Clinical trial · Interventional
Neoadjuvant HRS-4642 Plus Chemotherapy With or Without Immunotherapy for Pancreatic Cancer
An Exploratory Clinical Study of HRS-4642 in Combination With Chemotherapy With or Without Adebrelimab as Neoadjuvant Therapy for Pancreatic Cancer
NCT07691593CI-TRIAL-00117389not 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)
To evaluate the safety and efficacy of neoadjuvant HRS-4642 plus chemotherapy with or without adebrelimab in patients with pancreatic ductal adenocarcinoma.
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 |
|---|---|---|---|
| Pancreatic Cancer | Malignant Pancreatic Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| HRS-4642+NALIRIFOX | Drug | — | UNRESOLVED |
| HRS-4642+NALIRIFOX+Adebrelimab | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Arm 1:HRS-4642+NALIRIFOX
- interventionNames
- Drug: HRS-4642+NALIRIFOX
- type
- EXPERIMENTAL
- label
- Arm 2:HRS-4642+NALIRIFOX+Adebrelimab(4 cycles of neoadjuvant therapy)
- interventionNames
- Drug: HRS-4642+NALIRIFOX+Adebrelimab
- type
- EXPERIMENTAL
- label
- Arm 3:HRS-4642+NALIRIFOX+Adebrelimab(6 cycles of neoadjuvant therapy)
- interventionNames
- Drug: HRS-4642+NALIRIFOX+Adebrelimab
Primary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Male and female participants aged 18-70 (including those who are 18 and 70 years old); 2. Pathologically or cytologically confirmed ductal adenocarcinoma of the pancreas; and subjects must have at least one measurable lesion as defined by Response Evaluation Criteria in Solid Tumors (RECIST, version 1.1); 3. Life expectancy ≥ 12 weeks; 4. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1; 5. Adequate marrow and organ function; Exclusion Criteria: 1. Prior receipt of any anti-tumor therapy, including but not limited to systemic chemotherapy, radiotherapy, interventional therapy, immunotherapy, targeted therapy, and anti-tumor traditional Chinese medicine therapy; 2. Presence of distant metastatic lesions confirmed by imaging; 3. Known hypersensitivity to the investigational drug or any of its excipients; 4. Presence of any serious or uncontrolled systemic disease; 5. History of allogeneic hematopoietic stem cell transplantation or solid organ transplantation; 6. Clinically significant acute or chronic pancreatitis; 7. Participation in any interventional clinical trial involving drugs or medical devices within 4 weeks prior to the first administration of study treatment; 8. Vaccination with live or live-attenuated vaccines within 4 weeks prior to the first dose of the investigational drug; 9. Any other condition that, in the judgment of the investigator, makes the subject unsuitable for enrollment.
References
Publications (0)
Data not yet available
No reference posted for this study.