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WKN: A2P5PP | ISIN: US5171251003 | Ticker-Symbol: ZA71
Tradegate
18.11.24
17:49 Uhr
5,900 Euro
+0,100
+1,72 %
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Biotechnologie
Aktienmarkt
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LARIMAR THERAPEUTICS INC Chart 1 Jahr
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MoLarimar Therapeutics (NASDAQ:LRMR) Given "Buy" Rating at HC Wainwright7
MoLarimar Therapeutics Presents Additional Data from Phase 1 Studies and Phase 2 Dose Exploration Study Supporting the Nomlabofusp Clinical Program at ICAR 20241
LARIMAR THERAPEUTICS Aktie jetzt für 0€ handeln
MoLarimar Therapeutics, Inc. - 8-K, Current Report1
30.10.Larimar Therapeutics, Inc. - 10-Q, Quarterly Report3
30.10.Larimar Therapeutics GAAP EPS of -$0.24 beats by $0.141
30.10.Larimar Therapeutics Reports Third Quarter 2024 Operating and Financial Results88Nomlabofusp program update expected mid-December to include available safety, pharmacokinetic (PK) and frataxin data, as well as available clinical outcomes observations from patients with Friedreich's...
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30.10.Larimar Therapeutics, Inc. - 8-K, Current Report-
16.10.Larimar Therapeutics' New Drug Could Transform Treatment For Rare Neurological Disease, Analyst Sees Over 200% Upside For Stock3
16.10.Larimar initiated with bullish view at Oppenheimer on lead drug1
03.10.Larimar started at outperform by Wedbush on FA drug candidate10
03.10.Wedbush sees upside in Larimar, sets stock target on FDA pilot nod1
30.09.Larimar Therapeutics' SWOT analysis: nomlabofusp's potential drives stock outlook6
19.09.Larimar Therapeutics Announces Three Poster Presentations at the Upcoming International Congress for Ataxia Research6
12.09.Jones Research starts Larimar at buy, cites lead asset nomlabofusp2
08.08.Larimar Therapeutics, Inc. - 10-Q, Quarterly Report2
07.08.Larimar Therapeutics, Inc. - 8-K, Current Report-
10.06.Larimar Therapeutics, Inc. - 8-K, Current Report1
31.05.Larimar Therapeutics, Inc. - 8-K, Current Report1
31.05.Larimar's Friedreich's ataxia asset nomlabofusp chosen for FDA accelerated program2
20.05.Larimar Therapeutics Announces FDA has Removed Partial Clinical Hold for Nomlabofusp Program in Friedreich's Ataxia183Food and Drug Administration (FDA) removed partial clinical hold following review of Phase 2 dose exploration study data Ongoing open label extension (OLE) study initially evaluating 25 mg; Larimar...
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