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
0
Croissance des revenus (H/H)
--
--
--
--
--
--
Coût des ventes
--
--
--
--
--
--
Bénéfice brut
--
--
--
--
--
--
Vente, Général et Administration
20
18
21
18
11
2
Recherche et développement
57
--
57
48
24
6
Frais d'exploitation
77
62
78
67
35
8
Autres revenus (charges) non opérationnels
10
13
11
4
0
0
Bénéfice avant impôts
-67
-50
-67
-63
-35
-8
Charge d'impôt sur le revenu
--
--
--
--
--
--
Bénéfice net
-67
-50
-67
-63
-35
-8
Croissance du bénéfice net
43%
-25%
6%
80%
338%
300%
Actions en circulation (diluées)
56.95
57
56
55.71
45.94
53.82
Variation des actions (H-H)
1%
2%
1%
21%
-15%
0%
EPS (dilué)
-1.18
-0.88
-1.19
-1.14
-0.77
-0.15
Croissance du EPS
39%
-26%
4%
48%
413%
275%
Flux de trésorerie libre
-52
-43
-58
-52
-30
-8
Flux de trésorerie libre par action
--
--
--
--
--
--
Marge brute
--
--
--
--
--
--
Marge opérationnelle
0%
0%
0%
0%
0%
0%
Marge bénéficiaire
0%
0%
0%
0%
0%
0%
Marge du flux de trésorerie libre
0%
0%
0%
0%
0%
0%
EBITDA
-77
-62
-78
-67
-35
-8
Marge EBITDA
0%
0%
0%
0%
0%
0%
D&A pour le résultat opérationnel
0
0
0
0
0
0
EBIT
-77
-62
-78
-67
-35
-8
Marge EBIT
0%
0%
0%
0%
0%
0%
Taux d'imposition effectif
--
--
--
--
--
--
Statistiques clés
Clôture préc.
$10.07
Prix d'ouverture
$10.07
Plage de la journée
$9.95 - $10.23
Plage de 52 semaines
$2.6 - $10.97
Volume
134.1K
Volume moyen
437.4K
BPA (TTM)
-1.19
Rendement en dividend
--
Capitalisation boursière
$576.4M
Qu’est-ce que DSGN ?
Design Therapeutics, Inc. operates as a biotechnology company that develops therapies for serious degenerative disorders. The company is headquartered in Carlsbad, California and currently employs 55 full-time employees. The company went IPO on 2021-03-26. The company is engaged in the research and development of GeneTACT molecules, which are small-molecule gene targeted chimera therapeutic candidates designed to be disease-modifying by addressing the underlying cause of diseases caused by inherited nucleotide repeat expansion mutations. Its Friedreich ataxia (FA) program is focused on the development of a disease-modifying treatment. Its DT-216 is developed to overcome the FXN transcription impairment that causes FA. DT-216 is in Phase I clinical trial. The company is also engaged in developing DT-216 to enable higher exposure and chronic administration for treatment of FA, known as DT-216P2, which uses the same drug substance, DT-216. Its FECD program is focused on the development of a potentially disease-modifying medical treatment for FECD, DT-168, which is in Phase I clinical trial. Its Huntington's Disease program is focused on the development of a potentially disease-modifying treatment for HD.