Drug intelligence / Profile preview

LLP2A-alendronate (University of California, Davis)

Development stage
Phase 1
Lead developer
University of California, Davis
Modality
Peptide-Drug Conjugates → Peptide Conjugates → Peptides, Small Molecules
Administration
Intravenous
01

Overview

LLP2A-alendronate is a bone-targeted peptidomimetic conjugate designed to promote bone formation and repair by recruiting mesenchymal stem cells (MSCs) directly to the bone surface. The molecule consists of two functional moieties: **alendronate**, a bisphosphonate that provides high affinity for the bone mineral hydroxyapatite, and **LLP2A**, a high-affinity peptidomimetic ligand that specifically targets the active conformation of **integrin alpha-4 beta-1** (VLA-4) expressed on MSCs. By anchoring to the bone surface via the alendronate component, the conjugate creates a localized concentration of LLP2A that acts as a "homing beacon" for circulating or resident MSCs. Once recruited, these stem cells differentiate into osteoblasts, thereby increasing bone mass and strength. This approach is being investigated as an anabolic (bone-building) therapy for conditions characterized by bone loss or poor healing, such as osteoporosis and osteonecrosis.

Other names
LLP2A-alendronate conjugateLLP-2A-alendronate conjugateLLP 2A-alendronate conjugateLLP2A-bisphosphonate conjugateLLP-2A-bisphosphonate conjugateLLP 2A-bisphosphonate conjugate
02

Targets

FDPS (Farnesyl pyrophosphate synthase)α4β1 (Integrin α4β1)

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