Am besten 200 Mio auf den Tisch.......
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Die selben Ausübungsbedingungen wie bei den AEterna Nov. 16 Warrants.
For example, if (A) this Warrant then permits the Holder to acquire 100 Warrant Shares, (B) a Call Notice pertains to 75 Warrant Shares, and (C) prior to 6:30 p.m. (New York City time) on the Call Date the Holder tenders a Notice of Exercise in respect of 50 Warrant Shares, then (x) on the Call Date the right under this Warrant to acquire 25 Warrant Shares will be automatically cancelled, (y) the Company, in the time and manner required under this Warrant, will have issued and delivered to the Holder 50 Warrant Shares in respect of the exercises following receipt of the Call Notice, and (z) the Holder may, until the Termination Date, exercise this Warrant for 25 Warrant Shares (subject to adjustment as herein provided and subject to subsequent Call Notices).
https://ir.heatbio.com/sec-filings?page=2
Die haben eine Ausübungszeit von 5 Jahren. Den Spaß gönne ich mir und schau es an. Man lernt ja nie aus. :-))))
At June 30, 2018, we had $19.9 million of cash and cash equivalents.
As at August 9, 2018 we had 16,440,760, common shares issued and outstanding, as well as 161,000 deferred stock units and 973,717 stock options outstanding. Share purchase warrants outstanding as at August 9, 2018 represented a total of 3,417,840 equivalent common shares.
Mac:
>24 Mio$ Stongbridge Upfront gezahlt im Jan 18
>15% royalty on annual net sales up to $75.0 million and an 18% royalty on annual net sales above $75.0 million (On July 23, 2018, Strongbridge launched product sales of Macrilen) Im Nov 18 werden die ersten Verkaufszahlen im Q3 erscheinen.
> Einmalzahlung nach einem 1Jährigen Verkaufserlös (ersichtlich im Q3 2019 AEterna)
•$4.0 million on achieving $25.0 million annual net sales,
•$10.0 million on achieving $50.0 million annual net sales,
•$20.0 million on achieving $100.0 million annual net sales,
•$40.0 million on achieving $200.0 million annual net sales, and
•$100.0 million on achieving $500.0 million annual net sales.
>Upon approval by the FDA of a pediatric indication for Macrilen/ one-time milestone payment of $5.0 million
>Strongbridge agrees to fund 70% of the costs of a worldwide pediatric development program We are not currently conducting any clinical studies, but expect to start enrollment for the clinical trial for a pediatric indication of Macrilen™ (macimorelin) in late 2018.
>EMA
On November 27, 2017, we announced that the MAA for the use of MacrilenTM (macimorelin) for the evaluation of AGHD has been accepted by the EMA for regulatory review.
The start of the EMA review procedure for the MAA has been confirmed by EMA as November 23, 2017.
On March 23, 2018, we received from the EMA a Day 120 List of Questions, which was issued in connection with our MMA submission for MacrilenTM (macimorelin). We submitted our responses to the EMA for its Day 120 List of Questions on July 20, 2018.
EMA wird noch in 2018 entscheiden !
--------------------------------------------------
2018:
1. EMA Entscheid
2. Anfang pediaticstudie
3. Nov - Erste Verkaufszahlen für Mac
2019:
Lizensvereinbarung EU?
Strongebridge royality und einmaltahlung im Q3 ersichtlich
2020:
Q1- Q2 ende Cash ohne Strongbridgezahlungen aus 2019 (pediaticstudie mit eingerechnet)
1.5 Ablaufdatum Nov 16 Warrants (945T zu 4,7$) (call option)
9.12. Ablaufdatum Dez 15 Warrants (2,331Mio zu 7,1$)
Our results demonstrated the expression of splice variants and isoforms of receptor for LHRH in OCM3 UM cell line and its doxorubicin resistant form OCM3DOX320. It has been revealed by MTT assay that AN-152 inhibited cell proliferation in a dose dependent manner in OCM3DOX320 cells. Furthermore, receptor-mediated uptake of AN-152 was demonstrated using confocal laser scanning microscopy in both cell line.Our results suggest that the antiproliferative effect of AN-152 can be detected even if only LHRH receptor isoforms are expressed. Our study also demonstrates the LHRH receptor-mediated uptake of AN-152 in DOX resistant OCM3DOX320 cells. Our experiments provide new insights into a potential targeted therapy of UM and give further details about the accumulation of AN-152 in hormone-independent DOX-resistant cells expressing splice variants of the LHRH receptors.
Davon rede ich die ganze Zeit! Verkehrte Patientenpopulation.
Resistente Patienten profitieren!
Zopt ist mit dabei.
https://europepmc.org/articles/pmc6037002#SD2
Wieso wird Zopt in den Studien verwendet, wenn doch alles daran so schlecht ist?
Antitumor effects of cecropin B-LHRH’on drug-resistant ovarian and endometrial cancer cells.
https://www.researchgate.net/publication/..._endometrial_cancer_cells
OK Unicorn, stimmt schon.
Werde Zopt erst mal ruhen lassen bis es wieder ein aktuelles Thema wird!
Einer geht noch! ;-) Ich lese nichts von "Zopt auf den Müll geworfen"!
-We are currently not conducting any clinical trials but we may decide to do so in the future
-Our principal focus is on the licensing and development of Macrilen™
-In 2017, we completed a Phase 3 study of the internally developed compound Zoptrex™ (zoptarelin doxorubicin), in the indication for advanced, recurrent endometrial cancer, the results of which study are not supportive to pursue regulatory approval by the FDA. In light of the results of the Zoptrex™ study, our focus has shifted entirely to the commercialization, either directly or through third parties, of Macrilen™ (macimorelin).
-We may require significant additional capital to fund our commercial operations and may require additional capital to pursue planned clinical trials and regulatory approvals, as well as further R&D and marketing efforts for our product candidates and potential products
http://app.quotemedia.com/data/...+15%28d%29&dateFiled=2018-03-28
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