BridgeBio Pharma, Inc. (BBIO)
BridgeBio Pharma, Inc. is a pharmaceutical company dedicated to identifying, advancing, and providing medical solutions for various genetic conditions. The firm boasts an extensive portfolio comprising 30 distinct development initiatives, spanning the entire spectrum from initial discovery research to advanced clinical trial phases. Notable candidates within its development pipeline include: AG10 and BBP-265: A small molecule designed to stabilize transthyretin (TTR), currently in a pivotal Phase 3 clinical trial targeting transthyretin amyloidosis-cardiomyopathy (ATTR-CM). BBP-831: A selective small molecule inhibitor of FGFR1-3, which is undergoing Phase 2 clinical evaluation for treating achondroplasia in pediatric patients. BBP-631: An AAV5 gene transfer product candidate, also in Phase 2 clinical trials, aimed at congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency (21OHD). Furthermore, BridgeBio is developing: Encaleret: A small molecule antagonist of the calcium sensing receptor (CaSR), presently in a Phase 2 proof-of-concept study for Autosomal Dominant Hypocalcemia Type 1 (ADH1). BBP-711: Intended for the management of hyperoxaluria and individuals prone to recurring kidney stones. Beyond these specific programs, the company is actively engaged in developing therapies for a broader range of Mendelian disorders, oncological diseases, and gene therapy applications. BridgeBio Pharma, Inc. maintains strategic licensing and collaboration agreements with institutions such as Leland Stanford Junior University, The Regents of the University of California, and Leidos Biomedical Research, Inc. Established in 2015, the company's corporate headquarters are situated in Palo Alto, California.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
BridgeBio Pharma, Inc.
Trials need funding. See this company's dilution risk and cash position.
- $75M upfrontSep 30, 2026BEYONTTRA
- $75M upfrontJan 1, 1970acoramidis (BEYONTTRA)
- Phase 4Recruiting
Cardiac Magnetic Resonance and Echocardiography Study With Acoramidis
Acoramidis (AG10) oral tablet
Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM), Amyloidosis +2
NCT07695701Enrollment150StartJul 2026est.Primary CompletionAug 2030est.CompletionNov 2030est. - Phase 3Terminated
Phase 3 Study of BGJ398 (Oral Infigratinib) in First Line Cholangiocarcinoma With FGFR2 Gene Fusions/Translocations
BGJ398, Gemcitabine
Advanced Cholangiocarcinoma, FGFR2 Gene Mutation
NCT03773302Enrollment48StartDec 2019Primary CompletionMar 2023CompletionMar 2023 - Phase 3Completed
Efficacy and Safety of AG10 in Subjects With Transthyretin Amyloid Cardiomyopathy
acoramidis, Placebo Oral Tablet
Amyloidosis, Amyloid Cardiomyopathy +3
NCT03860935Enrollment632StartMar 2019Primary CompletionMay 2023CompletionMay 2023 - Phase 3Terminated
Oral Infigratinib for the Adjuvant Treatment of Subjects With Invasive Urothelial Carcinoma With Susceptible FGFR3 Genetic Alterations
Infigratinib, Placebo
Upper Tract Urothelial Carcinomas, Urothelial Bladder Cancer
NCT04197986Enrollment39StartMar 2020Primary CompletionFeb 2023CompletionFeb 2023 - Phase 3Withdrawn
Efficacy and Safety of AG10 in Subjects with Transthyretin Amyloid Polyneurophathy
AG10, Placebo
Transthyretin-Related (ATTR) Familial Amyloid Polyneuropathy
NCT04418024Enrollment0StartOct 2020Primary CompletionMar 2024est.CompletionApr 2024est. - Phase 3Withdrawn
Efficacy and Safety of Acoramidis (AG10) in Subjects with Transthyretin Amyloid Polyneurophathy (ATTRibute-PN)
Acoramidis
Transthyretin-Related (ATTR) Familial Amyloid Polyneuropathy
