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Details:

The net proceeds will be used for the clinical development of CGT9486 (bezuclastinib), which is a KIT mutant inhibitor for patients living with systemic mastocytosis and gastrointestinal stromal tumors.


Lead Product(s): Bezuclastinib,Sunitinib

Therapeutic Area: Oncology Product Name: CGT9486

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: J.P. Morgan

Deal Size: $225.0 million Upfront Cash: Undisclosed

Deal Type: Private Placement February 14, 2024

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Cogent intends to fund the development, regulatory and commercial preparation activities relating to CGT9486 (bezuclastinib), a selective tyrosine kinase inhibitor that is designed to potently inhibit the KIT D816V mutation as well as other mutations in KIT exon 17.


Lead Product(s): Bezuclastinib,Sunitinib

Therapeutic Area: Oncology Product Name: CGT9486

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: J.P. Morgan

Deal Size: $150.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering June 06, 2023

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Cabometyx (cabozantinib) is a multiple receptor tyrosine kinases inhibitor. These receptors are involved in both normal cellular function and pathologic processes such as oncogenesis, metastasis, tumor angiogenesis, maintenance of the tumor microenvironment, etc.


Lead Product(s): Cabozantinib,Nivolumab,Sunitinib

Therapeutic Area: Oncology Product Name: Cabometyx

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 13, 2023

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The net proceeds from the offering will be used for development, regulatory and commercial preparation activities relating to CGT9486 (bezuclastinib) and other product candidates, as well as for working capital and general corporate purposes.


Lead Product(s): Bezuclastinib,Sunitinib

Therapeutic Area: Oncology Product Name: CGT9486

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Jefferies

Deal Size: $172.6 million Upfront Cash: Undisclosed

Deal Type: Public Offering June 16, 2022

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Cogent intends to use the net proceeds from the offering for development, regulatory and commercial preparation activities relating to CGT9486 (bezuclastinib) and other product candidates, as well as for working capital and general corporate purposes.


Lead Product(s): Bezuclastinib,Sunitinib

Therapeutic Area: Oncology Product Name: CGT9486

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Jefferies

Deal Size: $150.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering June 14, 2022

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Updated outcomes from trial evaluating combination of Cabometyx (Cabozantinib) plus atezolizumab in an expanded patient population in NSCLC demonstrate encouraging clinical activity with manageable toxicity in people previously treated with an immune checkpoint inhibitor.


Lead Product(s): Cabozantinib,Nivolumab,Sunitinib

Therapeutic Area: Oncology Product Name: Cabometyx

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 26, 2022

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GB-102 is a microparticle formulation of a pan-VEGF inhibitor, sunitinib, for the treatment of wet age-related macular degeneration designed for a twice-per-year intravitreal injection. GB-102 has the potential to also benefit patients with diabetic retinopathy.


Lead Product(s): Sunitinib

Therapeutic Area: Ophthalmology Product Name: GB-102

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 19, 2022

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The MERECA study showed that the combination of ilixadencel with the tyrosine kinase inhibitor sunitinib was safe and associated with a positive trend for improved tumor response rate and overall survival, compared with sunitinib monotherapy (control group).


Lead Product(s): Ilixadencel,Sunitinib

Therapeutic Area: Oncology Product Name: Intuvax

Highest Development Status: Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 28, 2022

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Phase 2 study investigating CGT9486 for the treatment of patients with Advanced Systemic Mastocytosis (AdvSM), including patients with Aggressive SM (ASM), SM with Associated Hematologic Neoplasm (SM-AHN), and Mast Cell Leukemia (MCL).


Lead Product(s): Bezuclastinib,Sunitinib

Therapeutic Area: Oncology Product Name: CGT9486

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 08, 2022

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GB-102, a formulation of the pan-vascular endothelial growth factor (VEGF) inhibitor, sunitinib malate targeting a six-month or longer dosing regimen used for the treatment of wet age-related macular degeneration (wet AMD).


Lead Product(s): Sunitinib

Therapeutic Area: Ophthalmology Product Name: GB-102

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 28, 2021

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The ALTISSIMO trial is a masked and controlled Phase 2b dose-ranging study of two doses of GB-102 with a single control arm of patients on aflibercept. 48% of patients in the GB-102 1 mg arm were rescue-free for at least 6 months.


Lead Product(s): Sunitinib

Therapeutic Area: Ophthalmology Product Name: GB-102

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 09, 2021

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Sunitinib is an oral multi-kinase inhibitor (MKI), works by blocking several enzymes that promote cell growth. It is useful for the treatment of certain patients with gastrointestinal stromal tumors and advanced renal cell carcinoma.


Lead Product(s): Sunitinib

Therapeutic Area: Oncology Product Name: Sutib

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 16, 2021

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Graybug’s lead product candidate, GB-102, is a proprietary microparticle depot formulation of the pan-vascular endothelial growth factor (pan-VEGF) inhibitor, sunitinib malate, designed to be administered intravitreally twice per year.


Lead Product(s): Sunitinib

Therapeutic Area: Ophthalmology Product Name: GB-102

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 07, 2021

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Based on the updated survival data, the final median OS value was reached in the sunitinib control group, while the median OS has not yet been reached in the ilixadencel treatment group.


Lead Product(s): Ilixadencel,Sunitinib

Therapeutic Area: Oncology Product Name: Intuvax

Highest Development Status: Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 18, 2020

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  • Deals

Details:

Acquisition includes lead clinical-stage compound PLX9486, a potent and selective KIT D816V inhibitor.


Lead Product(s): Bezuclastinib,Sunitinib

Therapeutic Area: Oncology Product Name: PLX9486

Highest Development Status: Phase I/ Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Unum Therapeutics

Deal Size: $104.4 million Upfront Cash: Undisclosed

Deal Type: Acquisition July 06, 2020

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A limited interim safety analysis performed in February 2020 supports Graybug’s intention to take the 1 mg dose forward for further exploration in clinical trials.


Lead Product(s): Sunitinib

Therapeutic Area: Ophthalmology Product Name: Undisclosed

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 18, 2020

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Survival as of December 2019 was 54% in the ilixadencel treatment group compared with 37% of patients in the control group treated with sunitinib monotherapy.


Lead Product(s): Ilixadencel,Sunitinib

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 06, 2020

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The MERECA trial investigated Immunicum’s lead product, ilixadencel, in combination with Sutent® (sunitinib) as a first-line treatment in patients with metastatic kidney cancer.


Lead Product(s): Ilixadencel,Sunitinib

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 03, 2020

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