The financing was led by US-based Octave Life Sciences and included major Korean venture funds Smilegate Investment as co-lead, along with InterVest, Magna Investment and LB Investment, all series A investors.
Individual shareholders/co-founders and employees from US and Korea also participated in this financing.
The new round of financing adds to the USD 16.6m the company secured in March, 2018.
Proceeds will be used by Neuraly to advance a clinical candidate targeting neurodegenerative diseases into Phase II studies, by Precision Molecular to advance several neuroinflammation imaging agents into Phase I and Phase II trials, and by Theraly to advance a preclinical candidate targeting fibrosis into a Phase I/II trial.
Neuraly's lead asset is NLY01, a potent, long-acting glucagon-like peptide-1 receptor (GLP-1R) agonist.
NLY01 is being developed as an agent with the potential to slow the progression of neurodegenerative disorders including Parkinson's disease and Alzheimer's disease through inhibition of microglial activation and the resulting neuroinflammation.
Phase II clinical trials for Parkinson's and Alzheimer's are expected to be initiated in 2019 and 2020, respectively.
Precision Molecular is advancing four clinical stage and one IND-enabling stage PET imaging agents for early detection and management of neuroinflammation in Alzheimer's and Parkinson's patients.
Clinical agents include those targeting proteins expressed in activated microglia and proteins involved in neuroinflammation.
Non-invasive imaging of these cells and proteins may provide a direct approach to test new medications such as NLY01 for the therapeutic potential to reduce microglia-associated neuroinflammation and help identify early stage and asymptomatic patients.
The company aims to receive the first-ever FDA approval for such agents and open up new opportunities for the diagnostic market.
Theraly Fibrosis' lead candidate, TLY012, selectively targets myofibroblasts, cells believed to be the critical originators of fibrosis, a condition that affects a range of tissues.
TLY012 reversed established fibrosis in preclinical models of the disease in liver, pancreas and skin and has the potential to cure fibrotic diseases, including systemic sclerosis, liver fibrosis/cirrhosis, and chronic pancreatitis, as well as fibrosis-driven cancers.
Phase I/II trials are expected to be initiated in 2020 for chronic pancreatitis and NASH/liver fibrosis.
D and D Pharmatech is a clinical-stage global biotechnology company that funds the development of revolutionary medicines through disease-specific subsidiary companies founded and guided by top-tier medical research faculty.
This corporate structure creates a unique opportunity to accelerate translation of cutting-edge research into lifesaving therapeutic products for patients.
The company's product pipeline focuses on a range of indications including neurodegenerative and fibrotic diseases. D and D Pharmatech is the parent company of US-based Neuraly Inc., Theraly Fibrosis Inc., and Precision Molecular Inc.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA