BONAC is an organization that focuses on the research and development of nucleic acid medicines. They offer a range of services including the manufacturing of nucleic acid drug substances and the development of drugs. The company was established in 2010.

Tags

Respiratory Diseases

Infectious Diseases

Eye Diseases

siRNA

Disease domain score

A glimpse into the focused therapeutic areas

Technology Platform

Most used technologies in drug development

Targets

Most frequently developed targets

Disease Domain	Count

Infectious Diseases	3
Neoplasms	1
Endocrinology and Metabolic Disease	1

Top 5 Drug Type	Count

siRNA	8

Top 5 Target	Count

TGF-β1(Transforming growth factor beta 1)	2
renin receptor(ATPase H+ transporting accessory protein 2)	1

Drugs associated with BONAC Corp.

TRK-250

Target

TGF-β1

Mechanism

TGF-β1 inhibitors

Active Org.

Toray Industries, Inc. [+1]

Originator Org.

BONAC Corp.

Active Indication

Idiopathic Pulmonary Fibrosis

Inactive Indication-

Drug Highest PhasePhase 1

First Approval Ctry. / Loc.-

First Approval Date-

BNC-1251

Target-

Mechanism

RNA interference

Active Org.

BONAC Corp.

Originator Org.

BONAC Corp.

Active Indication

Neoplasms

Inactive Indication-

Drug Highest PhasePreclinical

First Approval Ctry. / Loc.-

First Approval Date-

BNC-1701

Target-

Mechanism-

Active Org.

BONAC Corp.

Originator Org.

BONAC Corp.

Active Indication

Hepatitis B

Inactive Indication-

Drug Highest PhasePreclinical

First Approval Ctry. / Loc.-

First Approval Date-

100 Clinical Results associated with BONAC Corp.

0 Patents (Medical) associated with BONAC Corp.

Literatures (Medical) associated with BONAC Corp.

01 Jun 2023·Molecular therapy. Nucleic acids

Terminal bridging of siRNA duplex at the ribose 2′ position controls strand bias and target sequence preference

Article

Author: Shibata, Atsushi ; Shirohzu, Hisao ; Emura, Chisato ; Abe, Tomoaki ; Ohgi, Tadaaki ; Iwakami, Yusuke ; Aoki, Eriko

Small interfering RNA (siRNA) and short hairpin RNA (shRNA) are widely used as RNA interference (RNAi) reagents. Recently, truncated shRNAs that trigger RNAi in a Dicer-independent manner have been developed. We generated a novel class of RNAi reagent, designated enforced strand bias (ESB) RNA, in which an siRNA duplex was chemically bridged between the 3' terminal overhang region of the guide strand and the 5' terminal nucleotide of the passenger strand. ESB RNA, which is chemically bridged at the 2' positions of ribose (2'-2' ESB RNA), functions in a Dicer-independent manner and was highly effective at triggering RNAi without the passenger strand-derived off-target effect. In addition, the 2'-2' ESB RNA exhibited a unique target sequence preference that differs from siRNA and silenced target sequences that could not be effectively suppressed by siRNA. Our results indicate that ESB RNA has the potential to be an effective RNAi reagent even when the target sequence is not suitable for siRNA.

01 Jun 2017·Molecular therapy. Nucleic acidsQ2 · MEDICINE

A Novel Single-Strand RNAi Therapeutic Agent Targeting the (Pro)renin Receptor Suppresses Ocular Inflammation

Q2 · MEDICINE

ArticleOA

Author: Ishizuka, Erdal Tan ; Noda, Kousuke ; Ishida, Susumu ; Toyofuku, Hidekazu ; Namba, Kenichi ; Matsumoto, Takahiro ; Kanda, Atsuhiro ; Shibata, Atsushi

The receptor-associated prorenin system (RAPS) refers to the pathogenic mechanism whereby prorenin binding to the (pro)renin receptor [(P)RR] dually activates the tissue renin-angiotensin system (RAS) and RAS-independent intracellular signaling. Here we revealed significant upregulation of prorenin and soluble (P)RR levels in the vitreous fluid of patients with uveitis compared to non-inflammatory controls, together with a positive correlation between these RAPS components and monocyte chemotactic protein-1 among several upregulated cytokines. Moreover, we developed a novel single-strand RNAi agent, proline-modified short hairpin RNA directed against human and mouse (P)RR [(P)RR-PshRNA], and we determined its safety and efficacy in vitro and in vivo. Application of (P)RR-PshRNA in mice caused significant amelioration of acute (uveitic) and chronic (diabetic) models of ocular inflammation with no apparent adverse effects. Our findings demonstrate the significant implication of RAPS in the pathogenesis of human uveitis and the potential usefulness of (P)RR-PshRNA as a therapeutic agent to reduce ocular inflammation.

