| Entry ID | 595 |
| INN | None |
| Status | Clinical |
| Drug code(s) | ELA026 |
| Brand name | None |
| mAb sequence source | mAb human |
| General Molecular Category | TBD |
| Format, general category | TBD |
| Format details | TBD |
| Isotype (Fc) | IgG1 |
| Light chain isotype | TBD |
| Linker | None |
| Ave. DAR | None |
| Conjugated/fused moiety | None |
| Discovery method/technology | None |
| Target(s) | SIRP alpha |
| Indications of clinical studies | Secondary Hemophagocytic Lymphohistiocytosis |
| Primary therapeutic area | Immune-mediated / inflammatory disorders |
| Most advanced stage of development (global) | Phase 2/3 |
| Status | Active |
| Start of clinical phase (IND filing or first Phase 1) | October 15, 2021 |
| Start of Phase 2 | May 19, 2022 |
| Start of Phase 3 | |
| Date BLA/NDA submitted to FDA | |
| Year of first approval (global) | None |
| Date of first US approval | |
| INN, US product name | None |
| US or EU approved indications | None |
| Company | Electra Therapeutics Inc. |
| Licensee/Partner | None |
| Comments about company or candidate | NCT05416307 Phase 1 study started in May 2023 converted to a Phase 2/3 study in Mar 2025. NCT05556863 Phase 1 study started in Oct 2021. |
| Full address of company | 201 Haskins Way, 5th Floor South San Francisco, CA 94080 North America United States of America https://electra-therapeutics.com/ |
ELA026 is a fully human IgG1 SIRP-directed monoclonal antibody designed to reduce the myeloid and T cells driving the inflammation.
| Anticipated events | None |
| Factor(s) contributing to discontinuation | None |