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                            Lead Product(s) : Marstacimab

                            Therapeutic Area : Genetic Disease

                            Study Phase : Approved

                            Sponsor : Not Applicable

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                            FDA Approves Pfizer’s HYMPAVZI™ For Hemophilia A Or B Without Inhibitors

                            Details : Hympavzi (marstacimab) is a human mAb IgG1 that targets TFPI approved as a subcutaneous treatment for severe hemophilia A or moderately severe to severe hemophilia B in 12 years and above patients.

                            Brand Name : Hympavzi

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            October 11, 2024

                            Lead Product(s) : Marstacimab

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Approved

                            Sponsor : Not Applicable

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                            Lead Product(s) : Enfortumab Vedotin,Pembrolizumab

                            Therapeutic Area : Oncology

                            Study Phase : Approved

                            Recipient : Astellas Pharma

                            Deal Size : Not Applicable

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                            Japan Approves PADCEV™ with KEYTRUDA® for Unresectable Urothelial Carcinoma

                            Details : Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.

                            Brand Name : Padcev

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            September 24, 2024

                            Lead Product(s) : Enfortumab Vedotin,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved

                            Recipient : Astellas Pharma

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            03

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
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                            Lead Product(s) : VLA15

                            Therapeutic Area : Infections and Infectious Diseases

                            Study Phase : Phase III

                            Recipient : Valneva

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            Valneva and Pfizer Report Positive Phase 2 Booster Results for Lyme Disease Vaccine

                            Details : VLA15, an alum-adjuvanted intramuscular vaccine, which is currently undergoing clinical development for the treatment of Lyme disease.

                            Brand Name : VLA15

                            Molecule Type : Vaccine

                            Upfront Cash : Not Applicable

                            September 03, 2024

                            Lead Product(s) : VLA15

                            Therapeutic Area : Infections and Infectious Diseases

                            Highest Development Status : Phase III

                            Recipient : Valneva

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            04

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
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                            Lead Product(s) : BNT162b2

                            Therapeutic Area : Infections and Infectious Diseases

                            Study Phase : Approved

                            Sponsor : BioNTech

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            Pfizer and BioNTech Get FDA Approval for Omicron-Adapted COVID-19 Vaccine

                            Details : Comirnaty JN.1 (Omi JN.1), a COVID-19 mRNA vaccine has achieved positive CHMP opinion by EMA for Omicron JN.1 lineage of SARS-CoV-2 infection in individuals 6 months of age and older.

                            Brand Name : Comirnaty JN.1

                            Molecule Type : Vaccine

                            Upfront Cash : Not Applicable

                            August 22, 2024

                            Lead Product(s) : BNT162b2

                            Therapeutic Area : Infections and Infectious Diseases

                            Highest Development Status : Approved

                            Sponsor : BioNTech

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            05

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : VLA15

                            Therapeutic Area : Infections and Infectious Diseases

                            Study Phase : Phase III

                            Recipient : Valneva

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            VALOR Trial: Valneva and Pfizer Announce Primary Vaccination Series Completion

                            Details : VLA15, an alum-adjuvanted formulation administered intramuscularly, is a vaccine candidate currently undergoing clinical development for the treatment of Lyme disease.

                            Brand Name : VLA15

                            Molecule Type : Vaccine

                            Upfront Cash : Not Applicable

                            July 17, 2024

                            Lead Product(s) : VLA15

                            Therapeutic Area : Infections and Infectious Diseases

                            Highest Development Status : Phase III

                            Recipient : Valneva

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            06

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Danuglipron

                            Therapeutic Area : Nutrition and Weight Loss

                            Study Phase : Phase II

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            Pfizer Advances Once-Daily Oral GLP-1 Agonist Danuglipron Development

                            Details : PF-06882961 (danuglipron) is an oral GLP-1R agonist smalll molecule candidate, which is being evaluated for the treatment of adults with obesity and without type 2 diabetes.

                            Brand Name : PF-06882961

                            Molecule Type : Small molecule

                            Upfront Cash : Not Applicable

                            July 11, 2024

                            Lead Product(s) : Danuglipron

                            Therapeutic Area : Nutrition and Weight Loss

                            Highest Development Status : Phase II

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            07

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Tisotumab Vedotin,Pembrolizumab,Carboplatin

                            Therapeutic Area : Oncology

                            Study Phase : Phase II

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            Tisotumab Vedotin Phase 2 Shows Antitumor Activity in Recurrent Head and Neck Cancer

                            Details : Tivdak (tisotumab vedotin) is an ADC that acts as coagulation factor III binding agent & tubulin inhibitor. It is being evaluated for the treatment of Head and Neck Squamous Cell Carcinoma.

                            Brand Name : Tivdak

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            June 03, 2024

                            Lead Product(s) : Tisotumab Vedotin,Pembrolizumab,Carboplatin

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            08

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
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                            Lead Product(s) : Tisotumab Vedotin

                            Therapeutic Area : Oncology

                            Study Phase : Approved

                            Sponsor : Genmab

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            FDA Grants Full Approval for TIVDAK® to Treat Recurrent or Metastatic Cervical Cancer

                            Details : Tivdak (tisotumab vedotin) is an antibody-drug conjugate that acts as coagulation factor III binding agent & tubulin inhibitor. It is approved for recurrent or metastatic cervical cancer.

                            Brand Name : Tivdak

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            April 29, 2024

                            Lead Product(s) : Tisotumab Vedotin

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved

                            Sponsor : Genmab

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            09

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Fidanacogene elaparvovec

                            Therapeutic Area : Genetic Disease

                            Study Phase : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            FDA Approves Pfizer’s BEQVEZ™ Gene Therapy for Hemophilia B

                            Details : Beqvez (fidanacogene elaparvovec) is an AAV-based gene therapy approved for adults with moderate to severe hemophilia B, introducing a functional copy of the high-activity FIX gene.

                            Brand Name : Beqvez

                            Molecule Type : Cell and Gene therapy

                            Upfront Cash : Not Applicable

                            April 26, 2024

                            Lead Product(s) : Fidanacogene elaparvovec

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            10

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Pfizer Inc

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Enfortumab Vedotin,Pembrolizumab

                            Therapeutic Area : Oncology

                            Study Phase : Approved

                            Recipient : Astellas Pharma

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            NMPA Accepts Astellas and Pfizer’s BLA for Enfortumab Vedotin and Keytruda

                            Details : Padcev (enfortumab vedotin-ejfv), a nectin-4 inhibitor ADC in combination with Keytruda (pembrolizumab), a PD-1 inhibitor. It is being evaluated for locally advanced or metastatic urothelial cancer.

                            Brand Name : Padcev

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            March 28, 2024

                            Lead Product(s) : Enfortumab Vedotin,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved

                            Recipient : Astellas Pharma

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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