BridgeBio Pharma (DB:2CL) - Cours de l'action, nouvelles et analyse

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2CL Aperçu des actions

BridgeBio Pharma, Inc. est une société biopharmaceutique à vocation commerciale qui découvre, crée, teste et fournit des médicaments transformateurs pour traiter les patients souffrant de maladies génétiques et de cancers.

A propos de l'entreprise

2CL analyse fondamentale
Score flocon de neige
Évaluation	2/6
Croissance future	2/6
Performances passées	0/6
Santé financière	1/6
Dividendes	0/6

Récompenses

Se négocie à 89.7% en dessous de notre estimation de sa juste valeur

Les revenus devraient augmenter 40.92% par an

Analyse des risques

Capitaux propres négatifs

A moins d'un an de piste de trésorerie

Les actionnaires ont été dilués au cours de l'année écoulée

Actuellement non rentable et ne devrait pas le devenir au cours des 3 prochaines années

+ 1 plus de risques

BridgeBio Pharma, Inc. Concurrents

MorphoSys

HMSE:MOR

€2.5b

Biotest

XTRA:BIO3

€1.4b

Formycon

XTRA:FYB

€944.6m

Heidelberg Pharma

XTRA:HPHA

€112.8m

Historique des prix et performances

Résumé des plus hauts, des changements et des baisses de prix pour BridgeBio Pharma
Historique des cours de bourse
Prix actuel de l'action	US$23.48
Plus haut sur 52 semaines	US$39.72
Plus bas sur 52 semaines	US$21.00
Bêta	1.08
1Variation sur 1 mois	-16.50%
Variation sur 3 mois	-0.21%
Variation sur 1 an	2.44%
3Variation sur 3 ans	-38.85%
Variation sur 5 ans	37.31%
Évolution depuis l'introduction en bourse	0.043%

Nouvelles et mises à jour récentes

Recent updates

Rendement pour les actionnaires

	2CL	DE Biotechs	DE Marché
7D	7.5%	2.2%	-1.9%
1Y	2.4%	-9.6%	12.3%

Rendement vs Industrie: 2CL a dépassé le secteur German Biotechs qui a rapporté -16.4 % au cours de l'année écoulée.

Rendement vs marché: 2CL a sous-performé le marché German qui a rapporté 3.9 % au cours de l'année écoulée.

Volatilité des prix

Is 2CL's price volatile compared to industry and market?
2CL volatility
2CL Average Weekly Movement	8.1%
Biotechs Industry Average Movement	6.4%
Market Average Movement	4.9%
10% most volatile stocks in DE Market	10.7%
10% least volatile stocks in DE Market	2.4%

Cours de l'action stable: Le cours de l'action de 2CL a été volatil au cours des 3 derniers mois.

Volatilité au fil du temps: La volatilité hebdomadaire de 2CL ( 9% ) est restée stable au cours de l'année écoulée, mais reste supérieure à 75 % des actions de German.

À propos de l'entreprise

Fondée	Salariés	PDG	Site web
2015	553	Neil Kumar	bridgebio.com

BridgeBio Pharma, Inc. est une société biopharmaceutique commerciale qui découvre, crée, teste et fournit des médicaments transformateurs pour traiter les patients souffrant de maladies génétiques et de cancers. Ses produits en cours de développement comprennent AG10, une petite molécule orale de nouvelle génération qui stabilise presque complètement la TTR et qui fait l'objet d'un essai clinique de phase 3 pour le traitement de l'amylose TTR, ou cardiomyopathie amyloïde à transthyrétine (ATTR-CM) ; l'infigratinib à faible dose, un inhibiteur oral sélectif de la tyrosine kinase FGFR1-3, qui fait l'objet d'une étude pivot de phase 3 en double aveugle et contrôlée par placebo pour le traitement des enfants atteints d'achondroplasie ; et le BBP-631, un produit candidat de transfert de gène AAV5 qui fait l'objet d'un essai clinique de phase 1/2 pour le traitement de l'hyperplasie congénitale des surrénales, ou HCS, due à une déficience en 21-hydroxylase, ou 21OHD. La société développe également Encaleret, une petite molécule antagoniste du récepteur de détection du calcium, ou CaSR, qui est en essai clinique de phase 3 pour le traitement de l'hypocalcémie autosomique dominante de type 1, ou ADH1 ; et BBP-418, un pro-médicament substrat de glycosylation qui est en essai clinique de phase 3 pour le traitement de la dystrophie musculaire des ceintures de type 2I/R9 (LGMD2I/R9).