01 Jul 2015·International journal of pharmaceuticsQ2 · MEDICINE

Functional peptide nanocarriers for delivery of novel anti-RelA RNA interference agents as a topical treatment of atopic dermatitis

Q2 · MEDICINE

Article

Author: Okada, Hiroaki ; Sogabe, Kana ; Kanazawa, Takanori ; Tamano, Kuniko ; Ohgi, Tadaaki ; Seta, Yasuo ; Endo, Takahiro ; Hamasaki, Tomohiro

Small interfering RNAs (siRNAs) are a potential treatment of atopic dermatitis (AD) because they can specifically silence the gene expression of AD-related factors. However, siRNA alone cannot exert a sufficiently strong therapeutic effect due to low delivery efficiency to the target tissues and cells; simply increasing the amount used is not possible due to the possibility of off-target effects. We previously reported a novel class of therapeutic RNA interference (RNAi) agents called nkRNA(®) and PnkRNA(®), which have been shown to be effective in several disease models, have greater resistance to nuclease degradation than canonical siRNAs, and do not induce any immunotoxicity. In the present study, we describe a non-invasive and effective transdermal RNAi therapeutic system for atopic dermatitis that uses the functional cell-penetrating stearoyl-oligopeptide OK-102 as a cytoplasm-responsive nanocarrier for nkRNA(®) and PnkRNA(®). The two RNAi agents were targeted against RelA, a subclass of NF-κB (nuclear factor kappa B), and, as part of OK-102 complexes, they strongly silenced RelA mRNA in macrophage cells and demonstrated a significant therapeutic effect in a mouse model of AD. It was shown that OK-102-complexed RNAi agents were an efficient therapeutic system for AD and caused no adverse reactions.

News (Medical) associated with BONAC Corp.

08 Mar 2023

·www.businesswire.com

Diabetic Retinopathy Pipeline Research Report 2022: Featuring Insights on 60+ Companies and Drugs in the Sector - ResearchAndMarkets.com

