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Farmas USA

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Farmas USA
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#78945

Re: Farmas USA

MNKD
Estaba subiendo un 8% en pre, y ya le están cascando un -15%. Todavía queda trecho hasta el $, por si alguien se atreve a meterle un corto.

#78947

Re: Farmas USA

MNKD

Bueno, como comentaba en el otro foro, yo me he animado esta tarde, y me he metido en 1.85.. de momento, la cosa va bien...

#78949

Re: Farmas USA

NVAX
Temporada blood sweat&tears, pero llegarán tiempos mejores, sin duda:)

#78950

Re: Farmas USA

ARNA

Otra info extraída de la rueda de prensa:

we continue to support Eisai's efforts in their active dialogue with the health authorities in Mexico and Brazil as well as Teva in Israel.

Regarding Taiwan, CY Biotech recently filed an application for the approval of BELVIQ with their health authority.

In Europe, Eisai and Arena have met with EU health authorities regarding the resubmission of BELVIQ MA and we are discussing the results of this meeting to how best to proceed. We no longer expect Eisai to make a resubmission by the end of March 2016 as previously anticipated and do not have a specific date as to when a potential MAA re-filing could occur.

Eisai expects slow growth for the obesity market in general and for BELVIQ to continue to grow slowly until the results of the cardiovascular outcome study or CVOT are known and if positive incorporated into the product label. Proof of reduced risk of hospitalization during cardiovascular event would allow BELVIQ to be differentiated from competing products. demonstrating a decrease risk of hospitalization in major cardiovascular event would enhance BELVIQ insurance coverage. result of the CVOT study is not expected until 2018

PD371, a highly selected and potent cannabinoid 2 receptor agonist and development for the treatment of pain, we recently announced start of our Phase 1 multiple ascending dose study. Top line results for this study are expected in the first quarter of 2016.

collaboration with Roivant Sciences for nelotanserin, inverse agonist of the serotonin 2A receptor. Axovant is responsible for all development cost and has announced that it intent to initiative two Phase 2 clinical trials with nelotanserin in the first quarter of 2016. The first trial was planned in patients with either dementia with Lewy bodies, or Parkinson's disease dementia in patients who suffer from visual hallucinations. The second trial is planned in patients with dementia with Lewy bodies who are experiencing REM Behavior Disorder.

we expect to incur charges primarily in the fourth quarter of 2015 of approximately $3.3 million in connection with one time employee termination cost.

«Después de nada, o después de todo/ supe que todo no era más que nada.»

#78952

Re: Farmas USA

Ana, ¿y tu como ves ARNA? No estaría mal que Eisai nos hiciera un BO... como le ha pasado a OCAT.... ehhhh... jejejejeje...