Clinical trial · Interventional
Evaluation of Safety and Efficacy of IBI318 Monotherapy for Relapsed/Refractory Extranodal NK/T Cell Lymphoma (Nasal Type) Trial
Evaluation of Safety and Efficacy of IBI318 Monotherapy for Relapsed/Refractory Extranodal NK/T Cell Lymphoma (Nasal Type), a Multicenter, Open-label Phase Ib/II Trial
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Due to the company's development strategy adjustment, Innovent Biologics has decided not to continue this study after consultation with investigators.
Summary
Brief summary (as posted)
The purpose of this study is to evaluate the safety and efficacy of IBI318 monotherapy for relapsed/refractory extranodal NK/T cell lymphoma (nasal type).
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 |
|---|---|---|---|
| Extranodal NK/T Cell Lymphoma, Nasal Type | Extranodal NK-/T-Cell Lymphoma, Nasal Type | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| IBI318(Recombinant human anti-PD1/PD-L1 bispecific antibody) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Previously received anti-PD1/PD-L1 antibodies
- description
- Patients previously received anti-PD1/PD-L1 antibodies, except for those were primarily refractory to them.
- interventionNames
- Drug: IBI318(Recombinant human anti-PD1/PD-L1 bispecific antibody)
- type
- EXPERIMENTAL
- label
- Patients previously never received anti-PD1/PD-L1 antibodies
- description
- Patients previously never received anti-PD1/PD-L1 antibodies.
- interventionNames
- Drug: IBI318(Recombinant human anti-PD1/PD-L1 bispecific antibody)
Primary outcomes (1)
- measure
- ORR(evaluated by the independent review committee according to Lyric 2016 criteria.)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically diagnosed as extra-nodal NK/T cell lymphoma (nasal type) according to WHO 2016 criteria; 2. Refractory and relapsed ENKTL patients, being relapsed is defined as re-occurrence of the same lymphoma lesions at the primary site or new sites after complete response (CR); being refractory is defined as having any of the following conditions: evaluated as stable disease (SD) or progression disease (PD) after 2 cycles of treatment; not being able to achieve partial response (PR) after 4 cycles of treatment; not being able to achieve complete response (CR) after 6 cycles of treatment. Patients that did not achieve remission, or relapsed/progressed after autologous stem cell transplantation (ASCT) could also be enrolled. 3. Patients must have received asparaginase-based chemotherapy previously (patients with phase I/II disease must have received radiotherapy previously). 4. With measurable foci, defined as: lymph nodes with long diameters\>15mm,extra-nodal foci\>10mm on CT scan; 5. ECOG PS (Eastern Cooperative Oncology Group Performance Status) point 0 or 1; Exclusion Criteria: 1. Invasive NK cell leukemia; 2. Primary CNS lymphoma or CNS-involved lymphoma; 3. Patients with hemophagocytic syndrome; 4. Patients with lymphoma invading large pulmonary vessels; 5. Patients primarily resistant to anti-PD1,PD-L1,PD-L2 antibodies (generally considered as those received anti- PD1,PD-L1,PD-L2 antibodies as monotherapy or in combination with chemotherapy, but did not achieve PR or CR in non-maintenance treatment).
References
Publications (0)
Data not yet available