Forum: Kiadis Pharma » Kiadis Pharma September 2018 » Pagina: 50

Forum: Kiadis Pharma » Kiadis Pharma September 2018 » Pagina: 50

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Forum: Kiadis Pharma » Kiadis Pharma September 2018

IEX.nl is hét beleggersplatform van Nederland. Blijf op de hoogte van alle relevante informatie over aandelen en andere beleggingsproducten. Beleggen – Koers – Aandelen – Discussie.

Forum: Kiadis Pharma » Kiadis Pharma September 2018

Ter kennisgeving: (CercleFinance.com) – Ipsen announces that the Committee for Medicinal Products for Human Use (CHMP) has provided a positive opinion on Cabomantx (cabozantinib) as a monotherapy for the treatment of hepatocellular carcinoma (HCC) in adults who have been previously treated with sorafenib. The CHMP positive opinion will now be reviewed by the European Commission (EC), which has

Forum: Kiadis Pharma » Molmed versus Kiadis Pharma en Sep 24, 2018
Forum: Kiadis Pharma » Oktober
Forum: Kiadis Pharma » Kiadis Pharma januari 2018

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Forum: Kiadis Pharma » Kiadis Pharma januari 2018

Kiadis Pharma januari 2018. September 29, 2017. Kiadis Pharma N.V.-Receive News & Ratings Via Email – Enter your email address below to receive a concise daily summary of the latest news and

Forum: Kiadis Pharma » Kiadis Pharma September 2018

Zou goed mogelijk zijn, aandeel heeft zeker veel potentie. Ben er maandag weer ingestapt.

Kiadis Pharma to attend upcoming investor conferences in

About Kiadis Pharma. Kiadis Pharma is initially developing its lead product candidate, ATIR101, for use in conjunction with haploidentical HSCT for adult blood cancers to address key limitations of haploidentical HSCT, without prophylactic immunosuppression and its associated morbidity and mortality.

Kiadis Pharma to attend upcoming investor conferences in

Kiadis Pharma to attend upcoming investor conferences in September 2018. Amsterdam, The Netherlands, August 28, 2018 – Kiadis Pharma N.V. (“Kiadis Pharma” or the “Company”) (Euronext Amsterdam and

Kiadis Pharma announces Financial Results for the six

Amsterdam, The Netherlands, August 31, 2018 – Kiadis Pharma N.V. The trial will be performed in 250 patients with acute leukemia and myelodysplastic syndrome, or MDS, at approximately 50 sites in the United States, Canada, Europe and certain additional countries. designation from the FDA in September 2017, which provides benefits that

Forum: Kiadis Pharma » In MEI, leggen alle kippen een ei

05-02-2018 03:19 PM CET – Health (DLBCL) • In September 2017, Kiadis pharma’s ATR101 was granted Regenerative Medicine Advanced Therapy (RMAT) designation by U.S.FDA and in April 2017, Kiadis pharma received regulatory approval from the national authority in Belgium to start pivotal Phase III trial with ATIR101™ and from the national

Forum: Kiadis Pharma » Molmed versus Kiadis Pharma en

Zalmoxis has been developed by the little-known Italian biotech MolMed, one of three companies – the others being Bellicum and Kiadis Pharma – known to be working on engineered T-cell products to improve the outcomes with haploidentical or partial matched HSCT.

Forum: Kiadis Pharma » Oktober op naar de 15 euro » Pagina

Kiadis Pharma is on track to potentially obtain (conditional) EMA approval for ATIR101™ in the second half of 2018, which would allow for a European launch in 2019.”

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