+ 12,3 % bei Geron (902213) Was ist los? o. T.
Zahlen für Q2/21
- keine Umsätze
- Verlust 30 Mio. $
- Cash 239 Mio. $
- MK 405 Mio. $
These financial resources, combined with expected future non-dilutive funding under the current debt facility, are now expected to fund operations through the end of the first quarter of 2023.
“We are pleased with the achievement of 91% of the planned enrollment in IMerge Phase 3 and expect the trial to be fully enrolled in the fourth quarter of 2021. In addition, the expected timing for top-line results in IMerge Phase 3 has been accelerated by three months to the first quarter of 2023,”
https://ir.geron.com/investors/press-releases/...of-2023/default.aspx
•Analyses Suggest Survival Benefit Associated with Imetelstat Treatment in Comparison to Best Available Therapy
•Overall Survival is Primary Endpoint for Ongoing Phase 3 Clinical Trial in Refractory MF
https://ir.geron.com/investors/press-releases/...atology/default.aspx
Zahlen für Q3/21
- kein Umsatz
- Verlust 27 Mio. $
- Cash 176 Mio. $
- MK 328 Mio. $
https://d18rn0p25nwr6d.cloudfront.net/...4835-9fc7-6576fce03f8c.html#
https://finance.yahoo.com/news/...nces-proposed-public-200100969.html
Und wir sind schon bei 323.73M outstanding shares.
All of the securities in the offering are being sold by Geron. The gross proceeds to Geron from this underwritten public offering are expected to be approximately $75.0 million, before deducting the underwriting discount and other estimated offering expenses payable by Geron. The offering is expected to close on or about April 1, 2022, subject to the satisfaction of customary closing conditions.
Geron currently intends to use the net proceeds from this public offering, together with its existing cash, cash equivalents, restricted cash and marketable securities to fund potential regulatory filings in the United States and European Union for imetelstat in lower risk myelodysplastic syndromes (MDS), assuming top-line results in the IMerge Phase 3 clinical trial are supportive, and to support toward the completion of the IMpactMF clinical trial in refractory myelofibrosis and the planned exploratory studies in new indications, including IMproveMF and investigator-led trials in acute myeloid leukemia and higher risk MDS, the preclinical work in lymphoid malignancies and the discovery research program related to next generation telomerase inhibitors.
https://www.stonkmoon.com/news/GERN/1242cffb229cc72c9f1cc5f4ee5461f2
75 Mio. $ Offering
- 53,3 Mio. Aktien + warrants zu 1,05$
https://ir.geron.com/investors/press-releases/...arrants/default.aspx
Rational nachvollziehbar ist dieser Kursananstieg (nach Bekanntgabe dieses Offerings) jedenfalls nicht.
Dr. Mascarenhas received research grant/funding from Incyte, Novartis, CTI BioPharma, Geron, PharmaEssentia, AbbVie, Bristol Myers Squibb, Celgene, Roche, Kartos, Promedior, and Merck in addition to many others. (Pay attention to big pharmas who are sponsoring the study)
The study designed to compare Imetelstat against two BAT; JAK inhibitors, ruxolitinib and fedratinib. An excellent study with no risk to patients.
Imetelstat vs. BAT, follow up visit after treatment ended. If progressive disease with BAT, patients were eligible for crossover to Imetelstat."
“They concluded that the study has the potential to change the treatment landscape in refractory MF and address a critical unmet need for disease-modifying therapies that will improve survival in this poor-prognosis patient population.”
(BAT is best available current treatments)
"Aus wettbewerblicher Sicht ist es ein Hindernis und ein Nachteil für $GERN und seine Entwicklung von imetelstat."
https://twitter.com/adamfeuerstein/status/...cxt=HHwWgMC4wZ3mpoYsAAAA
https://ir.geron.com/investors/press-releases/...Phase-3/default.aspx
...today announced that it intends to offer and sell $175 million of shares of its common stock in an underwritten public offering. All of the securities in the proposed offering are to be sold by Geron. Geron intends to grant the underwriters a 30-day option to purchase up to an additional 15% of the number of shares of its common stock offered in the public offering. The proposed offering is subject to market and other conditions, and there can be no assurance as to whether or when the offering may be completed, or as to the actual size or terms of the offering.
https://finance.yahoo.com/news/...nces-proposed-public-211900778.html
https://ir.geron.com/investors/press-releases/...n-Stock/default.aspx
Pricing
- 55,8 Mio. neue Aktien zu je 2,45$
- 25 Mio. warrants zu je 2,449$
- Volumen insgesamt 198 Mio. $
https://ir.geron.com/investors/press-releases/...arrants/default.aspx
Statistically significant and clinically meaningful efficacy results achieved across key MDS subgroups: ring sideroblast (RS) status, baseline transfusion burden and IPSS risk category
Safety results consistent with prior imetelstat clinical experience
Reduction in variant allele frequency (VAF) of genes commonly mutated in MDS and their correlation with clinical endpoints support disease-modifying potential of imetelstat
Data support NDA submission which is on track for June 2023 to support potential U.S. commercial launch in first half of 2024
https://finance.yahoo.com/news/...esentation-reporting-193000539.html
150 Mio. $ Offering
- 42 Mio. neue Aktien zu je 3$
https://ir.geron.com/investors/press-releases/...arrants/default.aspx