Clinical trial · Interventional
A Phase 1b/2 Study of Serabelisib in Combination With Canagliflozin in Patients With Advanced Solid Tumors
A Phase 1b/2 Study of Serabelisib in Combination With Canagliflozin in Patients With Advanced Solid Tumors With PIK3CA or KRAS Mutations
NCT04073680CI-TRIAL-00045198unknownPhase 1 / Phase 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 study aims to test the hypothesis that combining serabelisib, a PI3K alpha isoform inhibitor, with an SGLT2 inhibitor, canagliflozin will improve efficacy in the treatment of patients with advanced solid tumors.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Colo-rectal Cancer | — | UNRESOLVED | — |
| Endometrial Cancer | Malignant Endometrial Neoplasm | CURATED_BROADER | 0.80 |
| Head and Neck Cancer | Malignant Head and Neck Neoplasm | ALIAS | 0.90 |
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Canagliflozin 300mg | Drug | — | UNRESOLVED |
| Serabelisib | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Serabelisib
- description
- Part 1 is dose escalation of Serabelisib Cohort 1 = 600mg; Cohort 2 = 900mg; Cohort 3 = 1200mg Part 2 is expansion of mutational cohorts with selected dose as follows: Cohort 4 = PIK3CA-mutated breast cancer; Cohort 5 = PIK3CA-mutated Non breast cancer; Cohort 6 = KRAS mutated
- interventionNames
- Drug: Serabelisib
- Drug: Canagliflozin 300mg
Primary outcomes (4)
- measure
- Rate of Adverse Events
- timeFrame
- 30 days after last dose
- description
- Safety of serabelisib in combination with canagliflozin as evaluated by incidence of drug-related adverse events (AEs), serious adverse events (SAEs), adverse events leading to discontinuation, deaths and clinical laboratory test abnormalities.
- measure
- Rate of Laboratory Abnormalities
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Have histologically or cytologically confirmed locally advanced or metastatic solid tumors. 2. Have a tumor harboring a mutation in PIK3CA or KRAS genes. 3. Have received prior therapy and have recurrent or persistent disease without standard therapies available, or are ineligible to receive standard therapies. 4. Have measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 5. Have Eastern Cooperative Oncology Group performance status (ECOG PS) of ≤2 6. Have adequate organ function. 7. Have adequate birth control during the course of the study. 12\. Are able to receive canagliflozin Exclusion Criteria: 1. Diagnosis of primary brain tumor 2. Untreated brain metastasis or history of leptomeningeal disease 3. Have received prior chemotherapy within 28 days or other anticancer agents within 28 days of 5 half lives (whichever is the shorter duration) before the first administration of study drug. The exception is patients in Cohort 4 (PIK3CA-mutated breast cancer) are allowed to receive ongoing endocrine therapy. 4. Have diabetes mellitus requiring insulin therapy 5. Have diabetes mellitus requiring insulin secretagogue therapy 6. Have poorly controlled diabetes mellitus defined as glycosylated hemoglobin A1c (HbA1c) \>7.5% 7. Have a secondary malignancy requiring therapy or are unstable without therapy. 8. Known impaired cardiac function or clinically significant cardiac disease. 9. Myocardial infarction or unstable angina within 6 months before the first administration of study drug. 10. Pregnant (positive serum pregnancy test) or breastfeeding
References
Publications (0)
Data not yet available
No reference posted for this study.