Clinical trial · Interventional
Efficacy of PD-1 Inhibitor Combination Therapy in Non-small Cell Lung Cancer Patients Who Have Not Achieved Major Pathologic Response After Neoadjuvant Immunotherapy: a Multicenter, Phase II Clinical Trial
NCT06620822CI-TRIAL-00081219not yet recruitingPhase 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)
Exploring the efficacy of PD-1 inhibitor combination therapy strategies for adjuvant therapy in a population that has not achieved major pathological regression after neoadjuvant immunotherapy for non-small cell lung cancer: a multicenter, phase II clinical study
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 |
|---|---|---|---|
| Non Small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| IBI310+Sintilimab | Drug | — | UNRESOLVED |
| IBI363 | Drug | — | UNRESOLVED |
| LM-108+Sintilimab | Drug | — | UNRESOLVED |
| Sintilimab | Drug | Sintilimab | ALIAS |
Design
Arms and outcomes
Arms (4)
- type
- ACTIVE_COMPARATOR
- label
- Sintilimab
- interventionNames
- Drug: Sintilimab
- type
- EXPERIMENTAL
- label
- LM-108+Sintilimab
- interventionNames
- Drug: LM-108+Sintilimab
- type
- EXPERIMENTAL
- label
- IBI310+Sintilimab
- interventionNames
- Drug: IBI310+Sintilimab
- type
- EXPERIMENTAL
- label
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Subjects ≥ 18 years of age on the day of signed informed consent, male or female, and willing to follow study procedures; 2. ECOG score of 0 \~ 1; 3. Patients with resectable clinical stage II-IIIB (N2 only) NSCLC prior to neoadjuvant as assessed by the investigator (AJCC 8th ed.) and who are receiving 3 to 4 courses of standard PD-1 monoclonal antibody in combination with chemotherapy (platinum-containing two-agent chemotherapy) as neoadjuvant therapy during the neoadjuvant phase 4. Pathological evaluation of tumor for MPR (less than 10% residual tumor cells from the primary tumor) and specific remission rate (1 - residual tumor/primary tumor) 5. Subjects must have had complete resection of the NSCLC (no residual tumor and all surgical margins negative) 6. Histologically or cytologically confirmed squamous or non-squamous NSCLC. Exclusion Criteria: 1. Subjects who have undergone segmental lung resection or wedge resection only, and subjects who have not undergone systemic or lobe-specific lymph node dissection; 2. Postoperative treatment with off-protocol antitumor therapy (e.g., radiotherapy, chemotherapy, targeted therapy, other immunotherapies, etc.; antitumor herbal therapies require a 2-week washout period); 3. Severe grade 3 or higher irAE or severe organ damage during neoadjuvant immunotherapy; 4. Previous history of allogeneic bone marrow or organ transplantation; 5. Previous or current interstitial pneumonitis/lung disease requiring systemic hormone therapy; 6. Uncontrolled hypertension (blood pressure ≥150/90 mmHg at rest), with antihypertensive medications maintained at a stable dose for 7 days prior to the first dose of study drug; 7. Combination of other malignant tumors within 5 years prior to the first dose of study drug that require active treatment, except for tumors cured in the opinion of the investigator;
References
Publications (0)
Data not yet available
No reference posted for this study.