DUBLIN--( BUSINESS WIRE )--The "Diabetic Retinopathy - Pipeline Insight, 2022" clinical trials has been added to ResearchAndMarkets.com's offering. This "Diabetic Retinopathy - Pipeline Insight, 2022" report provides comprehensive insights about 60+ companies and 60+ pipeline drugs in Diabetic Retinopathy pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space. Geography Covered Global coverage Diabetic Retinopathy Understanding Diabetic Retinopathy: Overview Diabetic Retinopathy Emerging Drugs Chapters This segment of the Diabetic Retinopathy report encloses its detailed analysis of various drugs in different stages of clinical development, including phase II, I, preclinical and Discovery. It also helps to understand clinical trial details, expressive pharmacological action, agreements and collaborations, and the latest news and press releases. Diabetic Retinopathy Emerging Drugs KSI-301: Kodiak Sciences The Therapeutic candidate KSI-301, currently in clinical development, is a novel anti-VEGF biologic designed to have an extended ocular half-life. Ischemia due to vein occlusion results in secretion of vascular endothelial growth factor (VEGF) that causes further vascular leakage and edema. Anti-VEGF agents have become a very common treatment to improve the clinical outcomes in patients with diabetic retinopathy. As in wet AMD, an intensive treatment frequency is required to achieve optimal outcomes with currently-approved anti-VEGFs agents. However, many patients are lost to follow up due to the frequent injections and real-world outcomes in diabetic retinopathy do not meet the promise shown in clinical trials. By extending on mechanism treatment interval, KSI-301 may relieve the high treatment burden for patients, their family members, and physicians. KSI-301 is being developed in Phase III stage of development towards a once every four to six-month treatment regimen - a possible gamechanger that may provide the opportunity for real prevention. Brolucizumab: Novartis Brolucizumab (RTH258) is a humanized single-chain antibody fragment (scFv) and the most clinically advanced, humanized single-chain antibody fragment to reach this stage of development. Single-chain antibody fragments are highly sought after in drug development due to their small size, enhanced tissue penetration, rapid clearance from systemic circulation and drug delivery characteristics. The proprietary innovative structure results in a small molecule (26 kDa) with potent inhibition of, and high affinity to, all VEGF-A isoforms. In preclinical studies, brolucizumab inhibited activation of VEGF receptors through prevention of the ligand-receptor interaction. Increased signaling through the VEGF pathway is associated with pathologic ocular angiogenesis and retinal edema. Inhibition of the VEGF pathway has been shown to inhibit the growth of neovascular lesions, resolve retinal edema and improve vision in patients with chorioretinal vascular diseases. Currently, it is in Phase III stage of development to treat Diabetic Retinopathy. RGX 314: Regenxbio Inc. RGX-314 is being developed as a novel, one-time subretinal treatment that includes the NAV AAV8 vector containing a gene encoding for a monoclonal antibody fragment. The expressed protein is designed to neutralize vascular endothelial growth factor (VEGF) activity, modifying the pathway for formation of new leaky blood vessels and retinal fluid accumulation. The company is currently enrolling patients in ALTITUDETM, a Phase II trial for the treatment of diabetic retinopathy using suprachoroidal delivery of RGX-314. Diabetic Retinopathy: Therapeutic Assessment This segment of the report provides insights about the different Diabetic Retinopathy drugs segregated based on following parameters that define the scope of the report, such as: Major Players in Diabetic Retinopathy There are approx. 60+ key companies which are developing the therapies for Diabetic Retinopathy. The companies which have their Diabetic Retinopathy drug candidates in the mid to advanced stage, i.e. Phase III include, Kodiak Sciences Phases The report covers around 60+ products under different phases of clinical development like Late-stage products (Phase III ) Mid-Stage products (Phase II) Early-stage products ( Phase I) along with the details of Pre-clinical and Discovery stage candidates Discontinued & Inactive candidates ^- Route of Administration Diabetic Retinopathy pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as Intravenous Oral Molecule Type Products have been categorized under various Molecule types such as Small molecules Peptide Antibiotics Product Type Drugs have been categorized under various product types like Mono, Combination and Mono/Combination. Diabetic Retinopathy: Pipeline Development Activities The report provides insights into different therapeutic candidates in phase II, I, preclinical and discovery stage. It also analyses Diabetic Retinopathy therapeutic drugs key players involved in developing key drugs. Pipeline Development Activities The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging Diabetic Retinopathy drugs. Report Highlights The companies and academics are working to assess challenges and seek opportunities that could influence Diabetic Retinopathy R&D. The therapies under development are focused on novel approaches to treat/improve Diabetic Retinopathy. Diabetic Retinopathy Report Insights Diabetic Retinopathy Pipeline Analysis Therapeutic Assessment Unmet Needs Impact of Drugs Diabetic Retinopathy Report Assessment Pipeline Product Profiles Therapeutic Assessment Pipeline Assessment Inactive drugs assessment Unmet Needs Key Questions Answered Current Treatment Scenario and Emerging Therapies: How many companies are developing Diabetic Retinopathy drugs? How many Diabetic Retinopathy drugs are developed by each company? How many emerging drugs are in mid-stage, and late-stage of development for the treatment of Diabetic Retinopathy? What are the key collaborations (Industry-Industry, Industry-Academia), Mergers and acquisitions, licensing activities related to the Diabetic Retinopathy therapeutics? What are the recent trends, drug types and novel technologies developed to overcome the limitation of existing therapies? What are the clinical studies going on for Diabetic Retinopathy and their status? What are the key designations that have been granted to the emerging drugs? Key Products KSI-301 Brolucizumab Runcaciguat RC 28 E AKB-9778 RG7774 RGX-314 APX3330 ADVM-022 THR-687 OCX 063 BI 764524 MS-553 A selection of companies mentioned in this report includes Ascentage Pharma AptaBio BONAC corporation CCRP Therapeutics Curacle Co Ltd Emerald Bioscience, Inc. EnnovaBio Everglades Biopharma LUYE PHARMA MIRAE CELL BIO Novelty Nobility Inc Noveome Biotherapeutics, Inc. Palatin Technologies Inc PharmAbcine Inc PYC Therapeutics Retinset SL RIBOMIC Shanghai Henlius Biotech OccuRx Kodiak Sciences Novartis Bayer RemeGen Aerpio Therapeutics Hoffman-La-Roche Regenxbio Inc. Ocuphire Pharma, Inc. Adverum Biotechnologies Oxurion MingSight Relin Pharmaceuticals Boehringer Ingelheim NovaGo Therapeutics HanAll Biopharma For more information about this clinical trials report visit https://www.researchandmarkets.com/r/vy3xvo About ResearchAndMarkets.com ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

