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    [{"orgOrder":0,"company":"Pharmanovia","sponsor":"Aquestive Therapeutics","pharmaFlowCategory":"D","therapeuticArea":"Neurology","country":"U.S.A","productType":"Controlled Substance","year":"2022","type":"Licensing Agreement","leadProduct":"Diazepam","moa":"GABA-A receptor; anion channel","graph1":"Neurology","graph2":"Approved FDF","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Neurology","amount2New":0,"dosageForm":"Buccal Film","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"15","companyTruncated":"Pharmanovia \/ Pharmanovia"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Lindis Biotech","pharmaFlowCategory":"D","therapeuticArea":"Oncology","country":"GERMANY","productType":"Antibody","year":"2025","type":"Licensing Agreement","leadProduct":"Catumaxomab","moa":"T cell surface glycoprotein CD3 | Epithelial cell adhesion molecule","graph1":"Oncology","graph2":"Approved FDF","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intraperitoneal Infusion","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"15","companyTruncated":"Pharmanovia \/ Pharmanovia"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Lindis Biotech","pharmaFlowCategory":"DU","therapeuticArea":"Hepatology (Liver, Pancreatic, Gall Bladder)","country":"GERMANY","productType":"Antibody","year":"2025","type":"Inapplicable","leadProduct":"Catumaxomab","moa":"T cell surface glycoprotein CD3 | Epithelial cell adhesion molecule","graph1":"Hepatology (Liver, Pancreatic, Gall Bladder)","graph2":"Approved FDF","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Hepatology","amount2New":0,"dosageForm":"Intraperitoneal Injection","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"15","companyTruncated":"Pharmanovia \/ Pharmanovia"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Sanofi","pharmaFlowCategory":"D","therapeuticArea":"Psychiatry\/Psychology","country":"FRANCE","productType":"Controlled Substance","year":"2023","type":"Divestment","leadProduct":"Clobazam","moa":"GABA-A receptor; anion channel","graph1":"Psychiatry\/Psychology","graph2":"Approved FDF","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Psychiatry","amount2New":0,"dosageForm":"Oral Tablet","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"15","companyTruncated":"Pharmanovia \/ Pharmanovia"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Axsome Therapeutics","pharmaFlowCategory":"D","therapeuticArea":"Sleep","country":"U.S.A","productType":"Controlled Substance","year":"2023","type":"Licensing Agreement","leadProduct":"Solriamfetol Hydrochloride","moa":"Undisclosed","graph1":"Sleep","graph2":"Approved FDF","graph3":"Pharmanovia","amount2":0.17000000000000001,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Sleep","amount2New":0.17000000000000001,"dosageForm":"Oral Tablet","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"15","companyTruncated":"Pharmanovia \/ Pharmanovia"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Sleep","country":"UNITED KINGDOM","productType":"Other Small Molecule","year":"2023","type":"Inapplicable","leadProduct":"Chloral Hydrate","moa":"Undisclosed","graph1":"Sleep","graph2":"Phase IV","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Ph IV","therapeuticAreaShortName":"Sleep","amount2New":0,"dosageForm":"Oral","sponsorNew":"Pharmanovia \/ Inapplicable","highestDevelopmentStatusID":"11","companyTruncated":"Pharmanovia \/ Inapplicable"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Lindus Health","pharmaFlowCategory":"DU","therapeuticArea":"Sleep","country":"UNITED KINGDOM","productType":"Other Small Molecule","year":"2024","type":"Inapplicable","leadProduct":"Chloral Hydrate","moa":"Undisclosed","graph1":"Sleep","graph2":"Phase IV","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Ph IV","therapeuticAreaShortName":"Sleep","amount2New":0,"dosageForm":"Oral","sponsorNew":"Pharmanovia \/ Lindus Health","highestDevelopmentStatusID":"11","companyTruncated":"Pharmanovia \/ Lindus Health"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Closed Loop Medicine","pharmaFlowCategory":"D","therapeuticArea":"Cardiology\/Vascular Diseases","country":"UNITED KINGDOM","productType":"Undisclosed","year":"2023","type":"Partnership","leadProduct":"Undisclosed","moa":"Undisclosed","graph1":"Cardiology\/Vascular Diseases","graph2":"Preclinical","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Preclinical","therapeuticAreaShortName":"Cardiovascular Diseases","amount2New":0,"dosageForm":"Oral","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"4","companyTruncated":"Pharmanovia \/ Pharmanovia"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Stealth Biotherapeutics","pharmaFlowCategory":"D","therapeuticArea":"Rare Diseases and Disorders","country":"U.S.A","productType":"Peptide","year":"2023","type":"Licensing Agreement","leadProduct":"Elamipretide","moa":"peptides","graph1":"Rare Diseases and Disorders","graph2":"Phase III","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Ph III","therapeuticAreaShortName":"Rare Diseases","amount2New":0,"dosageForm":"Subcutaneous Injection","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"10","companyTruncated":"Pharmanovia \/ Pharmanovia"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"CSL","pharmaFlowCategory":"D","therapeuticArea":"Neurology","country":"AUSTRALIA","productType":"Other Small Molecule","year":"2024","type":"Licensing Agreement","leadProduct":"Safinamide Methanesulfonate","moa":"Monoamine oxidase B","graph1":"Neurology","graph2":"Approved FDF","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Neurology","amount2New":0,"dosageForm":"Undisclosed","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"15","companyTruncated":"Pharmanovia \/ Pharmanovia"},{"orgOrder":0,"company":"Pharmanovia","sponsor":"Lindis Biotech","pharmaFlowCategory":"D","therapeuticArea":"Oncology","country":"GERMANY","productType":"Antibody","year":"2024","type":"Licensing Agreement","leadProduct":"Catumaxomab","moa":"T cell surface glycoprotein CD3 | Epithelial cell adhesion molecule","graph1":"Oncology","graph2":"Phase III","graph3":"Pharmanovia","amount2":0,"highestDevelopmentShortName":"Ph III","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Undisclosed","sponsorNew":"Pharmanovia \/ Pharmanovia","highestDevelopmentStatusID":"10","companyTruncated":"Pharmanovia \/ Pharmanovia"}]

