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Probiodrug to attend International Conferences in June 2019

DGAP-Media / 2019-05-22 / 07:00 
 
*Probiodrug to attend International Conferences in June 2019* 
 
*HALLE (SAALE), Germany, 22 May 2019* - Probiodrug AG ("Probiodrug", 
Euronext: PBD), announces that the company is scheduled to attend the 
following conferences: 
 
*(1) *2019 BIO International Convention [1] 
June 3-6, 2019, Pennsylvania Convention Center, Philadelphia, PA, USA 
*Dr. Ulrich Dauer, CEO, and Dr. Michael Schaeffer, CBO, to attend and host 
meetings* 
 
*(2) Biotech CEO Summit Europe* 
June 17-19, 2019, Enniskerry, Ireland 
*Dr. Ulrich Dauer, CEO, to attend* 
 
### 
 
*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 novel inhibitors for disease relevant enzymes. The company 
has a successful track record in bringing drugs targeted to 
post-translational modifying enzymes to the market. Current projects are 
focusing on the two isoenzymes of Glutaminyl Cyclase, QPCT and QPCTL. QPCT 
is the crucial enzyme for the generation of highly neurotoxic pyroglutamate 
species of Abeta. Its inhibition by Probiodrug's lead molecule PQ912 is 
currently investigated in clinical Phase 2 trials (SAPHIR) for the treatment 
of Alzheimer's disease (AD). Whereas QPCTL has been identified as a 
potential target in cancer therapy. Blocking the enzymatic function of QPTCL 
by small molecule inhibitors is a novel therapeutic approach in cancer 
immunotherapy. Probiodrug has a unique and exceptionally strong patent 
position on QPCT and QPCTL inhibitors. 
www.probiodrug.com 
 
*About PQ912* 
PQ912, is a first in class, highly specific and potent inhibitor of 
Glutaminyl Cyclase (QPCT), - the enzyme that catalyses the formation of 
highly neurotoxic pGlu species. 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 that pGlu species of Abeta are especially neurotoxic and 
correlate with AD disease progression. The SAPHIR 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. 
 
*About Alzheimer's disease* 
Alzheimer's disease is a neurological disorder, which is the most common 
form of dementia. Today, 50 million people live with dementia worldwide, and 
this number is projected to treble to more than 152 million by 2050. 
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). 
 
*Glutaminyl-peptide cyclotransferase-like protein (QPCTL)* 
Glutaminyl-peptide cyclotransferase-like protein (QPCTL) is a 
posttranslational modifying enzyme that is responsible for the pyroglutamate 
formation on crucial proteins in the immune response to cancer. 
 
*Cancer immune checkpoint inhibitors* 
Checkpoint inhibitor therapy is a novel kind of cancer immunotherapy. The 
therapy targets immune checkpoints, key regulators of the immune system that 
stimulate or inhibit its actions, which tumors can use to protect themselves 
from attacks by the immune system. QPCTL inhibitor therapy can block 
inhibitory cancer checkpoints and thereby restore beneficial immune system 
functions. 
 
*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): Advertisement/Communication 
 
2019-05-22 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 
EQS News ID: 813797 
 
End of News DGAP Media 
 
813797 2019-05-22 
 
 
1: https://link.cockpit.eqs.com/cgi-bin/fncls.ssp?fn=redirect&url=a58f73b76e40c85c20ea2f1eedd4f6f5&application_id=813797&site_id=vwd&application_name=news 
 

(END) Dow Jones Newswires

May 22, 2019 01:00 ET (05:00 GMT)

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