Clinical trial · Interventional
A Study to Evaluate the Safety and Efficacy of Max-40279 and Toripalimab in Patients With Advanced Solid Tumors
A Phase 1 Study to Evaluate the Safety and Efficacy of Max-40279-01 in Combination With Toripalimab in Patients With Advanced Solid Tumors
NCT05369286CI-TRIAL-00058421unknownPhase 1ClinicalTrials.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 include two parts, part 1 is a dose escalation study and part 2 is a dose expansion study.
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 |
|---|---|---|---|
| Solid Tumor | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| "MAX-40279-01" and "Toripalimab" | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (5)
- type
- EXPERIMENTAL
- label
- dose level 1 of max-40279 combined dose level 1 of toripalimab
- description
- "MAX-40279-01" and "toripalimab"
- interventionNames
- Drug: "MAX-40279-01" and "Toripalimab"
- type
- EXPERIMENTAL
- label
- dose level 2 of max-40279 combined dose level 1 of toripalimab
- description
- "MAX-40279-01" and "toripalimab"
- interventionNames
- Drug: "MAX-40279-01" and "Toripalimab"
- type
- EXPERIMENTAL
- label
- dose level 2 of max-40279 combined dose level 2 of toripalimab
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Males and/or females over age 18 2. Histologically and/or cytologically documented local advanced or metastatic solid tumor. 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1. 4. Expected survival \>3 months. 5. Signed informed consent form. Exclusion Criteria: 1. Known uncontrolled or symptomatic central nervous system metastatic disease. 2. Adverse events (with exception of alopecia, peripheral sensory neuropathy grade ≤ 2 and those listed in specific exclusion criteria) from any prior anticancer therapy of grade \>1 (National Cancer Institute Common terminology Criteria \[NCI CTCAE\] v.5.0) at the time of randomization. 3. Inadequate organ or bone marrow function. 4. Medical history of difficulty swallowing, malabsorption or other chronic gastrointestinal disease, or conditions that may hamper compliance and/or absorption of the tested product. 5. Pregnant or breast-feeding woman. 6. Known allergies, hypersensitivity, or intolerance to Max-40279-01 the excipients of these treatments.
References
Publications (0)
Data not yet available
No reference posted for this study.