NCT04882735Enrollment0StartSep 2021Primary CompletionSep 2026est.CompletionOct 2026est. - Phase 3Active, not recruiting
Open-Label Safety Study of Acoramidis (AG10) in Symptomatic ATTR Participants
Acoramidis (AG10)
Amyloid Cardiomyopathy, Transthyretin-Related
NCT04988386Enrollment389StartOct 2021Primary CompletionApr 2028est.CompletionMay 2028est. - Phase 3Active, not recruiting
Efficacy and Safety of Encaleret Compared to Standard of Care in Participants With ADH1
Encaleret
Autosomal Dominant Hypocalcemia (ADH)
NCT05680818Enrollment67StartJan 2023Primary CompletionAug 2025CompletionAug 2029est. - Phase 3Completed
A Study to Evaluate the Efficacy and Safety of Infigratinib in Children and Adolescents With Achondroplasia
Infigratinib 0.25 mg/kg/day, Placebo Comparator 0.25 mg/kg/day
Achondroplasia
NCT06164951Enrollment114StartNov 2023Primary CompletionDec 2025CompletionDec 2025 - Phase 3Recruiting
Acoramidis Transthyretin Amyloidosis Prevention Trial in the Young (ACT-EARLY) Study in Asymptomatic Carriers of a Pathogenic TTR Variant
Acoramidis, Placebo oral tablet
Amyloidosis, Amyloid Cardiomyopathy +4
NCT06563895Enrollment587StartMay 2025Primary CompletionOct 2031est.CompletionDec 2032est. - Phase 3Not yet recruiting
To Evaluate the Long-term Safety and Tolerability of Acoramidis in Participants With Newly Diagnosed ATTR-CM (ACT-EARLY OLE)
Acoramidis (AG10)
Amyloidosis in Transthyretin (TTR), Amyloidosis, Familial +8
NCT07116473Enrollment250StartNov 2026est.Primary CompletionNov 2037est.CompletionDec 2037est. - Phase 3Recruiting
Efficacy, Safety, and Tolerability of Encaleret in Participants With Chronic Hypoparathyroidism
Encaleret, Placebo
Hypoparathyroidism, Chronic Hypoparathyroidism
NCT07805356Enrollment160StartAug 2026est.Primary CompletionJan 2028est.CompletionJan 2033est. - Phase 2/3Enrolling by invitation
An Interventional Study of Infigratinib in Children With Hypochondroplasia
infigratinib 0.128 mg/kg/day, infigratinib 0.25 mg/kg/day
Hypochondroplasia
NCT06873035Enrollment24StartApr 2025Primary CompletionJan 2027est.CompletionJan 2027est. - Phase 2/3Recruiting
Pharmacokinetics, Efficacy, and Safety of Encaleret in Pediatric Participants With Autosomal Dominant Hypocalcemia Type 1 (ADH1)
Encaleret
Autosomal Dominant Hypocalcemia Type 1 (ADH1)
NCT07080385Enrollment28StartJan 2026Primary CompletionDec 2028est.CompletionDec 2030est. - Phase 2Terminated
A Phase II, Single Arm Study of BGJ398 in Patients With Advanced Cholangiocarcinoma
BGJ398 (infigratinib)
Advanced Cholangiocarcinoma, FGFR2 Gene Mutation
NCT02150967Enrollment143StartJul 2014Primary CompletionMar 2021CompletionFeb 2022 - Phase 2Completed
Study of AG10 in Amyloid Cardiomyopathy
AG10, Placebo Oral Tablet
Familial ATTR-CM (ATTRm-CM, or FAC), Wild-type ATTR-CM (ATTRwt-CM)
NCT03458130Enrollment49StartApr 2018Primary CompletionOct 2018CompletionOct 2018 - Phase 2Terminated
Open-Label Study of AG10 in Patients With Cardiomyopathy
Acoramidis
Amyloid Cardiomyopathy
NCT03536767Enrollment47StartAug 2018Primary CompletionSep 2025CompletionSep 2025 - Phase 2Completed
Study of Infigratinib in Children With Achondroplasia
Infigratinib 0.016 mg/kg, Infigratinib 0.032 mg/kg
Achondroplasia
NCT04265651Enrollment84StartMar 2020Primary CompletionOct 2024CompletionOct 2024 - Phase 2Completed
Safety, Tolerability, and Efficacy of Encaleret in Participants With Autosomal Dominant Hypocalcemia (ADH) Type 1
Encaleret
Autosomal Dominant Hypocalcemia (ADH), Autosomal Dominant Hypocalcemia Type 1 (ADH1)
NCT04581629Enrollment13StartSep 2020Primary CompletionSep 2023CompletionSep 2023 - Phase 2Enrolling by invitation
