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Gedeon Richter: Cariprazine is well tolerated in the early stage of schizophrenia and has a positive effect on engagement compared to another antipsychotic


Gedeon Richter: Cariprazine is well tolerated in the early stage of schizophrenia and has a positive effect on engagement compared to another antipsychotic
Between the 10-13
was held virtually due to the COVID-19 pandemic situation -
new analysis of cariprazine studies with patients experiencing acute or predominant negative symptoms (PNS) of schizophrenia was presented by Gedeon Richter Plc. According to the scientific posters, cariprazine significantly improved patient engagement in individuals suffering from PNS compared to risperidone, and the co-administration of cariprazine with other antipsychotic medications did not show an unexpected safety profile nor overlapping toxicities. It was also shown that cariprazine was well-tolerated in the early stage of the illness (first five years) and the discontinuation rates due to unbearable side effects were also low. ....

United States , Italian Stock Exchange Reuters , Meeting Of The European Psychiatric Association , Gedeon Richter Plc , Gedeon Richter , Annual Meeting , European Psychiatric Association , Negative Syndrome Scale , Brand Name , Recordati Spa , Western European , Central Eastern Europe , Western Europe , Central Nervous System , Italian Stock Exchange , North Africa , South American , ஒன்றுபட்டது மாநிலங்களில் , இத்தாலிய ஸ்டாக் பரிமாற்றம் ராய்ட்டர்ஸ் , சந்தித்தல் ஆஃப் தி ஐரோப்பிய மனநல சங்கம் , கேதெோன் பணக்காரர் ப்ல் , கேதெோன் பணக்காரர் , ஆண்டு சந்தித்தல் , ஐரோப்பிய மனநல சங்கம் , எதிர்மறை நோய்க்குறி அளவு , பிராண்ட் பெயர் ,

Investegate |RECORDATI Announcements | RECORDATI: RECORDATI: LICENSE OBTAINED FOR THE COMMERCIALIZATION OF ELIGARD IN EUROPE AND OTHER COUNTRIES


RECORDATI: LICENSE OBTAINED FOR THE COMMERCIALIZATION OF ELIGARD IN EUROPE AND OTHER COUNTRIES
RECORDATI: LICENSE OBTAINED FOR THE COMMERCIALIZATION OF ELIGARD IN EUROPE AND OTHER COUNTRIES
 
Milan, 29 January 2021 – Recordati announces the closing of a License and Supply Agreement with Tolmar International Ltd, to commercialise Eligard® (leuprorelin acetate), in Europe, Turkey, Russia and other countries. Eligard® is a marketed medicinal product for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy.  
The active ingredient of Eligard® is leuprorelin acetate, a powder which is solubilized with a solvent for subcutaneous injection. Eligard® is available in three different dosages (for 1-month, 3-month and 6-month treatment, respectively) as a single kit containing two syringes. The development of a new device to admin ....

United States , Andrea Recordati , Noris Morano , Italian Stock Exchange Reuters , Astellas Pharma Inc , Tolmar International Ltd , Tolmar International , Supply Agreement , Italian Stock Exchange , North Africa , South American , Studio Noris Morano , ஒன்றுபட்டது மாநிலங்களில் , இத்தாலிய ஸ்டாக் பரிமாற்றம் ராய்ட்டர்ஸ் , இத்தாலிய ஸ்டாக் பரிமாற்றம் , தெற்கு அமெரிக்கன் ,

RECORDATI: LICENSE OBTAINED FOR THE COMMERCIALIZATION OF ELIGARD IN EUROPE AND OTHER COUNTRIES


 
Milan, 29 January 2021 – Recordati announces the closing of a License and Supply Agreement with Tolmar International Ltd, to commercialise Eligard® (leuprorelin acetate), in Europe, Turkey, Russia and other countries. Eligard® is a marketed medicinal product for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy.  
The active ingredient of Eligard® is leuprorelin acetate, a powder which is solubilized with a solvent for subcutaneous injection. Eligard® is available in three different dosages (for 1-month, 3-month and 6-month treatment, respectively) as a single kit containing two syringes. The development of a new device to administer the product which is easier to handle is currently ongoing, following the request from EMA. The regulatory variation is expected to be submitted by 31 October 2021. ....

United States , Andrea Recordati , Noris Morano , Italian Stock Exchange Reuters , Astellas Pharma Inc , Tolmar International Ltd , Tolmar International , Supply Agreement , Italian Stock Exchange , North Africa , South American , Studio Noris Morano , Private Securities Litigation Reform Act , ஒன்றுபட்டது மாநிலங்களில் , இத்தாலிய ஸ்டாக் பரிமாற்றம் ராய்ட்டர்ஸ் , இத்தாலிய ஸ்டாக் பரிமாற்றம் , தெற்கு அமெரிக்கன் , ப்ரைவேட் பத்திரங்கள் வழக்கு சீர்திருத்தம் நாடகம் ,