On #RareDiseaseDay & every day, we leverage AI to repurpose drugs to treat #RareDiseases like TTR Amyloidosis, Phenylketonuria, Tardive Dyskinesia or Duchenne Muscular Dystrophy.
ℹWe’re carrying out a Phase 2b clinical trial to treat Chorea in Huntington’s Disease. #CareForRare
Working with @caixabank to find investors in the European market and close a €32M #seriesb round to continue advancing in the development of drugs for the treatment of #rarediseases.
Article by @expansioncom : https://t.co/VmJPqOLlg0
SOM Biotech yesterday announced that it signed a licensing agreement with the University of Minnesota.
You can find out more about this by following the link: https://t.co/Fn6eMhPYy2
#drugdiscovery#licensing
@SOMBiotech will be presenting at the International #Duchenne Congress organized by @DPPSpain from the 13th to the 15th of May. The presentation will be dedicated to the repurposing strategies for this devastating muscle-wasting disease appearing in newborns.
#CongresoDPPS22
We are happy to attend Outsourcing in Clinical Trials Europe 2022 on the 4th and 5th of May in Barcelona. It is a great opportunity to learn about the latest innovations and insights.
https://t.co/y84YQcFG82
#clinicaltrials#OCT
We are attending this year’s BIO-Europe Spring Virtual Conference.
We look forward to hearing from industry experts and holding discussions with new partners.
To schedule a meeting with SOM Biotech, click here: https://t.co/6Sr1Dt0o4T
#BIOEurope22#SOMBiotech
Yesterday our CEO, Raúl Insa participated, as a former winner of #EmprendedorXXI Awards, in the round table “Launching and scaling tech companies in Europe. A view from Spanish and Israeli founders” at Day One Innovation Summit Catalonia in the framework of #4YFN22.
Currently approved treatments for #Huntington’s disease are associated with a number of severe side effects. That’s why #RareDiseaseDay is important, as we aim to encourage education and further research into Rare Diseases, to address these unmet needs. https://t.co/5cioz0B1i0
Phenylketonuria (PKU) occurs in an estimated 1 in 23,390 births globally.
This #RareDiseaseDay, PKU sufferer, Michelle teamed up with @Eurordis to tell her story. Read here: https://t.co/FTGJgB4c5o
#HuntingtonsDisease is a rare inherited neurodegenerative disorder of the central nervous system. Join us in supporting #RareDiseaseDay and raise awareness and generate change for those living with rare diseases, including Huntington’s. https://t.co/5cioz0B1i0
Today is #RareDiseaseDay 2022!
At SOM we recognize the importance of raising awareness and progressing scientific research in the field of #rarediseases.
Join us and get involved today: https://t.co/aeGTHI9tmy
We are soon approaching #RareDiseaseDay 2022!
Did you know that over 300 million people from around the world have a rare disease? Learn more and get involved at: https://t.co/5cioz0B1i0
We are excited to virtually attend this year’s BIO at J.P. Morgan and discuss our proprietary drug discovery platform SOMAIPRO.
#JPM22#healthcare#drugdiscovery
https://t.co/glsCpuHd1r
Our Newsletter for Q4 of 2021 has been launched. Find it here https://t.co/RSrBINHwtm
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We wish you a Merry Christmas and a Happy New Year!
We have signed a letter of intent with Megapharm regarding a potential distribution agreement for the commercialization of SOM3355 to treat chorea symptoms in Huntington’s disease in Israel and the Palestinian Authority. Read more here: https://t.co/KGmtBcuQRe
We are excited to present “SOM Biotech: Drug repurposing for Rare diseases” at the Open Innovation Madrid Norte Forum on science and technology today.
For more information, click here: https://t.co/y6f32lBzvJ