapy, radiotherapy) within 21 days of the first dose of study drug or 5 half-lives, whichever is shorter. 8. Major surgery within 28 days prior to the first dose of study drug. 9. Acute or chronic pancreatitis. 10. Diabetes mellitus requiring insulin treatment or subjects with a hemoglobin A1C (HbA1C) \>7%. 11. History or evidence of cardiac risk. 12. Known history of malignant hypertension.
References
Publications (0)
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