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                            01

                            Pharmanovia

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                            Lead Product(s) : Catumaxomab

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Recipient : Lindis Biotech

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Lindis Biotech and Pharmanovia Announce EMA Approval for a first-in-class Treatment

                            Details : Under a licensing agreement, LINDIS has granted Pharmanovia the exclusive rights to bring catumaxomab to market and spearhead its launch across Europe.

                            Product Name : Removab

                            Product Type : Antibody

                            Upfront Cash : Undisclosed

                            February 14, 2025

                            Lead Product(s) : Catumaxomab

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Recipient : Lindis Biotech

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

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                            02

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                            Lead Product(s) : Catumaxomab

                            Therapeutic Area : Hepatology (Liver, Pancreatic, Gall Bladder)

                            Study Phase : Approved FDF

                            Recipient : Lindis Biotech

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Lindis, Pharmanovia Secure EU Approval for Catumaxomab in Malignant Ascites

                            Details : Upon authorization by the European Commission, KORJUNY will be the only approved drug for malignant ascites in adults with epithelial cell adhesion molecule (EpCAM)-positive carcinomas

                            Product Name : Korjuny

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            February 13, 2025

                            Lead Product(s) : Catumaxomab

                            Therapeutic Area : Hepatology (Liver, Pancreatic, Gall Bladder)

                            Highest Development Status : Approved FDF

                            Recipient : Lindis Biotech

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            03

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                            Lead Product(s) : Catumaxomab

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Recipient : Lindis Biotech

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Pharmanovia In-Licenses Catumaxomab for Malignant Ascites from Lindis Biotech

                            Details : The agreement gives Pharmanovia the exclusive rights to market, Korjuny (catumaxomab), a first-in-class, trifunctional bi-specific monoclonal antibody, indicated for malignant ascites in adults.

                            Product Name : Korjuny

                            Product Type : Antibody

                            Upfront Cash : Undisclosed

                            November 19, 2024

                            Lead Product(s) : Catumaxomab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Recipient : Lindis Biotech

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

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                            04

                            Pharmanovia

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                            Lead Product(s) : Safinamide Methanesulfonate

                            Therapeutic Area : Neurology

                            Study Phase : Approved FDF

                            Recipient : CSL

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Pharmanovia Acquires Exclusive Rights to Treatment for Parkinson’s Disease

                            Details : Pharmanovia will take over rights from CSL and will be responsible for all commercial and regulatory activities of Xadago (safinamide), for adult patients with idiopathic Parkinson's disease.

                            Product Name : Xadago

                            Product Type : Other Small Molecule

                            Upfront Cash : Undisclosed

                            July 10, 2024

                            Lead Product(s) : Safinamide Methanesulfonate

                            Therapeutic Area : Neurology

                            Highest Development Status : Approved FDF

                            Recipient : CSL

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

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                            05

                            Pharmanovia

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                            Lead Product(s) : Chloral Hydrate

                            Therapeutic Area : Sleep

                            Study Phase : Phase IV

                            Sponsor : Lindus Health

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Pharmanovia Study Shows Chloral Hydrate Improves Severe Insomnia Within Two Weeks

                            Details : Chloral hydrate is converted rapidly to trichloroethanol, which is largely responsible for its hypnotic action. It is indicated for the treatment for severe insomnia.

