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Details:
Opuviz (aflibercept) is a vascular endothelial growth factor (VEGF) inhibitor indicated for the treatment of patients with Neovascular (Wet) Age-Related Macular Degeneration
Lead Product(s): Aflibercept
Therapeutic Area: Ophthalmology Brand Name: Opuviz
Study Phase: ApprovedProduct Type: Large molecule
Recipient: Samsung Bioepis
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 18, 2024
Lead Product(s) : Aflibercept
Therapeutic Area : Ophthalmology
Highest Development Status : Approved
Recipient : Samsung Bioepis
Deal Size : Not Applicable
Deal Type : Not Applicable
Samsung/Biogen EC Nod for OPUVIZ™ Aflibercept Biosimilar
Details : Opuviz (aflibercept) is a vascular endothelial growth factor (VEGF) inhibitor indicated for the treatment of patients with Neovascular (Wet) Age-Related Macular Degeneration
Brand Name : Opuviz
Molecule Type : Large molecule
Upfront Cash : Not Applicable
November 18, 2024
Details:
Leqembi (lecanemab) selectively binds to soluble Aβ aggregates (protofibrils), as well as insoluble amyloid beta aggregates (fibrils) which are a major component of amyloid beta plaques in AD.
Lead Product(s): Lecanemab
Therapeutic Area: Neurology Brand Name: Leqembi
Study Phase: ApprovedProduct Type: Large molecule
Recipient: Eisai
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable November 14, 2024
Eisai Gains CHMP Opinion for Lecanemab in Early Alzheimer's Disease in EU
Details : Leqembi (lecanemab) selectively binds to soluble Aβ aggregates (protofibrils), as well as insoluble amyloid beta aggregates (fibrils) which are a major component of amyloid beta plaques in AD.
Brand Name : Leqembi
Molecule Type : Large molecule
Upfront Cash : Not Applicable
November 14, 2024
Details:
The collaboration aims to leverage Neomorph's proprietary molecular glue discovery platform to expedite the identification and validation of new small-molecule therapeutics for Alzheimer’s disease.
Lead Product(s): Molecular Glue Degrader-based Therapy
Therapeutic Area: Neurology Brand Name: Undisclosed
Study Phase: Discovery PlatformProduct Type: Small molecule
Recipient: Neomorph
Deal Size: $1,450.0 million Upfront Cash: Undisclosed
Deal Type: Collaboration October 29, 2024
Lead Product(s) : Molecular Glue Degrader-based Therapy
Therapeutic Area : Neurology
Highest Development Status : Discovery Platform
Recipient : Neomorph
Deal Size : $1,450.0 million
Deal Type : Collaboration
Biogen & Neomorph Announce Collaboration to Discover and Develop Molecular Glue Degraders
Details : The collaboration aims to leverage Neomorph's proprietary molecular glue discovery platform to expedite the identification and validation of new small-molecule therapeutics for Alzheimer’s disease.
Brand Name : Undisclosed
Molecule Type : Small molecule
Upfront Cash : Undisclosed
October 29, 2024
Details:
MOR202 (felzartamab) is an investigational monoclonal antibody designed to specifically target and deplete CD38+ cells. It is being evaluated for late AMR in kidney transplant recipients.
Lead Product(s): Felzartamab
Therapeutic Area: Immunology Brand Name: MOR202
Study Phase: Phase IIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 09, 2024
Lead Product(s) : Felzartamab
Therapeutic Area : Immunology
Highest Development Status : Phase II
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Biogen's Felzartamab Receives FDA Breakthrough Designation For Kidney Transplant
Details : MOR202 (felzartamab) is an investigational monoclonal antibody designed to specifically target and deplete CD38+ cells. It is being evaluated for late AMR in kidney transplant recipients.
Brand Name : MOR202
Molecule Type : Large molecule
Upfront Cash : Not Applicable
October 09, 2024
Details:
Spinraza (nusinersen) is a survival motor neuron-2 (SMN2)-directed antisense oligonucleotide indicated for the treatment of spinal muscular atrophy (SMA) in pediatric and Toddlers.
Lead Product(s): Nusinersen Sodium
Therapeutic Area: Genetic Disease Brand Name: Spinraza
Study Phase: Phase II/ Phase IIIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 09, 2024
Lead Product(s) : Nusinersen Sodium
Therapeutic Area : Genetic Disease
Highest Development Status : Phase II/ Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Biogen Reports Promising Results For Higher Dose of Spinraza
Details : Spinraza (nusinersen) is a survival motor neuron-2 (SMN2)-directed antisense oligonucleotide indicated for the treatment of spinal muscular atrophy (SMA) in pediatric and Toddlers.
Brand Name : Spinraza
Molecule Type : Large molecule
Upfront Cash : Not Applicable
October 09, 2024
Details:
Following the termination of the agreement, Sage will regain full ownership of the SAGE-324 from Biogen. This asset is being evaluated for the treatment of patients with essential tremors.
