Non-narcotic Strong Analgesic (TRPV1 Antagonist)
Severe pain is an unbearable thing of mankind
 Non-narcotic Strong Analgesic (TRPV1 Antagonist)
Neuropathic pain is a chronic severe pain caused by damage to the nervous system due to diseases or accidents. So far, the most effective remedy for this disease is a narcotic analgesic drug as like morphine. The serious side effect of morphine is addiction.
TRPV1 Antagonist is more effective than conventional nonsteroidal antiinflammatory agents (aspirin, ibuprofen, etc.) and Tylenol. TRPV1 antagonist is not only less side effect than narcotic analgesics but also has comparable efficacy to narcotic analgesics.

GSK, Eli Lily
Pfizer pre-clinical
Postherpetic neuralgia
Diabetic neuropathy
Cancer pain
 Research & Development

 First In Class 
Agreement for out-license and joint development with Grünenthal (Germany): total deal package 40 million Euro
Showed hyperthermia
Non-clinical trial succeeded with non human primates
-  Solve the hyperthermia problem completely
-  Prove efficacy in non human primates
EMA Preparing Phase 1 clinical trial
 Neuropathic pain analgesics (TRPV1 agonist, topical cream/gel or patch)
New generation of analgesics from TRPV1 agonist not like antagonist

ENDO pharmaceuticals Lidoderm®
Astellas Europe ®
Purdue Pharma opioid patch®
Postherpetic neuralgia
Diabetic neuropathy
Neuropathic back pain
 Research & Development

Clinical candidate selection
Negotiation on going to make partnership with domestic and foreign pharmaceutical companies
  Developing disease modifying drugs for Alzheimer's disease (AD)
 AD Drug Development Strategy
 AD drug development (anti-oligomerization of beta-amyloid)
Mechanism to prevent brain neuronal cell death by blocking aggregation of Αβ in brain

Global pharmaceutical company such as Elan, Allon
 Research & Development

Joint development contract with Daewoong pharma
GLP toxicity study completed
Phase 1 human clinical trial SAD completed
Negotiation with Global Clinical Partner
 AD drug development (RAGE modulator)
Inhibition of interaction Αβ and RAGE(Receptor for Advanced Glycation Endproduct) that can block Αβ influx into brain from plasma

Global pharmaceutical company Pfizer
(vTv Therapeutics)
 Research & Development

Out-license deal with Roche, a multinational pharmaceutical company
(total package $ 290 million)
Efficacy test in animal study
 AD DRUG Development status
❶ α-Secretase activator
❷ β-Secretase Inhibitor
❸ γ-Secretase Inhibitor
Big Pharma has developed ❶and❸ expensing $ 200 to $ 300 million for each company over the past decade, but failed to overcome the side effects Merck, Astellas developing ❷BACE1 Inhibitor
❹ aggregation Inhibitor
A solution that minimizes side effects
Big Pharma's interest in aggregation Inhibitor
Only 6 to 7 bio-ventures developed aggregation Inhibitor worldwide
❺ RAGE antagonist
Worldwide Pfizer and Medifron (Roche) developed RAGE modulator only Preventing Αβ protein from entering the brain
(preventive and therapeutic effects)
❻ Αβ  antibodies
Johnson & Johnson, Lilly, Pfizer Phase Ⅲ failed clinical trial with antibody therapeutics
Roche gantenerumab phase Ⅲ failed
Roche crenezumab prevention therapy on going
❼ QC Inhibitor
Probiodrug (Germany) phase Ⅱ trial on going
Aβ and tau protein pathway block
Tau protein hyperphosphorylation inhibitor
TauRX(Singapore) phase Ⅲ failed
❾ O-GlcNAc Inhibitor
Merck & Co. pre-clinical stage
Tau Hyperphosphorylation inhibitor
  Development of AD Early Diagnosis Kit
Methods for diagnosing AD include cognitive testing mini-mental state examination (MMSE), Magnetic resonance imaging (MRI), positron emission tomography (PET), and spinal fluid examination.
MMSE has the disadvantage of poor accuracy and other methods have high accuracy but high cost. Our AD diagnostic Kit has a relatively high level of accuracy at a low cost. Now we are focused on upgrading for more accurate diagnostic efficacy.

The world's first Alzheimer's Disease Early Diagnosis Kit using human blood sample
 Research & Development
KFDA license for export
Clinical Validation is underway for the approval of domestic products