Clinical trial · Interventional
Dose Finding Study of TNO155 in Adult Patients With Advanced Solid Tumors
An Open-label, Multi-center, Phase I, Dose Finding Study of Oral TNO155 in Adult 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
Why stopped (as posted): Business reasons and not due to any safety concerns
Summary
Brief summary (as posted)
The purpose of this first in human (FIH) trial was to characterize the safety and tolerability of the SHP2 inhibitor TNO155 alone and in combination with EGF816 (nazartinib) and identify a recommended dose for future studies in adult patients with advanced solid tumors in selected indications.
Conditions
Conditions (7)
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 EGFR Mutant Non Small Cell LungCancer (NSCLC) | Lung Non-Small Cell Carcinoma | ALIAS | 0.85 |
| Advanced Gastrointestinal Stromal Tumors (GIST) | Gastrointestinal Stromal Tumor | CURATED_BROADER | 0.80 |
| Advanced NRAS/BRAFT wt Cutaneous Melanoma | — | UNRESOLVED | — |
| Esophageal Squamous Cell Cancer (SCC) | Esophageal Squamous Cell Carcinoma | ALIAS | 0.85 |
| Head/Neck SCC | — | UNRESOLVED | — |
| KRAS G12-mutant NSCLC | — | UNRESOLVED | — |
| Melanoma | Melanoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| TNO155 | Drug | — | UNRESOLVED |
| TNO155 in combination with EGF816 (nazartinib) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- TNO155
- description
- TNO155 for oral administration
- interventionNames
- Drug: TNO155
- type
- EXPERIMENTAL
- label
- TNO155 in combination with EGF816 (nazartinib)
- description
- TNO155 in combination with EGF816 (nazartinib) in patients with advanced EGFR mutant NSCLC
- interventionNames
- Drug: TNO155 in combination with EGF816 (nazartinib)
Primary outcomes (4)
- measure
- Number of participants with adverse events and serious adverse events
- timeFrame
- up to 5 years; at least once per treatment cycle
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 99 Years
Show eligibility criteria text
Inclusion Criteria: 1. Able to understand and voluntarily sign the ICF and able to comply with the study visit schedule and the other protocol requirements. 2. Patient (male or female) ≥18 years of age willing to agree to not father a child/become pregnant and comply with effective contraception criteria. 3. Must have progressed following standard therapy, or for whom, in the opinion of the Investigator, no effective standard therapy exists, is tolerated or is appropriate. 4. ECOG (Eastern cooperative oncology group) performance status ≤2 Additional criteria only appying to TNO155 in combination with EGF816 (nazartinib): 5. Patients must be screened for Hepatitis B virus and Hepatitis C virus Exclusion Criteria: 1. Tumors harboring known activating KRAS, NRAS, HRAS, BRAF or PTPN11 (SHP2) mutations. (Exceptions are KRAS G12-mutant NSCLC's) 2. History or current evidence of retinal vein occlusion (RVO) or current risk factors for RVO. 3. Any medical condition that would, in the investigator's judgment, prevent the patient's participation in the clinical study due to safety concerns or compliance with clinical study procedures. 4. Clinically significant cardiac disease. 5. Active diarrhea or inflammatory bowel disease 6. Insufficient bone marrow function 7. Insufficient hepatic and renal function. Additional criteria only appying to TNO155 in combination with EGF816 (nazartinib): 8. Patients with a known history of human immunodeficiency virus (HIV) seropositivity. 9. Patients receiving concomitant immunosuppressive agents or chronic corticosteroids use at the time of study entry. 10. Patients who have undergone a bone marrow or solid organ transplant 11. Patients with a history or presence of interstitial lung disease or interstitial pneumonitis 12. Bullous and exfoliative skin disorders at screening of any grade 13. Presence of clinically significant ophthalmological abnormalities that might increase the risk of corneal epithelial injury
References
Publications (0)
Data not yet available