Lead Product(s): SAGE-324
Therapeutic Area: Neurology Brand Name: SAGE-324
Study Phase: Phase II/ Phase IIIProduct Type: Small molecule
Recipient: Sage Therapeutics
Deal Size: $1,525.0 million Upfront Cash: $1,525.0 million
Deal Type: Termination September 26, 2024
Lead Product(s) : SAGE-324
Therapeutic Area : Neurology
Highest Development Status : Phase II/ Phase III
Recipient : Sage Therapeutics
Deal Size : $1,525.0 million
Deal Type : Termination
Sage Therapeutics Ends Collaboration with Biogen on SAGE-324 Program
Details : Following the termination of the agreement, Sage will regain full ownership of the SAGE-324 from Biogen. This asset is being evaluated for the treatment of patients with essential tremors.
Brand Name : SAGE-324
Molecule Type : Small molecule
Upfront Cash : $1,525.0 million
September 26, 2024
Details:
CDP7657 (dapirolizumab pegol), a novel Fc-free anti-CD40L drug candidate, investigated in people living with moderate-to-severe systemic lupus erythematosus (SLE).
Lead Product(s): Dapirolizumab Pegol
Therapeutic Area: Immunology Brand Name: CDP7657
Study Phase: Phase IIIProduct Type: Large molecule
Recipient: UCB Pharma S.A
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable September 24, 2024
Lead Product(s) : Dapirolizumab Pegol
Therapeutic Area : Immunology
Highest Development Status : Phase III
Recipient : UCB Pharma S.A
Deal Size : Not Applicable
Deal Type : Not Applicable
UCB and Biogen Announce Positive Phase 3 Results for Dapirolizumab Pegol in Lupus
Details : CDP7657 (dapirolizumab pegol), a novel Fc-free anti-CD40L drug candidate, investigated in people living with moderate-to-severe systemic lupus erythematosus (SLE).
Brand Name : CDP7657
Molecule Type : Large molecule
Upfront Cash : Not Applicable
September 24, 2024
Details:
Opuviz (aflibercept) is a vascular endothelial growth factor (VEGF) inhibitor indicated for the treatment of patients with Neovascular (Wet) Age-Related Macular Degeneration
Lead Product(s): Aflibercept
Therapeutic Area: Ophthalmology Brand Name: Opuviz
Study Phase: ApprovedProduct Type: Large molecule
Recipient: Samsung Bioepis
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable September 20, 2024
Lead Product(s) : Aflibercept
Therapeutic Area : Ophthalmology
Highest Development Status : Approved
Recipient : Samsung Bioepis
Deal Size : Not Applicable
Deal Type : Not Applicable
Samsung Bioepis and Biogen Receive CHMP Opinion for OPUVIZ™ Biosimilar
Details : Opuviz (aflibercept) is a vascular endothelial growth factor (VEGF) inhibitor indicated for the treatment of patients with Neovascular (Wet) Age-Related Macular Degeneration
Brand Name : Opuviz
Molecule Type : Large molecule
Upfront Cash : Not Applicable
September 20, 2024
Details:
The collaboration aims to investigate the use of C4T’s novel protein degradation platform to discover and develop potential new treatments for Alzheimer’s & Parkinson’s disease.
Lead Product(s): Undisclosed
Therapeutic Area: Neurology Brand Name: Undisclosed
Study Phase: DiscoveryProduct Type: Undisclosed
Recipient: C4 Therapeutics
Deal Size: $415.0 million Upfront Cash: Undisclosed
Deal Type: Collaboration September 10, 2024
Lead Product(s) : Undisclosed
Therapeutic Area : Neurology
Highest Development Status : Discovery
Recipient : C4 Therapeutics
Deal Size : $415.0 million
Deal Type : Collaboration
C4 Therapeutics Announces Delivery of Second Development Candidate to Biogen
Details : The collaboration aims to investigate the use of C4T’s novel protein degradation platform to discover and develop potential new treatments for Alzheimer’s & Parkinson’s disease.
Brand Name : Undisclosed
Molecule Type : Undisclosed
Upfront Cash : Undisclosed
September 10, 2024
Details:
Lantesens (nusinersen) is a generic of Spinraza, which is SMN2-directed antisense oligonucleotide investigated for the treatment of spinal muscular atrophy (SMA) in pediatrics.
Lead Product(s): Nusinersen Sodium
Therapeutic Area: Genetic Disease Brand Name: Spinraza
Study Phase: Phase II/ Phase IIIProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable September 04, 2024
Lead Product(s) : Nusinersen Sodium
Therapeutic Area : Genetic Disease
Highest Development Status : Phase II/ Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Biogen Reports Positive Topline Results For Higher Dose Of Nusinersen in SMA
Details : Lantesens (nusinersen) is a generic of Spinraza, which is SMN2-directed antisense oligonucleotide investigated for the treatment of spinal muscular atrophy (SMA) in pediatrics.
Brand Name : Spinraza
Molecule Type : Large molecule
Upfront Cash : Not Applicable
September 04, 2024
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