Drug intelligence / Profile preview

Opal (Cullinan Oncology)

Development stage
Preclinical
Lead developer
Cullinan Therapeutics
01

Overview

Opal (Cullinan Oncology): sourced facts only. name: "In a competition ELISA assay, Opal effectively blocked wt PD1 from binding to PDL1 and PDL2." [DOI:10.1158/1538-7445.am2022-2076]; target: "In a competition ELISA assay, Opal effectively blocked wt PD1 from binding to PDL1 and PDL2." [DOI:10.1158/1538-7445.am2022-2076]; target: "In a competition ELISA assay, Opal effectively blocked wt PD1 from binding to PDL1 and PDL2." [DOI:10.1158/1538-7445.am2022-2076]; developer: "1Cullinan Oncology, Inc., Cambridge, MA." [DOI:10.1158/1538-7445.am2022-2076]; modality: "Opal is a conditional 4-1BB agonistic fusion protein comprising trimerized 4-1BB ligand and a high affinity variant of the extracellular domain of PD-1" [DOI:10.1158/1538-7445.am2022-2076]; stage: "When tumor-bearing mice were treated IP with Opal at 1 mg/kg, 7/10 mice exhibited durable cures without significant body weight loss." [DOI:10.1158/1538-7445.am2022-2076]

02

Targets

CD274 (Programmed cell death protein 1 ligand 1)PDCD1LG2 (Programmed cell death 1 ligand 2)

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