BridgeBio Pharma, Inc. Résumé des fondamentaux

Comment les bénéfices et les revenus de BridgeBio Pharma se comparent-ils à sa capitalisation boursière ?
2CL statistiques fondamentales
Capitalisation boursière	€4.32b
Bénéfices(TTM)	-€413.47m
Recettes(TTM)	€199.64m

21.7x

Ratio P/S

-10.5x

Ratio P/E

Le site 2CL est-il surévalué ?

Voir Juste valeur et analyse de l'évaluation

Bénéfices et recettes

Principales statistiques de rentabilité tirées du dernier rapport sur les bénéfices (TTM)
2CL compte de résultat (TTM)
Recettes	US$219.12m
Coût des recettes	US$2.39m
Marge brute	US$216.73m
Autres dépenses	US$670.55m
Les revenus	-US$453.82m

Derniers bénéfices déclarés

Jun 30, 2024

Prochaine date de publication des résultats

s/o

Résultat par action (EPS)	-2.41
Marge brute	98.91%
Marge bénéficiaire nette	-207.11%
Ratio dettes/capitaux propres	-158.7%

Quelles ont été les performances à long terme de 2CL?

Voir les performances historiques et les comparaisons

2CL Aperçu des actions

Récompenses

Analyse des risques

BridgeBio Pharma, Inc. Concurrents

HMSE:MOR

€2.5b

XTRA:BIO3

€1.4b

XTRA:FYB

€944.6m

XTRA:HPHA

€112.8m

Historique des prix et performances

Nouvelles et mises à jour récentes

BridgeBio Pharma, Inc. Completes Enrollment of FORTIFY, Phase 3 Registrational Study of BBP-418 in Limb-girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9)

BridgeBio Pharma, Inc. Presents Additional Data from an Analysis of its Phase 3 ATTRibute-CM and Open-Label Extension Study of Acoramidis in ATTR-CM at the European Society of Cardiology 2024

BridgeBio Pharma, Inc. and QED Therapeutics Announce the Launch of the Initial Phase of MyAchonJourney

Second quarter 2024 earnings released: US$0.39 loss per share (vs US$0.98 loss in 2Q 2023)

BridgeBio Pharma, Inc. Announces Appointment of Thomas Trimarchi, Ph.D., as President and Chief Operating Officer

BridgeBio Pharma, Inc. Surpasses Interim Analysis Enrollment Target and Receives U.S. FDA Rare Pediatric Disease Designation for BBP-418, a Potential Treatment for Limb-Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9)

Recent updates

BridgeBio Pharma, Inc. Completes Enrollment of FORTIFY, Phase 3 Registrational Study of BBP-418 in Limb-girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9)

BridgeBio Pharma, Inc. Presents Additional Data from an Analysis of its Phase 3 ATTRibute-CM and Open-Label Extension Study of Acoramidis in ATTR-CM at the European Society of Cardiology 2024

BridgeBio Pharma, Inc. and QED Therapeutics Announce the Launch of the Initial Phase of MyAchonJourney

Second quarter 2024 earnings released: US$0.39 loss per share (vs US$0.98 loss in 2Q 2023)

BridgeBio Pharma, Inc. Announces Appointment of Thomas Trimarchi, Ph.D., as President and Chief Operating Officer

BridgeBio Pharma, Inc. Surpasses Interim Analysis Enrollment Target and Receives U.S. FDA Rare Pediatric Disease Designation for BBP-418, a Potential Treatment for Limb-Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9)

