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 |