                            Product Name : Undisclosed

                            Product Type : Other Small Molecule

                            Upfront Cash : Inapplicable

                            January 10, 2024

                            Lead Product(s) : Chloral Hydrate

                            Therapeutic Area : Sleep

                            Highest Development Status : Phase IV

                            Sponsor : Lindus Health

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            06

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                            Lead Product(s) : Chloral Hydrate

                            Therapeutic Area : Sleep

                            Study Phase : Phase IV

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            An Open-label Trial to Evaluate the Safety and Efficacy of Chloral Hydrate in Patients with Severe Insomnia

                            Details : Undisclosed

                            Product Name : Undisclosed

                            Product Type : Other Small Molecule

                            Upfront Cash : Inapplicable

                            September 26, 2023

                            Lead Product(s) : Chloral Hydrate

                            Therapeutic Area : Sleep

                            Highest Development Status : Phase IV

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            07

                            Pharmanovia

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                            Lead Product(s) : Clobazam

                            Therapeutic Area : Psychiatry/Psychology

                            Study Phase : Approved FDF

                            Recipient : Sanofi

                            Deal Size : Undisclosed

                            Deal Type : Divestment

                            DEALS_DEV arrow-down

                            Pharmanovia Acquires Global Central Nervous System (CNS) Portfolio from Sanofi

                            Details : Pharmanovia expands its neurology portfolio with the acquisition of 11 central nervous system (CNS) brands from Sanofi, including Frisium (clobazam), Gardenal (phenobarbital), Tercian (cyamemazine), Stemetil, Sentil, Urbanyl, Urbanil, Urbanol, Urbadan, N...

                            Product Name : Frisium

                            Product Type : Controlled Substance

                            Upfront Cash : Undisclosed

                            September 18, 2023

                            Lead Product(s) : Clobazam

                            Therapeutic Area : Psychiatry/Psychology

                            Highest Development Status : Approved FDF

                            Recipient : Sanofi

                            Deal Size : Undisclosed

                            Deal Type : Divestment

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                            08

                            Pharmanovia

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                            Lead Product(s) : Elamipretide

                            Therapeutic Area : Rare Diseases and Disorders

                            Study Phase : Phase III

                            Recipient : Stealth Biotherapeutics

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Stealth BioTherapeutics Enters into Exclusive Licensing Agreement with Pharmanovia to Commercialize Elamipreti...

                            Details : Pharmanovia will commercialize MTP-131 (elamipretide), an investigational mitochondrial protective agent, in Europe for the treatment of Barth syndrome, an ultra-rare cardiac condition caused by mitochondrial cardiolipin deficiency for which there are no...

                            Product Name : Bendavia

                            Product Type : Peptide

                            Upfront Cash : Undisclosed

                            May 30, 2023

                            Lead Product(s) : Elamipretide

                            Therapeutic Area : Rare Diseases and Disorders

                            Highest Development Status : Phase III

                            Recipient : Stealth Biotherapeutics

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

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                            09

                            Pharmanovia

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                            Lead Product(s) : Undisclosed

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Study Phase : Preclinical

                            Recipient : Closed Loop Medicine

                            Deal Size : Undisclosed

                            Deal Type : Partnership

                            DEALS_DEV arrow-down

                            Closed Loop Medicine and Pharmanovia Enter a Co-Development Partnership for Precision Medicine Combination The...

                            Details : Under the partnership, Closed Loop’s proprietary Software-as-a-Medical Device dosing optimization technology will be combined with Pharmanovia’s established anti-hypertensive medicines to develop drug + software product solutions for the treatment of...

                            Product Name : Undisclosed

                            Product Type : Undisclosed

                            Upfront Cash : Undisclosed

                            May 17, 2023

                            Lead Product(s) : Undisclosed

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Highest Development Status : Preclinical

                            Recipient : Closed Loop Medicine

                            Deal Size : Undisclosed

                            Deal Type : Partnership

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                            10

                            Pharmanovia

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                            Lead Product(s) : Solriamfetol Hydrochloride

                            Therapeutic Area : Sleep

                            Study Phase : Approved FDF

                            Recipient : Axsome Therapeutics

                            Deal Size : $167.0 million

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Axsome Therapeutics Enters into License Agreement with Pharmanovia to Expand Commercialization and Further Dev...

                            Details : Under the agreement, Pharmanovia will be responsible for the development and marketing of Sunosi (solriamfetol), a dual-acting dopamine and norepinephrine reuptake inhibitor shown to improve wakefulness in adults with EDS due to narcolepsy or OSA, in Eur...

                            Product Name : Sunosi

                            Product Type : Controlled Substance

                            Upfront Cash : $66.0 million

                            February 22, 2023

                            Lead Product(s) : Solriamfetol Hydrochloride

                            Therapeutic Area : Sleep

                            Highest Development Status : Approved FDF

                            Recipient : Axsome Therapeutics

                            Deal Size : $167.0 million

                            Deal Type : Licensing Agreement

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