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08 Jan 2025
// FIERCE BIOTECH
https://www.fiercebiotech.com/medtech/jj-pauses-varipulse-pulsed-field-ablation-debut-following-4-reports-strokes
Details:
Johnson gains an exclusive license to Kaken’s STAT6 program, including lead candidate KP-723, a preclinical STAT6 inhibitor, for autoimmune and allergic diseases, including atopic dermatitis.
Lead Product(s): KP-723
Therapeutic Area: Dermatology Brand Name: KP-723
Study Phase: PreclinicalProduct Type: Small molecule
Recipient: Kaken Pharmaceuticals
Deal Size: $1,247.5 million Upfront Cash: $30.0 million
Deal Type: Licensing Agreement December 26, 2024
Lead Product(s) : KP-723
Therapeutic Area : Dermatology
Highest Development Status : Preclinical
Recipient : Kaken Pharmaceuticals
Deal Size : $1,247.5 million
Deal Type : Licensing Agreement
Kaken, J&J Ink Potential $1.2B-Plus STAT6 Deal
Details : Johnson gains an exclusive license to Kaken’s STAT6 program, including lead candidate KP-723, a preclinical STAT6 inhibitor, for autoimmune and allergic diseases, including atopic dermatitis.
Brand Name : KP-723
Molecule Type : Small molecule
Upfront Cash : $30.0 million
December 26, 2024
Details:
Tremfya (guselkumab) is the first approved fully-human, monoclonal antibody that blocks IL-23. It is being evaluated for the treatment of adults with moderately to severely active ulcerative colitis.
Lead Product(s): Guselkumab
Therapeutic Area: Gastroenterology Brand Name: Tremfya
Study Phase: Phase IIIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 22, 2024
Lead Product(s) : Guselkumab
Therapeutic Area : Gastroenterology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
J&J Seeks FDA Nod for TREMFYA® Subcutaneous Use in Ulcerative Colitis Treatment
Details : Tremfya (guselkumab) is the first approved fully-human, monoclonal antibody that blocks IL-23. It is being evaluated for the treatment of adults with moderately to severely active ulcerative colitis.
Brand Name : Tremfya
Molecule Type : Large molecule
Upfront Cash : Not Applicable
November 22, 2024
Details:
JNJ-2113 (icotrokinra) is a first and only targeted oral peptide that is designed to selectively block the IL-23R. It is under clinical development for the treatment of moderate-to-severe psoriasis.
Lead Product(s): Icotrokinra
Therapeutic Area: Dermatology Brand Name: JNJ-2113
Study Phase: Phase IIIProduct Type: Peptide
Sponsor: Protagonist Therapeutics
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 18, 2024
Lead Product(s) : Icotrokinra
Therapeutic Area : Dermatology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Protagonist Therapeutics
Deal Size : Not Applicable
Deal Type : Not Applicable
Protagonist Announces Positive Results for Icotrokinra in Phase 3 Plaque Psoriasis
Details : JNJ-2113 (icotrokinra) is a first and only targeted oral peptide that is designed to selectively block the IL-23R. It is under clinical development for the treatment of moderate-to-severe psoriasis.
Brand Name : JNJ-2113
Molecule Type : Peptide
Upfront Cash : Not Applicable
November 18, 2024
Details:
Rybrevant (amivantamab) is a fully-human EGFR-MET bispecific antibody. It is indicated in combination with Lazertinib for the treatment of Advanced or Metastatic Non-small Cell Lung Cancer.
Lead Product(s): Amivantamab,Lazertinib,Dexamethasone
Therapeutic Area: Oncology Brand Name: Rybrevant
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 15, 2024
Lead Product(s) : Amivantamab,Lazertinib,Dexamethasone
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
CHMP Recommends RYBREVANT® and LAZCLUZE® for EGFR-Mutated Lung Cancer
Details : Rybrevant (amivantamab) is a fully-human EGFR-MET bispecific antibody. It is indicated in combination with Lazertinib for the treatment of Advanced or Metastatic Non-small Cell Lung Cancer.
Brand Name : Rybrevant
Molecule Type : Large molecule
Upfront Cash : Not Applicable
November 15, 2024
Details:
JNJ-80202135 (nipocalimab) is an investigational, high-affinity, fully human, aglycosylated, effectorless, monoclonal antibody that blocks FcRn. It is being evaluated for Sjögren's disease.
Lead Product(s): Nipocalimab
Therapeutic Area: Immunology Brand Name: JNJ-80202135
Study Phase: Phase IIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 14, 2024
Lead Product(s) : Nipocalimab
Therapeutic Area : Immunology
Highest Development Status : Phase II
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Nipocalimab Shows Clinical Gains in Phase 2 Study for Sjögren’s Disease
Details : JNJ-80202135 (nipocalimab) is an investigational, high-affinity, fully human, aglycosylated, effectorless, monoclonal antibody that blocks FcRn. It is being evaluated for Sjögren's disease.
Brand Name : JNJ-80202135
Molecule Type : Large molecule
Upfront Cash : Not Applicable
November 14, 2024
Details:
JNJ-80202135 (nipocalimab) is an investigational, high-affinity, fully human, aglycosylated, effectorless, monoclonal antibody that blocks FcRn. It is being evaluated for Sjögren's disease.
Lead Product(s): Nipocalimab
Therapeutic Area: Immunology Brand Name: JNJ-80202135
Study Phase: Phase IIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 11, 2024
Lead Product(s) : Nipocalimab
Therapeutic Area : Immunology
Highest Development Status : Phase II
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Nipocalimab Granted FDA Breakthrough Designation for Sjögren's Disease
Details : JNJ-80202135 (nipocalimab) is an investigational, high-affinity, fully human, aglycosylated, effectorless, monoclonal antibody that blocks FcRn. It is being evaluated for Sjögren's disease.
