Clinical trial · Interventional
A Study of Oncobax®-AK in Patients With Advanced Solid Tumors
A Phase 1/2 Study of Oncobax®-AK Administered in Combination With Immunotherapy To Patients With Advanced Solid Tumors
- 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)
Akkermansia muciniphila is a naturally occurring bacterium found in the healthy human gastrointestinal tract. Analysis of the gut microbiota of NSCLC or RCC patients shows that the presence of Akkermansia is associated with the clinical efficacy of immunotherapy. In preclinical models, oral administration of the Akkermansia p2261 strain reverses resistance to PD-1 blockade. In the clinical setting, it is therefore hypothesized that the oral administration of Oncobax®-AK to cancer patients under immunotherapy, but whose gut microbiota is deficient in Akkermansia will restore / improve the efficacy of immunotherapy in patients with NSCLC or RCC.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Carcinoma, Non-Small-Cell Lung | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| Carcinoma, Renal Cell | Renal Cell Carcinoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Live Bacterial Product - Akkermansia muciniphila | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Phase 2 - NSCLC
- description
- Oncobax-AK (1 capsule) will be administered daily until PD\< excessive toxicity or withdrawal of consent
- interventionNames
- Other: Live Bacterial Product - Akkermansia muciniphila
- type
- EXPERIMENTAL
- label
- Phase 2 -RCC
- description
- Oncobax-AK (1 capsule) will be administered daily until PD\< excessive toxicity or withdrawal of consent
- interventionNames
- Other: Live Bacterial Product - Akkermansia muciniphila
Primary outcomes (1)
- measure
- Objective Response Rate
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age \> 18 years 2. Histologically confirmed Stage IV non-squamous NSCLC or clear cell RCC 3. NSCLC-specific criterion: Best tumor response (by iRECIST) as Stable Disease 4. NSCLC-specific criterion: PD-L1 expression \> 50% 5. ECOG Performance Status = 0-1 6. Negative stool PCR test for Akkermansia 7. At least one measurable lesion per iRECIST 8. Hemoglobin ≥ 100 g/L 9. Albumin \> 35 g/L 10. Signed informed consent Exclusion Criteria: 1. Symptomatic brain metastases 2. AST or ALT \> 5 x ULN 3. Calculated creatinine clearance \< 45 ml/min 4. Auto-immune diseases requiring systemic therapy 5. Immunosuppressive therapy (\> 10 mg prednisone/day equivalent) 6. Radiotherapy (\> 30 Gy) to the lung(s) within 6 months of signed informed consent 7. Active infection 8. Co-morbidities that may increase the risk of treatment-related adverse events 9. Pregnancy 10. Inability to comply with protocol-specific assessments
References
Publications (2)
- BACKGROUNDDerosa L, Routy B, Thomas AM, Iebba V, Zalcman G, Friard S, Mazieres J, Audigier-Valette C, Moro-Sibilot D, Goldwasser F, Silva CAC, Terrisse S, Bonvalet M, Scherpereel A, Pegliasco H, Richard C, Ghiringhelli F, Elkrief A, Desilets A, Blanc-Durand F, Cumbo F, Blanco A, Boidot R, Chevrier S, Daillere R, Kroemer G, Alla L, Pons N, Le Chatelier E, Galleron N, Roume H, Dubuisson A, Bouchard N, Messaoudene M, Drubay D, Deutsch E, Barlesi F, Planchard D, Segata N, Martinez S, Zitvogel L, Soria JC, Besse B. Intestinal Akkermansia muciniphila predicts clinical response to PD-1 blockade in patients with advanced non-small-cell lung cancer. Nat Med. 2022 Feb;28(2):315-324. doi: 10.1038/s41591-021-01655-5. Epub 2022 Feb 3. PMID 35115705
- BACKGROUNDDerosa L, Routy B, Fidelle M, Iebba V, Alla L, Pasolli E, Segata N, Desnoyer A, Pietrantonio F, Ferrere G, Fahrner JE, Le Chatellier E, Pons N, Galleron N, Roume H, Duong CPM, Mondragon L, Iribarren K, Bonvalet M, Terrisse S, Rauber C, Goubet AG, Daillere R, Lemaitre F, Reni A, Casu B, Alou MT, Alves Costa Silva C, Raoult D, Fizazi K, Escudier B, Kroemer G, Albiges L, Zitvogel L. Gut Bacteria Composition Drives Primary Resistance to Cancer Immunotherapy in Renal Cell Carcinoma Patients. Eur Urol. 2020 Aug;78(2):195-206. doi: 10.1016/j.eururo.2020.04.044. Epub 2020 May 4. PMID 32376136