Chiffres en millions de dollars américains. L'exercice financier va de février à janvier.
Breakdown
TTM
06/30/2025
06/30/2024
06/30/2023
06/30/2022
06/30/2021
Revenus
0
0
0
0
0
0
Croissance des revenus (H/H)
--
--
--
--
--
--
Coût des ventes
--
0
0
0
0
0
Bénéfice brut
--
0
0
0
0
0
Vente, Général et Administration
31
23
6
6
6
6
Recherche et développement
26
18
15
12
11
7
Frais d'exploitation
45
41
22
19
17
13
Autres revenus (charges) non opérationnels
0
0
0
0
0
0
Bénéfice avant impôts
-41
-37
-21
-19
-18
-13
Charge d'impôt sur le revenu
--
--
--
--
--
--
Bénéfice net
-41
-37
-22
-19
-18
-13
Croissance du bénéfice net
95%
68%
16%
6%
38%
63%
Actions en circulation (diluées)
41.52
36.2
4.06
1.39
0.48
0.25
Variation des actions (H-H)
290%
792%
192%
190%
92%
317%
EPS (dilué)
-1
-1.04
-5.5
-14.07
-37.93
-55.52
Croissance du EPS
-50%
-81%
-61%
-63%
-32%
-60%
Flux de trésorerie libre
-22
-23
-19
-18
-15
-13
Flux de trésorerie libre par action
--
--
--
--
--
--
Marge brute
--
0%
0%
0%
0%
0%
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
-45
-41
-22
--
--
--
Marge EBITDA
0%
0%
0%
--
--
--
D&A pour le résultat opérationnel
0
0
0
--
--
--
EBIT
-45
-41
-22
-19
-17
-13
Marge EBIT
0%
0%
0%
0%
0%
0%
Taux d'imposition effectif
--
--
--
--
--
--
Statistiques clés
Clôture préc.
$11.34
Prix d'ouverture
$11.38
Plage de la journée
$10.38 - $11.45
Plage de 52 semaines
$9.8 - $17.15
Volume
170.3K
Volume moyen
184.0K
BPA (TTM)
-1.18
Rendement en dividend
--
Capitalisation boursière
$351.4M
Qu’est-ce que BNTC ?
Benitec Biopharma, Inc. is a development-stage biotechnology company, which engages in the advancement of novel genetic medicines. The company is headquartered in Hayward, California and currently employs 19 full-time employees. The company went IPO on 2012-07-11. The firm is focused on the advancement of novel genetic medicines. Its proprietary Silence and Replace deoxyribonucleic acid (DNA) -directed ribonucleic acid (RNA) interference platform combines RNA interference, or RNAi, with gene therapy to create medicines that simultaneously facilitate sustained silencing of disease-causing genes and concomitant delivery of wildtype replacement genes following a single administration of the therapeutic construct. The firm is developing Silence and Replace-based therapeutics (BB-301) for chronic and life-threatening human conditions including Oculopharyngeal Muscular Dystrophy (OPMD). BB-301 is an adeno-associated viral vector (AAV)-based gene therapy designed to silence the expression of disease-causing genes (to slow, or halt, the underlying mechanism of disease progression) and to simultaneously replace the mutant genes with normal, wildtype genes.