Brand Name : JNJ-80202135
Molecule Type : Large molecule
Upfront Cash : Not Applicable
November 11, 2024
Details:
Darzalex Faspro (daratumumab and hyaluronidase-fihj) in is being investgated as monotherapy for the treatment of adult patients with high-risk smouldering multiple myeloma.
Lead Product(s): Daratumumab,Hyaluronidase
Therapeutic Area: Oncology Brand Name: Darzalex Faspro
Study Phase: Phase IIIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 08, 2024
Lead Product(s) : Daratumumab,Hyaluronidase
Therapeutic Area : Oncology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Johnson & Johnson Submits DARZALEX® Applications for Myeloma Approval
Details : Darzalex Faspro (daratumumab and hyaluronidase-fihj) in is being investgated as monotherapy for the treatment of adult patients with high-risk smouldering multiple myeloma.
Brand Name : Darzalex Faspro
Molecule Type : Large molecule
Upfront Cash : Not Applicable
November 08, 2024
Details:
Tremfya (guselkumab) is the first approved fully-human, monoclonal antibody that blocks IL-23. It is being evaluated for the treatment of adults with moderately to severely active crohn's disease.
Lead Product(s): Guselkumab
Therapeutic Area: Gastroenterology Brand Name: Tremfya
Study Phase: Phase IIIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 28, 2024
Lead Product(s) : Guselkumab
Therapeutic Area : Gastroenterology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
TREMFYA® First IL-23 Inhibitor to Show Results in Crohn's Disease
Details : Tremfya (guselkumab) is the first approved fully-human, monoclonal antibody that blocks IL-23. It is being evaluated for the treatment of adults with moderately to severely active crohn's disease.
Brand Name : Tremfya
Molecule Type : Large molecule
Upfront Cash : Not Applicable
October 28, 2024
Details:
Tremfya (guselkumab) is the first approved fully-human, monoclonal antibody that blocks IL-23. It is being evaluated for the treatment of moderate plaque psoriasis with special site involvement.
Lead Product(s): Guselkumab
Therapeutic Area: Dermatology Brand Name: Tremfya
Study Phase: Phase IIIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 25, 2024
Lead Product(s) : Guselkumab
Therapeutic Area : Dermatology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
TREMFYA® Clears Plaque Psoriasis Effectively in New SPECTREM Study Findings
Details : Tremfya (guselkumab) is the first approved fully-human, monoclonal antibody that blocks IL-23. It is being evaluated for the treatment of moderate plaque psoriasis with special site involvement.
Brand Name : Tremfya
Molecule Type : Large molecule
Upfront Cash : Not Applicable
October 25, 2024
Details:
Darzalex (daratumumab) a CD38 inhibitor, being evaluated in combination with bortezomib, lenalidomide, dexamethasone for the treatment of newly diagnosed multiple myeloma.
Lead Product(s): Daratumumab,Lenalidomide,Bortezomib
Therapeutic Area: Oncology Brand Name: Darzalex
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 23, 2024
Lead Product(s) : Daratumumab,Lenalidomide,Bortezomib
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
DARZALEX Quadruplet Approved in EU for Newly Diagnosed Myeloma Patients
Details : Darzalex (daratumumab) a CD38 inhibitor, being evaluated in combination with bortezomib, lenalidomide, dexamethasone for the treatment of newly diagnosed multiple myeloma.
Brand Name : Darzalex
Molecule Type : Large molecule
Upfront Cash : Not Applicable
October 23, 2024
Regulatory Info :
Registration Country : USA
Dosage Form : INJECTABLE; INJECTION
Brand Name : REOPRO
Dosage Strength : 2MG/ML
Packaging :
Approval Date :
Application Number : 103575
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Johnson & Johnson Innovative Medicine
Dosage Form : INJEKTIONS-/INFUSIONSVÄ...
Brand Name : ReoPro
Dosage Strength : 2 MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Australia
Johnson & Johnson Innovative Medicine
Dosage Form :
Brand Name : Zytiga
Dosage Strength :
Packaging : 60
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Johnson & Johnson Innovative Medicine
Dosage Form : tablet
Brand Name : Zytiga
Dosage Strength : 250 mg
Packaging : 120
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Canada
Dosage Form : TABLET
Brand Name : AKEEGA
Dosage Strength : 500MG
Packaging :
Approval Date :
Application Number : 2538555
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : TABLET
Brand Name : AKEEGA
Dosage Strength : 500MG
Packaging :
Approval Date :
Application Number : 2538563
Regulatory Info :
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ZYTIGA
Dosage Strength : 500MG
Packaging :
Approval Date : 2017-04-14
Application Number : 202379
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Originator
Registration Country : South Africa
Johnson & Johnson Innovative Medicine
Dosage Form : FCT
Brand Name : ZYTIGA 500 MG
Dosage Strength : 500mg
Packaging : 60X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : Canada
Dosage Form : TABLET
Brand Name : ZYTIGA
Dosage Strength : 250MG
Packaging : 120
Approval Date :
Application Number : 2371065
Regulatory Info :
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Johnson & Johnson Innovative Medicine
Dosage Form : TAB
Brand Name : ZYTIGA 250 MG
Dosage Strength : 250MG
Packaging : 120X1MG
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Excipients
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12266
Submission : 1996-12-03
Status : Inactive
Type : IV
Inspections and registrations
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