Clinical trial · Interventional
A Phase 1/2a Study Evaluating Allocetra-OTS as Monotherapy or in Combination With Anti-PD-1 Therapy for the Treatment of Advanced Solid Tumor Malignancy
NCT05581719CI-TRIAL-00076164terminatedPhase 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
Why stopped (as posted): Sponsor decision
Summary
Brief summary (as posted)
This is an open-label, non-randomized, multicenter, Phase 1/2a study to evaluate the safety and potential efficacy of Allocetra-OTS in the treatment of advanced solid tumor malignancy as monotherapy or in combination with an anti-PD-1 therapy.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Peritoneal Cancer | Malignant Peritoneal Neoplasm | ALIAS | 0.90 |
| Peritoneal Metastases | — | UNRESOLVED | — |
| Solid Tumor | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Allocetra-OTS | Drug | — | UNRESOLVED |
| Nivolumab | Drug | Nivolumab | ALIAS |
| Tislelizumab | Drug | Tislelizumab | ALIAS |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Stage 1 (Allocetra-OTS monotherapy)
- description
- Dose escalation of Allocetra-OTS up to 10 x 10\^9 cells by IV or IP administration.
- interventionNames
- Drug: Allocetra-OTS
- type
- EXPERIMENTAL
- label
- Stage 2.1 (Allocetra-OTS in combination with anti-PD-1 therapy)
- description
- Dose escalation of Allocetra-OTS up to 10 x 10\^9 cells by IV or IP administration, with IV nivolumab 240 mg.
- interventionNames
- Drug: Allocetra-OTS
- Drug: Nivolumab
- type
- EXPERIMENTAL
- label
- Stage 2.2 (Allocetra-OTS in combination with anti-PD-1 therapy)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients must have histologically or cytologically confirmed locally advanced, unresectable or metastatic solid tumors, that have relapsed or have been refractory to available approved therapies, or patients who are not eligible for or declined additional standard of care systemic therapy. Patients with peritoneal carcinomatosis can be eligible if an appropriate IP catheter or port can be placed. 2. Patients must have measurable disease. 3. Age ≥ 18 years old. 4. ECOG performance status ≤1. 5. Adequate renal function, hepatic function, and bone marrow function. Exclusion Criteria: 1. Primary central nervous system (CNS) malignancy or CNS involvement, unless stable clinically. 2. Clinically significant uncontrolled infection, autoimmune or inflammatory diseases requiring systemic immunosuppression, clinically significant cardiovascular disease, severe pulmonary diseases or additional malignancies. 3. \[For patients in Stage 2\] Patients who previously experienced an ICI-related adverse reaction that resulted in discontinuation of the ICI.
References
Publications (0)
Data not yet available
No reference posted for this study.