Powered by NAi’s biology-first Bayesian causal AI, BPGbio has generated a deep and diversified discovery pipeline across wide-range disease areas. This pipeline demonstrates NAi’s capability to uncover novel, high-confidence targets and programs far beyond any single pathway or therapeutic area.
Novel Targets Discovered by NAi
High-confidence and Diversified Areas of Target Biology for Drug Discovery
The 75 targets discovered by the NAi platform span multiple biological mechanisms and disease pathways. Whether it’s mitochondrial metabolism, protein homeostasis, cytoskeletal regulation, signal transduction, or immune modulation, NAi’s causal modeling finds high-value biology across distinct therapeutic domains.
75 | 6 | 5 | 8 |
Target Validation Programs | Drug Discovery Programs | IND Approved | Clinical Development |
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BPGbio Robust Clinical Pipeline
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Indication | Molecule / Asset | Known Activity | Discovery | Hit to Lead | Lead | IND | Phase 1 | Phase 2 |
Clinical Programs | ||||||||
BPM31510-IV | Radiation Sensitizer | |||||||
BPM31510-IV | Chemotherapy Sensitizer | |||||||
BPM31510-IV | Direct Replacement | |||||||
Squamous Cell Carcinoma | BPM31510-T | Wound Healing | ||||||
BPM31510-T | Wound Healing | |||||||
BPM31510-Oral | Mitochondrial Respiration | |||||||
Solid and Liquid Tumors | BRG399 | Tubulin Polymerization | ||||||
Secondary CVD Prevention | BRG399 | Neutrophil Inflammation | ||||||
BPM31510, has received FDA Rare Pediatric Disease Designation for Primary Coenzyme Q10 Deficiency (PCQD) and Epidermolysis Bullosa (EB) respectively. The company is planning a potential pivotal trial in Primary CoQ10 Deficiency. Upon Approval, both designations provide BPGbio eligibility for a Priority Review Voucher (PRV). | ||||||||
Indication | Molecule / Asset | Target Class | Discovery | Hit to Lead | Lead | IND | Phase 1 | Phase 2 |
Drug Discovery Programs | ||||||||
Huntington Disease | BPG812 | Ubiquitin Proteosomal | ||||||
Oncology | BPG1438 | Targeted Protein Degradation | ||||||
Parkinson’s Disease | BRGP0811 | Oxidoreductase Target | ||||||
Oncology | Hit Molecules | DNA RNA Helicases | ||||||
Oncology | Hit Molecules | Ubiquitin Proteosomal | ||||||
Angiogenesis | BRG0001 | |||||||
Novel Target Biology Discovery by the NAi Platform
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Indication | Pathway / Biology Area | # of Targets |
Parkinson’s Disease (19 targets) | Cytoskeleton, adhesion, migration | 8 |
ECM & stromal biology | 2 | |
Stress & metabolic signaling | 4 | |
DNA damage & gene regulation | 2 | |
RNA processing & gene regulation | 3 | |
Alzheimer’s Disease (8 targets) | ER protein folding & UPR | 3 |
Mitochondrial ATP synthesis (OXPHOS) | 2 | |
Cytoskeleton & membrane trafficking | 3 | |
Huntington’s Disease | Autophagy-Proteostasis Cross-Talk | 1 |
Autism (11 targets) | Antigen processing & immunity | 4 |
Apoptosis | 1 | |
ER proteostasis / UPR | 2 | |
RNA metabolism & translation control | 2 | |
GPCR signaling | 1 | |
Mitochondrial ion/metabolic regulation | 1 | |
Oncology (28 Targets) | Protein folding, ER stress & proteostasis | 8 |
RNA processing & translational control | 7 | |
Mitochondrial biology & metabolism | 3 | |
Cytoskeleton & intracellular transport | 4 | |
Signal transduction (phosphatases) | 2 | |
ECM / developmental regulation & chomatin architecture | 4 | |
Diabetes (4 targets) | Energy metabolism: glycolysis & TCA | 3 |
Protein folding / molecular chaperones | 1 | |
Obesity (4 targets) | Extracellular Matrix / Structural Proteins | 2 |
Metabolism / Lipid Biosynthesis | 1 | |
Ubiquitin-Proteasome System / Protein Degradation | 1 | |