Chiffres en millions de dollars américains. L'exercice financier va de février à janvier.
Breakdown
TTM
12/31/2024
12/31/2023
12/31/2022
12/31/2021
12/31/2020
Revenus
0
0
0
0
0
1
Croissance des revenus (H/H)
--
--
--
--
-100%
0%
Coût des ventes
--
--
--
--
--
--
Bénéfice brut
--
--
--
--
--
--
Vente, Général et Administration
19
20
19
12
7
1
Recherche et développement
118
--
42
32
12
8
Frais d'exploitation
138
114
61
45
19
9
Autres revenus (charges) non opérationnels
0
12
0
0
-81
0
Bénéfice avant impôts
-133
-102
-52
-42
-100
-7
Charge d'impôt sur le revenu
--
--
--
--
--
--
Bénéfice net
-133
-102
-52
-42
-100
-7
Croissance du bénéfice net
62%
96%
24%
-57.99%
1,329%
0%
Actions en circulation (diluées)
60.57
60
49
40.6
20.06
38.65
Variation des actions (H-H)
1%
22%
21%
102%
-48%
0%
EPS (dilué)
-2.2
-1.71
-1.08
-1.06
-5.02
-0.19
Croissance du EPS
61%
57.99%
2%
-79%
2,542%
-5%
Flux de trésorerie libre
-123
-86
-43
-35
-18
-7
Flux de trésorerie libre par action
--
--
--
--
--
--
Marge brute
--
--
--
--
--
--
Marge opérationnelle
0%
0%
0%
0%
0%
-700%
Marge bénéficiaire
0%
0%
0%
0%
0%
-700%
Marge du flux de trésorerie libre
0%
0%
0%
0%
0%
-700%
EBITDA
-138
-114
-61
-45
-19
--
Marge EBITDA
0%
0%
0%
0%
0%
--
D&A pour le résultat opérationnel
0
0
0
0
0
--
EBIT
-138
-114
-61
-45
-19
-7
Marge EBIT
0%
0%
0%
0%
0%
-700%
Taux d'imposition effectif
--
--
--
--
--
--
Statistiques clés
Clôture préc.
--
Prix d'ouverture
--
Plage de la journée
-
Plage de 52 semaines
-
Volume
--
Volume moyen
504.4K
BPA (TTM)
-2.21
Rendement en dividend
--
Capitalisation boursière
--
Qu’est-ce que ABOS ?
Acumen Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company, which engages and develops medicines and diagnostics for Alzheimer's disease. The company is headquartered in Newton, Massachusetts and currently employs 61 full-time employees. The company went IPO on 2021-07-01. The firm is engaged in developing a disease-modifying approach to target underlying cause of Alzheimer's disease (AD). The firm is focused on advancing a targeted immunotherapy drug candidate, sabirnetug (ACU193), in its Phase II ALTITUDE-AD clinical trial following Phase I results in early AD patients (patients with mild cognitive impairment or mild dementia due to AD). Sabirnetug is a recombinant humanized immunoglobulin gamma 2 (IgG2), monoclonal antibody (mAb) that selectively targets the anti-amyloid-beta oligomer, has demonstrated functional and protective effects in in-vitro assays, and has demonstrated in-vivo safety and pharmacologic activity in multiple animal species including transgenic mouse models for AD. The firm is developing sabirnetug for IV administration once every four weeks (Q4W) for the treatment of early AD, and it has developing sabirnetug for subcutaneous administration.