Phase 2Phase 3

16 Nov 2022

·www.businesswire.com

Diabetic Retinopathy Drug Pipeline Market Insights Report 2022 - Comprehensive Insights About 60+ Companies and 60+ Pipeline Drugs - ResearchAndMarkets.com

DUBLIN--( BUSINESS WIRE )--The "Diabetic Retinopathy - Pipeline Insight, 2022" report has been added to ResearchAndMarkets.com's offering. This report provides comprehensive insights about 60+ companies and 60+ pipeline drugs in Diabetic Retinopathy pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space. Diabetic Retinopathy Emerging Drugs Chapters This segment of the Diabetic Retinopathy report encloses its detailed analysis of various drugs in different stages of clinical development, including phase II, I, preclinical and Discovery. It also helps to understand clinical trial details, expressive pharmacological action, agreements and collaborations, and the latest news and press releases. Diabetic Retinopathy Emerging Drugs KSI-301: Kodiak Sciences The Therapeutic candidate KSI-301, currently in clinical development, is a novel anti-VEGF biologic designed to have an extended ocular half-life. Ischemia due to vein occlusion results in secretion of vascular endothelial growth factor (VEGF) that causes further vascular leakage and edema. Anti-VEGF agents have become a very common treatment to improve the clinical outcomes in patients with diabetic retinopathy. As in wet AMD, an intensive treatment frequency is required to achieve optimal outcomes with currently-approved anti-VEGFs agents. However, many patients are lost to follow up due to the frequent injections and real-world outcomes in diabetic retinopathy do not meet the promise shown in clinical trials. By extending on mechanism treatment interval, KSI-301 may relieve the high treatment burden for patients, their family members, and physicians. KSI-301 is being developed in Phase III stage of development towards a once every four to six-month treatment regimen - a possible gamechanger that may provide the opportunity for real prevention. Brolucizumab: Novartis Brolucizumab (RTH258) is a humanized single-chain antibody fragment (scFv) and the most clinically advanced, humanized single-chain antibody fragment to reach this stage of development. Single-chain antibody fragments are highly sought after in drug development due to their small size, enhanced tissue penetration, rapid clearance from systemic circulation and drug delivery characteristics. The proprietary innovative structure results in a small molecule (26 kDa) with potent inhibition of, and high affinity to, all VEGF-A isoforms. In preclinical studies, brolucizumab inhibited activation of VEGF receptors through prevention of the ligand-receptor interaction. Increased signaling through the VEGF pathway is associated with pathologic ocular angiogenesis and retinal edema. Inhibition of the VEGF pathway has been shown to inhibit the growth of neovascular lesions, resolve retinal edema and improve vision in patients with chorioretinal vascular diseases. Currently, it is in Phase III stage of development to treat Diabetic Retinopathy. RGX 314: Regenxbio Inc. RGX-314 is being developed as a novel, one-time subretinal treatment that includes the NAV AAV8 vector containing a gene encoding for a monoclonal antibody fragment. The expressed protein is designed to neutralize vascular endothelial growth factor (VEGF) activity, modifying the pathway for formation of new leaky blood vessels and retinal fluid accumulation. The company is currently enrolling patients in ALTITUDETM, a Phase II trial for the treatment of diabetic retinopathy using suprachoroidal delivery of RGX-314. Diabetic Retinopathy: Therapeutic Assessment This segment of the report provides insights about the different Diabetic Retinopathy drugs segregated based on following parameters that define the scope of the report, such as: Major Players in Diabetic Retinopathy There are approx. 