Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2024-517952-37-00 | EU Trial (CTIS) Number |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This is a phase I trial with BYON4228, a humanized monoclonal antibody (mAb) directed against signal regulatory protein (SIRP)α in solid tumors, alone and in combination with pembrolizumab.
This study includes a dose escalation part (Part 1) in which the MTD or OBD and RDE(s) will be determined. This trial includes an expansion part (Part 2) to evaluate efficacy and safety of BYON4228 in combination with pembrolizumab in specific patient cohorts.
BYON4228 is a humanized IgG1 mAb directed against SIRPα. BYON4228 binds SIRPα expressed on innate immune cells, especially monocytes, macrophages and neutrophils. BYON4228 blocks binding of SIRPα to CD47 and inhibits signaling through the CD47-SIRPα axis.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| BYON4228 + Pembrolizumab | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BYON4228 + Pembrolizumab | Drug | BYON4228 is a humanized monoclonal antibody (mAb) directed against SIRPα. BYON4228 IV infusion every three weeks until disease progression or unacceptable toxicity. Different doses. Pembrolizumab IV infusion (200 mg) every three weeks from the second treatment cycle onwards. |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of Dose-Limiting Toxicities | 21 days | |
| Objective Response Rate | Part 2 (expansion): To evaluate the objective tumor response rate (ORR). | 2 years |
Not provided
Not provided
Inclusion Criteria:
Patient with histologically confirmed, locally advanced or metastatic cancer who has progressed on standard therapy or for whom no standard therapy exists:
Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1;
For Part 2 only: at least one measurable cancer lesion as defined by the Response Evaluation Criteria for Solid Tumors (RECIST version 1.1);
Adequate baseline organ function.
Exclusion Criteria:
Key inclusion and exclusion criteria details are listed here, additional requirements may apply.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Institut Jules Bordet | Brussels | Belgium | ||||
| UZ Leuven |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| Leuven |
| Belgium |
| CIOCC Hospital Universitario HM Sanchinarro | Madrid | Spain |
| Hospital Universitario Fundación Jiménez Díaz | Madrid | Spain |
| The Christie NHS Foundation Trust | Manchester | United Kingdom |
| The Royal Marsden | Sutton | United Kingdom |
| ID | Term |
|---|---|
| C582435 | pembrolizumab |
Not provided
Not provided
Not provided