Drug intelligence / Profile preview

CBP-4888

Development stage
Phase 1
Lead developer
Comanche Biopharma
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous
01

Overview

CBP-4888 is an investigational, placenta-targeted **small interfering RNA** therapy developed by Comanche Biopharma for **sFlt1-mediated preterm preeclampsia**. It is a fixed-dose combination of two chemically synthesized, lipid-conjugated siRNA duplex oligonucleotides designed to silence two soluble fms-like tyrosine kinase 1 messenger RNA isoforms in the placenta, thereby reducing pathological overproduction of soluble fms-like tyrosine kinase 1, a circulating anti-angiogenic driver of maternal vascular dysfunction in preeclampsia. The product is administered by subcutaneous injection and is in Phase 1 clinical development, including a study in hospitalized participants with preterm preeclampsia receiving standard-of-care expectant management. ([comanchebiopharma.com](https://comanchebiopharma.com/comanche-biopharma-receives-us-fda-fast-track-designation-for-cbp-4888-for-the-treatment-of-sflt-1-mediated-pre-term-preeclampsia/))

Other names
siRNA-2283siRNA2283siRNA 2283siRNA-2519siRNA2519siRNA 2519
02

Targets

sFlt-1 (Soluble VEGFR-1)

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