1.Product:FB704A
2.Mass production date:NA
3.Effect on company finances and business:
(1)New drug name or code:FB704A
(2)Purpose:
   A. For the treatment of severe asthma.
   B. Information Website: NA
(3)Planned development stages：Phase II clinical trial/ Phase III clinical trial/NDA
(4)Current development stage:
A.File application/approved/disapproved/Each of clinical trials (include interim analysis):FB704A, an anti-IL6 fully human monoclonal antibody developed by the proprietary platform of Oneness Bio, is safe to proceed with a phase 2 clinical trial in severe asthma under US FDA IND.
B.Once disapproved by competent authority or each of clinical trials (include  interim analysis) results less than statistically significant sense, the risks & the associated measures the Company may occur: NA
C.After obtaining official approval or the results of statistically significant sense, the future strategy: NA
D.Accumulated investment expenditure incurred:No disclosure of the investment expenditure at the moment in consideration of the future marketing strategies to protect the company and investors interests.
(5)Upcoming development plan:phase II / III clinical trial
    A.Scheduled completion date:The completion schedule will be subject to the trial timeline and regulatory review.
    B.Estimate responsibilities: NA
(6)Market:
    16.7 million population are affected by severe asthma which is refractory and causes huge medical burden. There are currently only a few biologics     approved for treatment of eosinophilic severe asthma whereas there remains no effective drugs to control neutrophilic and mixed granulocytic severe  asthma.IL-6 is the potential key cytokine to the pathogenesis of these two subtypes in severe asthma.
4.Any other matters that need to be specified:
(1)It is evaluated that FB704A (anti-IL6 mAb) may improve symptoms of neutrophilic and mixed granulocytic severe asthma by inhibition of classic and trans-signaling pathways of IL-6. Among the patients with these two subtypes of severe asthma, it is likely that FB704A may reduce Th1, Th2 and Th17 inflammation as well as airway hyper-responsiveness.
(2)The Company filed a phase 2 clinical trial application for FB704A in treatment of neutrophilic asthma to TFDA. TFDA has not approved it yet as it is under rebuttal procedure with regards to TFDA’s comments.
(3)According to Article 2 under Guidelines by Taipei Exchange on the Material Information Announced by Listed and OTC Companies, new drug development companies shall make public announcement when filing application for clinical trials or new drug application to domestic or overseas regulatory receiving approval or disapproval, obtaining the statistical date of endpoints authorities, in each clinical trial (including interim analysis), or receiving approval or disapproval on drug license application.
(4)It takes considerable time and expenses to develop a new drug of which success can’t be guaranteed. Investors shall bear such investment risk that warrants careful assessment before making investment decisions.