BridgeBio Pharma, Inc. Announces Durable Month 12 and 18 Phase 2 Cohort 5 Results of Oral Infigratinib in Achondroplasia, and First Participant Consented in ACCEL for Hypochondroplasia

First quarter 2024 earnings released: US$0.20 loss per share (vs US$0.92 loss in 1Q 2023)

BridgeBio Pharma, Inc., Annual General Meeting, Jun 21, 2024

BridgeBio Pharma, Inc. Presents Cardiac Magnetic Resonance (CMR) Imaging Evidence Consistent with Clinical Improvement

BridgeBio Pharma, Inc. has completed a Follow-on Equity Offering in the amount of $250.00001 million.

BridgeBio Pharma, Inc. has completed a Follow-on Equity Offering in the amount of $250.00001 million.

BridgeBio Pharma, Inc. has filed a Follow-on Equity Offering.

Full year 2023 earnings released: US$3.95 loss per share (vs US$3.26 loss in FY 2022)

New major risk - Financial position

BridgeBio Pharma, Inc. Announces U.S. Food and Drug Administration Acceptance of New Drug Application for Acoramidis for the Treatment of Patients with Transthyretin Amyloid Cardiomyopathy

BridgeBio Pharma, Inc. Shares Positive Results of Single-Arm Phase 3 Study of Acoramidis in Japanese Patients with Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Including No Mortality Reported in the Trial at 30 Months

BridgeBio Pharma, Inc. Announces Publication of Positive Results from Phase 3 ATTRibute-CM Study of Acoramidis for Patients with Transthyretin Amyloid Cardiomyopathy in the New England Journal of Medicine

BridgeBio Pharma, Inc. Announces First Child Dosed in PROPEL 3, its Phase 3 Clinical Trial for Infigratinib in Children with Achondroplasia

Now 21% undervalued

BridgeBio Pharma, Inc. Presents Additional Clinical Outcomes Data from the Phase 3 ATTRibute-CM Study of Acoramidis in Patients with Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM)

Third quarter 2023 earnings released: US$1.08 loss per share (vs US$0.93 loss in 3Q 2022)

BridgeBio Pharma, Inc. Shares Positive Long-Term Data from an Ongoing Phase 2 Study, Which Support the Potential Use of Glycosylated Alpha-dystroglycan (DG) Levels as a Surrogate Endpoint in Limb-Girdle Muscular Dystrophy Type 2I/R9

BridgeBio Pharma, Inc. announced that it expects to receive $250.003806 million in funding from Qatar Investment Authority and other investors

Bridgebio Pharma Announces Positive Feedback from the U.S. Fda and Eu Ema on the Regulatory Path for A Pivotal Phase 3 Trial of Infigratinib in Children with Achondroplasia

BridgeBio Pharma, Inc. Presents Detailed Positive Results from Phase 3 Attribute-CM Study of Acoramidis for Patients with Transthyretin Amyloid Cardiomyopathy (ATTR-CM) At European Society of Cardiology Congress 2023

New minor risk - Financial position

Second quarter 2023 earnings released: US$0.98 loss per share (vs US$0.067 loss in 2Q 2022)

Bridgebio Pharma Announces Opportunity for Accelerated Approval Pathway in Limb-Girdle Muscular Dystrophy Type 2I (Lgmd2i/R9) Based on Glycosylated Alpha-Dystroglycan (Dg) Levels and Announces First Patient Dosed in Fortify Phase 3 Study

Bridgebio Announces Consistently Positive Results from Phase 3 Attribute-Cm Study of Acoramidis for Patients with Transthyretin Amyloid Cardiomyopathy

BridgeBio Pharma, Inc. Presents Updated Six Month Results from Its Phase 2 Cohort 5 Trial of Infigratinib in Achondroplasia

First quarter 2023 earnings released: US$0.92 loss per share (vs US$1.35 loss in 1Q 2022)

Full year 2022 earnings released: US$3.26 loss per share (vs US$3.90 loss in FY 2021)

