Clinical trial · Interventional
A Study to Evaluate the Efficacy and Safety of QLF31907 Combination Therapy in Patients With Advanced Malignant Tumors
A Phase 1b/2 Trial to Evaluate the Efficacy and Safety of QLF31907 (PD-L1/4-1BB Bi-specific Antibody) Combination Therapy in Patients With Advanced Malignant Tumors
NCT06394713CI-TRIAL-00076621not yet recruitingPhase 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 is designed to evaluate the safety and efficacy of QLF31907 combination therapy in advanced malignant tumors.
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 |
|---|---|---|---|
| Advanced Malignant Neoplasm | Malignant Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Docetaxel | Drug | Docetaxel | ALIAS |
| Irinotecan | Drug | Irinotecan | ALIAS |
| QLF31907 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- QLF31907 in combination with Irinotecan
- interventionNames
- Drug: QLF31907
- Drug: Irinotecan
- type
- EXPERIMENTAL
- label
- QLF31907 in combination with Docetaxel
- interventionNames
- Drug: QLF31907
- Drug: Docetaxel
Primary outcomes (2)
- measure
- phase Ib: Dose-limiting toxicity(DLT)
- timeFrame
- 28 days
- description
- The DLT of QLF31907 combination therapy will be determined
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. subjects voluntarily participated and signed a written informed consent form; 2. age ≥18 years, male or female; 3. ECOG PS 0-1; 4. histopathologically diagnosed advanced malignant tumors; 5. at least 1 measurable lesion according to RECIST v1.1 criteria or Lugano (2014) criteria; 6. adequate organ function; Exclusion Criteria: 1. previous treatment with 4-1BB agonist or 4-1BB recombinant fusion protein; 2. received anti-tumor therapy within 4 weeks prior to the first study treatment; 3. history of autoimmune disease; 4. history of other active malignancies within 3 years prior to the first treatment; 5. history of serous cardiovascular events;
References
Publications (0)
Data not yet available
No reference posted for this study.