Extension Study of Infigratinib in Children With Achondroplasia (ACH)
Infigratinib, Infigratinib
Achondroplasia
NCT05145010Enrollment325StartDec 2021Primary CompletionDec 2031est.CompletionFeb 2032est. - Phase 2Recruiting
Interventional Study of Infigratinib in Children < 3 Years Old With Achondroplasia (ACH)
Infigratinib is provided as a single dose of minitablets for oral administration, Infigratinib is provided as sprinkle capsules for daily oral administration
Achondroplasia
NCT07169279Enrollment77StartNov 2025Primary CompletionMar 2030est.CompletionMar 2032est. - Phase 2Enrolling by invitation
Open-Label, Long-Term, Extension Study of Infigratinib in Children With Hypochondroplasia
Infigratinib
Hypochondroplasia
NCT07393373Enrollment135StartApr 2026Primary CompletionMay 2036est.CompletionMay 2036est. - Phase 1/2Terminated
First in Human Trial of Topical VT30 in Pts With Venous/Lymphatic Malformations Assoc With PIK3CA or TEK Gene Mutations
VT30
Venous Malformation, Lymphatic Malformation +1
NCT04409145Enrollment15StartOct 2020Primary CompletionApr 2022CompletionApr 2022 - Phase 1Completed
Single and Multiple Ascending Dose Study Assessing the Safety, Tolerability, PK and PD of AG10
AG10 oral tablet, Placebo Oral Tablet
Amyloid Cardiomyopathy, Transthyretin-Related
NCT03294707Enrollment56StartSep 2017Primary CompletionFeb 2018CompletionMay 2018 - Phase 1Terminated
First-in-Human Study of the SHP2 Inhibitor BBP-398 in Patients With Advanced Solid Tumors
BBP-398 (Formerly known as IACS-15509)
Tumor, Solid
NCT04528836Enrollment72StartNov 2020Primary CompletionMar 2024CompletionJul 2024
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 4 | Recruiting | Acoramidis (AG10) oral tablet | NCT07695701 |
| Phase 3 | Terminated | BGJ398, Gemcitabine | NCT03773302 |
| Phase 3 | Completed | acoramidis, Placebo Oral Tablet | NCT03860935 |
| Phase 3 | Terminated | Infigratinib, Placebo | NCT04197986 |
| Phase 3 | Withdrawn | AG10, Placebo | NCT04418024 |
| Phase 3 | Withdrawn | Acoramidis | NCT04882735 |
| Phase 3 | Active, not recruiting | Acoramidis (AG10) | NCT04988386 |
| Phase 3 | Active, not recruiting | Encaleret | NCT05680818 |
| Phase 3 | Completed | Infigratinib 0.25 mg/kg/day, Placebo Comparator 0.25 mg/kg/day | NCT06164951 |
| Phase 3 | Recruiting | Acoramidis, Placebo oral tablet | NCT06563895 |
| Phase 3 | Not yet recruiting | Acoramidis (AG10) | NCT07116473 |
| Phase 3 | Recruiting | Encaleret, Placebo | NCT07805356 |
| Phase 2/3 | Enrolling by invitation | infigratinib 0.128 mg/kg/day, infigratinib 0.25 mg/kg/day | NCT06873035 |
| Phase 2/3 | Recruiting | Encaleret | NCT07080385 |
| Phase 2 | Terminated | BGJ398 (infigratinib) | NCT02150967 |
| Phase 2 | Completed | AG10, Placebo Oral Tablet | NCT03458130 |
| Phase 2 | Terminated | Acoramidis | NCT03536767 |
| Phase 2 | Completed | Infigratinib 0.016 mg/kg, Infigratinib 0.032 mg/kg | NCT04265651 |
| Phase 2 | Completed | Encaleret | NCT04581629 |
| Phase 2 | Enrolling by invitation | Infigratinib, Infigratinib | NCT05145010 |
| Phase 2 | Recruiting | Infigratinib is provided as a single dose of minitablets for oral administration, Infigratinib is provided as sprinkle capsules for daily oral administration | NCT07169279 |
| Phase 2 | Enrolling by invitation | Infigratinib | NCT07393373 |
| Phase 1/2 | Terminated | VT30 | NCT04409145 |
| Phase 1 | Completed | AG10 oral tablet, Placebo Oral Tablet | NCT03294707 |
| Phase 1 | Terminated | BBP-398 (Formerly known as IACS-15509) | NCT04528836 |
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