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Dow Jones News
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Probiodrug to attend BIO Europe Spring in March 2019

Dow Jones received a payment from EQS/DGAP to publish this press release.

DGAP-Media / 2019-03-12 / 07:00 
 
*Probiodrug to attend BIO Europe Spring in March 2019* 
 
*HALLE (SAALE), Germany, 12 March 2019* - Probiodrug AG ("Probiodrug", 
Euronext: PBD), a clinical stage biopharmaceutical company developing novel 
therapeutic solutions to treat Alzheimer's disease, announces that the 
company is scheduled to attend the following conference: 
 
*(1) *BIO Europe Spring [1] 
 
March 25-27, 2019, Messe Wien Exhibition and Congress Center, Vienna, 
Austria 
*Dr. Ulrich Dauer, CEO, and Dr. Michael Schaeffer, CBO, to attend and host 
meetings* 
 
At BIO-Europe Spring, there are plenty of opportunities to network - between 
partnering meetings, program sessions, during lunch, receptions, in the 
exhibition, and our special evening networking receptions. 
 
### 
 
*For more information, please contact:* 
*Probiodrug * 
Dr. Ulrich Dauer, CEO 
Email: contact@probiodrug.com 
 
*MC Services AG* 
Anne Hennecke, Susanne Kutter 
Tel: +49 (0) 211 529 252 27 
Email: probiodrug@mc-services.eu 
 
*Notes to Editors: 
About Probiodrug AG* 
Headquartered in Halle (Saale), Germany, Probiodrug AG (Euronext Amsterdam: 
PBD) is a clinical stage biopharmaceutical company focused on the 
development of new therapeutic products for the treatment of Alzheimer's 
disease (AD). Probiodrug has identified a new therapeutic concept linked to 
disease initiation and progression. The development approaches are targeting 
a key neuro-/synaptotoxic component of the pathology, pyroglutamate-Abeta 
(pGlu-Abeta) as a therapeutic strategy. The enzyme Glutaminyl Cyclase (QC) 
plays a central role in this process. 
 
Its lead product, PQ912, has successfully completed a Phase 2a (SAPHIR) 
study. The company's pipeline also includes PBD-C06, an 
anti-pGlu-Abeta-specific monoclonal antibody, in preclinical development. 
Probiodrug has medical use and composition of matter patents related to the 
inhibition of QC and anti-pGlu-Abeta-specific monoclonal antibodies, and 
has, in the Company's view, a leading position in this field of research. 
 
*About PQ912* 
PQ912, is a first-in-class, highly specific and potent inhibitor of 
Glutaminyl Cyclase (QC), the enzyme catalyzing the formation of synaptotoxic 
pGlu-Abeta. PQ912 has shown therapeutic effects in AD animal models. A 
Phase-1 study in healthy young and elderly volunteers revealed a dose 
dependent exposure and showed good safety and tolerability up to the highest 
dose resulting in >90% target occupancy in the spinal fluid. In June 2017, 
Probiodrug announced top-line data of the Phase 2a SAPHIR trial of PQ912 and 
presented the study results at CTAD 2017. Results strongly support (a) the 
hypothesis of pGlu-Abeta being synaptotoxic and (b) the therapeutic concept 
pursued by Probiodrug. The study provides important guidance how to move 
forward with the development of PQ912 as a disease-modifying drug for AD. 
Altogether, the results make the program highly attractive for further 
development; the company has initiated the preparation of a Phase 2b core 
program. 
www.probiodrug.com [2] 
 
*About Alzheimer's disease* 
Alzheimer's disease is a neurological disorder, which is the most common 
form of dementia, and ultimately leads to death. Today, 50 million people 
live with dementia worldwide, and this number is projected to treble to more 
than 152 million by 2050, as the global population ages. Dementia also has a 
huge economic impact. Alzheimer's has an estimated, global societal cost of 
US$ 1 trillion, and it will become 2 trillion dollar disease by 2030. (World 
Alzheimer Report 2018). 
 
*Forward Looking Statements* 
Information set forth in this press release contains forward-looking 
statements, which involve a number of risks and uncertainties. The 
forward-looking statements contained herein represent the judgment of 
Probiodrug AG as of the date of this press release. Such forward-looking 
statements are neither promises nor guarantees, but are subject to a variety 
of risks and uncertainties, many of which are beyond our control, and which 
could cause actual results to differ materially from those contemplated in 
these forward-looking statements. We expressly disclaim any obligation or 
undertaking to release publicly any updates or revisions to any such 
statements to reflect any change in our expectations or any change in 
events, conditions or circumstances on which any such statement is based. 
 
End of Media Release 
 
Issuer: Probiodrug AG 
Key word(s): Events 
 
2019-03-12 Dissemination of a Press Release, transmitted by DGAP - a service 
of EQS Group AG. 
The issuer is solely responsible for the content of this announcement. 
 
The DGAP Distribution Services include Regulatory Announcements, 
Financial/Corporate News and Press Releases. 
Archive at www.dgap.de 
Language: English 
Company:  Probiodrug AG 
          Weinbergweg 22 
          06120 Halle/Saale 
          Germany 
Phone:    +49 (0)345 555 9900 
Fax:      +49 (0)345 555 9901 
E-mail:   contact@probiodrug.de 
Internet: www.probiodrug.de 
ISIN:     DE0007921835 
WKN:      792183 
Listed:   Regulated Unofficial Market in Berlin, Frankfurt, Munich, 
          Stuttgart; Amsterdam 
 
End of News DGAP Media 
 
786049 2019-03-12 
 
 
1: https://link.cockpit.eqs.com/cgi-bin/fncls.ssp?fn=redirect&url=e79c5669117b1e03b0f2344537b241cb&application_id=786049&site_id=vwd&application_name=news 
2: https://link.cockpit.eqs.com/cgi-bin/fncls.ssp?fn=redirect&url=d41768cf065bad2dae80502271452537&application_id=786049&site_id=vwd&application_name=news 
 

(END) Dow Jones Newswires

March 12, 2019 02:00 ET (06:00 GMT)

© 2019 Dow Jones News
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