Clinical trial · Interventional
SHR1459 in Combination With YY-20394 in Recurrent and Refractory B-cell Non-Hodgkin's Lymphoma
A Phase I/ II Study of SHR1459 in Combination With YY-20394 in Recurrent and Refractory B-cell Non-Hodgkin's Lymphoma in Adults
NCT04948788CI-TRIAL-00054111unknownPhase 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)
The study is evaluating the efficacy, and safety of SHR1459 combined with YY-20394 for Recurrent and refractory B-cell non-Hodgkin's lymphoma in adults.
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 |
|---|---|---|---|
| Recurrent and Refractory B-cell Non-Hodgkin's Lymphoma | B-Cell Malignant Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Gemcitabine-Oxaliplatin | Drug | — | UNRESOLVED |
| SHR1459 ;YY-20394 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- SHR1459 + YY-20394 (Stage 1)
- interventionNames
- Drug: SHR1459 ;YY-20394
- type
- EXPERIMENTAL
- label
- SHR1459 + YY-20394 (Stage 2)
- interventionNames
- Drug: SHR1459 ;YY-20394
- type
- EXPERIMENTAL
- label
- GemOx (Stage 2)
- interventionNames
- Drug: Gemcitabine-Oxaliplatin
Primary outcomes (2)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically confirmed diagnosis of B-cell NHL such as DLBCL, FL and MCL 2. Patients received at least 2 lines of systemic therapy 3. Previously received anti- CD20 treatment 4. Patients in stage II should also be unsuitable or unwilling to receive allogeneic hematopoietic stem cell transplantation 5. Patients must have an acceptable organ function Exclusion Criteria: 1. Previously treated with PI3K inhibitors or BTK inhibitors 2. Unresolved toxicity of CTCAE grade \> 1 from prior anti-lymphoma therapy 3. Chemotherapy or other investigational therapy within 28 days (or 5 times the half-life time, whichever is shorter) before starting cycle 1 4. Significant concurrent medical disease or condition which according to the investigators' judgement 5. Active hepatitis B, C or HIV infection 6. Infection requiring treatment 2 weeks prior to the first dosing
References
Publications (0)
Data not yet available
No reference posted for this study.