60+ key companies which are developing the therapies for Diabetic Retinopathy. The companies which have their Diabetic Retinopathy drug candidates in the mid to advanced stage, i.e. Phase III include, Kodiak Sciences Phases This report covers around 60+ products under different phases of clinical development like Late-stage products (Phase III ) Mid-Stage products (Phase II) Early-stage products ( Phase I) along with the details of Pre-clinical and Discovery stage candidates Discontinued & Inactive candidates Route of Administration Diabetic Retinopathy pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as Intravenous Oral Molecule Type Products have been categorized under various Molecule types such as Small molecules Peptide Antibiotics Product Type Drugs have been categorized under various product types like Mono, Combination and Mono/Combination. Diabetic Retinopathy: Pipeline Development Activities The report provides insights into different therapeutic candidates in phase II, I, preclinical and discovery stage. It also analyses Diabetic Retinopathy therapeutic drugs key players involved in developing key drugs. Pipeline Development Activities The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging Diabetic Retinopathy drugs. Report Highlights The companies and academics are working to assess challenges and seek opportunities that could influence Diabetic Retinopathy R&D. The therapies under development are focused on novel approaches to treat/improve Diabetic Retinopathy. Diabetic Retinopathy Report Insights Diabetic Retinopathy Pipeline Analysis Therapeutic Assessment Unmet Needs Impact of Drugs Diabetic Retinopathy Report Assessment Pipeline Product Profiles Therapeutic Assessment Pipeline Assessment Inactive drugs assessment Unmet Needs Key Questions Current Treatment Scenario and Emerging Therapies: How many companies are developing Diabetic Retinopathy drugs? How many Diabetic Retinopathy drugs are developed by each company? How many emerging drugs are in mid-stage, and late-stage of development for the treatment of Diabetic Retinopathy? What are the key collaborations (Industry-Industry, Industry-Academia), Mergers and acquisitions, licensing activities related to the Diabetic Retinopathy therapeutics? What are the recent trends, drug types and novel technologies developed to overcome the limitation of existing therapies? What are the clinical studies going on for Diabetic Retinopathy and their status? What are the key designations that have been granted to the emerging drugs? Key Players Kodiak Sciences Novartis Bayer RemeGen Aerpio Therapeutics Hoffman-La-Roche Regenxbio Inc. Ocuphire Pharma, Inc. Adverum Biotechnologies Oxurion MingSight Relin Pharmaceuticals Boehringer Ingelheim NovaGo Therapeutics HanAll Biopharma Ascentage Pharma AptaBio BONAC corporation CCRP Therapeutics Curacle Co Ltd Emerald Bioscience, Inc. EnnovaBio Everglades Biopharma LUYE PHARMA MIRAE CELL BIO Novelty Nobility Inc Noveome Biotherapeutics, Inc. Palatin Technologies Inc PharmAbcine Inc PYC Therapeutics Retinset SL RIBOMIC Shanghai Henlius Biotech OccuRx Key Products KSI-301 Brolucizumab Runcaciguat RC 28 E AKB-9778 RG7774 RGX-314 APX3330 ADVM-022 THR-687 OCX 063 BI 764524 MS-553 For more information about this report visit https://www.researchandmarkets.com/r/lg24xg

Phase 2Phase 3

100 Deals associated with BONAC Corp.

100 Translational Medicine associated with BONAC Corp.

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Pipeline

Pipeline Snapshot as of 03 Oct 2024

The statistics for drugs in the Pipeline is the current organization and its subsidiaries are counted as organizations,Early Phase 1 is incorporated into Phase 1, Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3

Discovery

Preclinical

Phase 1

Other

Current Projects

Drug(Targets)	Indications	Global Highest Phase

TRK-250 ( TGF-β1 )	Idiopathic Pulmonary Fibrosis More	Phase 1
BNC-1601 ( renin receptor )	Dystrophy, Macular More	Preclinical
BNC-1602	Liver Cirrhosis More	Preclinical
BNC-1322	COVID-19 More	Preclinical
BNC-1251	Neoplasms More	Preclinical

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