Clinical trial · Interventional
Clinical Trial of BT02 in Patients With Advanced Solid Tumors
A First-in-Human, Open Label, Phase I/II Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity and Preliminary Antitumor Activity of BT02 in Patients With Advanced Solid Tumors
NCT06404905CI-TRIAL-00084058BT02recruitingPhase 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)
A First-in-Human, Open Label, Phase I/II Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity and Preliminary Antitumor Activity of BT02 in Patients with Advanced Solid 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 Solid Tumor | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| BT02 monoclonal antibody injection | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- BT02 treatment
- description
- BT02 given intravenously administer in patients with advanced solid tumors.
- interventionNames
- Drug: BT02 monoclonal antibody injection
Primary outcomes (3)
- measure
- Dose Limiting Toxicity
- timeFrame
- Within day 28 after administration
- description
- safety
- measure
- Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)
- timeFrame
- Within day 28 after administration
- description
- Safety
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age ≥18 at the time of signing the informed consent form, male or female; 2. Patients must have histologically or cytologically confirmed diagnosis of advanced solid tumor; 3. Adequate organ and hematologic function; 4. Patients must have at least measurable or evaluable lesion in phase I and measurable lesion in phase II according to RECIST 1.1; 5. ECOG performance status 0\~1; 6. Life expectancy ≥ 3 months; 7. Good compliance and be willing to follow-up visit. Exclusion Criteria: 1. Receive treatment before study as below: a) Previous systematic anti-cancer therapy; 2. Active or prior documented autoimmune disease within past 2 years; 3. History of clinically significant cardiovascular disease; 4. Significant acute or chronic infections; 5. Prior toxicities from anti-cancer therapies have not regressed to grade ≤1 severity; 6. Any prior Grade≥3 irAE while receiving immunotherapy; 7. Unstable brain metastasis or meningeal metastasis with clinical symptoms; 8. Patients with mental disorders or poor compliance; 9. Known alcohol or drug abuse; 10. Other severe systemic diseases or conditions that unsuitable for participating in this study in the opinion of the investigator.
References
Publications (0)
Data not yet available
No reference posted for this study.