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Molecule","year":"2025","type":"Inapplicable","leadProduct":"Vamifeport","moa":"SLC40A1","graph1":"Undisclosed","graph2":"Phase I","graph3":"CSL Behring","amount2":0,"highestDevelopmentShortName":"Ph I","therapeuticAreaShortName":"","amount2New":0,"dosageForm":"Undisclosed","sponsorNew":"CSL Behring \/ Undisclosed","highestDevelopmentStatusID":"6","companyTruncated":"CSL Behring \/ Undisclosed"},{"orgOrder":0,"company":"CSL Behring","sponsor":"Undisclosed","pharmaFlowCategory":"DU","therapeuticArea":"Pulmonary\/Respiratory Diseases","country":"U.S.A","productType":"Protein","year":"2025","type":"Inapplicable","leadProduct":"CSL787","moa":"Undisclosed","graph1":"Pulmonary\/Respiratory Diseases","graph2":"Phase II","graph3":"CSL Behring","amount2":0,"highestDevelopmentShortName":"Ph II","therapeuticAreaShortName":"Respiratory Diseases","amount2New":0,"dosageForm":"Undisclosed","sponsorNew":"CSL Behring \/ Undisclosed","highestDevelopmentStatusID":"8","companyTruncated":"CSL Behring \/ Undisclosed"}]

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                            01

                            CSL Behring

                            U.S.A arrow
                            World Drug Safety EU
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                            CSL Behring

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                            Lead Product(s) : BE1116

                            Therapeutic Area : Undisclosed

                            Study Phase : Phase III

                            Sponsor : Undisclosed

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            4F-PCC Safety & Efficacy In Adults Undergoing Complex Cardiovascular Surgery with CPB

                            Details : BE1116 is a drug candidate, which is currently being evaluated in Phase III clinical studies for the treatment of unspecified medical condition.

                            Product Name : Undisclosed

                            Product Type : Undisclosed

                            Upfront Cash : Inapplicable

                            July 30, 2025

                            Lead Product(s) : BE1116

                            Therapeutic Area : Undisclosed

                            Highest Development Status : Phase III

                            Sponsor : Undisclosed

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            02

                            CSL Behring

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                            CSL Behring

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                            World Drug Safety EU
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                            Lead Product(s) : CSL787

                            Therapeutic Area : Pulmonary/Respiratory Diseases

                            Study Phase : Phase II

                            Sponsor : Undisclosed

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Dose-Finding and Safety of CSL787 In Non-CF Bronchiectasis

                            Details : CSL787 is a Protein drug candidate, which is currently being evaluated in Phase II clinical studies for the treatment of Bronchiectasis.

                            Product Name : Undisclosed

                            Product Type : Protein

                            Upfront Cash : Inapplicable

                            July 02, 2025

                            Lead Product(s) : CSL787

                            Therapeutic Area : Pulmonary/Respiratory Diseases

                            Highest Development Status : Phase II

                            Sponsor : Undisclosed

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            03

                            CSL

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                            World Drug Safety EU
                            Not Confirmed

                            CSL

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                            Not Confirmed
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                            Lead Product(s) : Garadacimab

                            Therapeutic Area : Genetic Disease

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            FDA Approves CSL’s ANDEMBRY for HAE with Monthly Factor XIIa Targeting

                            Details : Andembry (garadacimab) uniquely inhibits the plasma protein, FXIIa. It is approved for hereditary angioedema (HAE) in adult and pediatric patients aged 12 years and older.

                            Product Name : Andembry

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            June 16, 2025

                            Lead Product(s) : Garadacimab

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            04

                            CSL Behring

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                            World Drug Safety EU
                            Not Confirmed

                            CSL Behring

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                            World Drug Safety EU
                            Not Confirmed
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                            Lead Product(s) : Vamifeport

                            Therapeutic Area : Undisclosed

                            Study Phase : Phase I

                            Sponsor : Undisclosed

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Effect of Food on Oral Bioavailability of Prolonged-Release Vamifeport in Healthy Adults

                            Details : Vamifeport is a Other Small Molecule drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of unspecified medical condition.

                            Product Name : Undisclosed

                            Product Type : Other Small Molecule

                            Upfront Cash : Inapplicable

                            May 30, 2025

                            Lead Product(s) : Vamifeport

                            Therapeutic Area : Undisclosed

                            Highest Development Status : Phase I

                            Sponsor : Undisclosed

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            05

                            CSL Vifor

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                            World Drug Safety EU
                            Not Confirmed

                            CSL Vifor

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                            World Drug Safety EU
                            Not Confirmed
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                            Lead Product(s) : Sparsentan

                            Therapeutic Area : Nephrology

                            Study Phase : Approved FDF

                            Recipient : Travere Therapeutics

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Travere, CSL Vifor Gain EU Approval for FILSPARI to Treat IgA Nephropathy

                            Details : Filspari (sparsentan) is an oral drug designed to selectively target two critical pathways - endothelin-1 and angiotensin II. It is approved for the treatment of IgA Nephropathy.