Bridgebio Pharma, Inc. Initiates CALIBRATE, A Pivotal Phase 3 Study of Encaleret in Autosomal Dominant Hypocalcemia Type 1

Third quarter 2022 earnings released: US$0.93 loss per share (vs US$1.06 loss in 3Q 2021)

BridgeBio Pharm and ML Bio Solutions Present 12-month Results from Phase 2 Study of BBP-418 in Limb-Girdle Muscular Dystrophy Type 2i (LGMD2i)

BridgeBio Pharma, Inc Presents Updated Positive Data from Its BBP-812 Canavan Disease Gene Therapy Program At the 51st Annual Meeting of the Child Neurology Society

BridgeBio Pharma Announces First Lung Cancer Patient Dosed in Phase 1/2 Trial and US FDA Fast Track Designation for SHP2 Inhibitor BBP-398 in Combination with Amgen's Lumakras(R) (Sotorasib)

BridgeBio Pharma, Inc. to Present New Data on its Novel Approaches to RAS-driven Cancers at the Fourth RAS Initiative Symposium

BridgeBio Pharma and Sentynl Therapeutics Receive Marketing Authorization in the EU for NULIBRY® (fosdenopterin) for the Treatment of MoCD Type A

BridgeBio Pharma, Inc Announces Dosing of First Patient in Phase 1 Trial of BBP-671

BridgeBio Pharma, Sentynl Therapeutics and Medison Pharma Announce Approval in Israel for NULIBRY® (fosdenopterin) for the Treatment of MoCD Type A

Second quarter 2022 earnings released: US$0.067 loss per share (vs US$0.66 loss in 2Q 2021)

BridgeBio Pharma, Inc. Announces Positive Interim Results from PROPEL 2

BridgeBio Pharma, Inc. and Sentynl Therapeutics, Inc. Receive Positive CHMP Opinion for NULIBRY® (Fosdenopterin) for Treatment of MoCD Type A

BridgeBio Pharma Announces Positive Phase 1 Data and Phase 2/3 Trial Design for BBP-711, a Potentially Best-In-Class GO Inhibitor for Primary Hyperoxaluria Type 1 (PH1) and Recurrent Kidney Stone Formers

BridgeBio Pharma Announces Early Positive Data for BBP-812, its Investigational AAV9 Gene Therapy for Canavan Disease

BridgeBio Pharma, Inc. Shares Positive Phase 2B Data and Announces Pivotal Study Design for Phase 3 Trial of Encaleret in Autosomal Dominant Hypocalcemia Type 1 (ADH1)

BridgeBio Pharma, Inc. and Venthera, Inc. Presents Preliminary Results from Clinical Trial of VT30 (BBP-681) for Venous, Lymphatic, and Venolymphatic Malformations

BridgeBio Pharma Presents Positive Phase 1 Data in Healthy Volunteers, Advancing Development of BBP-671 for Pantothenate Kinase-Associated Neurodegeneration (PKAN) and Organic Acidemias

BridgeBio Pharma, Inc. and Phoenix Tissue Repair, Inc Announce Positive Results from Phase 2 Trial of PTR-01

BridgeBio Pharma, Inc., Annual General Meeting, Jun 22, 2022

BridgeBio Pharma Presents Updated Results from Phase 2 Open-label Extension Study of Acoramidis in Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

Insider recently bought €75k worth of stock

Sentynl Therapeutics Inc. entered into an asset purchase agreement to acquire Global Rights to NULIBRY from BridgeBio Pharma, Inc. (NasdaqGS:BBIO).

Full year 2021 earnings: EPS in line with expectations, revenues disappoint

BridgeBio Pharma Announces Dosing of First Patient in Phase 1/2 Trial of Investigational Gene Therapy for Congenital Adrenal Hyperplasia (CAH)

Independent Director recently bought €264k worth of stock

BridgeBio Pharma Reports Month 12 Topline Results from Phase 3 ATTRibute-CM Study