                            Product Name : Filspari

                            Product Type : Other Small Molecule

                            Upfront Cash : Inapplicable

                            April 29, 2025

                            Lead Product(s) : Sparsentan

                            Therapeutic Area : Nephrology

                            Highest Development Status : Approved FDF

                            Recipient : Travere Therapeutics

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            06

                            CSL

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                            Not Confirmed

                            CSL

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                            Lead Product(s) : Bempedoic Acid,Ezetimibe

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Study Phase : Approved FDF

                            Recipient : Esperion Therapeutics

                            Deal Size : $5.0 million

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Esperion Partners with CSL Seqirus to Commercialize Nexletol and Nexlizet in Australia

                            Details : CSL Seqirus gains exclusive rights to commercialize Nexletol (bempedoic acid) and Nexlizet (bempedoic acid and ezetimibe) in Australia and New Zealand for cardiovascular disease.

                            Product Name : Nexlizet

                            Product Type : Other Small Molecule

                            Upfront Cash : Undisclosed

                            March 03, 2025

                            Lead Product(s) : Bempedoic Acid,Ezetimibe

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Highest Development Status : Approved FDF

                            Recipient : Esperion Therapeutics

                            Deal Size : $5.0 million

                            Deal Type : Licensing Agreement

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                            07

                            CSL

                            Australia arrow
                            World Drug Safety EU
                            Not Confirmed

                            CSL

                            Australia arrow
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                            Not Confirmed
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                            Lead Product(s) : Garadacimab

                            Therapeutic Area : Genetic Disease

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            CSL Gets Japan Approval for ANDEMBRY® Subcutaneous Injection

                            Details : Andembry (garadacimab) is a novel Factor XIIa-inhibitory monoclonal antibody. It is under development as a once-monthly subcutaneous prophylactic treatment for attacks related to HAE.

                            Product Name : Andembry

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            February 20, 2025

                            Lead Product(s) : Garadacimab

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            08

                            CSL

                            Australia arrow
                            World Drug Safety EU
                            Not Confirmed

                            CSL

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                            Not Confirmed
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                            Lead Product(s) : Self-Amplifying Mrna Vaccine

                            Therapeutic Area : Infections and Infectious Diseases

                            Study Phase : Approved FDF

                            Sponsor : Arcturus Therapeutics

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            EU Approves CSL, Arcturus’ KOSTAIVE®, First Self-Amplifying mRNA COVID Vaccine

                            Details : Kostaive is an self-amplifying mRNA (sa-mRNA) vaccine based on the SARS-CoV-2 D614G variant spike protein. This covid-19 vaccine for initial vaccination and booster for adults 18 years and older.

                            Product Name : Kostaive

                            Product Type : Vaccine

                            Upfront Cash : Inapplicable

                            February 14, 2025

                            Lead Product(s) : Self-Amplifying Mrna Vaccine

                            Therapeutic Area : Infections and Infectious Diseases

                            Highest Development Status : Approved FDF

                            Sponsor : Arcturus Therapeutics

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            09

                            CSL

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                            World Drug Safety EU
                            Not Confirmed

                            CSL

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                            Not Confirmed
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                            Lead Product(s) : Garadacimab

                            Therapeutic Area : Genetic Disease

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            EU Commission Approves CSL's ANDEMBRY® for Preventing Hereditary Angioedema Attacks

                            Details : Andembry (garadacimab) is a novel Factor XIIa-inhibitory monoclonal antibody. It is under development as a once-monthly subcutaneous prophylactic treatment for attacks related to HAE.

                            Product Name : Undisclosed

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            February 13, 2025

                            Lead Product(s) : Garadacimab

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            10

                            CSL Behring

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                            Not Confirmed

                            CSL Behring

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                            Lead Product(s) : Lonoctocog Alfa

                            Therapeutic Area : Genetic Disease

                            Study Phase : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Recombinant Single-chain Factor VIII (rVIII-SingleChain) in Chinese Participants With Hemophilia A Previously ...

                            Details : Undisclosed

                            Product Name : Undisclosed

                            Product Type : Undisclosed

                            Upfront Cash : Inapplicable

                            December 17, 2024

                            Lead Product(s) : Lonoctocog Alfa

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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